CN112062857A - Eta抗体与bnp的融合蛋白质,及其药物组合物和应用 - Google Patents
Eta抗体与bnp的融合蛋白质,及其药物组合物和应用 Download PDFInfo
- Publication number
- CN112062857A CN112062857A CN201910496142.4A CN201910496142A CN112062857A CN 112062857 A CN112062857 A CN 112062857A CN 201910496142 A CN201910496142 A CN 201910496142A CN 112062857 A CN112062857 A CN 112062857A
- Authority
- CN
- China
- Prior art keywords
- seq
- amino acid
- acid sequence
- ser
- fusion protein
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 102000037865 fusion proteins Human genes 0.000 title claims abstract description 256
- 108020001507 fusion proteins Proteins 0.000 title claims abstract description 256
- 239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 13
- 208000002815 pulmonary hypertension Diseases 0.000 claims abstract description 45
- 206010019280 Heart failures Diseases 0.000 claims abstract description 19
- 125000003275 alpha amino acid group Chemical group 0.000 claims description 368
- 101800000407 Brain natriuretic peptide 32 Proteins 0.000 claims description 263
- 102400000667 Brain natriuretic peptide 32 Human genes 0.000 claims description 261
- 101800002247 Brain natriuretic peptide 45 Proteins 0.000 claims description 261
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 180
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 109
- 229920001184 polypeptide Polymers 0.000 claims description 98
- 210000004027 cell Anatomy 0.000 claims description 82
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 61
- 210000004899 c-terminal region Anatomy 0.000 claims description 53
- 230000027455 binding Effects 0.000 claims description 52
- 102000040430 polynucleotide Human genes 0.000 claims description 51
- 108091033319 polynucleotide Proteins 0.000 claims description 51
- 239000002157 polynucleotide Substances 0.000 claims description 51
- ZUBDGKVDJUIMQQ-UBFCDGJISA-N endothelin-1 Chemical compound C([C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(O)=O)NC(=O)[C@H]1NC(=O)[C@H](CC=2C=CC=CC=2)NC(=O)[C@@H](CC=2C=CC(O)=CC=2)NC(=O)[C@H](C(C)C)NC(=O)[C@H]2CSSC[C@@H](C(N[C@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@H](CC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N2)=O)NC(=O)[C@@H](CO)NC(=O)[C@H](N)CSSC1)C1=CNC=N1 ZUBDGKVDJUIMQQ-UBFCDGJISA-N 0.000 claims description 42
- 102000010180 Endothelin receptor Human genes 0.000 claims description 34
- 108050001739 Endothelin receptor Proteins 0.000 claims description 34
- 239000003814 drug Substances 0.000 claims description 29
- 239000013598 vector Substances 0.000 claims description 24
- 238000011282 treatment Methods 0.000 claims description 22
- 108091026890 Coding region Proteins 0.000 claims description 19
- 102000002045 Endothelin Human genes 0.000 claims description 15
- 108050009340 Endothelin Proteins 0.000 claims description 15
- 241001529936 Murinae Species 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 11
- 238000002360 preparation method Methods 0.000 claims description 11
- 230000002265 prevention Effects 0.000 claims description 10
- 230000002401 inhibitory effect Effects 0.000 claims description 9
- 230000004913 activation Effects 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 3
- 238000010253 intravenous injection Methods 0.000 claims description 3
- 238000010254 subcutaneous injection Methods 0.000 claims description 3
- 239000007929 subcutaneous injection Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 abstract description 63
- 208000024891 symptom Diseases 0.000 abstract description 22
- 206010064911 Pulmonary arterial hypertension Diseases 0.000 abstract description 16
- 108010090549 Endothelin A Receptor Proteins 0.000 description 248
- 102000030168 Endothelin A Receptor Human genes 0.000 description 248
- HPNRHPKXQZSDFX-OAQDCNSJSA-N nesiritide Chemical compound C([C@H]1C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H](C(N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CSSC[C@@H](C(=O)N1)NC(=O)CNC(=O)[C@H](CO)NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H]1N(CCC1)C(=O)[C@@H](N)CO)C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=1N=CNC=1)C(O)=O)=O)[C@@H](C)CC)C1=CC=CC=C1 HPNRHPKXQZSDFX-OAQDCNSJSA-N 0.000 description 214
- 241000699666 Mus <mouse, genus> Species 0.000 description 189
- 108020004414 DNA Proteins 0.000 description 122
- 150000007523 nucleic acids Chemical class 0.000 description 61
- 108090000623 proteins and genes Proteins 0.000 description 61
- 102100035360 Cerebellar degeneration-related antigen 1 Human genes 0.000 description 58
- 101100112922 Candida albicans CDR3 gene Proteins 0.000 description 54
- 235000001014 amino acid Nutrition 0.000 description 54
- 102000039446 nucleic acids Human genes 0.000 description 54
- 108020004707 nucleic acids Proteins 0.000 description 54
- 102000004169 proteins and genes Human genes 0.000 description 47
- 239000012634 fragment Substances 0.000 description 43
- 102100035361 Cerebellar degeneration-related protein 2 Human genes 0.000 description 41
- 101000737796 Homo sapiens Cerebellar degeneration-related protein 2 Proteins 0.000 description 41
- 235000018102 proteins Nutrition 0.000 description 41
- 101000737793 Homo sapiens Cerebellar degeneration-related antigen 1 Proteins 0.000 description 39
- 150000001413 amino acids Chemical class 0.000 description 39
- 229940024606 amino acid Drugs 0.000 description 37
- 238000006467 substitution reaction Methods 0.000 description 37
- 108010047041 Complementarity Determining Regions Proteins 0.000 description 34
- 241000282414 Homo sapiens Species 0.000 description 34
- 241000880493 Leptailurus serval Species 0.000 description 33
- 239000000427 antigen Substances 0.000 description 33
- 102000036639 antigens Human genes 0.000 description 32
- 108091007433 antigens Proteins 0.000 description 32
- 230000000694 effects Effects 0.000 description 26
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 23
- 125000000539 amino acid group Chemical group 0.000 description 23
- 108010037850 glycylvaline Proteins 0.000 description 22
- 230000014509 gene expression Effects 0.000 description 21
- 108010003137 tyrosyltyrosine Proteins 0.000 description 21
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 20
- HTONZBWRYUKUKC-RCWTZXSCSA-N Val-Thr-Val Chemical compound CC(C)[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(O)=O HTONZBWRYUKUKC-RCWTZXSCSA-N 0.000 description 18
- 230000004071 biological effect Effects 0.000 description 17
- 108010050848 glycylleucine Proteins 0.000 description 17
- 239000000203 mixture Substances 0.000 description 17
- 230000037430 deletion Effects 0.000 description 16
- 238000012217 deletion Methods 0.000 description 16
- 125000003729 nucleotide group Chemical group 0.000 description 16
- 102000005962 receptors Human genes 0.000 description 16
- 108020003175 receptors Proteins 0.000 description 16
- CCBIBMKQNXHNIN-ZETCQYMHSA-N Gly-Leu-Gly Chemical compound NCC(=O)N[C@@H](CC(C)C)C(=O)NCC(O)=O CCBIBMKQNXHNIN-ZETCQYMHSA-N 0.000 description 15
- 241001465754 Metazoa Species 0.000 description 15
- 108010068265 aspartyltyrosine Proteins 0.000 description 15
- 239000013604 expression vector Substances 0.000 description 15
- XKUKSGPZAADMRA-UHFFFAOYSA-N glycyl-glycyl-glycine Chemical compound NCC(=O)NCC(=O)NCC(O)=O XKUKSGPZAADMRA-UHFFFAOYSA-N 0.000 description 15
- 239000002773 nucleotide Substances 0.000 description 15
- LINKCQUOMUDLKN-KATARQTJSA-N Leu-Thr-Cys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CC(C)C)N)O LINKCQUOMUDLKN-KATARQTJSA-N 0.000 description 14
- 108010078144 glutaminyl-glycine Proteins 0.000 description 14
- 230000001603 reducing effect Effects 0.000 description 14
- SOEGEPHNZOISMT-BYPYZUCNSA-N Gly-Ser-Gly Chemical compound NCC(=O)N[C@@H](CO)C(=O)NCC(O)=O SOEGEPHNZOISMT-BYPYZUCNSA-N 0.000 description 13
- 108010021625 Immunoglobulin Fragments Proteins 0.000 description 13
- 102000008394 Immunoglobulin Fragments Human genes 0.000 description 13
- CREYEAPXISDKSB-FQPOAREZSA-N Ala-Thr-Tyr Chemical compound [H]N[C@@H](C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O CREYEAPXISDKSB-FQPOAREZSA-N 0.000 description 12
- 241000282693 Cercopithecidae Species 0.000 description 12
- GGAPHLIUUTVYMX-QWRGUYRKSA-N Gly-Phe-Ser Chemical compound OC[C@@H](C([O-])=O)NC(=O)[C@@H](NC(=O)C[NH3+])CC1=CC=CC=C1 GGAPHLIUUTVYMX-QWRGUYRKSA-N 0.000 description 12
- WNZOCXUOGVYYBJ-CDMKHQONSA-N Gly-Phe-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN)O WNZOCXUOGVYYBJ-CDMKHQONSA-N 0.000 description 12
- WZBLRQQCDYYRTD-SIXJUCDHSA-N His-Ile-Trp Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)O)NC(=O)[C@H](CC3=CN=CN3)N WZBLRQQCDYYRTD-SIXJUCDHSA-N 0.000 description 12
- 108010073969 valyllysine Proteins 0.000 description 12
- 102100039339 Atrial natriuretic peptide receptor 1 Human genes 0.000 description 11
- HAOUOFNNJJLVNS-BQBZGAKWSA-N Gly-Pro-Ser Chemical compound NCC(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(O)=O HAOUOFNNJJLVNS-BQBZGAKWSA-N 0.000 description 11
- 101000961044 Homo sapiens Atrial natriuretic peptide receptor 1 Proteins 0.000 description 11
- 108060003951 Immunoglobulin Proteins 0.000 description 11
- 108010065920 Insulin Lispro Proteins 0.000 description 11
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 11
- QJUWBDPGGYVRHY-YUMQZZPRSA-N Leu-Gly-Cys Chemical compound CC(C)C[C@@H](C(=O)NCC(=O)N[C@@H](CS)C(=O)O)N QJUWBDPGGYVRHY-YUMQZZPRSA-N 0.000 description 11
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 11
- SRSPTFBENMJHMR-WHFBIAKZSA-N Ser-Ser-Gly Chemical compound OC[C@H](N)C(=O)N[C@@H](CO)C(=O)NCC(O)=O SRSPTFBENMJHMR-WHFBIAKZSA-N 0.000 description 11
- SYSWVVCYSXBVJG-RHYQMDGZSA-N Val-Leu-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C(C)C)N)O SYSWVVCYSXBVJG-RHYQMDGZSA-N 0.000 description 11
- 230000036772 blood pressure Effects 0.000 description 11
- 201000010099 disease Diseases 0.000 description 11
- 238000009396 hybridization Methods 0.000 description 11
- 102000018358 immunoglobulin Human genes 0.000 description 11
- ZXCAQANTQWBICD-DCAQKATOSA-N Cys-Lys-Val Chemical compound CC(C)[C@@H](C(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CS)N ZXCAQANTQWBICD-DCAQKATOSA-N 0.000 description 10
- HNAUFGBKJLTWQE-IFFSRLJSSA-N Gln-Val-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCC(=O)N)N)O HNAUFGBKJLTWQE-IFFSRLJSSA-N 0.000 description 10
- SABZDFAAOJATBR-QWRGUYRKSA-N Gly-Cys-Phe Chemical compound [H]NCC(=O)N[C@@H](CS)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O SABZDFAAOJATBR-QWRGUYRKSA-N 0.000 description 10
- GZRABTMNWJXFMH-UVOCVTCTSA-N Leu-Thr-Thr Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O GZRABTMNWJXFMH-UVOCVTCTSA-N 0.000 description 10
- SPSSJSICDYYTQN-HJGDQZAQSA-N Met-Thr-Gln Chemical compound CSCC[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@H](C(O)=O)CCC(N)=O SPSSJSICDYYTQN-HJGDQZAQSA-N 0.000 description 10
- TUYWCHPXKQTISF-LPEHRKFASA-N Pro-Cys-Pro Chemical compound C1C[C@H](NC1)C(=O)N[C@@H](CS)C(=O)N2CCC[C@@H]2C(=O)O TUYWCHPXKQTISF-LPEHRKFASA-N 0.000 description 10
- 241000700159 Rattus Species 0.000 description 10
- BNFVPSRLHHPQKS-WHFBIAKZSA-N Ser-Asp-Gly Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(=O)NCC(O)=O BNFVPSRLHHPQKS-WHFBIAKZSA-N 0.000 description 10
- KDGARKCAKHBEDB-NKWVEPMBSA-N Ser-Gly-Pro Chemical compound C1C[C@@H](N(C1)C(=O)CNC(=O)[C@H](CO)N)C(=O)O KDGARKCAKHBEDB-NKWVEPMBSA-N 0.000 description 10
- YUJLIIRMIAGMCQ-CIUDSAMLSA-N Ser-Leu-Ser Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(O)=O YUJLIIRMIAGMCQ-CIUDSAMLSA-N 0.000 description 10
- VGQVAVQWKJLIRM-FXQIFTODSA-N Ser-Ser-Val Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(O)=O VGQVAVQWKJLIRM-FXQIFTODSA-N 0.000 description 10
- 230000006229 amino acid addition Effects 0.000 description 10
- 230000000295 complement effect Effects 0.000 description 10
- 108010049041 glutamylalanine Proteins 0.000 description 10
- 108010064235 lysylglycine Proteins 0.000 description 10
- JSOQIZDOEIKRLY-UHFFFAOYSA-N n-propylnitrous amide Chemical compound CCCNN=O JSOQIZDOEIKRLY-UHFFFAOYSA-N 0.000 description 10
- 238000003752 polymerase chain reaction Methods 0.000 description 10
- 108010072986 threonyl-seryl-lysine Proteins 0.000 description 10
- JEOCWTUOMKEEMF-RHYQMDGZSA-N Arg-Leu-Thr Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O JEOCWTUOMKEEMF-RHYQMDGZSA-N 0.000 description 9
- GCACQYDBDHRVGE-LKXGYXEUSA-N Asp-Thr-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H]([C@H](O)C)NC(=O)[C@@H](N)CC(O)=O GCACQYDBDHRVGE-LKXGYXEUSA-N 0.000 description 9
- ASCFJMSGKUIRDU-ZPFDUUQYSA-N Ile-Arg-Gln Chemical compound CC[C@H](C)[C@H](N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(N)=O)C(O)=O ASCFJMSGKUIRDU-ZPFDUUQYSA-N 0.000 description 9
- HVHRPWQEQHIQJF-AVGNSLFASA-N Leu-Lys-Glu Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(O)=O HVHRPWQEQHIQJF-AVGNSLFASA-N 0.000 description 9
- IHCXPSYCHXFXKT-DCAQKATOSA-N Pro-Arg-Glu Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(O)=O IHCXPSYCHXFXKT-DCAQKATOSA-N 0.000 description 9
- CXPJPTFWKXNDKV-NUTKFTJISA-N Trp-Leu-Ala Chemical compound C1=CC=C2C(C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(O)=O)=CNC2=C1 CXPJPTFWKXNDKV-NUTKFTJISA-N 0.000 description 9
- 108010070944 alanylhistidine Proteins 0.000 description 9
- 230000004872 arterial blood pressure Effects 0.000 description 9
- 108010069205 aspartyl-phenylalanine Proteins 0.000 description 9
- 230000008859 change Effects 0.000 description 9
- 208000035475 disorder Diseases 0.000 description 9
- 108010015792 glycyllysine Proteins 0.000 description 9
- 238000000746 purification Methods 0.000 description 9
- 230000002829 reductive effect Effects 0.000 description 9
- 230000001105 regulatory effect Effects 0.000 description 9
- AOHKLEBWKMKITA-IHRRRGAJSA-N Arg-Phe-Ser Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](CCCN=C(N)N)N AOHKLEBWKMKITA-IHRRRGAJSA-N 0.000 description 8
- UVTGNSWSRSCPLP-UHFFFAOYSA-N Arg-Tyr Natural products NC(CCNC(=N)N)C(=O)NC(Cc1ccc(O)cc1)C(=O)O UVTGNSWSRSCPLP-UHFFFAOYSA-N 0.000 description 8
- QSFHZPQUAAQHAQ-CIUDSAMLSA-N Asp-Ser-Leu Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(O)=O QSFHZPQUAAQHAQ-CIUDSAMLSA-N 0.000 description 8
- MJJIHRWNWSQTOI-VEVYYDQMSA-N Asp-Thr-Arg Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H]([C@H](O)C)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O MJJIHRWNWSQTOI-VEVYYDQMSA-N 0.000 description 8
- KFMBRBPXHVMDFN-UWVGGRQHSA-N Gly-Arg-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)CN)CCCNC(N)=N KFMBRBPXHVMDFN-UWVGGRQHSA-N 0.000 description 8
- LHSGPCFBGJHPCY-UHFFFAOYSA-N L-leucine-L-tyrosine Natural products CC(C)CC(N)C(=O)NC(C(O)=O)CC1=CC=C(O)C=C1 LHSGPCFBGJHPCY-UHFFFAOYSA-N 0.000 description 8
- SQUTUWHAAWJYES-GUBZILKMSA-N Met-Asp-Arg Chemical compound [H]N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O SQUTUWHAAWJYES-GUBZILKMSA-N 0.000 description 8
- YYEIFXZOBZVDPH-DCAQKATOSA-N Met-Lys-Asp Chemical compound CSCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(O)=O YYEIFXZOBZVDPH-DCAQKATOSA-N 0.000 description 8
- SITLTJHOQZFJGG-UHFFFAOYSA-N N-L-alpha-glutamyl-L-valine Natural products CC(C)C(C(O)=O)NC(=O)C(N)CCC(O)=O SITLTJHOQZFJGG-UHFFFAOYSA-N 0.000 description 8
- JURQXQBJKUHGJS-UHFFFAOYSA-N Ser-Ser-Ser-Ser Chemical compound OCC(N)C(=O)NC(CO)C(=O)NC(CO)C(=O)NC(CO)C(O)=O JURQXQBJKUHGJS-UHFFFAOYSA-N 0.000 description 8
- FIFDDJFLNVAVMS-RHYQMDGZSA-N Thr-Leu-Met Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(O)=O FIFDDJFLNVAVMS-RHYQMDGZSA-N 0.000 description 8
- LMKKMCGTDANZTR-BZSNNMDCSA-N Tyr-Phe-Asp Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC(O)=O)C(O)=O)C1=CC=C(O)C=C1 LMKKMCGTDANZTR-BZSNNMDCSA-N 0.000 description 8
- MQGGXGKQSVEQHR-KKUMJFAQSA-N Tyr-Ser-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 MQGGXGKQSVEQHR-KKUMJFAQSA-N 0.000 description 8
- KHPLUFDSWGDRHD-SLFFLAALSA-N Tyr-Tyr-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CC=C(C=C2)O)NC(=O)[C@H](CC3=CC=C(C=C3)O)N)C(=O)O KHPLUFDSWGDRHD-SLFFLAALSA-N 0.000 description 8
- OVLIFGQSBSNGHY-KKHAAJSZSA-N Val-Asp-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](C(C)C)N)O OVLIFGQSBSNGHY-KKHAAJSZSA-N 0.000 description 8
- ZOOGRGPOEVQQDX-KHLHZJAASA-N cyclic guanosine monophosphate Chemical compound C([C@H]1O2)O[P@](O)(=O)O[C@@H]1[C@H](O)[C@H]2N1C(N=C(NC2=O)N)=C2N=C1 ZOOGRGPOEVQQDX-KHLHZJAASA-N 0.000 description 8
- 229940079593 drug Drugs 0.000 description 8
- 108010089804 glycyl-threonine Proteins 0.000 description 8
- 108010025306 histidylleucine Proteins 0.000 description 8
- 238000001727 in vivo Methods 0.000 description 8
- 108010012058 leucyltyrosine Proteins 0.000 description 8
- 108010003700 lysyl aspartic acid Proteins 0.000 description 8
- 230000004048 modification Effects 0.000 description 8
- 238000012986 modification Methods 0.000 description 8
- 108010051242 phenylalanylserine Proteins 0.000 description 8
- 239000006228 supernatant Substances 0.000 description 8
- 108010044292 tryptophyltyrosine Proteins 0.000 description 8
- HKZAAJSTFUZYTO-LURJTMIESA-N (2s)-2-[[2-[[2-[[2-[(2-aminoacetyl)amino]acetyl]amino]acetyl]amino]acetyl]amino]-3-hydroxypropanoic acid Chemical compound NCC(=O)NCC(=O)NCC(=O)NCC(=O)N[C@@H](CO)C(O)=O HKZAAJSTFUZYTO-LURJTMIESA-N 0.000 description 7
- GXXWTNKNFFKTJB-NAKRPEOUSA-N Arg-Ile-Ser Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(O)=O GXXWTNKNFFKTJB-NAKRPEOUSA-N 0.000 description 7
- DAYDURRBMDCCFL-AAEUAGOBSA-N Asn-Trp-Gly Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)NCC(=O)O)NC(=O)[C@H](CC(=O)N)N DAYDURRBMDCCFL-AAEUAGOBSA-N 0.000 description 7
- UZFHNLYQWMGUHU-DCAQKATOSA-N Asp-Lys-Arg Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O UZFHNLYQWMGUHU-DCAQKATOSA-N 0.000 description 7
- SZQCDCKIGWQAQN-FXQIFTODSA-N Cys-Arg-Ala Chemical compound [H]N[C@@H](CS)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(O)=O SZQCDCKIGWQAQN-FXQIFTODSA-N 0.000 description 7
- ZZWUYQXMIFTIIY-WEDXCCLWSA-N Gly-Thr-Leu Chemical compound [H]NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(O)=O ZZWUYQXMIFTIIY-WEDXCCLWSA-N 0.000 description 7
- XHVONGZZVUUORG-WEDXCCLWSA-N Gly-Thr-Lys Chemical compound NCC(=O)N[C@@H]([C@H](O)C)C(=O)N[C@H](C(O)=O)CCCCN XHVONGZZVUUORG-WEDXCCLWSA-N 0.000 description 7
- NZGTYCMLUGYMCV-XUXIUFHCSA-N Ile-Lys-Arg Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)N NZGTYCMLUGYMCV-XUXIUFHCSA-N 0.000 description 7
- PXKACEXYLPBMAD-JBDRJPRFSA-N Ile-Ser-Ser Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)O)N PXKACEXYLPBMAD-JBDRJPRFSA-N 0.000 description 7
- PMGDADKJMCOXHX-UHFFFAOYSA-N L-Arginyl-L-glutamin-acetat Natural products NC(=N)NCCCC(N)C(=O)NC(CCC(N)=O)C(O)=O PMGDADKJMCOXHX-UHFFFAOYSA-N 0.000 description 7
- FQZPTCNSNPWHLJ-AVGNSLFASA-N Leu-Gln-Lys Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN)C(O)=O FQZPTCNSNPWHLJ-AVGNSLFASA-N 0.000 description 7
- FEHQLKKBVJHSEC-SZMVWBNQSA-N Leu-Glu-Trp Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](N)CC(C)C)C(O)=O)=CNC2=C1 FEHQLKKBVJHSEC-SZMVWBNQSA-N 0.000 description 7
- WXUOJXIGOPMDJM-SRVKXCTJSA-N Leu-Lys-Asn Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(O)=O WXUOJXIGOPMDJM-SRVKXCTJSA-N 0.000 description 7
- KIZIOFNVSOSKJI-CIUDSAMLSA-N Leu-Ser-Cys Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CS)C(=O)O)N KIZIOFNVSOSKJI-CIUDSAMLSA-N 0.000 description 7
- AIQWYVFNBNNOLU-RHYQMDGZSA-N Leu-Thr-Val Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(O)=O AIQWYVFNBNNOLU-RHYQMDGZSA-N 0.000 description 7
- 241000282567 Macaca fascicularis Species 0.000 description 7
- 241000699670 Mus sp. Species 0.000 description 7
- 108091028043 Nucleic acid sequence Proteins 0.000 description 7
- GZFAWAQTEYDKII-YUMQZZPRSA-N Ser-Gly-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)CO GZFAWAQTEYDKII-YUMQZZPRSA-N 0.000 description 7
- XXXAXOWMBOKTRN-XPUUQOCRSA-N Ser-Gly-Val Chemical compound [H]N[C@@H](CO)C(=O)NCC(=O)N[C@@H](C(C)C)C(O)=O XXXAXOWMBOKTRN-XPUUQOCRSA-N 0.000 description 7
- NMZXJDSKEGFDLJ-DCAQKATOSA-N Ser-Pro-Lys Chemical compound C1C[C@H](N(C1)C(=O)[C@H](CO)N)C(=O)N[C@@H](CCCCN)C(=O)O NMZXJDSKEGFDLJ-DCAQKATOSA-N 0.000 description 7
- XQJCEKXQUJQNNK-ZLUOBGJFSA-N Ser-Ser-Ser Chemical compound OC[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O XQJCEKXQUJQNNK-ZLUOBGJFSA-N 0.000 description 7
- BIBYEFRASCNLAA-CDMKHQONSA-N Thr-Phe-Gly Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@H](C(=O)NCC(O)=O)CC1=CC=CC=C1 BIBYEFRASCNLAA-CDMKHQONSA-N 0.000 description 7
- XHWCDRUPDNSDAZ-XKBZYTNZSA-N Thr-Ser-Glu Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(=O)O)C(=O)O)N)O XHWCDRUPDNSDAZ-XKBZYTNZSA-N 0.000 description 7
- JAWUQFCGNVEDRN-MEYUZBJRSA-N Thr-Tyr-Leu Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](CC(C)C)C(=O)O)N)O JAWUQFCGNVEDRN-MEYUZBJRSA-N 0.000 description 7
- MNYNCKZAEIAONY-XGEHTFHBSA-N Thr-Val-Ser Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CO)C(O)=O MNYNCKZAEIAONY-XGEHTFHBSA-N 0.000 description 7
- QOIKZODVIPOPDD-AVGNSLFASA-N Tyr-Cys-Gln Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCC(N)=O)C(O)=O QOIKZODVIPOPDD-AVGNSLFASA-N 0.000 description 7
- QUILOGWWLXMSAT-IHRRRGAJSA-N Tyr-Gln-Gln Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O QUILOGWWLXMSAT-IHRRRGAJSA-N 0.000 description 7
- VJOWWOGRNXRQMF-UVBJJODRSA-N Val-Ala-Trp Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@H](C)NC(=O)[C@@H](N)C(C)C)C(O)=O)=CNC2=C1 VJOWWOGRNXRQMF-UVBJJODRSA-N 0.000 description 7
- SSYBNWFXCFNRFN-GUBZILKMSA-N Val-Pro-Ser Chemical compound CC(C)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(O)=O SSYBNWFXCFNRFN-GUBZILKMSA-N 0.000 description 7
- 108010086434 alanyl-seryl-glycine Proteins 0.000 description 7
- 108010008355 arginyl-glutamine Proteins 0.000 description 7
- 108010052670 arginyl-glutamyl-glutamic acid Proteins 0.000 description 7
- 108010063718 gamma-glutamylaspartic acid Proteins 0.000 description 7
- 108010000434 glycyl-alanyl-leucine Proteins 0.000 description 7
- 108010050475 glycyl-leucyl-tyrosine Proteins 0.000 description 7
- 210000004408 hybridoma Anatomy 0.000 description 7
- 230000001965 increasing effect Effects 0.000 description 7
- 108010034529 leucyl-lysine Proteins 0.000 description 7
- 108010017391 lysylvaline Proteins 0.000 description 7
- 230000035772 mutation Effects 0.000 description 7
- 108010070409 phenylalanyl-glycyl-glycine Proteins 0.000 description 7
- 108010024654 phenylalanyl-prolyl-alanine Proteins 0.000 description 7
- 108010070643 prolylglutamic acid Proteins 0.000 description 7
- 230000002685 pulmonary effect Effects 0.000 description 7
- 239000000523 sample Substances 0.000 description 7
- HUZGPXBILPMCHM-IHRRRGAJSA-N Asn-Arg-Phe Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O HUZGPXBILPMCHM-IHRRRGAJSA-N 0.000 description 6
- MNQMTYSEKZHIDF-GCJQMDKQSA-N Asp-Thr-Ala Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C)C(O)=O MNQMTYSEKZHIDF-GCJQMDKQSA-N 0.000 description 6
- XEEIQMGZRFFSRD-XVYDVKMFSA-N Cys-Ala-His Chemical compound C[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)[C@H](CS)N XEEIQMGZRFFSRD-XVYDVKMFSA-N 0.000 description 6
- HEPLXMBVMCXTBP-QWRGUYRKSA-N Cys-Phe-Gly Chemical compound [H]N[C@@H](CS)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)NCC(O)=O HEPLXMBVMCXTBP-QWRGUYRKSA-N 0.000 description 6
- QDMVXRNLOPTPIE-WDCWCFNPSA-N Glu-Lys-Thr Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(O)=O QDMVXRNLOPTPIE-WDCWCFNPSA-N 0.000 description 6
- BYYNJRSNDARRBX-YFKPBYRVSA-N Gly-Gln-Gly Chemical compound NCC(=O)N[C@@H](CCC(N)=O)C(=O)NCC(O)=O BYYNJRSNDARRBX-YFKPBYRVSA-N 0.000 description 6
- UQJNXZSSGQIPIQ-FBCQKBJTSA-N Gly-Gly-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)CNC(=O)CN UQJNXZSSGQIPIQ-FBCQKBJTSA-N 0.000 description 6
- MQFGXJNSUJTXDT-QSFUFRPTSA-N Ile-Gly-Ile Chemical compound N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H]([C@@H](C)CC)C(=O)O MQFGXJNSUJTXDT-QSFUFRPTSA-N 0.000 description 6
- QGXQHJQPAPMACW-PPCPHDFISA-N Ile-Thr-Lys Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)O)N QGXQHJQPAPMACW-PPCPHDFISA-N 0.000 description 6
- SENJXOPIZNYLHU-UHFFFAOYSA-N L-leucyl-L-arginine Natural products CC(C)CC(N)C(=O)NC(C(O)=O)CCCN=C(N)N SENJXOPIZNYLHU-UHFFFAOYSA-N 0.000 description 6
- TYYLDKGBCJGJGW-UHFFFAOYSA-N L-tryptophan-L-tyrosine Natural products C=1NC2=CC=CC=C2C=1CC(N)C(=O)NC(C(O)=O)CC1=CC=C(O)C=C1 TYYLDKGBCJGJGW-UHFFFAOYSA-N 0.000 description 6
- GPICTNQYKHHHTH-GUBZILKMSA-N Leu-Gln-Ser Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CO)C(O)=O GPICTNQYKHHHTH-GUBZILKMSA-N 0.000 description 6
- YQFZRHYZLARWDY-IHRRRGAJSA-N Leu-Val-Lys Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(O)=O)CCCCN YQFZRHYZLARWDY-IHRRRGAJSA-N 0.000 description 6
- KCXUCYYZNZFGLL-SRVKXCTJSA-N Lys-Ala-Leu Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(O)=O KCXUCYYZNZFGLL-SRVKXCTJSA-N 0.000 description 6
- YKIRNDPUWONXQN-GUBZILKMSA-N Lys-Asn-Gln Chemical compound C(CCN)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CCC(=O)N)C(=O)O)N YKIRNDPUWONXQN-GUBZILKMSA-N 0.000 description 6
- LOGFVTREOLYCPF-RHYQMDGZSA-N Lys-Pro-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCCN LOGFVTREOLYCPF-RHYQMDGZSA-N 0.000 description 6
- GILLQRYAWOMHED-DCAQKATOSA-N Lys-Val-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)CCCCN GILLQRYAWOMHED-DCAQKATOSA-N 0.000 description 6
- DNDVVILEHVMWIS-LPEHRKFASA-N Met-Asp-Pro Chemical compound CSCC[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N1CCC[C@@H]1C(=O)O)N DNDVVILEHVMWIS-LPEHRKFASA-N 0.000 description 6
- RIIFMEBFDDXGCV-VEVYYDQMSA-N Met-Thr-Asn Chemical compound CSCC[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@H](C(O)=O)CC(N)=O RIIFMEBFDDXGCV-VEVYYDQMSA-N 0.000 description 6
- YBAFDPFAUTYYRW-UHFFFAOYSA-N N-L-alpha-glutamyl-L-leucine Natural products CC(C)CC(C(O)=O)NC(=O)C(N)CCC(O)=O YBAFDPFAUTYYRW-UHFFFAOYSA-N 0.000 description 6
- JDMKQHSHKJHAHR-UHFFFAOYSA-N Phe-Phe-Leu-Tyr Natural products C=1C=C(O)C=CC=1CC(C(O)=O)NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)CC1=CC=CC=C1 JDMKQHSHKJHAHR-UHFFFAOYSA-N 0.000 description 6
- SPLBRAKYXGOFSO-UNQGMJICSA-N Pro-Phe-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)[C@@H]2CCCN2)O SPLBRAKYXGOFSO-UNQGMJICSA-N 0.000 description 6
- LEIKGVHQTKHOLM-IUCAKERBSA-N Pro-Pro-Gly Chemical compound OC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@H]1NCCC1 LEIKGVHQTKHOLM-IUCAKERBSA-N 0.000 description 6
- QVOGDCQNGLBNCR-FXQIFTODSA-N Ser-Arg-Ser Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(O)=O QVOGDCQNGLBNCR-FXQIFTODSA-N 0.000 description 6
- YMTLKLXDFCSCNX-BYPYZUCNSA-N Ser-Gly-Gly Chemical compound OC[C@H](N)C(=O)NCC(=O)NCC(O)=O YMTLKLXDFCSCNX-BYPYZUCNSA-N 0.000 description 6
- UIGMAMGZOJVTDN-WHFBIAKZSA-N Ser-Gly-Ser Chemical compound OC[C@H](N)C(=O)NCC(=O)N[C@@H](CO)C(O)=O UIGMAMGZOJVTDN-WHFBIAKZSA-N 0.000 description 6
- UBRMZSHOOIVJPW-SRVKXCTJSA-N Ser-Leu-Lys Chemical compound OC[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(O)=O UBRMZSHOOIVJPW-SRVKXCTJSA-N 0.000 description 6
- MUJQWSAWLLRJCE-KATARQTJSA-N Ser-Leu-Thr Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O MUJQWSAWLLRJCE-KATARQTJSA-N 0.000 description 6
- FPCGZYMRFFIYIH-CIUDSAMLSA-N Ser-Lys-Ser Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(O)=O FPCGZYMRFFIYIH-CIUDSAMLSA-N 0.000 description 6
- HHJFMHQYEAAOBM-ZLUOBGJFSA-N Ser-Ser-Ala Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(O)=O HHJFMHQYEAAOBM-ZLUOBGJFSA-N 0.000 description 6
- XJDMUQCLVSCRSJ-VZFHVOOUSA-N Ser-Thr-Ala Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C)C(O)=O XJDMUQCLVSCRSJ-VZFHVOOUSA-N 0.000 description 6
- GXUWHVZYDAHFSV-FLBSBUHZSA-N Thr-Ile-Thr Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(O)=O GXUWHVZYDAHFSV-FLBSBUHZSA-N 0.000 description 6
- YOOAQCZYZHGUAZ-KATARQTJSA-N Thr-Leu-Ser Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(O)=O YOOAQCZYZHGUAZ-KATARQTJSA-N 0.000 description 6
- VRUFCJZQDACGLH-UVOCVTCTSA-N Thr-Leu-Thr Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O VRUFCJZQDACGLH-UVOCVTCTSA-N 0.000 description 6
- KZSYAEWQMJEGRZ-RHYQMDGZSA-N Thr-Leu-Val Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(O)=O KZSYAEWQMJEGRZ-RHYQMDGZSA-N 0.000 description 6
- ABWNZPOIUJMNKT-IXOXFDKPSA-N Thr-Phe-Ser Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(O)=O ABWNZPOIUJMNKT-IXOXFDKPSA-N 0.000 description 6
- YOPQYBJJNSIQGZ-JNPHEJMOSA-N Thr-Tyr-Tyr Chemical compound C([C@H](NC(=O)[C@@H](N)[C@H](O)C)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(O)=O)C1=CC=C(O)C=C1 YOPQYBJJNSIQGZ-JNPHEJMOSA-N 0.000 description 6
- PWKMJDQXKCENMF-MEYUZBJRSA-N Tyr-Thr-Leu Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(O)=O PWKMJDQXKCENMF-MEYUZBJRSA-N 0.000 description 6
- OWFGFHQMSBTKLX-UFYCRDLUSA-N Val-Tyr-Tyr Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](CC2=CC=C(C=C2)O)C(=O)O)N OWFGFHQMSBTKLX-UFYCRDLUSA-N 0.000 description 6
- 108010076324 alanyl-glycyl-glycine Proteins 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 6
- 238000003776 cleavage reaction Methods 0.000 description 6
- 239000002299 complementary DNA Substances 0.000 description 6
- 230000003247 decreasing effect Effects 0.000 description 6
- 238000001514 detection method Methods 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 6
- 230000006870 function Effects 0.000 description 6
- 108010013768 glutamyl-aspartyl-proline Proteins 0.000 description 6
- 230000013595 glycosylation Effects 0.000 description 6
- 238000006206 glycosylation reaction Methods 0.000 description 6
- VPZXBVLAVMBEQI-UHFFFAOYSA-N glycyl-DL-alpha-alanine Natural products OC(=O)C(C)NC(=O)CN VPZXBVLAVMBEQI-UHFFFAOYSA-N 0.000 description 6
- 238000000338 in vitro Methods 0.000 description 6
- 108010044374 isoleucyl-tyrosine Proteins 0.000 description 6
- 108010000761 leucylarginine Proteins 0.000 description 6
- 108010020755 prolyl-glycyl-glycine Proteins 0.000 description 6
- 108010087846 prolyl-prolyl-glycine Proteins 0.000 description 6
- 230000009467 reduction Effects 0.000 description 6
- 238000001890 transfection Methods 0.000 description 6
- 108010051110 tyrosyl-lysine Proteins 0.000 description 6
- 108010052774 valyl-lysyl-glycyl-phenylalanyl-tyrosine Proteins 0.000 description 6
- 210000003462 vein Anatomy 0.000 description 6
- RLMISHABBKUNFO-WHFBIAKZSA-N Ala-Ala-Gly Chemical compound C[C@H](N)C(=O)N[C@@H](C)C(=O)NCC(O)=O RLMISHABBKUNFO-WHFBIAKZSA-N 0.000 description 5
- YYSWCHMLFJLLBJ-ZLUOBGJFSA-N Ala-Ala-Ser Chemical compound C[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(O)=O YYSWCHMLFJLLBJ-ZLUOBGJFSA-N 0.000 description 5
- MNZHHDPWDWQJCQ-YUMQZZPRSA-N Ala-Leu-Gly Chemical compound C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)NCC(O)=O MNZHHDPWDWQJCQ-YUMQZZPRSA-N 0.000 description 5
- DYJJJCHDHLEFDW-FXQIFTODSA-N Ala-Pro-Cys Chemical compound C[C@@H](C(=O)N1CCC[C@H]1C(=O)N[C@@H](CS)C(=O)O)N DYJJJCHDHLEFDW-FXQIFTODSA-N 0.000 description 5
- IORKCNUBHNIMKY-CIUDSAMLSA-N Ala-Pro-Glu Chemical compound C[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(O)=O IORKCNUBHNIMKY-CIUDSAMLSA-N 0.000 description 5
- VNFSAYFQLXPHPY-CIQUZCHMSA-N Ala-Thr-Ile Chemical compound [H]N[C@@H](C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O VNFSAYFQLXPHPY-CIQUZCHMSA-N 0.000 description 5
- GIVATXIGCXFQQA-FXQIFTODSA-N Arg-Ala-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCCN=C(N)N GIVATXIGCXFQQA-FXQIFTODSA-N 0.000 description 5
- UXJCMQFPDWCHKX-DCAQKATOSA-N Arg-Arg-Glu Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(O)=O)C(O)=O UXJCMQFPDWCHKX-DCAQKATOSA-N 0.000 description 5
- MTYLORHAQXVQOW-AVGNSLFASA-N Arg-Lys-Met Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCSC)C(O)=O MTYLORHAQXVQOW-AVGNSLFASA-N 0.000 description 5
- SLKLLQWZQHXYSV-CIUDSAMLSA-N Asn-Ala-Lys Chemical compound NC(=O)C[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(O)=O SLKLLQWZQHXYSV-CIUDSAMLSA-N 0.000 description 5
- DPNWSMBUYCLEDG-CIUDSAMLSA-N Asp-Lys-Ser Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(O)=O DPNWSMBUYCLEDG-CIUDSAMLSA-N 0.000 description 5
- SQIARYGNVQWOSB-BZSNNMDCSA-N Asp-Tyr-Phe Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O SQIARYGNVQWOSB-BZSNNMDCSA-N 0.000 description 5
- 102000004190 Enzymes Human genes 0.000 description 5
- 108090000790 Enzymes Proteins 0.000 description 5
- -1 FR3 Proteins 0.000 description 5
- DHNWZLGBTPUTQQ-QEJZJMRPSA-N Gln-Asp-Trp Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCC(=O)N)N DHNWZLGBTPUTQQ-QEJZJMRPSA-N 0.000 description 5
- SMLDOQHTOAAFJQ-WDSKDSINSA-N Gln-Gly-Ser Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)NCC(=O)N[C@@H](CO)C(O)=O SMLDOQHTOAAFJQ-WDSKDSINSA-N 0.000 description 5
- FQCILXROGNOZON-YUMQZZPRSA-N Gln-Pro-Gly Chemical compound NC(=O)CC[C@H](N)C(=O)N1CCC[C@H]1C(=O)NCC(O)=O FQCILXROGNOZON-YUMQZZPRSA-N 0.000 description 5
- VLOLPWWCNKWRNB-LOKLDPHHSA-N Gln-Thr-Pro Chemical compound C[C@H]([C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CCC(=O)N)N)O VLOLPWWCNKWRNB-LOKLDPHHSA-N 0.000 description 5
- FITIQFSXXBKFFM-NRPADANISA-N Gln-Val-Ser Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CO)C(O)=O FITIQFSXXBKFFM-NRPADANISA-N 0.000 description 5
- CKOFNWCLWRYUHK-XHNCKOQMSA-N Glu-Asp-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCC(=O)O)N)C(=O)O CKOFNWCLWRYUHK-XHNCKOQMSA-N 0.000 description 5
- INGJLBQKTRJLFO-UKJIMTQDSA-N Glu-Ile-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@@H](N)CCC(O)=O INGJLBQKTRJLFO-UKJIMTQDSA-N 0.000 description 5
- BPCLDCNZBUYGOD-BPUTZDHNSA-N Glu-Trp-Glu Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@H](CCC(O)=O)N)C(=O)N[C@@H](CCC(O)=O)C(O)=O)=CNC2=C1 BPCLDCNZBUYGOD-BPUTZDHNSA-N 0.000 description 5
- VSVZIEVNUYDAFR-YUMQZZPRSA-N Gly-Ala-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)CN VSVZIEVNUYDAFR-YUMQZZPRSA-N 0.000 description 5
- PABFFPWEJMEVEC-JGVFFNPUSA-N Gly-Gln-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CCC(=O)N)NC(=O)CN)C(=O)O PABFFPWEJMEVEC-JGVFFNPUSA-N 0.000 description 5
- MIIVFRCYJABHTQ-ONGXEEELSA-N Gly-Leu-Val Chemical compound [H]NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(O)=O MIIVFRCYJABHTQ-ONGXEEELSA-N 0.000 description 5
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 5
- MAABHGXCIBEYQR-XVYDVKMFSA-N His-Asn-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CC1=CN=CN1)N MAABHGXCIBEYQR-XVYDVKMFSA-N 0.000 description 5
- HIAHVKLTHNOENC-HGNGGELXSA-N His-Glu-Ala Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(O)=O HIAHVKLTHNOENC-HGNGGELXSA-N 0.000 description 5
- MKWSZEHGHSLNPF-NAKRPEOUSA-N Ile-Ala-Val Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)O)N MKWSZEHGHSLNPF-NAKRPEOUSA-N 0.000 description 5
- JHNJNTMTZHEDLJ-NAKRPEOUSA-N Ile-Ser-Arg Chemical compound CC[C@H](C)[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O JHNJNTMTZHEDLJ-NAKRPEOUSA-N 0.000 description 5
- 108010054477 Immunoglobulin Fab Fragments Proteins 0.000 description 5
- 102000001706 Immunoglobulin Fab Fragments Human genes 0.000 description 5
- OIARJGNVARWKFP-YUMQZZPRSA-N Leu-Asn-Gly Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)NCC(O)=O OIARJGNVARWKFP-YUMQZZPRSA-N 0.000 description 5
- AXZGZMGRBDQTEY-SRVKXCTJSA-N Leu-Gln-Met Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCSC)C(O)=O AXZGZMGRBDQTEY-SRVKXCTJSA-N 0.000 description 5
- HPBCTWSUJOGJSH-MNXVOIDGSA-N Leu-Glu-Ile Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O HPBCTWSUJOGJSH-MNXVOIDGSA-N 0.000 description 5
- HYMLKESRWLZDBR-WEDXCCLWSA-N Leu-Gly-Thr Chemical compound CC(C)C[C@H](N)C(=O)NCC(=O)N[C@@H]([C@@H](C)O)C(O)=O HYMLKESRWLZDBR-WEDXCCLWSA-N 0.000 description 5
- NRFGTHFONZYFNY-MGHWNKPDSA-N Leu-Ile-Tyr Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 NRFGTHFONZYFNY-MGHWNKPDSA-N 0.000 description 5
- LCNASHSOFMRYFO-WDCWCFNPSA-N Leu-Thr-Gln Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@H](C(O)=O)CCC(N)=O LCNASHSOFMRYFO-WDCWCFNPSA-N 0.000 description 5
- ODUQLUADRKMHOZ-JYJNAYRXSA-N Lys-Glu-Tyr Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)N)O ODUQLUADRKMHOZ-JYJNAYRXSA-N 0.000 description 5
- GQZMPWBZQALKJO-UWVGGRQHSA-N Lys-Gly-Arg Chemical compound [H]N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(O)=O GQZMPWBZQALKJO-UWVGGRQHSA-N 0.000 description 5
- KFSALEZVQJYHCE-AVGNSLFASA-N Lys-Met-Val Chemical compound CC(C)[C@@H](C(=O)O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)N KFSALEZVQJYHCE-AVGNSLFASA-N 0.000 description 5
- YFQSSOAGMZGXFT-MEYUZBJRSA-N Lys-Thr-Tyr Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O YFQSSOAGMZGXFT-MEYUZBJRSA-N 0.000 description 5
- SUZVLFWOCKHWET-CQDKDKBSSA-N Lys-Tyr-Ala Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](C)C(O)=O SUZVLFWOCKHWET-CQDKDKBSSA-N 0.000 description 5
- RQILLQOQXLZTCK-KBPBESRZSA-N Lys-Tyr-Gly Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)NCC(O)=O RQILLQOQXLZTCK-KBPBESRZSA-N 0.000 description 5
- CNFMPVYIVQUJOO-NHCYSSNCSA-N Met-Val-Gln Chemical compound CSCC[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(O)=O)CCC(N)=O CNFMPVYIVQUJOO-NHCYSSNCSA-N 0.000 description 5
- KZNQNBZMBZJQJO-UHFFFAOYSA-N N-glycyl-L-proline Natural products NCC(=O)N1CCCC1C(O)=O KZNQNBZMBZJQJO-UHFFFAOYSA-N 0.000 description 5
- 108010079364 N-glycylalanine Proteins 0.000 description 5
- MSHZERMPZKCODG-ACRUOGEOSA-N Phe-Leu-Phe Chemical compound C([C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=CC=C1 MSHZERMPZKCODG-ACRUOGEOSA-N 0.000 description 5
- JLLJTMHNXQTMCK-UBHSHLNASA-N Phe-Pro-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CC1=CC=CC=C1 JLLJTMHNXQTMCK-UBHSHLNASA-N 0.000 description 5
- WWPAHTZOWURIMR-ULQDDVLXSA-N Phe-Pro-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CC1=CC=CC=C1 WWPAHTZOWURIMR-ULQDDVLXSA-N 0.000 description 5
- MCIXMYKSPQUMJG-SRVKXCTJSA-N Phe-Ser-Ser Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O MCIXMYKSPQUMJG-SRVKXCTJSA-N 0.000 description 5
- FGWUALWGCZJQDJ-URLPEUOOSA-N Phe-Thr-Ile Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O FGWUALWGCZJQDJ-URLPEUOOSA-N 0.000 description 5
- UAYHMOIGIQZLFR-NHCYSSNCSA-N Pro-Gln-Val Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C(C)C)C(O)=O UAYHMOIGIQZLFR-NHCYSSNCSA-N 0.000 description 5
- LGSANCBHSMDFDY-GARJFASQSA-N Pro-Glu-Pro Chemical compound C1C[C@H](NC1)C(=O)N[C@@H](CCC(=O)O)C(=O)N2CCC[C@@H]2C(=O)O LGSANCBHSMDFDY-GARJFASQSA-N 0.000 description 5
- VPEVBAUSTBWQHN-NHCYSSNCSA-N Pro-Glu-Val Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(O)=O VPEVBAUSTBWQHN-NHCYSSNCSA-N 0.000 description 5
- JMVQDLDPDBXAAX-YUMQZZPRSA-N Pro-Gly-Gln Chemical compound NC(=O)CC[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H]1CCCN1 JMVQDLDPDBXAAX-YUMQZZPRSA-N 0.000 description 5
- ZLXKLMHAMDENIO-DCAQKATOSA-N Pro-Lys-Asp Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(O)=O ZLXKLMHAMDENIO-DCAQKATOSA-N 0.000 description 5
- PCWLNNZTBJTZRN-AVGNSLFASA-N Pro-Pro-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H]1NCCC1 PCWLNNZTBJTZRN-AVGNSLFASA-N 0.000 description 5
- OWQXAJQZLWHPBH-FXQIFTODSA-N Pro-Ser-Asn Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(O)=O OWQXAJQZLWHPBH-FXQIFTODSA-N 0.000 description 5
- GMJDSFYVTAMIBF-FXQIFTODSA-N Pro-Ser-Asp Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(O)=O GMJDSFYVTAMIBF-FXQIFTODSA-N 0.000 description 5
- QEDMOZUJTGEIBF-FXQIFTODSA-N Ser-Arg-Asp Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(O)=O QEDMOZUJTGEIBF-FXQIFTODSA-N 0.000 description 5
- CDVFZMOFNJPUDD-ACZMJKKPSA-N Ser-Gln-Asn Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O CDVFZMOFNJPUDD-ACZMJKKPSA-N 0.000 description 5
- MOQDPPUMFSMYOM-KKUMJFAQSA-N Ser-His-Phe Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)O)NC(=O)[C@H](CC2=CN=CN2)NC(=O)[C@H](CO)N MOQDPPUMFSMYOM-KKUMJFAQSA-N 0.000 description 5
- UIPXCLNLUUAMJU-JBDRJPRFSA-N Ser-Ile-Ser Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(O)=O UIPXCLNLUUAMJU-JBDRJPRFSA-N 0.000 description 5
- QYSFWUIXDFJUDW-DCAQKATOSA-N Ser-Leu-Arg Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O QYSFWUIXDFJUDW-DCAQKATOSA-N 0.000 description 5
- GZSZPKSBVAOGIE-CIUDSAMLSA-N Ser-Lys-Ala Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(O)=O GZSZPKSBVAOGIE-CIUDSAMLSA-N 0.000 description 5
- ADJDNJCSPNFFPI-FXQIFTODSA-N Ser-Pro-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CO ADJDNJCSPNFFPI-FXQIFTODSA-N 0.000 description 5
- BMKNXTJLHFIAAH-CIUDSAMLSA-N Ser-Ser-Leu Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(O)=O BMKNXTJLHFIAAH-CIUDSAMLSA-N 0.000 description 5
- PCJLFYBAQZQOFE-KATARQTJSA-N Ser-Thr-Lys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CO)N)O PCJLFYBAQZQOFE-KATARQTJSA-N 0.000 description 5
- RCOUFINCYASMDN-GUBZILKMSA-N Ser-Val-Met Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCSC)C(O)=O RCOUFINCYASMDN-GUBZILKMSA-N 0.000 description 5
- KRPKYGOFYUNIGM-XVSYOHENSA-N Thr-Asp-Phe Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)N)O KRPKYGOFYUNIGM-XVSYOHENSA-N 0.000 description 5
- ODSAPYVQSLDRSR-LKXGYXEUSA-N Thr-Cys-Asn Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CS)C(=O)N[C@@H](CC(N)=O)C(O)=O ODSAPYVQSLDRSR-LKXGYXEUSA-N 0.000 description 5
- DJDSEDOKJTZBAR-ZDLURKLDSA-N Thr-Gly-Ser Chemical compound C[C@@H](O)[C@H](N)C(=O)NCC(=O)N[C@@H](CO)C(O)=O DJDSEDOKJTZBAR-ZDLURKLDSA-N 0.000 description 5
- PAXANSWUSVPFNK-IUKAMOBKSA-N Thr-Ile-Asn Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)[C@H]([C@@H](C)O)N PAXANSWUSVPFNK-IUKAMOBKSA-N 0.000 description 5
- DXPURPNJDFCKKO-RHYQMDGZSA-N Thr-Lys-Val Chemical compound CC(C)[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)[C@@H](C)O)C(O)=O DXPURPNJDFCKKO-RHYQMDGZSA-N 0.000 description 5
- MROIJTGJGIDEEJ-RCWTZXSCSA-N Thr-Pro-Pro Chemical compound C[C@@H](O)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1[C@H](C(O)=O)CCC1 MROIJTGJGIDEEJ-RCWTZXSCSA-N 0.000 description 5
- SGAOHNPSEPVAFP-ZDLURKLDSA-N Thr-Ser-Gly Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)NCC(O)=O SGAOHNPSEPVAFP-ZDLURKLDSA-N 0.000 description 5
- UKINEYBQXPMOJO-UBHSHLNASA-N Trp-Asn-Ser Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CO)C(=O)O)N UKINEYBQXPMOJO-UBHSHLNASA-N 0.000 description 5
- MBLJBGZWLHTJBH-SZMVWBNQSA-N Trp-Val-Arg Chemical compound C1=CC=C2C(C[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O)=CNC2=C1 MBLJBGZWLHTJBH-SZMVWBNQSA-N 0.000 description 5
- ZQGPWORGSNRQLN-NHCYSSNCSA-N Val-Asp-His Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)N ZQGPWORGSNRQLN-NHCYSSNCSA-N 0.000 description 5
- OQWNEUXPKHIEJO-NRPADANISA-N Val-Glu-Ser Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CO)C(=O)O)N OQWNEUXPKHIEJO-NRPADANISA-N 0.000 description 5
- UEHRGZCNLSWGHK-DLOVCJGASA-N Val-Glu-Val Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(O)=O UEHRGZCNLSWGHK-DLOVCJGASA-N 0.000 description 5
- ZIGZPYJXIWLQFC-QTKMDUPCSA-N Val-His-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC1=CN=CN1)NC(=O)[C@H](C(C)C)N)O ZIGZPYJXIWLQFC-QTKMDUPCSA-N 0.000 description 5
- LLJLBRRXKZTTRD-GUBZILKMSA-N Val-Val-Ser Chemical compound CC(C)[C@@H](C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CO)C(=O)O)N LLJLBRRXKZTTRD-GUBZILKMSA-N 0.000 description 5
- 108010081404 acein-2 Proteins 0.000 description 5
- 238000001042 affinity chromatography Methods 0.000 description 5
- 235000018417 cysteine Nutrition 0.000 description 5
- 239000000539 dimer Substances 0.000 description 5
- 229940088598 enzyme Drugs 0.000 description 5
- 108010079547 glutamylmethionine Proteins 0.000 description 5
- 108010077515 glycylproline Proteins 0.000 description 5
- 108010057821 leucylproline Proteins 0.000 description 5
- 108020004999 messenger RNA Proteins 0.000 description 5
- 229920001223 polyethylene glycol Polymers 0.000 description 5
- 108010031719 prolyl-serine Proteins 0.000 description 5
- 108010053725 prolylvaline Proteins 0.000 description 5
- 238000003259 recombinant expression Methods 0.000 description 5
- 230000007017 scission Effects 0.000 description 5
- 108010069117 seryl-lysyl-aspartic acid Proteins 0.000 description 5
- 108010071207 serylmethionine Proteins 0.000 description 5
- 230000011664 signaling Effects 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 241000894007 species Species 0.000 description 5
- 108010080629 tryptophan-leucine Proteins 0.000 description 5
- 108010027345 wheylin-1 peptide Proteins 0.000 description 5
- IESDGNYHXIOKRW-YXMSTPNBSA-N (2s)-2-[[(2s)-1-[(2s)-6-amino-2-[[(2s,3r)-2-amino-3-hydroxybutanoyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-5-(diaminomethylideneamino)pentanoic acid Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O IESDGNYHXIOKRW-YXMSTPNBSA-N 0.000 description 4
- DIBLBAURNYJYBF-XLXZRNDBSA-N (2s)-2-[[(2s)-2-[[2-[[(2s)-6-amino-2-[[(2s)-2-amino-3-methylbutanoyl]amino]hexanoyl]amino]acetyl]amino]-3-phenylpropanoyl]amino]-3-(4-hydroxyphenyl)propanoic acid Chemical compound C([C@H](NC(=O)CNC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)C(C)C)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(O)=O)C1=CC=CC=C1 DIBLBAURNYJYBF-XLXZRNDBSA-N 0.000 description 4
- OINVDEKBKBCPLX-JXUBOQSCSA-N Ala-Lys-Thr Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(O)=O OINVDEKBKBCPLX-JXUBOQSCSA-N 0.000 description 4
- 206010002091 Anaesthesia Diseases 0.000 description 4
- JGDGLDNAQJJGJI-AVGNSLFASA-N Arg-Arg-His Chemical compound C1=C(NC=N1)C[C@@H](C(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCN=C(N)N)N JGDGLDNAQJJGJI-AVGNSLFASA-N 0.000 description 4
- PNHQRQTVBRDIEF-CIUDSAMLSA-N Asn-Leu-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)N)N PNHQRQTVBRDIEF-CIUDSAMLSA-N 0.000 description 4
- JBDLMLZNDRLDIX-HJGDQZAQSA-N Asn-Thr-Leu Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(O)=O JBDLMLZNDRLDIX-HJGDQZAQSA-N 0.000 description 4
- LGCVSPFCFXWUEY-IHPCNDPISA-N Asn-Trp-Tyr Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CC3=CC=C(C=C3)O)C(=O)O)NC(=O)[C@H](CC(=O)N)N LGCVSPFCFXWUEY-IHPCNDPISA-N 0.000 description 4
- MRQQMVZUHXUPEV-IHRRRGAJSA-N Asp-Arg-Phe Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O MRQQMVZUHXUPEV-IHRRRGAJSA-N 0.000 description 4
- SNDBKTFJWVEVPO-WHFBIAKZSA-N Asp-Gly-Ser Chemical compound [H]N[C@@H](CC(O)=O)C(=O)NCC(=O)N[C@@H](CO)C(O)=O SNDBKTFJWVEVPO-WHFBIAKZSA-N 0.000 description 4
- AYFVRYXNDHBECD-YUMQZZPRSA-N Asp-Leu-Gly Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)NCC(O)=O AYFVRYXNDHBECD-YUMQZZPRSA-N 0.000 description 4
- RXBGWGRSWXOBGK-KKUMJFAQSA-N Asp-Lys-Tyr Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O RXBGWGRSWXOBGK-KKUMJFAQSA-N 0.000 description 4
- GEEXORWTBTUOHC-FXQIFTODSA-N Cys-Arg-Ser Chemical compound C(C[C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](CS)N)CN=C(N)N GEEXORWTBTUOHC-FXQIFTODSA-N 0.000 description 4
- BBQIWFFTTQTNOC-AVGNSLFASA-N Cys-Phe-Gln Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](CS)N BBQIWFFTTQTNOC-AVGNSLFASA-N 0.000 description 4
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 4
- JXFLPKSDLDEOQK-JHEQGTHGSA-N Gln-Gly-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)CCC(N)=O JXFLPKSDLDEOQK-JHEQGTHGSA-N 0.000 description 4
- LKDIBBOKUAASNP-FXQIFTODSA-N Glu-Ala-Glu Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(O)=O LKDIBBOKUAASNP-FXQIFTODSA-N 0.000 description 4
- GLWXKFRTOHKGIT-ACZMJKKPSA-N Glu-Asn-Asn Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O GLWXKFRTOHKGIT-ACZMJKKPSA-N 0.000 description 4
- HNVFSTLPVJWIDV-CIUDSAMLSA-N Glu-Glu-Gln Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O HNVFSTLPVJWIDV-CIUDSAMLSA-N 0.000 description 4
- KASDBWKLWJKTLJ-GUBZILKMSA-N Glu-Glu-Met Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCSC)C(O)=O KASDBWKLWJKTLJ-GUBZILKMSA-N 0.000 description 4
- SUIAHERNFYRBDZ-GVXVVHGQSA-N Glu-Lys-Val Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(O)=O SUIAHERNFYRBDZ-GVXVVHGQSA-N 0.000 description 4
- CGWHAXBNGYQBBK-JBACZVJFSA-N Glu-Trp-Tyr Chemical compound C([C@H](NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CCC(O)=O)N)C(O)=O)C1=CC=C(O)C=C1 CGWHAXBNGYQBBK-JBACZVJFSA-N 0.000 description 4
- YQPFCZVKMUVZIN-AUTRQRHGSA-N Glu-Val-Gln Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O YQPFCZVKMUVZIN-AUTRQRHGSA-N 0.000 description 4
- GRIRDMVMJJDZKV-RCOVLWMOSA-N Gly-Asn-Val Chemical compound [H]NCC(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](C(C)C)C(O)=O GRIRDMVMJJDZKV-RCOVLWMOSA-N 0.000 description 4
- YWAQATDNEKZFFK-BYPYZUCNSA-N Gly-Gly-Ser Chemical compound NCC(=O)NCC(=O)N[C@@H](CO)C(O)=O YWAQATDNEKZFFK-BYPYZUCNSA-N 0.000 description 4
- UUYBFNKHOCJCHT-VHSXEESVSA-N Gly-Leu-Pro Chemical compound CC(C)C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)CN UUYBFNKHOCJCHT-VHSXEESVSA-N 0.000 description 4
- OMOZPGCHVWOXHN-BQBZGAKWSA-N Gly-Met-Ser Chemical compound CSCC[C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)CN OMOZPGCHVWOXHN-BQBZGAKWSA-N 0.000 description 4
- FFALDIDGPLUDKV-ZDLURKLDSA-N Gly-Thr-Ser Chemical compound [H]NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(O)=O FFALDIDGPLUDKV-ZDLURKLDSA-N 0.000 description 4
- WMKXFMUJRCEGRP-SRVKXCTJSA-N His-Asn-His Chemical compound C1=C(NC=N1)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC2=CN=CN2)C(=O)O)N WMKXFMUJRCEGRP-SRVKXCTJSA-N 0.000 description 4
- ZLFNNVATRMCAKN-ZKWXMUAHSA-N Ile-Ser-Gly Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CO)C(=O)NCC(=O)O)N ZLFNNVATRMCAKN-ZKWXMUAHSA-N 0.000 description 4
- VGSPNSSCMOHRRR-BJDJZHNGSA-N Ile-Ser-Lys Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)O)N VGSPNSSCMOHRRR-BJDJZHNGSA-N 0.000 description 4
- PVMPDMIKUVNOBD-CIUDSAMLSA-N Leu-Asp-Ser Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(O)=O PVMPDMIKUVNOBD-CIUDSAMLSA-N 0.000 description 4
- QVFGXCVIXXBFHO-AVGNSLFASA-N Leu-Glu-Leu Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(O)=O QVFGXCVIXXBFHO-AVGNSLFASA-N 0.000 description 4
- IWMJFLJQHIDZQW-KKUMJFAQSA-N Leu-Ser-Phe Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 IWMJFLJQHIDZQW-KKUMJFAQSA-N 0.000 description 4
- MVJRBCJCRYGCKV-GVXVVHGQSA-N Leu-Val-Gln Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O MVJRBCJCRYGCKV-GVXVVHGQSA-N 0.000 description 4
- XNKDCYABMBBEKN-IUCAKERBSA-N Lys-Gly-Gln Chemical compound NCCCC[C@H](N)C(=O)NCC(=O)N[C@H](C(O)=O)CCC(N)=O XNKDCYABMBBEKN-IUCAKERBSA-N 0.000 description 4
- GQFDWEDHOQRNLC-QWRGUYRKSA-N Lys-Gly-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)CCCCN GQFDWEDHOQRNLC-QWRGUYRKSA-N 0.000 description 4
- SKRGVGLIRUGANF-AVGNSLFASA-N Lys-Leu-Glu Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O SKRGVGLIRUGANF-AVGNSLFASA-N 0.000 description 4
- PDIDTSZKKFEDMB-UWVGGRQHSA-N Lys-Pro-Gly Chemical compound [H]N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)NCC(O)=O PDIDTSZKKFEDMB-UWVGGRQHSA-N 0.000 description 4
- IOQWIOPSKJOEKI-SRVKXCTJSA-N Lys-Ser-Leu Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(O)=O IOQWIOPSKJOEKI-SRVKXCTJSA-N 0.000 description 4
- DRRXXZBXDMLGFC-IHRRRGAJSA-N Lys-Val-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)CCCCN DRRXXZBXDMLGFC-IHRRRGAJSA-N 0.000 description 4
- PNDCUTDWYVKBHX-IHRRRGAJSA-N Met-Asp-Tyr Chemical compound CSCC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 PNDCUTDWYVKBHX-IHRRRGAJSA-N 0.000 description 4
- GHQFLTYXGUETFD-UFYCRDLUSA-N Met-Tyr-Tyr Chemical compound CSCC[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](CC2=CC=C(C=C2)O)C(=O)O)N GHQFLTYXGUETFD-UFYCRDLUSA-N 0.000 description 4
- CDNPIRSCAFMMBE-SRVKXCTJSA-N Phe-Asn-Ser Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(O)=O CDNPIRSCAFMMBE-SRVKXCTJSA-N 0.000 description 4
- XDMMOISUAHXXFD-SRVKXCTJSA-N Phe-Ser-Asp Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(O)=O XDMMOISUAHXXFD-SRVKXCTJSA-N 0.000 description 4
- IIEOLPMQYRBZCN-SRVKXCTJSA-N Phe-Ser-Cys Chemical compound N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CS)C(=O)O IIEOLPMQYRBZCN-SRVKXCTJSA-N 0.000 description 4
- KLYYKKGCPOGDPE-OEAJRASXSA-N Phe-Thr-Leu Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(O)=O KLYYKKGCPOGDPE-OEAJRASXSA-N 0.000 description 4
- 229920002873 Polyethylenimine Polymers 0.000 description 4
- FDMKYQQYJKYCLV-GUBZILKMSA-N Pro-Pro-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H]1NCCC1 FDMKYQQYJKYCLV-GUBZILKMSA-N 0.000 description 4
- SEZGGSHLMROBFX-CIUDSAMLSA-N Pro-Ser-Gln Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(O)=O SEZGGSHLMROBFX-CIUDSAMLSA-N 0.000 description 4
- 241000700157 Rattus norvegicus Species 0.000 description 4
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 4
- HBOABDXGTMMDSE-GUBZILKMSA-N Ser-Arg-Val Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(O)=O HBOABDXGTMMDSE-GUBZILKMSA-N 0.000 description 4
- VAUMZJHYZQXZBQ-WHFBIAKZSA-N Ser-Asn-Gly Chemical compound OC[C@H](N)C(=O)N[C@@H](CC(N)=O)C(=O)NCC(O)=O VAUMZJHYZQXZBQ-WHFBIAKZSA-N 0.000 description 4
- VGNYHOBZJKWRGI-CIUDSAMLSA-N Ser-Asn-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](N)CO VGNYHOBZJKWRGI-CIUDSAMLSA-N 0.000 description 4
- MQUZANJDFOQOBX-SRVKXCTJSA-N Ser-Phe-Ser Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(O)=O MQUZANJDFOQOBX-SRVKXCTJSA-N 0.000 description 4
- JCLAFVNDBJMLBC-JBDRJPRFSA-N Ser-Ser-Ile Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O JCLAFVNDBJMLBC-JBDRJPRFSA-N 0.000 description 4
- DSLHSTIUAPKERR-XGEHTFHBSA-N Thr-Cys-Val Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CS)C(=O)N[C@@H](C(C)C)C(O)=O DSLHSTIUAPKERR-XGEHTFHBSA-N 0.000 description 4
- FQPDRTDDEZXCEC-SVSWQMSJSA-N Thr-Ile-Ser Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(O)=O FQPDRTDDEZXCEC-SVSWQMSJSA-N 0.000 description 4
- MECLEFZMPPOEAC-VOAKCMCISA-N Thr-Leu-Lys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)O)N)O MECLEFZMPPOEAC-VOAKCMCISA-N 0.000 description 4
- BDGBHYCAZJPLHX-HJGDQZAQSA-N Thr-Lys-Asn Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(O)=O BDGBHYCAZJPLHX-HJGDQZAQSA-N 0.000 description 4
- DEGCBBCMYWNJNA-RHYQMDGZSA-N Thr-Pro-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)[C@@H](C)O DEGCBBCMYWNJNA-RHYQMDGZSA-N 0.000 description 4
- IEZVHOULSUULHD-XGEHTFHBSA-N Thr-Ser-Val Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(O)=O IEZVHOULSUULHD-XGEHTFHBSA-N 0.000 description 4
- BEZTUFWTPVOROW-KJEVXHAQSA-N Thr-Tyr-Arg Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)N)O BEZTUFWTPVOROW-KJEVXHAQSA-N 0.000 description 4
- 101710120037 Toxin CcdB Proteins 0.000 description 4
- VEYXZZGMIBKXCN-UBHSHLNASA-N Trp-Asp-Asp Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)O)N VEYXZZGMIBKXCN-UBHSHLNASA-N 0.000 description 4
- VTHNLRXALGUDBS-BPUTZDHNSA-N Trp-Gln-Glu Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCC(=O)O)C(=O)O)N VTHNLRXALGUDBS-BPUTZDHNSA-N 0.000 description 4
- SVGAWGVHFIYAEE-JSGCOSHPSA-N Trp-Gly-Gln Chemical compound C1=CC=C2C(C[C@H](N)C(=O)NCC(=O)N[C@@H](CCC(N)=O)C(O)=O)=CNC2=C1 SVGAWGVHFIYAEE-JSGCOSHPSA-N 0.000 description 4
- VTFWAGGJDRSQFG-MELADBBJSA-N Tyr-Asn-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC(=O)N)NC(=O)[C@H](CC2=CC=C(C=C2)O)N)C(=O)O VTFWAGGJDRSQFG-MELADBBJSA-N 0.000 description 4
- NXRGXTBPMOGFID-CFMVVWHZSA-N Tyr-Ile-Asn Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(N)=O)C(O)=O NXRGXTBPMOGFID-CFMVVWHZSA-N 0.000 description 4
- SINRIKQYQJRGDQ-MEYUZBJRSA-N Tyr-Lys-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 SINRIKQYQJRGDQ-MEYUZBJRSA-N 0.000 description 4
- RWOKVQUCENPXGE-IHRRRGAJSA-N Tyr-Ser-Arg Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O RWOKVQUCENPXGE-IHRRRGAJSA-N 0.000 description 4
- RIVVDNTUSRVTQT-IRIUXVKKSA-N Tyr-Thr-Gln Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)N)O RIVVDNTUSRVTQT-IRIUXVKKSA-N 0.000 description 4
- QHDXUYOYTPWCSK-RCOVLWMOSA-N Val-Asp-Gly Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)NCC(=O)O)N QHDXUYOYTPWCSK-RCOVLWMOSA-N 0.000 description 4
- XEYUMGGWQCIWAR-XVKPBYJWSA-N Val-Gln-Gly Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)NCC(=O)O)N XEYUMGGWQCIWAR-XVKPBYJWSA-N 0.000 description 4
- JXGWQYWDUOWQHA-DZKIICNBSA-N Val-Gln-Phe Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)N JXGWQYWDUOWQHA-DZKIICNBSA-N 0.000 description 4
- XTDDIVQWDXMRJL-IHRRRGAJSA-N Val-Leu-His Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)[C@H](C(C)C)N XTDDIVQWDXMRJL-IHRRRGAJSA-N 0.000 description 4
- RYHUIHUOYRNNIE-NRPADANISA-N Val-Ser-Gln Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(=O)N)C(=O)O)N RYHUIHUOYRNNIE-NRPADANISA-N 0.000 description 4
- DVLWZWNAQUBZBC-ZNSHCXBVSA-N Val-Thr-Pro Chemical compound C[C@H]([C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](C(C)C)N)O DVLWZWNAQUBZBC-ZNSHCXBVSA-N 0.000 description 4
- ZLNYBMWGPOKSLW-LSJOCFKGSA-N Val-Val-Asp Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(O)=O ZLNYBMWGPOKSLW-LSJOCFKGSA-N 0.000 description 4
- 230000003213 activating effect Effects 0.000 description 4
- 239000002671 adjuvant Substances 0.000 description 4
- 108010047495 alanylglycine Proteins 0.000 description 4
- 108010087924 alanylproline Proteins 0.000 description 4
- 230000037005 anaesthesia Effects 0.000 description 4
- 108010009111 arginyl-glycyl-glutamic acid Proteins 0.000 description 4
- 108010077245 asparaginyl-proline Proteins 0.000 description 4
- 108010040443 aspartyl-aspartic acid Proteins 0.000 description 4
- 108010047857 aspartylglycine Proteins 0.000 description 4
- 238000003556 assay Methods 0.000 description 4
- 230000000747 cardiac effect Effects 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 238000004113 cell culture Methods 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 description 4
- 108010004073 cysteinylcysteine Proteins 0.000 description 4
- 230000002068 genetic effect Effects 0.000 description 4
- 108010057083 glutamyl-aspartyl-leucine Proteins 0.000 description 4
- XBGGUPMXALFZOT-UHFFFAOYSA-N glycyl-L-tyrosine hemihydrate Natural products NCC(=O)NC(C(O)=O)CC1=CC=C(O)C=C1 XBGGUPMXALFZOT-UHFFFAOYSA-N 0.000 description 4
- 108010067216 glycyl-glycyl-glycine Proteins 0.000 description 4
- 108010087823 glycyltyrosine Proteins 0.000 description 4
- 230000037431 insertion Effects 0.000 description 4
- 238000003780 insertion Methods 0.000 description 4
- 210000004072 lung Anatomy 0.000 description 4
- 239000013612 plasmid Substances 0.000 description 4
- 210000001147 pulmonary artery Anatomy 0.000 description 4
- 230000035945 sensitivity Effects 0.000 description 4
- 108010026333 seryl-proline Proteins 0.000 description 4
- 230000000638 stimulation Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229940124597 therapeutic agent Drugs 0.000 description 4
- 230000001225 therapeutic effect Effects 0.000 description 4
- 108010038745 tryptophylglycine Proteins 0.000 description 4
- 108010045269 tryptophyltryptophan Proteins 0.000 description 4
- 230000002861 ventricular Effects 0.000 description 4
- AXFMEGAFCUULFV-BLFANLJRSA-N (2s)-2-[[(2s)-1-[(2s,3r)-2-amino-3-methylpentanoyl]pyrrolidine-2-carbonyl]amino]pentanedioic acid Chemical compound CC[C@@H](C)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(O)=O AXFMEGAFCUULFV-BLFANLJRSA-N 0.000 description 3
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 3
- SSSROGPPPVTHLX-FXQIFTODSA-N Ala-Arg-Asp Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(O)=O SSSROGPPPVTHLX-FXQIFTODSA-N 0.000 description 3
- DVJSJDDYCYSMFR-ZKWXMUAHSA-N Ala-Ile-Gly Chemical compound [H]N[C@@H](C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(O)=O DVJSJDDYCYSMFR-ZKWXMUAHSA-N 0.000 description 3
- HOVPGJUNRLMIOZ-CIUDSAMLSA-N Ala-Ser-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CO)NC(=O)[C@H](C)N HOVPGJUNRLMIOZ-CIUDSAMLSA-N 0.000 description 3
- LSMDIAAALJJLRO-XQXXSGGOSA-N Ala-Thr-Glu Chemical compound [H]N[C@@H](C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCC(O)=O)C(O)=O LSMDIAAALJJLRO-XQXXSGGOSA-N 0.000 description 3
- KTXKIYXZQFWJKB-VZFHVOOUSA-N Ala-Thr-Ser Chemical compound [H]N[C@@H](C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(O)=O KTXKIYXZQFWJKB-VZFHVOOUSA-N 0.000 description 3
- VWVPYNGMOCSSGK-GUBZILKMSA-N Arg-Arg-Asn Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(N)=O)C(O)=O VWVPYNGMOCSSGK-GUBZILKMSA-N 0.000 description 3
- HKRXJBBCQBAGIM-FXQIFTODSA-N Arg-Asp-Ser Chemical compound C(C[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CO)C(=O)O)N)CN=C(N)N HKRXJBBCQBAGIM-FXQIFTODSA-N 0.000 description 3
- GDVDRMUYICMNFJ-CIUDSAMLSA-N Arg-Cys-Glu Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCC(O)=O)C(O)=O GDVDRMUYICMNFJ-CIUDSAMLSA-N 0.000 description 3
- FFEUXEAKYRCACT-PEDHHIEDSA-N Arg-Ile-Ile Chemical compound CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@@H](N)CCCNC(N)=N)[C@@H](C)CC)C(O)=O FFEUXEAKYRCACT-PEDHHIEDSA-N 0.000 description 3
- FRBAHXABMQXSJQ-FXQIFTODSA-N Arg-Ser-Ser Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O FRBAHXABMQXSJQ-FXQIFTODSA-N 0.000 description 3
- PYDIIVKGTBRIEL-SZMVWBNQSA-N Arg-Trp-Pro Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N1CCC[C@H]1C(O)=O PYDIIVKGTBRIEL-SZMVWBNQSA-N 0.000 description 3
- XYOVHPDDWCEUDY-CIUDSAMLSA-N Asn-Ala-Leu Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(O)=O XYOVHPDDWCEUDY-CIUDSAMLSA-N 0.000 description 3
- JZRLLSOWDYUKOK-SRVKXCTJSA-N Asn-Asp-Phe Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(=O)N)N JZRLLSOWDYUKOK-SRVKXCTJSA-N 0.000 description 3
- FJIRXKVEDFLLOQ-SRVKXCTJSA-N Asn-Cys-Phe Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)O)NC(=O)[C@H](CS)NC(=O)[C@H](CC(=O)N)N FJIRXKVEDFLLOQ-SRVKXCTJSA-N 0.000 description 3
- GJFYPBDMUGGLFR-NKWVEPMBSA-N Asn-Gly-Pro Chemical compound C1C[C@@H](N(C1)C(=O)CNC(=O)[C@H](CC(=O)N)N)C(=O)O GJFYPBDMUGGLFR-NKWVEPMBSA-N 0.000 description 3
- RAQMSGVCGSJKCL-FOHZUACHSA-N Asn-Gly-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)CC(N)=O RAQMSGVCGSJKCL-FOHZUACHSA-N 0.000 description 3
- DJIMLSXHXKWADV-CIUDSAMLSA-N Asn-Leu-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CC(N)=O DJIMLSXHXKWADV-CIUDSAMLSA-N 0.000 description 3
- NJSNXIOKBHPFMB-GMOBBJLQSA-N Asn-Pro-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(=O)N)N NJSNXIOKBHPFMB-GMOBBJLQSA-N 0.000 description 3
- MKJBPDLENBUHQU-CIUDSAMLSA-N Asn-Ser-Leu Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(O)=O MKJBPDLENBUHQU-CIUDSAMLSA-N 0.000 description 3
- XYBJLTKSGFBLCS-QXEWZRGKSA-N Asp-Arg-Val Chemical compound NC(N)=NCCC[C@@H](C(=O)N[C@@H](C(C)C)C(O)=O)NC(=O)[C@@H](N)CC(O)=O XYBJLTKSGFBLCS-QXEWZRGKSA-N 0.000 description 3
- QNFRBNZGVVKBNJ-PEFMBERDSA-N Asp-Ile-Gln Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](CC(=O)O)N QNFRBNZGVVKBNJ-PEFMBERDSA-N 0.000 description 3
- RQHLMGCXCZUOGT-ZPFDUUQYSA-N Asp-Leu-Ile Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O RQHLMGCXCZUOGT-ZPFDUUQYSA-N 0.000 description 3
- XWSIYTYNLKCLJB-CIUDSAMLSA-N Asp-Lys-Asn Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(O)=O XWSIYTYNLKCLJB-CIUDSAMLSA-N 0.000 description 3
- USNJAPJZSGTTPX-XVSYOHENSA-N Asp-Phe-Thr Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)O)C(O)=O USNJAPJZSGTTPX-XVSYOHENSA-N 0.000 description 3
- WMLFFCRUSPNENW-ZLUOBGJFSA-N Asp-Ser-Ala Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(O)=O WMLFFCRUSPNENW-ZLUOBGJFSA-N 0.000 description 3
- MGSVBZIBCCKGCY-ZLUOBGJFSA-N Asp-Ser-Ser Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O MGSVBZIBCCKGCY-ZLUOBGJFSA-N 0.000 description 3
- GGBQDSHTXKQSLP-NHCYSSNCSA-N Asp-Val-Lys Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CC(=O)O)N GGBQDSHTXKQSLP-NHCYSSNCSA-N 0.000 description 3
- 206010007556 Cardiac failure acute Diseases 0.000 description 3
- 102000014914 Carrier Proteins Human genes 0.000 description 3
- AMRLSQGGERHDHJ-FXQIFTODSA-N Cys-Ala-Arg Chemical compound [H]N[C@@H](CS)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O AMRLSQGGERHDHJ-FXQIFTODSA-N 0.000 description 3
- SMYXEYRYCLIPIL-ZLUOBGJFSA-N Cys-Cys-Cys Chemical compound SC[C@H](N)C(=O)N[C@@H](CS)C(=O)N[C@@H](CS)C(O)=O SMYXEYRYCLIPIL-ZLUOBGJFSA-N 0.000 description 3
- OHLLDUNVMPPUMD-DCAQKATOSA-N Cys-Leu-Val Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](C(C)C)C(=O)O)NC(=O)[C@H](CS)N OHLLDUNVMPPUMD-DCAQKATOSA-N 0.000 description 3
- NMPSRDYYNIYOSJ-IHPCNDPISA-N Cys-Trp-Phe Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)O)NC(=O)[C@H](CC2=CNC3=CC=CC=C32)NC(=O)[C@H](CS)N NMPSRDYYNIYOSJ-IHPCNDPISA-N 0.000 description 3
- 108010090461 DFG peptide Proteins 0.000 description 3
- 101100012887 Drosophila melanogaster btl gene Proteins 0.000 description 3
- 101100012878 Drosophila melanogaster htl gene Proteins 0.000 description 3
- 241000588724 Escherichia coli Species 0.000 description 3
- 108010020195 FLAG peptide Proteins 0.000 description 3
- XZWYTXMRWQJBGX-VXBMVYAYSA-N FLAG peptide Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](NC(=O)[C@@H](N)CC(O)=O)CC1=CC=C(O)C=C1 XZWYTXMRWQJBGX-VXBMVYAYSA-N 0.000 description 3
- NPTGGVQJYRSMCM-GLLZPBPUSA-N Gln-Gln-Thr Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O NPTGGVQJYRSMCM-GLLZPBPUSA-N 0.000 description 3
- GQZDDFRXSDGUNG-YVNDNENWSA-N Gln-Ile-Gln Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCC(N)=O)C(O)=O GQZDDFRXSDGUNG-YVNDNENWSA-N 0.000 description 3
- MFHVAWMMKZBSRQ-ACZMJKKPSA-N Gln-Ser-Cys Chemical compound C(CC(=O)N)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CS)C(=O)O)N MFHVAWMMKZBSRQ-ACZMJKKPSA-N 0.000 description 3
- IESFZVCAVACGPH-PEFMBERDSA-N Glu-Asp-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H](N)CCC(O)=O IESFZVCAVACGPH-PEFMBERDSA-N 0.000 description 3
- CJWANNXUTOATSJ-DCAQKATOSA-N Glu-Gln-His Chemical compound C1=C(NC=N1)C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CCC(=O)O)N CJWANNXUTOATSJ-DCAQKATOSA-N 0.000 description 3
- RJIVPOXLQFJRTG-LURJTMIESA-N Gly-Arg-Gly Chemical compound OC(=O)CNC(=O)[C@@H](NC(=O)CN)CCCN=C(N)N RJIVPOXLQFJRTG-LURJTMIESA-N 0.000 description 3
- UXJHNZODTMHWRD-WHFBIAKZSA-N Gly-Asn-Ala Chemical compound [H]NCC(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](C)C(O)=O UXJHNZODTMHWRD-WHFBIAKZSA-N 0.000 description 3
- LGQZOQRDEUIZJY-YUMQZZPRSA-N Gly-Cys-Lys Chemical compound NCCCC[C@H](NC(=O)[C@H](CS)NC(=O)CN)C(O)=O LGQZOQRDEUIZJY-YUMQZZPRSA-N 0.000 description 3
- UESJMAMHDLEHGM-NHCYSSNCSA-N Gly-Ile-Leu Chemical compound NCC(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(O)=O UESJMAMHDLEHGM-NHCYSSNCSA-N 0.000 description 3
- SCWYHUQOOFRVHP-MBLNEYKQSA-N Gly-Ile-Thr Chemical compound NCC(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(O)=O SCWYHUQOOFRVHP-MBLNEYKQSA-N 0.000 description 3
- IUZGUFAJDBHQQV-YUMQZZPRSA-N Gly-Leu-Asn Chemical compound NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(O)=O IUZGUFAJDBHQQV-YUMQZZPRSA-N 0.000 description 3
- NVTPVQLIZCOJFK-FOHZUACHSA-N Gly-Thr-Asp Chemical compound [H]NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(O)=O NVTPVQLIZCOJFK-FOHZUACHSA-N 0.000 description 3
- DBUNZBWUWCIELX-JHEQGTHGSA-N Gly-Thr-Glu Chemical compound [H]NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCC(O)=O)C(O)=O DBUNZBWUWCIELX-JHEQGTHGSA-N 0.000 description 3
- GBYYQVBXFVDJPJ-WLTAIBSBSA-N Gly-Tyr-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)NC(=O)CN)O GBYYQVBXFVDJPJ-WLTAIBSBSA-N 0.000 description 3
- BNMRSWQOHIQTFL-JSGCOSHPSA-N Gly-Val-Phe Chemical compound NCC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 BNMRSWQOHIQTFL-JSGCOSHPSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- JBCLFWXMTIKCCB-UHFFFAOYSA-N H-Gly-Phe-OH Natural products NCC(=O)NC(C(O)=O)CC1=CC=CC=C1 JBCLFWXMTIKCCB-UHFFFAOYSA-N 0.000 description 3
- FFKJUTZARGRVTH-KKUMJFAQSA-N His-Ser-Tyr Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O FFKJUTZARGRVTH-KKUMJFAQSA-N 0.000 description 3
- 101500026735 Homo sapiens Brain natriuretic peptide 32 Proteins 0.000 description 3
- 101000613820 Homo sapiens Osteopontin Proteins 0.000 description 3
- VAXBXNPRXPHGHG-BJDJZHNGSA-N Ile-Ala-Leu Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)O)N VAXBXNPRXPHGHG-BJDJZHNGSA-N 0.000 description 3
- HDOYNXLPTRQLAD-JBDRJPRFSA-N Ile-Ala-Ser Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(=O)O)N HDOYNXLPTRQLAD-JBDRJPRFSA-N 0.000 description 3
- DFFTXLCCDFYRKD-MBLNEYKQSA-N Ile-Gly-Thr Chemical compound CC[C@H](C)[C@@H](C(=O)NCC(=O)N[C@@H]([C@@H](C)O)C(=O)O)N DFFTXLCCDFYRKD-MBLNEYKQSA-N 0.000 description 3
- GTSAALPQZASLPW-KJYZGMDISA-N Ile-His-Trp Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N[C@@H](CC2=CNC3=CC=CC=C32)C(=O)O)N GTSAALPQZASLPW-KJYZGMDISA-N 0.000 description 3
- KLBVGHCGHUNHEA-BJDJZHNGSA-N Ile-Leu-Ala Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)O)N KLBVGHCGHUNHEA-BJDJZHNGSA-N 0.000 description 3
- TVYWVSJGSHQWMT-AJNGGQMLSA-N Ile-Leu-Lys Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)O)N TVYWVSJGSHQWMT-AJNGGQMLSA-N 0.000 description 3
- WYUHAXJAMDTOAU-IAVJCBSLSA-N Ile-Phe-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)CC)C(=O)O)N WYUHAXJAMDTOAU-IAVJCBSLSA-N 0.000 description 3
- VZSDQFZFTCVEGF-ZEWNOJEFSA-N Ile-Phe-Tyr Chemical compound CC[C@H](C)[C@H](N)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O VZSDQFZFTCVEGF-ZEWNOJEFSA-N 0.000 description 3
- XVUAQNRNFMVWBR-BLMTYFJBSA-N Ile-Trp-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)N[C@@H]([C@@H](C)CC)C(=O)O)N XVUAQNRNFMVWBR-BLMTYFJBSA-N 0.000 description 3
- JCGMFFQQHJQASB-PYJNHQTQSA-N Ile-Val-His Chemical compound N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC1=CNC=N1)C(=O)O JCGMFFQQHJQASB-PYJNHQTQSA-N 0.000 description 3
- FADYJNXDPBKVCA-UHFFFAOYSA-N L-Phenylalanyl-L-lysin Natural products NCCCCC(C(O)=O)NC(=O)C(N)CC1=CC=CC=C1 FADYJNXDPBKVCA-UHFFFAOYSA-N 0.000 description 3
- NTRAGDHVSGKUSF-AVGNSLFASA-N Leu-Arg-Arg Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O NTRAGDHVSGKUSF-AVGNSLFASA-N 0.000 description 3
- WUFYAPWIHCUMLL-CIUDSAMLSA-N Leu-Asn-Ala Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](C)C(O)=O WUFYAPWIHCUMLL-CIUDSAMLSA-N 0.000 description 3
- NHHKSOGJYNQENP-SRVKXCTJSA-N Leu-Cys-Lys Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CS)C(=O)N[C@@H](CCCCN)C(=O)O)N NHHKSOGJYNQENP-SRVKXCTJSA-N 0.000 description 3
- KAFOIVJDVSZUMD-DCAQKATOSA-N Leu-Gln-Gln Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O KAFOIVJDVSZUMD-DCAQKATOSA-N 0.000 description 3
- KAFOIVJDVSZUMD-UHFFFAOYSA-N Leu-Gln-Gln Natural products CC(C)CC(N)C(=O)NC(CCC(N)=O)C(=O)NC(CCC(N)=O)C(O)=O KAFOIVJDVSZUMD-UHFFFAOYSA-N 0.000 description 3
- PPQRKXHCLYCBSP-IHRRRGAJSA-N Leu-Leu-Met Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)O)N PPQRKXHCLYCBSP-IHRRRGAJSA-N 0.000 description 3
- RXGLHDWAZQECBI-SRVKXCTJSA-N Leu-Leu-Ser Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(O)=O RXGLHDWAZQECBI-SRVKXCTJSA-N 0.000 description 3
- ZGUMORRUBUCXEH-AVGNSLFASA-N Leu-Lys-Gln Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(O)=O ZGUMORRUBUCXEH-AVGNSLFASA-N 0.000 description 3
- VCHVSKNMTXWIIP-SRVKXCTJSA-N Leu-Lys-Ser Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(O)=O VCHVSKNMTXWIIP-SRVKXCTJSA-N 0.000 description 3
- JVTYXRRFZCEPPK-RHYQMDGZSA-N Leu-Met-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(C)C)N)O JVTYXRRFZCEPPK-RHYQMDGZSA-N 0.000 description 3
- IDGZVZJLYFTXSL-DCAQKATOSA-N Leu-Ser-Arg Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CCCN=C(N)N IDGZVZJLYFTXSL-DCAQKATOSA-N 0.000 description 3
- BRTVHXHCUSXYRI-CIUDSAMLSA-N Leu-Ser-Ser Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O BRTVHXHCUSXYRI-CIUDSAMLSA-N 0.000 description 3
- RDFIVFHPOSOXMW-ACRUOGEOSA-N Leu-Tyr-Phe Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O RDFIVFHPOSOXMW-ACRUOGEOSA-N 0.000 description 3
- VUBIPAHVHMZHCM-KKUMJFAQSA-N Leu-Tyr-Ser Chemical compound CC(C)C[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CO)C(O)=O)CC1=CC=C(O)C=C1 VUBIPAHVHMZHCM-KKUMJFAQSA-N 0.000 description 3
- AIMGJYMCTAABEN-GVXVVHGQSA-N Leu-Val-Glu Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O AIMGJYMCTAABEN-GVXVVHGQSA-N 0.000 description 3
- NRQRKMYZONPCTM-CIUDSAMLSA-N Lys-Asp-Ser Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(O)=O NRQRKMYZONPCTM-CIUDSAMLSA-N 0.000 description 3
- NDSNUWJPZKTFAR-DCAQKATOSA-N Lys-Cys-Met Chemical compound CSCC[C@@H](C(O)=O)NC(=O)[C@H](CS)NC(=O)[C@@H](N)CCCCN NDSNUWJPZKTFAR-DCAQKATOSA-N 0.000 description 3
- ITWQLSZTLBKWJM-YUMQZZPRSA-N Lys-Gly-Ala Chemical compound OC(=O)[C@H](C)NC(=O)CNC(=O)[C@@H](N)CCCCN ITWQLSZTLBKWJM-YUMQZZPRSA-N 0.000 description 3
- NCZIQZYZPUPMKY-PPCPHDFISA-N Lys-Ile-Thr Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(O)=O NCZIQZYZPUPMKY-PPCPHDFISA-N 0.000 description 3
- GZGWILAQHOVXTD-DCAQKATOSA-N Lys-Met-Asp Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(O)=O GZGWILAQHOVXTD-DCAQKATOSA-N 0.000 description 3
- AZOFEHCPMBRNFD-BZSNNMDCSA-N Lys-Phe-Lys Chemical compound NCCCC[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(O)=O)CC1=CC=CC=C1 AZOFEHCPMBRNFD-BZSNNMDCSA-N 0.000 description 3
- WGILOYIKJVQUPT-DCAQKATOSA-N Lys-Pro-Asp Chemical compound [H]N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(O)=O)C(O)=O WGILOYIKJVQUPT-DCAQKATOSA-N 0.000 description 3
- JMNRXRPBHFGXQX-GUBZILKMSA-N Lys-Ser-Glu Chemical compound NCCCC[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CCC(O)=O JMNRXRPBHFGXQX-GUBZILKMSA-N 0.000 description 3
- VHTOGMKQXXJOHG-RHYQMDGZSA-N Lys-Thr-Val Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(O)=O VHTOGMKQXXJOHG-RHYQMDGZSA-N 0.000 description 3
- 241000124008 Mammalia Species 0.000 description 3
- QZPXMHVKPHJNTR-DCAQKATOSA-N Met-Leu-Asn Chemical compound CSCC[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(O)=O QZPXMHVKPHJNTR-DCAQKATOSA-N 0.000 description 3
- YLDSJJOGQNEQJK-AVGNSLFASA-N Met-Pro-Leu Chemical compound CSCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(O)=O YLDSJJOGQNEQJK-AVGNSLFASA-N 0.000 description 3
- XMBSYZWANAQXEV-UHFFFAOYSA-N N-alpha-L-glutamyl-L-phenylalanine Natural products OC(=O)CCC(N)C(=O)NC(C(O)=O)CC1=CC=CC=C1 XMBSYZWANAQXEV-UHFFFAOYSA-N 0.000 description 3
- 108091034117 Oligonucleotide Proteins 0.000 description 3
- 102100040557 Osteopontin Human genes 0.000 description 3
- BBDSZDHUCPSYAC-QEJZJMRPSA-N Phe-Ala-Leu Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(O)=O BBDSZDHUCPSYAC-QEJZJMRPSA-N 0.000 description 3
- VUYCNYVLKACHPA-KKUMJFAQSA-N Phe-Asp-His Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC2=CN=CN2)C(=O)O)N VUYCNYVLKACHPA-KKUMJFAQSA-N 0.000 description 3
- NHCKESBLOMHIIE-IRXDYDNUSA-N Phe-Gly-Phe Chemical compound C([C@H](N)C(=O)NCC(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=CC=C1 NHCKESBLOMHIIE-IRXDYDNUSA-N 0.000 description 3
- BIYWZVCPZIFGPY-QWRGUYRKSA-N Phe-Gly-Ser Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)NCC(=O)N[C@@H](CO)C(O)=O BIYWZVCPZIFGPY-QWRGUYRKSA-N 0.000 description 3
- RTUWVJVJSMOGPL-KKUMJFAQSA-N Phe-Met-Glu Chemical compound CSCC[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)O)NC(=O)[C@H](CC1=CC=CC=C1)N RTUWVJVJSMOGPL-KKUMJFAQSA-N 0.000 description 3
- CKJACGQPCPMWIT-UFYCRDLUSA-N Phe-Pro-Phe Chemical compound C([C@H](N)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=CC=C1 CKJACGQPCPMWIT-UFYCRDLUSA-N 0.000 description 3
- BPCLGWHVPVTTFM-QWRGUYRKSA-N Phe-Ser-Gly Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(=O)NCC(O)=O BPCLGWHVPVTTFM-QWRGUYRKSA-N 0.000 description 3
- IAOZOFPONWDXNT-IXOXFDKPSA-N Phe-Ser-Thr Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(O)=O IAOZOFPONWDXNT-IXOXFDKPSA-N 0.000 description 3
- QUUCAHIYARMNBL-FHWLQOOXSA-N Phe-Tyr-Gln Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CC2=CC=C(C=C2)O)C(=O)N[C@@H](CCC(=O)N)C(=O)O)N QUUCAHIYARMNBL-FHWLQOOXSA-N 0.000 description 3
- SJRQWEDYTKYHHL-SLFFLAALSA-N Phe-Tyr-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CC=C(C=C2)O)NC(=O)[C@H](CC3=CC=CC=C3)N)C(=O)O SJRQWEDYTKYHHL-SLFFLAALSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- FYPGHGXAOZTOBO-IHRRRGAJSA-N Pro-Leu-His Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)[C@@H]2CCCN2 FYPGHGXAOZTOBO-IHRRRGAJSA-N 0.000 description 3
- JIWJRKNYLSHONY-KKUMJFAQSA-N Pro-Phe-Glu Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCC(O)=O)C(O)=O JIWJRKNYLSHONY-KKUMJFAQSA-N 0.000 description 3
- BGWKULMLUIUPKY-BQBZGAKWSA-N Pro-Ser-Gly Chemical compound OC(=O)CNC(=O)[C@H](CO)NC(=O)[C@@H]1CCCN1 BGWKULMLUIUPKY-BQBZGAKWSA-N 0.000 description 3
- VBZXFFYOBDLLFE-HSHDSVGOSA-N Pro-Trp-Thr Chemical compound N([C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H]([C@H](O)C)C(O)=O)C(=O)[C@@H]1CCCN1 VBZXFFYOBDLLFE-HSHDSVGOSA-N 0.000 description 3
- 108020004511 Recombinant DNA Proteins 0.000 description 3
- 102000007056 Recombinant Fusion Proteins Human genes 0.000 description 3
- 108010008281 Recombinant Fusion Proteins Proteins 0.000 description 3
- OHKLFYXEOGGGCK-ZLUOBGJFSA-N Ser-Asp-Asn Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O OHKLFYXEOGGGCK-ZLUOBGJFSA-N 0.000 description 3
- INCNPLPRPOYTJI-JBDRJPRFSA-N Ser-Cys-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CS)NC(=O)[C@H](CO)N INCNPLPRPOYTJI-JBDRJPRFSA-N 0.000 description 3
- MPPHJZYXDVDGOF-BWBBJGPYSA-N Ser-Cys-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H](CS)NC(=O)[C@@H](N)CO MPPHJZYXDVDGOF-BWBBJGPYSA-N 0.000 description 3
- FMDHKPRACUXATF-ACZMJKKPSA-N Ser-Gln-Ser Chemical compound OC[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CO)C(O)=O FMDHKPRACUXATF-ACZMJKKPSA-N 0.000 description 3
- UICKAKRRRBTILH-GUBZILKMSA-N Ser-Glu-His Chemical compound C1=C(NC=N1)C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CO)N UICKAKRRRBTILH-GUBZILKMSA-N 0.000 description 3
- UQFYNFTYDHUIMI-WHFBIAKZSA-N Ser-Gly-Ala Chemical compound OC(=O)[C@H](C)NC(=O)CNC(=O)[C@@H](N)CO UQFYNFTYDHUIMI-WHFBIAKZSA-N 0.000 description 3
- CJINPXGSKSZQNE-KBIXCLLPSA-N Ser-Ile-Gln Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCC(N)=O)C(O)=O CJINPXGSKSZQNE-KBIXCLLPSA-N 0.000 description 3
- ZIFYDQAFEMIZII-GUBZILKMSA-N Ser-Leu-Glu Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O ZIFYDQAFEMIZII-GUBZILKMSA-N 0.000 description 3
- KCGIREHVWRXNDH-GARJFASQSA-N Ser-Leu-Pro Chemical compound CC(C)C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CO)N KCGIREHVWRXNDH-GARJFASQSA-N 0.000 description 3
- RWDVVSKYZBNDCO-MELADBBJSA-N Ser-Phe-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CO)N)C(=O)O RWDVVSKYZBNDCO-MELADBBJSA-N 0.000 description 3
- CUXJENOFJXOSOZ-BIIVOSGPSA-N Ser-Ser-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CO)NC(=O)[C@H](CO)N)C(=O)O CUXJENOFJXOSOZ-BIIVOSGPSA-N 0.000 description 3
- SQHKXWODKJDZRC-LKXGYXEUSA-N Ser-Thr-Asn Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(O)=O SQHKXWODKJDZRC-LKXGYXEUSA-N 0.000 description 3
- NADLKBTYNKUJEP-KATARQTJSA-N Ser-Thr-Leu Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(O)=O NADLKBTYNKUJEP-KATARQTJSA-N 0.000 description 3
- BEBVVQPDSHHWQL-NRPADANISA-N Ser-Val-Glu Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O BEBVVQPDSHHWQL-NRPADANISA-N 0.000 description 3
- LGIMRDKGABDMBN-DCAQKATOSA-N Ser-Val-Lys Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CO)N LGIMRDKGABDMBN-DCAQKATOSA-N 0.000 description 3
- HNDMFDBQXYZSRM-IHRRRGAJSA-N Ser-Val-Phe Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O HNDMFDBQXYZSRM-IHRRRGAJSA-N 0.000 description 3
- ANOQEBQWIAYIMV-AEJSXWLSSA-N Ser-Val-Pro Chemical compound CC(C)[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CO)N ANOQEBQWIAYIMV-AEJSXWLSSA-N 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- PXQUBKWZENPDGE-CIQUZCHMSA-N Thr-Ala-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](C)NC(=O)[C@H]([C@@H](C)O)N PXQUBKWZENPDGE-CIQUZCHMSA-N 0.000 description 3
- TZKPNGDGUVREEB-FOHZUACHSA-N Thr-Asn-Gly Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC(N)=O)C(=O)NCC(O)=O TZKPNGDGUVREEB-FOHZUACHSA-N 0.000 description 3
- DHPPWTOLRWYIDS-XKBZYTNZSA-N Thr-Cys-Glu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCC(O)=O)C(O)=O DHPPWTOLRWYIDS-XKBZYTNZSA-N 0.000 description 3
- XFTYVCHLARBHBQ-FOHZUACHSA-N Thr-Gly-Asn Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N[C@@H](CC(N)=O)C(O)=O XFTYVCHLARBHBQ-FOHZUACHSA-N 0.000 description 3
- MEJHFIOYJHTWMK-VOAKCMCISA-N Thr-Leu-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)[C@@H](C)O MEJHFIOYJHTWMK-VOAKCMCISA-N 0.000 description 3
- PCMDGXKXVMBIFP-VEVYYDQMSA-N Thr-Met-Asn Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(O)=O PCMDGXKXVMBIFP-VEVYYDQMSA-N 0.000 description 3
- JMBRNXUOLJFURW-BEAPCOKYSA-N Thr-Phe-Pro Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N2CCC[C@@H]2C(=O)O)N)O JMBRNXUOLJFURW-BEAPCOKYSA-N 0.000 description 3
- OGOYMQWIWHGTGH-KZVJFYERSA-N Thr-Val-Ala Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C)C(O)=O OGOYMQWIWHGTGH-KZVJFYERSA-N 0.000 description 3
- ILUOMMDDGREELW-OSUNSFLBSA-N Thr-Val-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)[C@@H](C)O ILUOMMDDGREELW-OSUNSFLBSA-N 0.000 description 3
- YPBYQWFZAAQMGW-XIRDDKMYSA-N Trp-Lys-Asn Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(=O)N)C(=O)O)N YPBYQWFZAAQMGW-XIRDDKMYSA-N 0.000 description 3
- FBHHJGOJWXHGDO-TUSQITKMSA-N Trp-Trp-Leu Chemical compound C1=CC=C2C(C[C@H](N)C(=O)N[C@@H](CC=3C4=CC=CC=C4NC=3)C(=O)N[C@@H](CC(C)C)C(O)=O)=CNC2=C1 FBHHJGOJWXHGDO-TUSQITKMSA-N 0.000 description 3
- GHUNBABNQPIETG-MELADBBJSA-N Tyr-Cys-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CS)NC(=O)[C@H](CC2=CC=C(C=C2)O)N)C(=O)O GHUNBABNQPIETG-MELADBBJSA-N 0.000 description 3
- CRHFOYCJGVJPLE-AVGNSLFASA-N Tyr-Gln-Asn Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC(=O)N)C(=O)O)N)O CRHFOYCJGVJPLE-AVGNSLFASA-N 0.000 description 3
- CNLKDWSAORJEMW-KWQFWETISA-N Tyr-Gly-Ala Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)NCC(=O)N[C@@H](C)C(O)=O CNLKDWSAORJEMW-KWQFWETISA-N 0.000 description 3
- UPODKYBYUBTWSV-BZSNNMDCSA-N Tyr-Phe-Cys Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CS)C(O)=O)C1=CC=C(O)C=C1 UPODKYBYUBTWSV-BZSNNMDCSA-N 0.000 description 3
- MDXLPNRXCFOBTL-BZSNNMDCSA-N Tyr-Ser-Tyr Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O MDXLPNRXCFOBTL-BZSNNMDCSA-N 0.000 description 3
- IRLYZKKNBFPQBW-XGEHTFHBSA-N Val-Cys-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CS)NC(=O)[C@H](C(C)C)N)O IRLYZKKNBFPQBW-XGEHTFHBSA-N 0.000 description 3
- FXVDGDZRYLFQKY-WPRPVWTQSA-N Val-Gly-Met Chemical compound CSCC[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)C(C)C FXVDGDZRYLFQKY-WPRPVWTQSA-N 0.000 description 3
- FEXILLGKGGTLRI-NHCYSSNCSA-N Val-Leu-Asn Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)[C@H](C(C)C)N FEXILLGKGGTLRI-NHCYSSNCSA-N 0.000 description 3
- MJFSRZZJQWZHFQ-SRVKXCTJSA-N Val-Met-Val Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCSC)C(=O)N[C@@H](C(C)C)C(=O)O)N MJFSRZZJQWZHFQ-SRVKXCTJSA-N 0.000 description 3
- YQMILNREHKTFBS-IHRRRGAJSA-N Val-Phe-Cys Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CS)C(=O)O)N YQMILNREHKTFBS-IHRRRGAJSA-N 0.000 description 3
- VHIZXDZMTDVFGX-DCAQKATOSA-N Val-Ser-Leu Chemical compound CC(C)C[C@@H](C(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](C(C)C)N VHIZXDZMTDVFGX-DCAQKATOSA-N 0.000 description 3
- QTPQHINADBYBNA-DCAQKATOSA-N Val-Ser-Lys Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CCCCN QTPQHINADBYBNA-DCAQKATOSA-N 0.000 description 3
- WBPFYNYTYASCQP-CYDGBPFRSA-N Val-Val-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](C(C)C)N WBPFYNYTYASCQP-CYDGBPFRSA-N 0.000 description 3
- 238000010171 animal model Methods 0.000 description 3
- 108010092854 aspartyllysine Proteins 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 108091008324 binding proteins Proteins 0.000 description 3
- 210000004369 blood Anatomy 0.000 description 3
- 239000008280 blood Substances 0.000 description 3
- 230000036770 blood supply Effects 0.000 description 3
- 230000037396 body weight Effects 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 230000003185 calcium uptake Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000004587 chromatography analysis Methods 0.000 description 3
- 238000010367 cloning Methods 0.000 description 3
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 230000002255 enzymatic effect Effects 0.000 description 3
- 210000003527 eukaryotic cell Anatomy 0.000 description 3
- 238000010353 genetic engineering Methods 0.000 description 3
- 108010010147 glycylglutamine Proteins 0.000 description 3
- 108010081551 glycylphenylalanine Proteins 0.000 description 3
- 230000036541 health Effects 0.000 description 3
- 230000004217 heart function Effects 0.000 description 3
- 108010018006 histidylserine Proteins 0.000 description 3
- 229940027941 immunoglobulin g Drugs 0.000 description 3
- 238000005462 in vivo assay Methods 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 238000001990 intravenous administration Methods 0.000 description 3
- 238000002955 isolation Methods 0.000 description 3
- 210000003292 kidney cell Anatomy 0.000 description 3
- 239000003446 ligand Substances 0.000 description 3
- 108010054155 lysyllysine Proteins 0.000 description 3
- 108010038320 lysylphenylalanine Proteins 0.000 description 3
- 238000006384 oligomerization reaction Methods 0.000 description 3
- 108010029020 prolylglycine Proteins 0.000 description 3
- 230000002797 proteolythic effect Effects 0.000 description 3
- 238000002741 site-directed mutagenesis Methods 0.000 description 3
- 210000001519 tissue Anatomy 0.000 description 3
- 230000002792 vascular Effects 0.000 description 3
- NFGXHKASABOEEW-UHFFFAOYSA-N 1-methylethyl 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate Chemical compound COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C NFGXHKASABOEEW-UHFFFAOYSA-N 0.000 description 2
- XWTNPSHCJMZAHQ-QMMMGPOBSA-N 2-[[2-[[2-[[(2s)-2-amino-4-methylpentanoyl]amino]acetyl]amino]acetyl]amino]acetic acid Chemical compound CC(C)C[C@H](N)C(=O)NCC(=O)NCC(=O)NCC(O)=O XWTNPSHCJMZAHQ-QMMMGPOBSA-N 0.000 description 2
- BTYTYHBSJKQBQA-GCJQMDKQSA-N Ala-Asp-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](C)N)O BTYTYHBSJKQBQA-GCJQMDKQSA-N 0.000 description 2
- NWVVKQZOVSTDBQ-CIUDSAMLSA-N Ala-Glu-Arg Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O NWVVKQZOVSTDBQ-CIUDSAMLSA-N 0.000 description 2
- MEFILNJXAVSUTO-JXUBOQSCSA-N Ala-Leu-Thr Chemical compound C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O MEFILNJXAVSUTO-JXUBOQSCSA-N 0.000 description 2
- DCVYRWFAMZFSDA-ZLUOBGJFSA-N Ala-Ser-Ala Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(O)=O DCVYRWFAMZFSDA-ZLUOBGJFSA-N 0.000 description 2
- NZGRHTKZFSVPAN-BIIVOSGPSA-N Ala-Ser-Pro Chemical compound C[C@@H](C(=O)N[C@@H](CO)C(=O)N1CCC[C@@H]1C(=O)O)N NZGRHTKZFSVPAN-BIIVOSGPSA-N 0.000 description 2
- NCQMBSJGJMYKCK-ZLUOBGJFSA-N Ala-Ser-Ser Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O NCQMBSJGJMYKCK-ZLUOBGJFSA-N 0.000 description 2
- WQKAQKZRDIZYNV-VZFHVOOUSA-N Ala-Ser-Thr Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(O)=O WQKAQKZRDIZYNV-VZFHVOOUSA-N 0.000 description 2
- SYIFFFHSXBNPMC-UWJYBYFXSA-N Ala-Ser-Tyr Chemical compound C[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O)N SYIFFFHSXBNPMC-UWJYBYFXSA-N 0.000 description 2
- 108010088751 Albumins Proteins 0.000 description 2
- 102000009027 Albumins Human genes 0.000 description 2
- 241001156002 Anthonomus pomorum Species 0.000 description 2
- 108010032595 Antibody Binding Sites Proteins 0.000 description 2
- IASNWHAGGYTEKX-IUCAKERBSA-N Arg-Arg-Gly Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCC(O)=O IASNWHAGGYTEKX-IUCAKERBSA-N 0.000 description 2
- CPSHGRGUPZBMOK-CIUDSAMLSA-N Arg-Asn-Gln Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O CPSHGRGUPZBMOK-CIUDSAMLSA-N 0.000 description 2
- UAOSDDXCTBIPCA-QXEWZRGKSA-N Arg-Ile-Gly Chemical compound CC[C@H](C)[C@@H](C(=O)NCC(=O)O)NC(=O)[C@H](CCCN=C(N)N)N UAOSDDXCTBIPCA-QXEWZRGKSA-N 0.000 description 2
- HGKHPCFTRQDHCU-IUCAKERBSA-N Arg-Pro-Gly Chemical compound NC(N)=NCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)NCC(O)=O HGKHPCFTRQDHCU-IUCAKERBSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- AYZAWXAPBAYCHO-CIUDSAMLSA-N Asn-Asn-His Chemical compound C1=C(NC=N1)C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CC(=O)N)N AYZAWXAPBAYCHO-CIUDSAMLSA-N 0.000 description 2
- BVLIJXXSXBUGEC-SRVKXCTJSA-N Asn-Asn-Tyr Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O BVLIJXXSXBUGEC-SRVKXCTJSA-N 0.000 description 2
- QNJIRRVTOXNGMH-GUBZILKMSA-N Asn-Gln-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)CC(N)=O QNJIRRVTOXNGMH-GUBZILKMSA-N 0.000 description 2
- DXVMJJNAOVECBA-WHFBIAKZSA-N Asn-Gly-Asn Chemical compound NC(=O)C[C@H](N)C(=O)NCC(=O)N[C@@H](CC(N)=O)C(O)=O DXVMJJNAOVECBA-WHFBIAKZSA-N 0.000 description 2
- MDDXKBHIMYYJLW-FXQIFTODSA-N Asn-Met-Asp Chemical compound CSCC[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)O)NC(=O)[C@H](CC(=O)N)N MDDXKBHIMYYJLW-FXQIFTODSA-N 0.000 description 2
- VCJCPARXDBEGNE-GUBZILKMSA-N Asn-Pro-Pro Chemical compound NC(=O)C[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1[C@H](C(O)=O)CCC1 VCJCPARXDBEGNE-GUBZILKMSA-N 0.000 description 2
- HPBNLFLSSQDFQW-WHFBIAKZSA-N Asn-Ser-Gly Chemical compound NC(=O)C[C@H](N)C(=O)N[C@@H](CO)C(=O)NCC(O)=O HPBNLFLSSQDFQW-WHFBIAKZSA-N 0.000 description 2
- QYRMBFWDSFGSFC-OLHMAJIHSA-N Asn-Thr-Asn Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)[C@H](CC(=O)N)N)O QYRMBFWDSFGSFC-OLHMAJIHSA-N 0.000 description 2
- JZLFYAAGGYMRIK-BYULHYEWSA-N Asn-Val-Asp Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(O)=O JZLFYAAGGYMRIK-BYULHYEWSA-N 0.000 description 2
- KRXIWXCXOARFNT-ZLUOBGJFSA-N Asp-Ala-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC(O)=O KRXIWXCXOARFNT-ZLUOBGJFSA-N 0.000 description 2
- HMQDRBKQMLRCCG-GMOBBJLQSA-N Asp-Arg-Ile Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O HMQDRBKQMLRCCG-GMOBBJLQSA-N 0.000 description 2
- NYQHSUGFEWDWPD-ACZMJKKPSA-N Asp-Gln-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CC(=O)O)N NYQHSUGFEWDWPD-ACZMJKKPSA-N 0.000 description 2
- HSWYMWGDMPLTTH-FXQIFTODSA-N Asp-Glu-Gln Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O HSWYMWGDMPLTTH-FXQIFTODSA-N 0.000 description 2
- PZXPWHFYZXTFBI-YUMQZZPRSA-N Asp-Gly-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)CC(O)=O PZXPWHFYZXTFBI-YUMQZZPRSA-N 0.000 description 2
- ICZWAZVKLACMKR-CIUDSAMLSA-N Asp-His-Ser Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CO)C(O)=O)CC1=CN=CN1 ICZWAZVKLACMKR-CIUDSAMLSA-N 0.000 description 2
- KYQNAIMCTRZLNP-QSFUFRPTSA-N Asp-Ile-Val Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C(C)C)C(O)=O KYQNAIMCTRZLNP-QSFUFRPTSA-N 0.000 description 2
- JSHWXQIZOCVWIA-ZKWXMUAHSA-N Asp-Ser-Val Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(O)=O JSHWXQIZOCVWIA-ZKWXMUAHSA-N 0.000 description 2
- HTSSXFASOUSJQG-IHPCNDPISA-N Asp-Tyr-Trp Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O HTSSXFASOUSJQG-IHPCNDPISA-N 0.000 description 2
- ALMIMUZAWTUNIO-BZSNNMDCSA-N Asp-Tyr-Tyr Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O ALMIMUZAWTUNIO-BZSNNMDCSA-N 0.000 description 2
- GIKOVDMXBAFXDF-NHCYSSNCSA-N Asp-Val-Leu Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(O)=O GIKOVDMXBAFXDF-NHCYSSNCSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 208000024172 Cardiovascular disease Diseases 0.000 description 2
- 108091006146 Channels Proteins 0.000 description 2
- 241000699802 Cricetulus griseus Species 0.000 description 2
- VTJLJQGUMBWHBP-GUBZILKMSA-N Cys-His-Gln Chemical compound C1=C(NC=N1)C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](CS)N VTJLJQGUMBWHBP-GUBZILKMSA-N 0.000 description 2
- SMEYEQDCCBHTEF-FXQIFTODSA-N Cys-Pro-Ala Chemical compound [H]N[C@@H](CS)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(O)=O SMEYEQDCCBHTEF-FXQIFTODSA-N 0.000 description 2
- KSMSFCBQBQPFAD-GUBZILKMSA-N Cys-Pro-Pro Chemical compound SC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1[C@H](C(O)=O)CCC1 KSMSFCBQBQPFAD-GUBZILKMSA-N 0.000 description 2
- CMYVIUWVYHOLRD-ZLUOBGJFSA-N Cys-Ser-Ala Chemical compound [H]N[C@@H](CS)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(O)=O CMYVIUWVYHOLRD-ZLUOBGJFSA-N 0.000 description 2
- NDNZRWUDUMTITL-FXQIFTODSA-N Cys-Ser-Val Chemical compound [H]N[C@@H](CS)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(O)=O NDNZRWUDUMTITL-FXQIFTODSA-N 0.000 description 2
- IRDBEBCCTCNXGZ-AVGNSLFASA-N Cys-Tyr-Gln Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](CS)N)O IRDBEBCCTCNXGZ-AVGNSLFASA-N 0.000 description 2
- NGOIQDYZMIKCOK-NAKRPEOUSA-N Cys-Val-Ile Chemical compound [H]N[C@@H](CS)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O NGOIQDYZMIKCOK-NAKRPEOUSA-N 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 241000206602 Eukaryota Species 0.000 description 2
- 102000016359 Fibronectins Human genes 0.000 description 2
- 108010067306 Fibronectins Proteins 0.000 description 2
- 108091006027 G proteins Proteins 0.000 description 2
- XOKGKOQWADCLFQ-GARJFASQSA-N Gln-Arg-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCC(=O)N)N)C(=O)O XOKGKOQWADCLFQ-GARJFASQSA-N 0.000 description 2
- WMOMPXKOKASNBK-PEFMBERDSA-N Gln-Asn-Ile Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O WMOMPXKOKASNBK-PEFMBERDSA-N 0.000 description 2
- MADFVRSKEIEZHZ-DCAQKATOSA-N Gln-Gln-Lys Chemical compound C(CCN)C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CCC(=O)N)N MADFVRSKEIEZHZ-DCAQKATOSA-N 0.000 description 2
- ICDIMQAMJGDHSE-GUBZILKMSA-N Gln-His-Ser Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CO)C(O)=O ICDIMQAMJGDHSE-GUBZILKMSA-N 0.000 description 2
- FFVXLVGUJBCKRX-UKJIMTQDSA-N Gln-Ile-Val Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](C(C)C)C(=O)O)NC(=O)[C@H](CCC(=O)N)N FFVXLVGUJBCKRX-UKJIMTQDSA-N 0.000 description 2
- FNAJNWPDTIXYJN-CIUDSAMLSA-N Gln-Pro-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCC(N)=O FNAJNWPDTIXYJN-CIUDSAMLSA-N 0.000 description 2
- OSCLNNWLKKIQJM-WDSKDSINSA-N Gln-Ser-Gly Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CO)C(=O)NCC(O)=O OSCLNNWLKKIQJM-WDSKDSINSA-N 0.000 description 2
- RDPOETHPAQEGDP-ACZMJKKPSA-N Glu-Asp-Ala Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(O)=O RDPOETHPAQEGDP-ACZMJKKPSA-N 0.000 description 2
- PAQUJCSYVIBPLC-AVGNSLFASA-N Glu-Asp-Phe Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 PAQUJCSYVIBPLC-AVGNSLFASA-N 0.000 description 2
- WATXSTJXNBOHKD-LAEOZQHASA-N Glu-Asp-Val Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(O)=O WATXSTJXNBOHKD-LAEOZQHASA-N 0.000 description 2
- RFDHKPSHTXZKLL-IHRRRGAJSA-N Glu-Gln-Phe Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CCC(=O)O)N RFDHKPSHTXZKLL-IHRRRGAJSA-N 0.000 description 2
- JWNZHMSRZXXGTM-XKBZYTNZSA-N Glu-Ser-Thr Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(O)=O JWNZHMSRZXXGTM-XKBZYTNZSA-N 0.000 description 2
- ZYRXTRTUCAVNBQ-GVXVVHGQSA-N Glu-Val-Lys Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CCC(=O)O)N ZYRXTRTUCAVNBQ-GVXVVHGQSA-N 0.000 description 2
- WGYHAAXZWPEBDQ-IFFSRLJSSA-N Glu-Val-Thr Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O WGYHAAXZWPEBDQ-IFFSRLJSSA-N 0.000 description 2
- QSDKBRMVXSWAQE-BFHQHQDPSA-N Gly-Ala-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)CN QSDKBRMVXSWAQE-BFHQHQDPSA-N 0.000 description 2
- XCLCVBYNGXEVDU-WHFBIAKZSA-N Gly-Asn-Ser Chemical compound NCC(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(O)=O XCLCVBYNGXEVDU-WHFBIAKZSA-N 0.000 description 2
- DGKBSGNCMCLDSL-BYULHYEWSA-N Gly-Ile-Asn Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)CN DGKBSGNCMCLDSL-BYULHYEWSA-N 0.000 description 2
- FXGRXIATVXUAHO-WEDXCCLWSA-N Gly-Lys-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)CN)CCCCN FXGRXIATVXUAHO-WEDXCCLWSA-N 0.000 description 2
- JSLVAHYTAJJEQH-QWRGUYRKSA-N Gly-Ser-Phe Chemical compound NCC(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 JSLVAHYTAJJEQH-QWRGUYRKSA-N 0.000 description 2
- RHRLHXQWHCNJKR-PMVVWTBXSA-N Gly-Thr-His Chemical compound NCC(=O)N[C@@H]([C@H](O)C)C(=O)N[C@H](C(O)=O)CC1=CN=CN1 RHRLHXQWHCNJKR-PMVVWTBXSA-N 0.000 description 2
- HUFUVTYGPOUCBN-MBLNEYKQSA-N Gly-Thr-Ile Chemical compound [H]NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O HUFUVTYGPOUCBN-MBLNEYKQSA-N 0.000 description 2
- TVTZEOHWHUVYCG-KYNKHSRBSA-N Gly-Thr-Thr Chemical compound [H]NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O TVTZEOHWHUVYCG-KYNKHSRBSA-N 0.000 description 2
- OCRQUYDOYKCOQG-IRXDYDNUSA-N Gly-Tyr-Phe Chemical compound C([C@H](NC(=O)CN)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=C(O)C=C1 OCRQUYDOYKCOQG-IRXDYDNUSA-N 0.000 description 2
- DNAZKGFYFRGZIH-QWRGUYRKSA-N Gly-Tyr-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)CN)CC1=CC=C(O)C=C1 DNAZKGFYFRGZIH-QWRGUYRKSA-N 0.000 description 2
- NGBGZCUWFVVJKC-IRXDYDNUSA-N Gly-Tyr-Tyr Chemical compound C([C@H](NC(=O)CN)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(O)=O)C1=CC=C(O)C=C1 NGBGZCUWFVVJKC-IRXDYDNUSA-N 0.000 description 2
- SYOJVRNQCXYEOV-XVKPBYJWSA-N Gly-Val-Glu Chemical compound [H]NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O SYOJVRNQCXYEOV-XVKPBYJWSA-N 0.000 description 2
- RYAOJUMWLWUGNW-QMMMGPOBSA-N Gly-Val-Gly Chemical compound NCC(=O)N[C@@H](C(C)C)C(=O)NCC(O)=O RYAOJUMWLWUGNW-QMMMGPOBSA-N 0.000 description 2
- FULZDMOZUZKGQU-ONGXEEELSA-N Gly-Val-His Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)CN FULZDMOZUZKGQU-ONGXEEELSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- NELVFWFDOKRTOR-SDDRHHMPSA-N His-Gln-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CC2=CN=CN2)N)C(=O)O NELVFWFDOKRTOR-SDDRHHMPSA-N 0.000 description 2
- TTYKEFZRLKQTHH-MELADBBJSA-N His-Lys-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CCCCN)NC(=O)[C@H](CC2=CN=CN2)N)C(=O)O TTYKEFZRLKQTHH-MELADBBJSA-N 0.000 description 2
- TVMNTHXFRSXZGR-IHRRRGAJSA-N His-Lys-Val Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(O)=O TVMNTHXFRSXZGR-IHRRRGAJSA-N 0.000 description 2
- KDDKJKKQODQQBR-NHCYSSNCSA-N His-Val-Asp Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)O)NC(=O)[C@H](CC1=CN=CN1)N KDDKJKKQODQQBR-NHCYSSNCSA-N 0.000 description 2
- RMNMUUCYTMLWNA-ZPFDUUQYSA-N Ile-Lys-Asp Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(=O)O)C(=O)O)N RMNMUUCYTMLWNA-ZPFDUUQYSA-N 0.000 description 2
- NXRNRBOKDBIVKQ-CXTHYWKRSA-N Ile-Tyr-Tyr Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](CC2=CC=C(C=C2)O)C(=O)O)N NXRNRBOKDBIVKQ-CXTHYWKRSA-N 0.000 description 2
- 235000003332 Ilex aquifolium Nutrition 0.000 description 2
- 241000209027 Ilex aquifolium Species 0.000 description 2
- 108010091135 Immunoglobulin Fc Fragments Proteins 0.000 description 2
- IBMVEYRWAWIOTN-UHFFFAOYSA-N L-Leucyl-L-Arginyl-L-Proline Natural products CC(C)CC(N)C(=O)NC(CCCN=C(N)N)C(=O)N1CCCC1C(O)=O IBMVEYRWAWIOTN-UHFFFAOYSA-N 0.000 description 2
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 2
- HXWALXSAVBLTPK-NUTKFTJISA-N Leu-Ala-Trp Chemical compound C[C@@H](C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)O)NC(=O)[C@H](CC(C)C)N HXWALXSAVBLTPK-NUTKFTJISA-N 0.000 description 2
- USTCFDAQCLDPBD-XIRDDKMYSA-N Leu-Asn-Trp Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)O)N USTCFDAQCLDPBD-XIRDDKMYSA-N 0.000 description 2
- CQGSYZCULZMEDE-UHFFFAOYSA-N Leu-Gln-Pro Natural products CC(C)CC(N)C(=O)NC(CCC(N)=O)C(=O)N1CCCC1C(O)=O CQGSYZCULZMEDE-UHFFFAOYSA-N 0.000 description 2
- XOWMDXHFSBCAKQ-SRVKXCTJSA-N Leu-Ser-Leu Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CC(C)C XOWMDXHFSBCAKQ-SRVKXCTJSA-N 0.000 description 2
- PPGBXYKMUMHFBF-KATARQTJSA-N Leu-Ser-Thr Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(O)=O PPGBXYKMUMHFBF-KATARQTJSA-N 0.000 description 2
- FBNPMTNBFFAMMH-UHFFFAOYSA-N Leu-Val-Arg Natural products CC(C)CC(N)C(=O)NC(C(C)C)C(=O)NC(C(O)=O)CCCN=C(N)N FBNPMTNBFFAMMH-UHFFFAOYSA-N 0.000 description 2
- 102000019298 Lipocalin Human genes 0.000 description 2
- 108050006654 Lipocalin Proteins 0.000 description 2
- LMVOVCYVZBBWQB-SRVKXCTJSA-N Lys-Asp-Lys Chemical compound NCCCC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(O)=O)CCCCN LMVOVCYVZBBWQB-SRVKXCTJSA-N 0.000 description 2
- NTBFKPBULZGXQL-KKUMJFAQSA-N Lys-Asp-Tyr Chemical compound NCCCC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 NTBFKPBULZGXQL-KKUMJFAQSA-N 0.000 description 2
- RFQATBGBLDAKGI-VHSXEESVSA-N Lys-Gly-Pro Chemical compound C1C[C@@H](N(C1)C(=O)CNC(=O)[C@H](CCCCN)N)C(=O)O RFQATBGBLDAKGI-VHSXEESVSA-N 0.000 description 2
- MYZMQWHPDAYKIE-SRVKXCTJSA-N Lys-Leu-Ala Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(O)=O MYZMQWHPDAYKIE-SRVKXCTJSA-N 0.000 description 2
- AIRZWUMAHCDDHR-KKUMJFAQSA-N Lys-Leu-Leu Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(O)=O AIRZWUMAHCDDHR-KKUMJFAQSA-N 0.000 description 2
- YTJFXEDRUOQGSP-DCAQKATOSA-N Lys-Pro-Ser Chemical compound [H]N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(O)=O YTJFXEDRUOQGSP-DCAQKATOSA-N 0.000 description 2
- TVOOGUNBIWAURO-KATARQTJSA-N Lys-Thr-Cys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CCCCN)N)O TVOOGUNBIWAURO-KATARQTJSA-N 0.000 description 2
- QLFAPXUXEBAWEK-NHCYSSNCSA-N Lys-Val-Asp Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(O)=O QLFAPXUXEBAWEK-NHCYSSNCSA-N 0.000 description 2
- UGCIQUYEJIEHKX-GVXVVHGQSA-N Lys-Val-Glu Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O UGCIQUYEJIEHKX-GVXVVHGQSA-N 0.000 description 2
- 241000282560 Macaca mulatta Species 0.000 description 2
- UYAKZHGIPRCGPF-CIUDSAMLSA-N Met-Glu-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCSC)N UYAKZHGIPRCGPF-CIUDSAMLSA-N 0.000 description 2
- BCRQJDMZQUHQSV-STQMWFEESA-N Met-Gly-Tyr Chemical compound [H]N[C@@H](CCSC)C(=O)NCC(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O BCRQJDMZQUHQSV-STQMWFEESA-N 0.000 description 2
- FGAMAYQCWQCUNF-DCAQKATOSA-N Met-His-Asn Chemical compound CSCC[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N[C@@H](CC(=O)N)C(=O)O)N FGAMAYQCWQCUNF-DCAQKATOSA-N 0.000 description 2
- AUEJLPRZGVVDNU-UHFFFAOYSA-N N-L-tyrosyl-L-leucine Natural products CC(C)CC(C(O)=O)NC(=O)C(N)CC1=CC=C(O)C=C1 AUEJLPRZGVVDNU-UHFFFAOYSA-N 0.000 description 2
- 108090000526 Papain Proteins 0.000 description 2
- 102000057297 Pepsin A Human genes 0.000 description 2
- 108090000284 Pepsin A Proteins 0.000 description 2
- 108091093037 Peptide nucleic acid Proteins 0.000 description 2
- OPEVYHFJXLCCRT-AVGNSLFASA-N Phe-Gln-Ser Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CO)C(O)=O OPEVYHFJXLCCRT-AVGNSLFASA-N 0.000 description 2
- JJHVFCUWLSKADD-ONGXEEELSA-N Phe-Gly-Ala Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)NCC(=O)N[C@@H](C)C(O)=O JJHVFCUWLSKADD-ONGXEEELSA-N 0.000 description 2
- RFEXGCASCQGGHZ-STQMWFEESA-N Phe-Gly-Arg Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(O)=O RFEXGCASCQGGHZ-STQMWFEESA-N 0.000 description 2
- NAXPHWZXEXNDIW-JTQLQIEISA-N Phe-Gly-Gly Chemical compound OC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=CC=C1 NAXPHWZXEXNDIW-JTQLQIEISA-N 0.000 description 2
- LRBSWBVUCLLRLU-BZSNNMDCSA-N Phe-Leu-Lys Chemical compound CC(C)C[C@H](NC(=O)[C@@H](N)Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(O)=O LRBSWBVUCLLRLU-BZSNNMDCSA-N 0.000 description 2
- KAJLHCWRWDSROH-BZSNNMDCSA-N Phe-Phe-Asp Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC(O)=O)C(O)=O)C1=CC=CC=C1 KAJLHCWRWDSROH-BZSNNMDCSA-N 0.000 description 2
- QARPMYDMYVLFMW-KKUMJFAQSA-N Phe-Pro-Glu Chemical compound C([C@H](N)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCC(O)=O)C(O)=O)C1=CC=CC=C1 QARPMYDMYVLFMW-KKUMJFAQSA-N 0.000 description 2
- UNBFGVQVQGXXCK-KKUMJFAQSA-N Phe-Ser-Leu Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(O)=O UNBFGVQVQGXXCK-KKUMJFAQSA-N 0.000 description 2
- JHSRGEODDALISP-XVSYOHENSA-N Phe-Thr-Asn Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(O)=O JHSRGEODDALISP-XVSYOHENSA-N 0.000 description 2
- GNRMAQSIROFNMI-IXOXFDKPSA-N Phe-Thr-Ser Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(O)=O GNRMAQSIROFNMI-IXOXFDKPSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- VXCHGLYSIOOZIS-GUBZILKMSA-N Pro-Ala-Arg Chemical compound NC(N)=NCCC[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1 VXCHGLYSIOOZIS-GUBZILKMSA-N 0.000 description 2
- ZCXQTRXYZOSGJR-FXQIFTODSA-N Pro-Asp-Ser Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(O)=O ZCXQTRXYZOSGJR-FXQIFTODSA-N 0.000 description 2
- HQVPQXMCQKXARZ-FXQIFTODSA-N Pro-Cys-Ser Chemical compound C1C[C@H](NC1)C(=O)N[C@@H](CS)C(=O)N[C@@H](CO)C(=O)O HQVPQXMCQKXARZ-FXQIFTODSA-N 0.000 description 2
- HJSCRFZVGXAGNG-SRVKXCTJSA-N Pro-Gln-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]1CCCN1 HJSCRFZVGXAGNG-SRVKXCTJSA-N 0.000 description 2
- FMLRRBDLBJLJIK-DCAQKATOSA-N Pro-Leu-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1 FMLRRBDLBJLJIK-DCAQKATOSA-N 0.000 description 2
- VTFXTWDFPTWNJY-RHYQMDGZSA-N Pro-Leu-Thr Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O VTFXTWDFPTWNJY-RHYQMDGZSA-N 0.000 description 2
- SUENWIFTSTWUKD-AVGNSLFASA-N Pro-Leu-Val Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(O)=O SUENWIFTSTWUKD-AVGNSLFASA-N 0.000 description 2
- RMODQFBNDDENCP-IHRRRGAJSA-N Pro-Lys-Leu Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(O)=O RMODQFBNDDENCP-IHRRRGAJSA-N 0.000 description 2
- RCYUBVHMVUHEBM-RCWTZXSCSA-N Pro-Pro-Thr Chemical compound [H]N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H]([C@@H](C)O)C(O)=O RCYUBVHMVUHEBM-RCWTZXSCSA-N 0.000 description 2
- PRKWBYCXBBSLSK-GUBZILKMSA-N Pro-Ser-Val Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(O)=O PRKWBYCXBBSLSK-GUBZILKMSA-N 0.000 description 2
- YDTUEBLEAVANFH-RCWTZXSCSA-N Pro-Val-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H]1CCCN1 YDTUEBLEAVANFH-RCWTZXSCSA-N 0.000 description 2
- 239000004365 Protease Substances 0.000 description 2
- 108010076504 Protein Sorting Signals Proteins 0.000 description 2
- 108010007127 Pulmonary Surfactant-Associated Protein D Proteins 0.000 description 2
- 102100027845 Pulmonary surfactant-associated protein D Human genes 0.000 description 2
- IDQFQFVEWMWRQQ-DLOVCJGASA-N Ser-Ala-Phe Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O IDQFQFVEWMWRQQ-DLOVCJGASA-N 0.000 description 2
- UGJRQLURDVGULT-LKXGYXEUSA-N Ser-Asn-Thr Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O UGJRQLURDVGULT-LKXGYXEUSA-N 0.000 description 2
- PJIQEIFXZPCWOJ-FXQIFTODSA-N Ser-Pro-Asp Chemical compound [H]N[C@@H](CO)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(O)=O)C(O)=O PJIQEIFXZPCWOJ-FXQIFTODSA-N 0.000 description 2
- NVNPWELENFJOHH-CIUDSAMLSA-N Ser-Ser-His Chemical compound C1=C(NC=N1)C[C@@H](C(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](CO)N NVNPWELENFJOHH-CIUDSAMLSA-N 0.000 description 2
- PYTKULIABVRXSC-BWBBJGPYSA-N Ser-Ser-Thr Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(O)=O PYTKULIABVRXSC-BWBBJGPYSA-N 0.000 description 2
- SNXUIBACCONSOH-BWBBJGPYSA-N Ser-Thr-Ser Chemical compound OC[C@H](N)C(=O)N[C@@H]([C@H](O)C)C(=O)N[C@@H](CO)C(O)=O SNXUIBACCONSOH-BWBBJGPYSA-N 0.000 description 2
- 101150052859 Slc9a1 gene Proteins 0.000 description 2
- DGDCHPCRMWEOJR-FQPOAREZSA-N Thr-Ala-Tyr Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 DGDCHPCRMWEOJR-FQPOAREZSA-N 0.000 description 2
- PKXHGEXFMIZSER-QTKMDUPCSA-N Thr-Arg-His Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)N)O PKXHGEXFMIZSER-QTKMDUPCSA-N 0.000 description 2
- SKHPKKYKDYULDH-HJGDQZAQSA-N Thr-Asn-Leu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(O)=O SKHPKKYKDYULDH-HJGDQZAQSA-N 0.000 description 2
- VXMHQKHDKCATDV-VEVYYDQMSA-N Thr-Asp-Arg Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O VXMHQKHDKCATDV-VEVYYDQMSA-N 0.000 description 2
- KBBRNEDOYWMIJP-KYNKHSRBSA-N Thr-Gly-Thr Chemical compound C[C@H]([C@@H](C(=O)NCC(=O)N[C@@H]([C@@H](C)O)C(=O)O)N)O KBBRNEDOYWMIJP-KYNKHSRBSA-N 0.000 description 2
- UDNVOQMPQBEITB-MEYUZBJRSA-N Thr-His-Phe Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O UDNVOQMPQBEITB-MEYUZBJRSA-N 0.000 description 2
- AMXMBCAXAZUCFA-RHYQMDGZSA-N Thr-Leu-Arg Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O AMXMBCAXAZUCFA-RHYQMDGZSA-N 0.000 description 2
- KPNSNVTUVKSBFL-ZJDVBMNYSA-N Thr-Met-Thr Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCSC)C(=O)N[C@@H]([C@@H](C)O)C(=O)O)N)O KPNSNVTUVKSBFL-ZJDVBMNYSA-N 0.000 description 2
- IQPWNQRRAJHOKV-KATARQTJSA-N Thr-Ser-Lys Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CCCCN IQPWNQRRAJHOKV-KATARQTJSA-N 0.000 description 2
- HUPLKEHTTQBXSC-YJRXYDGGSA-N Thr-Ser-Tyr Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 HUPLKEHTTQBXSC-YJRXYDGGSA-N 0.000 description 2
- BBPCSGKKPJUYRB-UVOCVTCTSA-N Thr-Thr-Leu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(O)=O BBPCSGKKPJUYRB-UVOCVTCTSA-N 0.000 description 2
- KVEWWQRTAVMOFT-KJEVXHAQSA-N Thr-Tyr-Val Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](C(C)C)C(O)=O KVEWWQRTAVMOFT-KJEVXHAQSA-N 0.000 description 2
- MKDXQPMIQPTTAW-SIXJUCDHSA-N Trp-Ile-His Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)[C@H](CC2=CNC3=CC=CC=C32)N MKDXQPMIQPTTAW-SIXJUCDHSA-N 0.000 description 2
- UOXPLPBMEPLZBW-WDSOQIARSA-N Trp-Val-Lys Chemical compound C1=CC=C2C(C[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(O)=O)=CNC2=C1 UOXPLPBMEPLZBW-WDSOQIARSA-N 0.000 description 2
- 102000011016 Type 5 Cyclic Nucleotide Phosphodiesterases Human genes 0.000 description 2
- 108010037581 Type 5 Cyclic Nucleotide Phosphodiesterases Proteins 0.000 description 2
- LGEYOIQBBIPHQN-UWJYBYFXSA-N Tyr-Ala-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 LGEYOIQBBIPHQN-UWJYBYFXSA-N 0.000 description 2
- AKXBNSZMYAOGLS-STQMWFEESA-N Tyr-Arg-Gly Chemical compound NC(N)=NCCC[C@@H](C(=O)NCC(O)=O)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 AKXBNSZMYAOGLS-STQMWFEESA-N 0.000 description 2
- PEVVXUGSAKEPEN-AVGNSLFASA-N Tyr-Asn-Glu Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(O)=O PEVVXUGSAKEPEN-AVGNSLFASA-N 0.000 description 2
- UABYBEBXFFNCIR-YDHLFZDLSA-N Tyr-Asp-Val Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(O)=O UABYBEBXFFNCIR-YDHLFZDLSA-N 0.000 description 2
- OLWFDNLLBWQWCP-STQMWFEESA-N Tyr-Gly-Met Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)NCC(=O)N[C@@H](CCSC)C(O)=O OLWFDNLLBWQWCP-STQMWFEESA-N 0.000 description 2
- OSXNCKRGMSHWSQ-ACRUOGEOSA-N Tyr-His-Tyr Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O OSXNCKRGMSHWSQ-ACRUOGEOSA-N 0.000 description 2
- LUMQYLVYUIRHHU-YJRXYDGGSA-N Tyr-Ser-Thr Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(O)=O LUMQYLVYUIRHHU-YJRXYDGGSA-N 0.000 description 2
- QFHRUCJIRVILCK-YJRXYDGGSA-N Tyr-Thr-Cys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)N)O QFHRUCJIRVILCK-YJRXYDGGSA-N 0.000 description 2
- KUXCBJFJURINGF-PXDAIIFMSA-N Tyr-Trp-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CC1=CNC2=CC=CC=C21)NC(=O)[C@H](CC3=CC=C(C=C3)O)N KUXCBJFJURINGF-PXDAIIFMSA-N 0.000 description 2
- RMRFSFXLFWWAJZ-HJOGWXRNSA-N Tyr-Tyr-Tyr Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(O)=O)C1=CC=C(O)C=C1 RMRFSFXLFWWAJZ-HJOGWXRNSA-N 0.000 description 2
- QGFPYRPIUXBYGR-YDHLFZDLSA-N Val-Asn-Phe Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)N QGFPYRPIUXBYGR-YDHLFZDLSA-N 0.000 description 2
- JVYIGCARISMLMV-HOCLYGCPSA-N Val-Gly-Trp Chemical compound CC(C)[C@@H](C(=O)NCC(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)O)N JVYIGCARISMLMV-HOCLYGCPSA-N 0.000 description 2
- HQYVQDRYODWONX-DCAQKATOSA-N Val-His-Ser Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N[C@@H](CO)C(=O)O)N HQYVQDRYODWONX-DCAQKATOSA-N 0.000 description 2
- OTJMMKPMLUNTQT-AVGNSLFASA-N Val-Leu-Arg Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)NC(=O)[C@H](C(C)C)N OTJMMKPMLUNTQT-AVGNSLFASA-N 0.000 description 2
- HGJRMXOWUWVUOA-GVXVVHGQSA-N Val-Leu-Gln Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](C(C)C)N HGJRMXOWUWVUOA-GVXVVHGQSA-N 0.000 description 2
- ZHQWPWQNVRCXAX-XQQFMLRXSA-N Val-Leu-Pro Chemical compound CC(C)C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](C(C)C)N ZHQWPWQNVRCXAX-XQQFMLRXSA-N 0.000 description 2
- PZTZYZUTCPZWJH-FXQIFTODSA-N Val-Ser-Ser Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)O)N PZTZYZUTCPZWJH-FXQIFTODSA-N 0.000 description 2
- SDHZOOIGIUEPDY-JYJNAYRXSA-N Val-Ser-Trp Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@H](CO)NC(=O)[C@@H](N)C(C)C)C(O)=O)=CNC2=C1 SDHZOOIGIUEPDY-JYJNAYRXSA-N 0.000 description 2
- HWNYVQMOLCYHEA-IHRRRGAJSA-N Val-Ser-Tyr Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O)N HWNYVQMOLCYHEA-IHRRRGAJSA-N 0.000 description 2
- GVNLOVJNNDZUHS-RHYQMDGZSA-N Val-Thr-Lys Chemical compound [H]N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(O)=O GVNLOVJNNDZUHS-RHYQMDGZSA-N 0.000 description 2
- JAIZPWVHPQRYOU-ZJDVBMNYSA-N Val-Thr-Thr Chemical compound C[C@H]([C@@H](C(=O)N[C@@H]([C@@H](C)O)C(=O)O)NC(=O)[C@H](C(C)C)N)O JAIZPWVHPQRYOU-ZJDVBMNYSA-N 0.000 description 2
- JVGDAEKKZKKZFO-RCWTZXSCSA-N Val-Val-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](C(C)C)N)O JVGDAEKKZKKZFO-RCWTZXSCSA-N 0.000 description 2
- 208000032594 Vascular Remodeling Diseases 0.000 description 2
- 206010047139 Vasoconstriction Diseases 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 230000001154 acute effect Effects 0.000 description 2
- 230000009824 affinity maturation Effects 0.000 description 2
- 235000004279 alanine Nutrition 0.000 description 2
- 108010024078 alanyl-glycyl-serine Proteins 0.000 description 2
- 210000004102 animal cell Anatomy 0.000 description 2
- 239000005557 antagonist Substances 0.000 description 2
- 108010062796 arginyllysine Proteins 0.000 description 2
- 108010093581 aspartyl-proline Proteins 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009530 blood pressure measurement Methods 0.000 description 2
- 210000004204 blood vessel Anatomy 0.000 description 2
- 210000001124 body fluid Anatomy 0.000 description 2
- 239000010839 body fluid Substances 0.000 description 2
- 238000000423 cell based assay Methods 0.000 description 2
- 230000007960 cellular response to stress Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000001684 chronic effect Effects 0.000 description 2
- 238000012875 competitive assay Methods 0.000 description 2
- 238000004590 computer program Methods 0.000 description 2
- 210000004748 cultured cell Anatomy 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 239000003623 enhancer Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 108010080575 glutamyl-aspartyl-alanine Proteins 0.000 description 2
- RWSXRVCMGQZWBV-WDSKDSINSA-N glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- 230000000004 hemodynamic effect Effects 0.000 description 2
- 108010040030 histidinoalanine Proteins 0.000 description 2
- 230000001900 immune effect Effects 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 230000003834 intracellular effect Effects 0.000 description 2
- 108010073093 leucyl-glycyl-glycyl-glycine Proteins 0.000 description 2
- 108010090333 leucyl-lysyl-proline Proteins 0.000 description 2
- 108010073472 leucyl-prolyl-proline Proteins 0.000 description 2
- 210000004962 mammalian cell Anatomy 0.000 description 2
- 230000001404 mediated effect Effects 0.000 description 2
- 210000004379 membrane Anatomy 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 238000002703 mutagenesis Methods 0.000 description 2
- 231100000350 mutagenesis Toxicity 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 229940055729 papain Drugs 0.000 description 2
- 235000019834 papain Nutrition 0.000 description 2
- 229940111202 pepsin Drugs 0.000 description 2
- 239000000816 peptidomimetic Substances 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- 108010018625 phenylalanylarginine Proteins 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- XOJVVFBFDXDTEG-UHFFFAOYSA-N pristane Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)C XOJVVFBFDXDTEG-UHFFFAOYSA-N 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 210000001236 prokaryotic cell Anatomy 0.000 description 2
- 108010077112 prolyl-proline Proteins 0.000 description 2
- 238000002708 random mutagenesis Methods 0.000 description 2
- 238000007634 remodeling Methods 0.000 description 2
- 230000010076 replication Effects 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 210000005241 right ventricle Anatomy 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- 230000035488 systolic blood pressure Effects 0.000 description 2
- 150000003573 thiols Chemical class 0.000 description 2
- 108010033670 threonyl-aspartyl-tyrosine Proteins 0.000 description 2
- 108010071097 threonyl-lysyl-proline Proteins 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- 238000011269 treatment regimen Methods 0.000 description 2
- 239000013638 trimer Substances 0.000 description 2
- 108010077037 tyrosyl-tyrosyl-phenylalanine Proteins 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 210000003556 vascular endothelial cell Anatomy 0.000 description 2
- 230000025033 vasoconstriction Effects 0.000 description 2
- 230000024883 vasodilation Effects 0.000 description 2
- 239000013603 viral vector Substances 0.000 description 2
- 229920003169 water-soluble polymer Polymers 0.000 description 2
- 210000005253 yeast cell Anatomy 0.000 description 2
- MGTUVUVRFJVHAL-UHFFFAOYSA-N 2,8-dibenzyl-6-(4-hydroxyphenyl)imidazo[1,2-a]pyrazin-3-ol Chemical compound Oc1c(Cc2ccccc2)nc2c(Cc3ccccc3)nc(cn12)-c1ccc(O)cc1 MGTUVUVRFJVHAL-UHFFFAOYSA-N 0.000 description 1
- SKPQXOSVPKPXML-ULQDDVLXSA-N 2-[[(2s)-1-[(2s)-3-phenyl-2-[[(2s)-pyrrolidine-2-carbonyl]amino]propanoyl]pyrrolidine-2-carbonyl]amino]acetic acid Chemical compound OC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H](NC(=O)[C@H]1NCCC1)CC1=CC=CC=C1 SKPQXOSVPKPXML-ULQDDVLXSA-N 0.000 description 1
- QKNYBSVHEMOAJP-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;hydron;chloride Chemical compound Cl.OCC(N)(CO)CO QKNYBSVHEMOAJP-UHFFFAOYSA-N 0.000 description 1
- UPXRTVAIJMUAQR-UHFFFAOYSA-N 4-(9h-fluoren-9-ylmethoxycarbonylamino)-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid Chemical compound C1C(C(O)=O)N(C(=O)OC(C)(C)C)CC1NC(=O)OCC1C2=CC=CC=C2C2=CC=CC=C21 UPXRTVAIJMUAQR-UHFFFAOYSA-N 0.000 description 1
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 description 1
- UGLPMYSCWHTZQU-AUTRQRHGSA-N Ala-Ala-Tyr Chemical compound C[C@H]([NH3+])C(=O)N[C@@H](C)C(=O)N[C@H](C([O-])=O)CC1=CC=C(O)C=C1 UGLPMYSCWHTZQU-AUTRQRHGSA-N 0.000 description 1
- CVGNCMIULZNYES-WHFBIAKZSA-N Ala-Asn-Gly Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)NCC(O)=O CVGNCMIULZNYES-WHFBIAKZSA-N 0.000 description 1
- XQJAFSDFQZPYCU-UWJYBYFXSA-N Ala-Asn-Tyr Chemical compound C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O)N XQJAFSDFQZPYCU-UWJYBYFXSA-N 0.000 description 1
- GSCLWXDNIMNIJE-ZLUOBGJFSA-N Ala-Asp-Asn Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O GSCLWXDNIMNIJE-ZLUOBGJFSA-N 0.000 description 1
- LSLIRHLIUDVNBN-CIUDSAMLSA-N Ala-Asp-Lys Chemical compound C[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(O)=O)CCCCN LSLIRHLIUDVNBN-CIUDSAMLSA-N 0.000 description 1
- BUDNAJYVCUHLSV-ZLUOBGJFSA-N Ala-Asp-Ser Chemical compound C[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(O)=O BUDNAJYVCUHLSV-ZLUOBGJFSA-N 0.000 description 1
- WCBVQNZTOKJWJS-ACZMJKKPSA-N Ala-Cys-Glu Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCC(O)=O)C(O)=O WCBVQNZTOKJWJS-ACZMJKKPSA-N 0.000 description 1
- PAIHPOGPJVUFJY-WDSKDSINSA-N Ala-Glu-Gly Chemical compound C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)NCC(O)=O PAIHPOGPJVUFJY-WDSKDSINSA-N 0.000 description 1
- XYTNPQNAZREREP-XQXXSGGOSA-N Ala-Glu-Thr Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O XYTNPQNAZREREP-XQXXSGGOSA-N 0.000 description 1
- NBTGEURICRTMGL-WHFBIAKZSA-N Ala-Gly-Ser Chemical compound C[C@H](N)C(=O)NCC(=O)N[C@@H](CO)C(O)=O NBTGEURICRTMGL-WHFBIAKZSA-N 0.000 description 1
- OBVSBEYOMDWLRJ-BFHQHQDPSA-N Ala-Gly-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)CNC(=O)[C@H](C)N OBVSBEYOMDWLRJ-BFHQHQDPSA-N 0.000 description 1
- GRIFPSOFWFIICX-GOPGUHFVSA-N Ala-His-Trp Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O GRIFPSOFWFIICX-GOPGUHFVSA-N 0.000 description 1
- SUMYEVXWCAYLLJ-GUBZILKMSA-N Ala-Leu-Gln Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O SUMYEVXWCAYLLJ-GUBZILKMSA-N 0.000 description 1
- DPNZTBKGAUAZQU-DLOVCJGASA-N Ala-Leu-His Chemical compound C[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)N DPNZTBKGAUAZQU-DLOVCJGASA-N 0.000 description 1
- AWZKCUCQJNTBAD-SRVKXCTJSA-N Ala-Leu-Lys Chemical compound C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(O)=O)CCCCN AWZKCUCQJNTBAD-SRVKXCTJSA-N 0.000 description 1
- OYJCVIGKMXUVKB-GARJFASQSA-N Ala-Leu-Pro Chemical compound C[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@@H]1C(=O)O)N OYJCVIGKMXUVKB-GARJFASQSA-N 0.000 description 1
- LDLSENBXQNDTPB-DCAQKATOSA-N Ala-Lys-Arg Chemical compound NCCCC[C@H](NC(=O)[C@@H](N)C)C(=O)N[C@H](C(O)=O)CCCN=C(N)N LDLSENBXQNDTPB-DCAQKATOSA-N 0.000 description 1
- MDNAVFBZPROEHO-DCAQKATOSA-N Ala-Lys-Val Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(O)=O MDNAVFBZPROEHO-DCAQKATOSA-N 0.000 description 1
- MDNAVFBZPROEHO-UHFFFAOYSA-N Ala-Lys-Val Natural products CC(C)C(C(O)=O)NC(=O)C(NC(=O)C(C)N)CCCCN MDNAVFBZPROEHO-UHFFFAOYSA-N 0.000 description 1
- REAQAWSENITKJL-DDWPSWQVSA-N Ala-Met-Asp-Tyr Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O REAQAWSENITKJL-DDWPSWQVSA-N 0.000 description 1
- WQLDNOCHHRISMS-NAKRPEOUSA-N Ala-Pro-Ile Chemical compound [H]N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N[C@@H]([C@@H](C)CC)C(O)=O WQLDNOCHHRISMS-NAKRPEOUSA-N 0.000 description 1
- XWFWAXPOLRTDFZ-FXQIFTODSA-N Ala-Pro-Ser Chemical compound C[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(O)=O XWFWAXPOLRTDFZ-FXQIFTODSA-N 0.000 description 1
- OEVCHROQUIVQFZ-YTLHQDLWSA-N Ala-Thr-Ala Chemical compound C[C@H](N)C(=O)N[C@@H]([C@H](O)C)C(=O)N[C@@H](C)C(O)=O OEVCHROQUIVQFZ-YTLHQDLWSA-N 0.000 description 1
- IOFVWPYSRSCWHI-JXUBOQSCSA-N Ala-Thr-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](C)N IOFVWPYSRSCWHI-JXUBOQSCSA-N 0.000 description 1
- YCTIYBUTCKNOTI-UWJYBYFXSA-N Ala-Tyr-Asp Chemical compound C[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](CC(=O)O)C(=O)O)N YCTIYBUTCKNOTI-UWJYBYFXSA-N 0.000 description 1
- MUGAESARFRGOTQ-IGNZVWTISA-N Ala-Tyr-Tyr Chemical compound C[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](CC2=CC=C(C=C2)O)C(=O)O)N MUGAESARFRGOTQ-IGNZVWTISA-N 0.000 description 1
- YEBZNKPPOHFZJM-BPNCWPANSA-N Ala-Tyr-Val Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](C(C)C)C(O)=O YEBZNKPPOHFZJM-BPNCWPANSA-N 0.000 description 1
- 229940122816 Amylase inhibitor Drugs 0.000 description 1
- 102000008102 Ankyrins Human genes 0.000 description 1
- 108010049777 Ankyrins Proteins 0.000 description 1
- DFCIPNHFKOQAME-FXQIFTODSA-N Arg-Ala-Asn Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(O)=O DFCIPNHFKOQAME-FXQIFTODSA-N 0.000 description 1
- VKKYFICVTYKFIO-CIUDSAMLSA-N Arg-Ala-Glu Chemical compound OC(=O)CC[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCCN=C(N)N VKKYFICVTYKFIO-CIUDSAMLSA-N 0.000 description 1
- NABSCJGZKWSNHX-RCWTZXSCSA-N Arg-Arg-Thr Chemical compound NC(N)=NCCC[C@@H](C(=O)N[C@@H]([C@H](O)C)C(O)=O)NC(=O)[C@@H](N)CCCN=C(N)N NABSCJGZKWSNHX-RCWTZXSCSA-N 0.000 description 1
- DPXDVGDLWJYZBH-GUBZILKMSA-N Arg-Asn-Arg Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O DPXDVGDLWJYZBH-GUBZILKMSA-N 0.000 description 1
- PQWTZSNVWSOFFK-FXQIFTODSA-N Arg-Asp-Asn Chemical compound C(C[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)N)C(=O)O)N)CN=C(N)N PQWTZSNVWSOFFK-FXQIFTODSA-N 0.000 description 1
- JUWQNWXEGDYCIE-YUMQZZPRSA-N Arg-Gln-Gly Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(O)=O JUWQNWXEGDYCIE-YUMQZZPRSA-N 0.000 description 1
- PNQWAUXQDBIJDY-GUBZILKMSA-N Arg-Glu-Glu Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(O)=O PNQWAUXQDBIJDY-GUBZILKMSA-N 0.000 description 1
- AUFHLLPVPSMEOG-YUMQZZPRSA-N Arg-Gly-Glu Chemical compound NC(N)=NCCC[C@H](N)C(=O)NCC(=O)N[C@@H](CCC(O)=O)C(O)=O AUFHLLPVPSMEOG-YUMQZZPRSA-N 0.000 description 1
- OQCWXQJLCDPRHV-UWVGGRQHSA-N Arg-Gly-Leu Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](CC(C)C)C(O)=O OQCWXQJLCDPRHV-UWVGGRQHSA-N 0.000 description 1
- WVNFNPGXYADPPO-BQBZGAKWSA-N Arg-Gly-Ser Chemical compound NC(N)=NCCC[C@H](N)C(=O)NCC(=O)N[C@@H](CO)C(O)=O WVNFNPGXYADPPO-BQBZGAKWSA-N 0.000 description 1
- YKBHOXLMMPZPHQ-GMOBBJLQSA-N Arg-Ile-Asp Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(O)=O)C(O)=O YKBHOXLMMPZPHQ-GMOBBJLQSA-N 0.000 description 1
- GIMTZGADWZTZGV-DCAQKATOSA-N Arg-Lys-Cys Chemical compound C(CCN)C[C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CCCN=C(N)N)N GIMTZGADWZTZGV-DCAQKATOSA-N 0.000 description 1
- DNLQVHBBMPZUGJ-BQBZGAKWSA-N Arg-Ser-Gly Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)NCC(O)=O DNLQVHBBMPZUGJ-BQBZGAKWSA-N 0.000 description 1
- KMFPQTITXUKJOV-DCAQKATOSA-N Arg-Ser-Leu Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(O)=O KMFPQTITXUKJOV-DCAQKATOSA-N 0.000 description 1
- SYFHFLGAROUHNT-VEVYYDQMSA-N Arg-Thr-Asn Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(O)=O SYFHFLGAROUHNT-VEVYYDQMSA-N 0.000 description 1
- HRCIIMCTUIAKQB-XGEHTFHBSA-N Arg-Thr-Cys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CCCN=C(N)N)N)O HRCIIMCTUIAKQB-XGEHTFHBSA-N 0.000 description 1
- AUZAXCPWMDBWEE-HJGDQZAQSA-N Arg-Thr-Glu Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCC(O)=O)C(O)=O AUZAXCPWMDBWEE-HJGDQZAQSA-N 0.000 description 1
- ZJBUILVYSXQNSW-YTWAJWBKSA-N Arg-Thr-Pro Chemical compound C[C@H]([C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CCCN=C(N)N)N)O ZJBUILVYSXQNSW-YTWAJWBKSA-N 0.000 description 1
- ZUVMUOOHJYNJPP-XIRDDKMYSA-N Arg-Trp-Gln Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CCC(N)=O)C(O)=O ZUVMUOOHJYNJPP-XIRDDKMYSA-N 0.000 description 1
- POZKLUIXMHIULG-FDARSICLSA-N Arg-Trp-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CC1=CNC2=CC=CC=C21)NC(=O)[C@H](CCCN=C(N)N)N POZKLUIXMHIULG-FDARSICLSA-N 0.000 description 1
- ULBHWNVWSCJLCO-NHCYSSNCSA-N Arg-Val-Glu Chemical compound OC(=O)CC[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)CCCN=C(N)N ULBHWNVWSCJLCO-NHCYSSNCSA-N 0.000 description 1
- 239000004475 Arginine Substances 0.000 description 1
- 206010003445 Ascites Diseases 0.000 description 1
- NUHQMYUWLUSRJX-BIIVOSGPSA-N Asn-Ala-Pro Chemical compound C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CC(=O)N)N NUHQMYUWLUSRJX-BIIVOSGPSA-N 0.000 description 1
- ZZXMOQIUIJJOKZ-ZLUOBGJFSA-N Asn-Asn-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](N)CC(N)=O ZZXMOQIUIJJOKZ-ZLUOBGJFSA-N 0.000 description 1
- NVGWESORMHFISY-SRVKXCTJSA-N Asn-Asn-Phe Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O NVGWESORMHFISY-SRVKXCTJSA-N 0.000 description 1
- SRUUBQBAVNQZGJ-LAEOZQHASA-N Asn-Gln-Val Chemical compound CC(C)[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CC(=O)N)N SRUUBQBAVNQZGJ-LAEOZQHASA-N 0.000 description 1
- WONGRTVAMHFGBE-WDSKDSINSA-N Asn-Gly-Gln Chemical compound C(CC(=O)N)[C@@H](C(=O)O)NC(=O)CNC(=O)[C@H](CC(=O)N)N WONGRTVAMHFGBE-WDSKDSINSA-N 0.000 description 1
- OLVIPTLKNSAYRJ-YUMQZZPRSA-N Asn-Gly-Lys Chemical compound C(CCN)C[C@@H](C(=O)O)NC(=O)CNC(=O)[C@H](CC(=O)N)N OLVIPTLKNSAYRJ-YUMQZZPRSA-N 0.000 description 1
- ODBSSLHUFPJRED-CIUDSAMLSA-N Asn-His-Asn Chemical compound C1=C(NC=N1)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)[C@H](CC(=O)N)N ODBSSLHUFPJRED-CIUDSAMLSA-N 0.000 description 1
- WQLJRNRLHWJIRW-KKUMJFAQSA-N Asn-His-Tyr Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)O)NC(=O)[C@H](CC2=CN=CN2)NC(=O)[C@H](CC(=O)N)N)O WQLJRNRLHWJIRW-KKUMJFAQSA-N 0.000 description 1
- HDHZCEDPLTVHFZ-GUBZILKMSA-N Asn-Leu-Glu Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O HDHZCEDPLTVHFZ-GUBZILKMSA-N 0.000 description 1
- NYGILGUOUOXGMJ-YUMQZZPRSA-N Asn-Lys-Gly Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)NCC(O)=O NYGILGUOUOXGMJ-YUMQZZPRSA-N 0.000 description 1
- RBOBTTLFPRSXKZ-BZSNNMDCSA-N Asn-Phe-Tyr Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O RBOBTTLFPRSXKZ-BZSNNMDCSA-N 0.000 description 1
- YRTOMUMWSTUQAX-FXQIFTODSA-N Asn-Pro-Asp Chemical compound NC(=O)C[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(O)=O)C(O)=O YRTOMUMWSTUQAX-FXQIFTODSA-N 0.000 description 1
- UGXYFDQFLVCDFC-CIUDSAMLSA-N Asn-Ser-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC(N)=O UGXYFDQFLVCDFC-CIUDSAMLSA-N 0.000 description 1
- VLDRQOHCMKCXLY-SRVKXCTJSA-N Asn-Ser-Phe Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O VLDRQOHCMKCXLY-SRVKXCTJSA-N 0.000 description 1
- HNXWVVHIGTZTBO-LKXGYXEUSA-N Asn-Ser-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC(N)=O HNXWVVHIGTZTBO-LKXGYXEUSA-N 0.000 description 1
- PIABYSIYPGLLDQ-XVSYOHENSA-N Asn-Thr-Phe Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O PIABYSIYPGLLDQ-XVSYOHENSA-N 0.000 description 1
- RDLYUKRPEJERMM-XIRDDKMYSA-N Asn-Trp-Leu Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CC(C)C)C(O)=O RDLYUKRPEJERMM-XIRDDKMYSA-N 0.000 description 1
- QNNBHTFDFFFHGC-KKUMJFAQSA-N Asn-Tyr-Lys Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CC(=O)N)N)O QNNBHTFDFFFHGC-KKUMJFAQSA-N 0.000 description 1
- DXHINQUXBZNUCF-MELADBBJSA-N Asn-Tyr-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CC=C(C=C2)O)NC(=O)[C@H](CC(=O)N)N)C(=O)O DXHINQUXBZNUCF-MELADBBJSA-N 0.000 description 1
- KBQOUDLMWYWXNP-YDHLFZDLSA-N Asn-Val-Phe Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)NC(=O)[C@H](CC(=O)N)N KBQOUDLMWYWXNP-YDHLFZDLSA-N 0.000 description 1
- XEDQMTWEYFBOIK-ACZMJKKPSA-N Asp-Ala-Glu Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(O)=O XEDQMTWEYFBOIK-ACZMJKKPSA-N 0.000 description 1
- YNQIDCRRTWGHJD-ZLUOBGJFSA-N Asp-Asn-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](N)CC(O)=O YNQIDCRRTWGHJD-ZLUOBGJFSA-N 0.000 description 1
- RDRMWJBLOSRRAW-BYULHYEWSA-N Asp-Asn-Val Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](C(C)C)C(O)=O RDRMWJBLOSRRAW-BYULHYEWSA-N 0.000 description 1
- LDGUZSIPGSPBJP-XVYDVKMFSA-N Asp-His-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CC1=CN=CN1)NC(=O)[C@H](CC(=O)O)N LDGUZSIPGSPBJP-XVYDVKMFSA-N 0.000 description 1
- OOXKFYNWRVGYFM-XIRDDKMYSA-N Asp-His-Trp Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)O)NC(=O)[C@H](CC3=CN=CN3)NC(=O)[C@H](CC(=O)O)N OOXKFYNWRVGYFM-XIRDDKMYSA-N 0.000 description 1
- HOBNTSHITVVNBN-ZPFDUUQYSA-N Asp-Ile-Leu Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)O)NC(=O)[C@H](CC(=O)O)N HOBNTSHITVVNBN-ZPFDUUQYSA-N 0.000 description 1
- CJUKAWUWBZCTDQ-SRVKXCTJSA-N Asp-Leu-Lys Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(O)=O CJUKAWUWBZCTDQ-SRVKXCTJSA-N 0.000 description 1
- QNMKWNONJGKJJC-NHCYSSNCSA-N Asp-Leu-Val Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(O)=O QNMKWNONJGKJJC-NHCYSSNCSA-N 0.000 description 1
- LTCKTLYKRMCFOC-KKUMJFAQSA-N Asp-Phe-Leu Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC(C)C)C(O)=O LTCKTLYKRMCFOC-KKUMJFAQSA-N 0.000 description 1
- KPSHWSWFPUDEGF-FXQIFTODSA-N Asp-Pro-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CC(O)=O KPSHWSWFPUDEGF-FXQIFTODSA-N 0.000 description 1
- FAUPLTGRUBTXNU-FXQIFTODSA-N Asp-Pro-Ser Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(O)=O FAUPLTGRUBTXNU-FXQIFTODSA-N 0.000 description 1
- CUQDCPXNZPDYFQ-ZLUOBGJFSA-N Asp-Ser-Asp Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(O)=O CUQDCPXNZPDYFQ-ZLUOBGJFSA-N 0.000 description 1
- KGHLGJAXYSVNJP-WHFBIAKZSA-N Asp-Ser-Gly Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H](CO)C(=O)NCC(O)=O KGHLGJAXYSVNJP-WHFBIAKZSA-N 0.000 description 1
- VNXQRBXEQXLERQ-CIUDSAMLSA-N Asp-Ser-Lys Chemical compound C(CCN)C[C@@H](C(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(=O)O)N VNXQRBXEQXLERQ-CIUDSAMLSA-N 0.000 description 1
- OFYVKOXTTDCUIL-FXQIFTODSA-N Asp-Ser-Met Chemical compound CSCC[C@@H](C(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(=O)O)N OFYVKOXTTDCUIL-FXQIFTODSA-N 0.000 description 1
- YIDFBWRHIYOYAA-LKXGYXEUSA-N Asp-Ser-Thr Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(O)=O YIDFBWRHIYOYAA-LKXGYXEUSA-N 0.000 description 1
- JSNWZMFSLIWAHS-HJGDQZAQSA-N Asp-Thr-Leu Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(C)C)C(=O)O)NC(=O)[C@H](CC(=O)O)N)O JSNWZMFSLIWAHS-HJGDQZAQSA-N 0.000 description 1
- NALWOULWGHTVDA-UWVGGRQHSA-N Asp-Tyr Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 NALWOULWGHTVDA-UWVGGRQHSA-N 0.000 description 1
- KNDCWFXCFKSEBM-AVGNSLFASA-N Asp-Tyr-Glu Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CCC(O)=O)C(O)=O KNDCWFXCFKSEBM-AVGNSLFASA-N 0.000 description 1
- CZIVKMOEXPILDK-SRVKXCTJSA-N Asp-Tyr-Ser Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CO)C(O)=O CZIVKMOEXPILDK-SRVKXCTJSA-N 0.000 description 1
- XWKPSMRPIKKDDU-RCOVLWMOSA-N Asp-Val-Gly Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)NCC(O)=O XWKPSMRPIKKDDU-RCOVLWMOSA-N 0.000 description 1
- XQFLFQWOBXPMHW-NHCYSSNCSA-N Asp-Val-His Chemical compound N[C@@H](CC(=O)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC1=CNC=N1)C(=O)O XQFLFQWOBXPMHW-NHCYSSNCSA-N 0.000 description 1
- QOJJMJKTMKNFEF-ZKWXMUAHSA-N Asp-Val-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)CC(O)=O QOJJMJKTMKNFEF-ZKWXMUAHSA-N 0.000 description 1
- GYNUXDMCDILYIQ-QRTARXTBSA-N Asp-Val-Trp Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)O)NC(=O)[C@H](CC(=O)O)N GYNUXDMCDILYIQ-QRTARXTBSA-N 0.000 description 1
- ZUNMTUPRQMWMHX-LSJOCFKGSA-N Asp-Val-Val Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(O)=O ZUNMTUPRQMWMHX-LSJOCFKGSA-N 0.000 description 1
- 235000018185 Betula X alpestris Nutrition 0.000 description 1
- 235000018212 Betula X uliginosa Nutrition 0.000 description 1
- 125000001433 C-terminal amino-acid group Chemical group 0.000 description 1
- 238000011740 C57BL/6 mouse Methods 0.000 description 1
- 102100021786 CMP-N-acetylneuraminate-poly-alpha-2,8-sialyltransferase Human genes 0.000 description 1
- 229940127291 Calcium channel antagonist Drugs 0.000 description 1
- 102000005367 Carboxypeptidases Human genes 0.000 description 1
- 108010006303 Carboxypeptidases Proteins 0.000 description 1
- 206010007572 Cardiac hypertrophy Diseases 0.000 description 1
- 208000006029 Cardiomegaly Diseases 0.000 description 1
- 206010008479 Chest Pain Diseases 0.000 description 1
- 241000282552 Chlorocebus aethiops Species 0.000 description 1
- 108020004635 Complementary DNA Proteins 0.000 description 1
- 241000557626 Corvus corax Species 0.000 description 1
- 241000699800 Cricetinae Species 0.000 description 1
- 102220554102 Cyclic GMP-AMP synthase_L13H_mutation Human genes 0.000 description 1
- CPTUXCUWQIBZIF-ZLUOBGJFSA-N Cys-Asn-Ser Chemical compound SC[C@H](N)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(O)=O CPTUXCUWQIBZIF-ZLUOBGJFSA-N 0.000 description 1
- BPHKULHWEIUDOB-FXQIFTODSA-N Cys-Gln-Gln Chemical compound SC[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O BPHKULHWEIUDOB-FXQIFTODSA-N 0.000 description 1
- SFRQEQGPRTVDPO-NRPADANISA-N Cys-Gln-Val Chemical compound [H]N[C@@H](CS)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C(C)C)C(O)=O SFRQEQGPRTVDPO-NRPADANISA-N 0.000 description 1
- WVLZTXGTNGHPBO-SRVKXCTJSA-N Cys-Leu-Leu Chemical compound [H]N[C@@H](CS)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(O)=O WVLZTXGTNGHPBO-SRVKXCTJSA-N 0.000 description 1
- NIXHTNJAGGFBAW-CIUDSAMLSA-N Cys-Lys-Ser Chemical compound C(CCN)C[C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](CS)N NIXHTNJAGGFBAW-CIUDSAMLSA-N 0.000 description 1
- XKDHARKYRGHLKO-QEJZJMRPSA-N Cys-Trp-Gln Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](CS)N XKDHARKYRGHLKO-QEJZJMRPSA-N 0.000 description 1
- RIONIAPMMKVUCX-IHPCNDPISA-N Cys-Trp-Tyr Chemical compound C([C@H](NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CS)N)C(O)=O)C1=CC=C(O)C=C1 RIONIAPMMKVUCX-IHPCNDPISA-N 0.000 description 1
- VIOQRFNAZDMVLO-NRPADANISA-N Cys-Val-Glu Chemical compound [H]N[C@@H](CS)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O VIOQRFNAZDMVLO-NRPADANISA-N 0.000 description 1
- ALTQTAKGRFLRLR-GUBZILKMSA-N Cys-Val-Val Chemical compound CC(C)[C@@H](C(=O)N[C@@H](C(C)C)C(=O)O)NC(=O)[C@H](CS)N ALTQTAKGRFLRLR-GUBZILKMSA-N 0.000 description 1
- 102100025287 Cytochrome b Human genes 0.000 description 1
- 108010075028 Cytochromes b Proteins 0.000 description 1
- 241000701022 Cytomegalovirus Species 0.000 description 1
- 102000053602 DNA Human genes 0.000 description 1
- 108010008286 DNA nucleotidylexotransferase Proteins 0.000 description 1
- 102000052510 DNA-Binding Proteins Human genes 0.000 description 1
- 108700020911 DNA-Binding Proteins Proteins 0.000 description 1
- 102100029764 DNA-directed DNA/RNA polymerase mu Human genes 0.000 description 1
- 241000702421 Dependoparvovirus Species 0.000 description 1
- 229920002307 Dextran Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 102100024746 Dihydrofolate reductase Human genes 0.000 description 1
- 206010061818 Disease progression Diseases 0.000 description 1
- 208000000059 Dyspnea Diseases 0.000 description 1
- 206010013975 Dyspnoeas Diseases 0.000 description 1
- 238000002965 ELISA Methods 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 229940118365 Endothelin receptor antagonist Drugs 0.000 description 1
- 102400000686 Endothelin-1 Human genes 0.000 description 1
- 101800004490 Endothelin-1 Proteins 0.000 description 1
- YQYJSBFKSSDGFO-UHFFFAOYSA-N Epihygromycin Natural products OC1C(O)C(C(=O)C)OC1OC(C(=C1)O)=CC=C1C=C(C)C(=O)NC1C(O)C(O)C2OCOC2C1O YQYJSBFKSSDGFO-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 102000009109 Fc receptors Human genes 0.000 description 1
- 108010087819 Fc receptors Proteins 0.000 description 1
- 108010008177 Fd immunoglobulins Proteins 0.000 description 1
- 102000009123 Fibrin Human genes 0.000 description 1
- 108010073385 Fibrin Proteins 0.000 description 1
- 206010016803 Fluid overload Diseases 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 102000034286 G proteins Human genes 0.000 description 1
- 102000030782 GTP binding Human genes 0.000 description 1
- 108091000058 GTP-Binding Proteins 0.000 description 1
- WUAYFMZULZDSLB-ACZMJKKPSA-N Gln-Ala-Asn Chemical compound NC(=O)C[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCC(N)=O WUAYFMZULZDSLB-ACZMJKKPSA-N 0.000 description 1
- MLZRSFQRBDNJON-GUBZILKMSA-N Gln-Ala-Lys Chemical compound C[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CCC(=O)N)N MLZRSFQRBDNJON-GUBZILKMSA-N 0.000 description 1
- OYTPNWYZORARHL-XHNCKOQMSA-N Gln-Ala-Pro Chemical compound C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CCC(=O)N)N OYTPNWYZORARHL-XHNCKOQMSA-N 0.000 description 1
- CRRFJBGUGNNOCS-PEFMBERDSA-N Gln-Asp-Ile Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O CRRFJBGUGNNOCS-PEFMBERDSA-N 0.000 description 1
- WLODHVXYKYHLJD-ACZMJKKPSA-N Gln-Asp-Ser Chemical compound C(CC(=O)N)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CO)C(=O)O)N WLODHVXYKYHLJD-ACZMJKKPSA-N 0.000 description 1
- LOJYQMFIIJVETK-WDSKDSINSA-N Gln-Gln Chemical compound NC(=O)CC[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(O)=O LOJYQMFIIJVETK-WDSKDSINSA-N 0.000 description 1
- LVNILKSSFHCSJZ-IHRRRGAJSA-N Gln-Gln-Phe Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CCC(=O)N)N LVNILKSSFHCSJZ-IHRRRGAJSA-N 0.000 description 1
- QFJPFPCSXOXMKI-BPUTZDHNSA-N Gln-Gln-Trp Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CCC(=O)N)N QFJPFPCSXOXMKI-BPUTZDHNSA-N 0.000 description 1
- CGVWDTRDPLOMHZ-FXQIFTODSA-N Gln-Glu-Asp Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(O)=O CGVWDTRDPLOMHZ-FXQIFTODSA-N 0.000 description 1
- ZQPOVSJFBBETHQ-CIUDSAMLSA-N Gln-Glu-Gln Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O ZQPOVSJFBBETHQ-CIUDSAMLSA-N 0.000 description 1
- KCJJFESQRXGTGC-BQBZGAKWSA-N Gln-Glu-Gly Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)NCC(O)=O KCJJFESQRXGTGC-BQBZGAKWSA-N 0.000 description 1
- ZNZPKVQURDQFFS-FXQIFTODSA-N Gln-Glu-Ser Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(O)=O ZNZPKVQURDQFFS-FXQIFTODSA-N 0.000 description 1
- XKBASPWPBXNVLQ-WDSKDSINSA-N Gln-Gly-Asn Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)NCC(=O)N[C@@H](CC(N)=O)C(O)=O XKBASPWPBXNVLQ-WDSKDSINSA-N 0.000 description 1
- GNMQDOGFWYWPNM-LAEOZQHASA-N Gln-Gly-Ile Chemical compound CC[C@H](C)[C@H](NC(=O)CNC(=O)[C@@H](N)CCC(N)=O)C(O)=O GNMQDOGFWYWPNM-LAEOZQHASA-N 0.000 description 1
- FGYPOQPQTUNESW-IUCAKERBSA-N Gln-Gly-Leu Chemical compound CC(C)C[C@@H](C(=O)O)NC(=O)CNC(=O)[C@H](CCC(=O)N)N FGYPOQPQTUNESW-IUCAKERBSA-N 0.000 description 1
- GFLNKSQHOBOMNM-AVGNSLFASA-N Gln-His-His Chemical compound C1=C(NC=N1)C[C@@H](C(=O)N[C@@H](CC2=CN=CN2)C(=O)O)NC(=O)[C@H](CCC(=O)N)N GFLNKSQHOBOMNM-AVGNSLFASA-N 0.000 description 1
- ZNTDJIMJKNNSLR-RWRJDSDZSA-N Gln-Ile-Thr Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H]([C@@H](C)O)C(=O)O)NC(=O)[C@H](CCC(=O)N)N ZNTDJIMJKNNSLR-RWRJDSDZSA-N 0.000 description 1
- IOFDDSNZJDIGPB-GVXVVHGQSA-N Gln-Leu-Val Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(O)=O IOFDDSNZJDIGPB-GVXVVHGQSA-N 0.000 description 1
- ZEEPYMXTJWIMSN-GUBZILKMSA-N Gln-Lys-Ser Chemical compound NCCCC[C@@H](C(=O)N[C@@H](CO)C(O)=O)NC(=O)[C@@H](N)CCC(N)=O ZEEPYMXTJWIMSN-GUBZILKMSA-N 0.000 description 1
- AQPZYBSRDRZBAG-AVGNSLFASA-N Gln-Phe-Asn Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)[C@H](CCC(=O)N)N AQPZYBSRDRZBAG-AVGNSLFASA-N 0.000 description 1
- UESYBOXFJWJVSB-AVGNSLFASA-N Gln-Phe-Ser Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(O)=O UESYBOXFJWJVSB-AVGNSLFASA-N 0.000 description 1
- HMIXCETWRYDVMO-GUBZILKMSA-N Gln-Pro-Glu Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(O)=O HMIXCETWRYDVMO-GUBZILKMSA-N 0.000 description 1
- VNTGPISAOMAXRK-CIUDSAMLSA-N Gln-Pro-Ser Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(O)=O VNTGPISAOMAXRK-CIUDSAMLSA-N 0.000 description 1
- OKARHJKJTKFQBM-ACZMJKKPSA-N Gln-Ser-Asn Chemical compound C(CC(=O)N)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(=O)N)C(=O)O)N OKARHJKJTKFQBM-ACZMJKKPSA-N 0.000 description 1
- SXFPZRRVWSUYII-KBIXCLLPSA-N Gln-Ser-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(=O)N)N SXFPZRRVWSUYII-KBIXCLLPSA-N 0.000 description 1
- LPIKVBWNNVFHCQ-GUBZILKMSA-N Gln-Ser-Leu Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(O)=O LPIKVBWNNVFHCQ-GUBZILKMSA-N 0.000 description 1
- SYZZMPFLOLSMHL-XHNCKOQMSA-N Gln-Ser-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CO)NC(=O)[C@H](CCC(=O)N)N)C(=O)O SYZZMPFLOLSMHL-XHNCKOQMSA-N 0.000 description 1
- UEILCTONAMOGBR-RWRJDSDZSA-N Gln-Thr-Ile Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O UEILCTONAMOGBR-RWRJDSDZSA-N 0.000 description 1
- BETSEXMYBWCDAE-SZMVWBNQSA-N Gln-Trp-Lys Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CCC(=O)N)N BETSEXMYBWCDAE-SZMVWBNQSA-N 0.000 description 1
- WTJIWXMJESRHMM-XDTLVQLUSA-N Gln-Tyr-Ala Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](C)C(O)=O WTJIWXMJESRHMM-XDTLVQLUSA-N 0.000 description 1
- GTBXHETZPUURJE-KKUMJFAQSA-N Gln-Tyr-Arg Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O GTBXHETZPUURJE-KKUMJFAQSA-N 0.000 description 1
- AKDOUBMVLRCHBD-SIUGBPQLSA-N Gln-Tyr-Ile Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O AKDOUBMVLRCHBD-SIUGBPQLSA-N 0.000 description 1
- JTWZNMUVQWWGOX-SOUVJXGZSA-N Gln-Tyr-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CC=C(C=C2)O)NC(=O)[C@H](CCC(=O)N)N)C(=O)O JTWZNMUVQWWGOX-SOUVJXGZSA-N 0.000 description 1
- RUFHOVYUYSNDNY-ACZMJKKPSA-N Glu-Ala-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCC(O)=O RUFHOVYUYSNDNY-ACZMJKKPSA-N 0.000 description 1
- MXOODARRORARSU-ACZMJKKPSA-N Glu-Ala-Ser Chemical compound C[C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](CCC(=O)O)N MXOODARRORARSU-ACZMJKKPSA-N 0.000 description 1
- VPKBCVUDBNINAH-GARJFASQSA-N Glu-Arg-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCC(=O)O)N)C(=O)O VPKBCVUDBNINAH-GARJFASQSA-N 0.000 description 1
- WOSRKEJQESVHGA-CIUDSAMLSA-N Glu-Arg-Ser Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(O)=O WOSRKEJQESVHGA-CIUDSAMLSA-N 0.000 description 1
- DYFJZDDQPNIPAB-NHCYSSNCSA-N Glu-Arg-Val Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(O)=O DYFJZDDQPNIPAB-NHCYSSNCSA-N 0.000 description 1
- AFODTOLGSZQDSL-PEFMBERDSA-N Glu-Asn-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CCC(=O)O)N AFODTOLGSZQDSL-PEFMBERDSA-N 0.000 description 1
- PXHABOCPJVTGEK-BQBZGAKWSA-N Glu-Gln-Gly Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(O)=O PXHABOCPJVTGEK-BQBZGAKWSA-N 0.000 description 1
- MIQCYAJSDGNCNK-BPUTZDHNSA-N Glu-Gln-Trp Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O MIQCYAJSDGNCNK-BPUTZDHNSA-N 0.000 description 1
- MUSGDMDGNGXULI-DCAQKATOSA-N Glu-Glu-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](N)CCC(O)=O MUSGDMDGNGXULI-DCAQKATOSA-N 0.000 description 1
- WVYJNPCWJYBHJG-YVNDNENWSA-N Glu-Ile-Gln Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCC(N)=O)C(O)=O WVYJNPCWJYBHJG-YVNDNENWSA-N 0.000 description 1
- HVYWQYLBVXMXSV-GUBZILKMSA-N Glu-Leu-Ala Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(O)=O HVYWQYLBVXMXSV-GUBZILKMSA-N 0.000 description 1
- PJBVXVBTTFZPHJ-GUBZILKMSA-N Glu-Leu-Asp Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)O)NC(=O)[C@H](CCC(=O)O)N PJBVXVBTTFZPHJ-GUBZILKMSA-N 0.000 description 1
- GJBUAAAIZSRCDC-GVXVVHGQSA-N Glu-Leu-Val Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(O)=O GJBUAAAIZSRCDC-GVXVVHGQSA-N 0.000 description 1
- SJJHXJDSNQJMMW-SRVKXCTJSA-N Glu-Lys-Arg Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O SJJHXJDSNQJMMW-SRVKXCTJSA-N 0.000 description 1
- YHOJJFFTSMWVGR-HJGDQZAQSA-N Glu-Met-Thr Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCSC)C(=O)N[C@@H]([C@@H](C)O)C(O)=O YHOJJFFTSMWVGR-HJGDQZAQSA-N 0.000 description 1
- AAJHGGDRKHYSDH-GUBZILKMSA-N Glu-Pro-Gln Chemical compound C1C[C@H](N(C1)C(=O)[C@H](CCC(=O)O)N)C(=O)N[C@@H](CCC(=O)N)C(=O)O AAJHGGDRKHYSDH-GUBZILKMSA-N 0.000 description 1
- GMVCSRBOSIUTFC-FXQIFTODSA-N Glu-Ser-Glu Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(O)=O GMVCSRBOSIUTFC-FXQIFTODSA-N 0.000 description 1
- HMJULNMJWOZNFI-XHNCKOQMSA-N Glu-Ser-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CO)NC(=O)[C@H](CCC(=O)O)N)C(=O)O HMJULNMJWOZNFI-XHNCKOQMSA-N 0.000 description 1
- DMYACXMQUABZIQ-NRPADANISA-N Glu-Ser-Val Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(O)=O DMYACXMQUABZIQ-NRPADANISA-N 0.000 description 1
- ZGXGVBYEJGVJMV-HJGDQZAQSA-N Glu-Thr-Met Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCSC)C(=O)O)NC(=O)[C@H](CCC(=O)O)N)O ZGXGVBYEJGVJMV-HJGDQZAQSA-N 0.000 description 1
- MXJYXYDREQWUMS-XKBZYTNZSA-N Glu-Thr-Ser Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(O)=O MXJYXYDREQWUMS-XKBZYTNZSA-N 0.000 description 1
- DLISPGXMKZTWQG-IFFSRLJSSA-N Glu-Thr-Val Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(O)=O DLISPGXMKZTWQG-IFFSRLJSSA-N 0.000 description 1
- UCZXXMREFIETQW-AVGNSLFASA-N Glu-Tyr-Asn Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC(N)=O)C(O)=O UCZXXMREFIETQW-AVGNSLFASA-N 0.000 description 1
- VXEFAWJTFAUDJK-AVGNSLFASA-N Glu-Tyr-Ser Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](CCC(=O)O)N)O VXEFAWJTFAUDJK-AVGNSLFASA-N 0.000 description 1
- ZALGPUWUVHOGAE-GVXVVHGQSA-N Glu-Val-His Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)[C@H](CCC(=O)O)N ZALGPUWUVHOGAE-GVXVVHGQSA-N 0.000 description 1
- SOYWRINXUSUWEQ-DLOVCJGASA-N Glu-Val-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)CCC(O)=O SOYWRINXUSUWEQ-DLOVCJGASA-N 0.000 description 1
- 108010024636 Glutathione Proteins 0.000 description 1
- PYTZFYUXZZHOAD-WHFBIAKZSA-N Gly-Ala-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)CN PYTZFYUXZZHOAD-WHFBIAKZSA-N 0.000 description 1
- YMUFWNJHVPQNQD-ZKWXMUAHSA-N Gly-Ala-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)CN YMUFWNJHVPQNQD-ZKWXMUAHSA-N 0.000 description 1
- JRDYDYXZKFNNRQ-XPUUQOCRSA-N Gly-Ala-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)CN JRDYDYXZKFNNRQ-XPUUQOCRSA-N 0.000 description 1
- JXYMPBCYRKWJEE-BQBZGAKWSA-N Gly-Arg-Ala Chemical compound [H]NCC(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(O)=O JXYMPBCYRKWJEE-BQBZGAKWSA-N 0.000 description 1
- OCQUNKSFDYDXBG-QXEWZRGKSA-N Gly-Arg-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)CN)CCCN=C(N)N OCQUNKSFDYDXBG-QXEWZRGKSA-N 0.000 description 1
- KRRMJKMGWWXWDW-STQMWFEESA-N Gly-Arg-Phe Chemical compound NC(=N)NCCC[C@H](NC(=O)CN)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 KRRMJKMGWWXWDW-STQMWFEESA-N 0.000 description 1
- FMNHBTKMRFVGRO-FOHZUACHSA-N Gly-Asn-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)CN FMNHBTKMRFVGRO-FOHZUACHSA-N 0.000 description 1
- BIRKKBCSAIHDDF-WDSKDSINSA-N Gly-Glu-Cys Chemical compound NCC(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CS)C(O)=O BIRKKBCSAIHDDF-WDSKDSINSA-N 0.000 description 1
- KMSGYZQRXPUKGI-BYPYZUCNSA-N Gly-Gly-Asn Chemical compound NCC(=O)NCC(=O)N[C@H](C(O)=O)CC(N)=O KMSGYZQRXPUKGI-BYPYZUCNSA-N 0.000 description 1
- BUEFQXUHTUZXHR-LURJTMIESA-N Gly-Gly-Pro zwitterion Chemical compound NCC(=O)NCC(=O)N1CCC[C@H]1C(O)=O BUEFQXUHTUZXHR-LURJTMIESA-N 0.000 description 1
- BHPQOIPBLYJNAW-NGZCFLSTSA-N Gly-Ile-Pro Chemical compound CC[C@H](C)[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)CN BHPQOIPBLYJNAW-NGZCFLSTSA-N 0.000 description 1
- TWTPDFFBLQEBOE-IUCAKERBSA-N Gly-Leu-Gln Chemical compound [H]NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O TWTPDFFBLQEBOE-IUCAKERBSA-N 0.000 description 1
- LOEANKRDMMVOGZ-YUMQZZPRSA-N Gly-Lys-Asp Chemical compound NCCCC[C@H](NC(=O)CN)C(=O)N[C@@H](CC(O)=O)C(O)=O LOEANKRDMMVOGZ-YUMQZZPRSA-N 0.000 description 1
- GMTXWRIDLGTVFC-IUCAKERBSA-N Gly-Lys-Glu Chemical compound [H]NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(O)=O GMTXWRIDLGTVFC-IUCAKERBSA-N 0.000 description 1
- PDUHNKAFQXQNLH-ZETCQYMHSA-N Gly-Lys-Gly Chemical compound NCCCC[C@H](NC(=O)CN)C(=O)NCC(O)=O PDUHNKAFQXQNLH-ZETCQYMHSA-N 0.000 description 1
- HHRODZSXDXMUHS-LURJTMIESA-N Gly-Met-Gly Chemical compound CSCC[C@H](NC(=O)C[NH3+])C(=O)NCC([O-])=O HHRODZSXDXMUHS-LURJTMIESA-N 0.000 description 1
- LPHQAFLNEHWKFF-QXEWZRGKSA-N Gly-Met-Ile Chemical compound [H]NCC(=O)N[C@@H](CCSC)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O LPHQAFLNEHWKFF-QXEWZRGKSA-N 0.000 description 1
- 108010009504 Gly-Phe-Leu-Gly Proteins 0.000 description 1
- OOCFXNOVSLSHAB-IUCAKERBSA-N Gly-Pro-Pro Chemical compound NCC(=O)N1CCC[C@H]1C(=O)N1[C@H](C(O)=O)CCC1 OOCFXNOVSLSHAB-IUCAKERBSA-N 0.000 description 1
- OHUKZZYSJBKFRR-WHFBIAKZSA-N Gly-Ser-Asp Chemical compound [H]NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(O)=O OHUKZZYSJBKFRR-WHFBIAKZSA-N 0.000 description 1
- ABPRMMYHROQBLY-NKWVEPMBSA-N Gly-Ser-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CO)NC(=O)CN)C(=O)O ABPRMMYHROQBLY-NKWVEPMBSA-N 0.000 description 1
- LCRDMSSAKLTKBU-ZDLURKLDSA-N Gly-Ser-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H](CO)NC(=O)CN LCRDMSSAKLTKBU-ZDLURKLDSA-N 0.000 description 1
- FKYQEVBRZSFAMJ-QWRGUYRKSA-N Gly-Ser-Tyr Chemical compound NCC(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 FKYQEVBRZSFAMJ-QWRGUYRKSA-N 0.000 description 1
- ZLCLYFGMKFCDCN-XPUUQOCRSA-N Gly-Ser-Val Chemical compound CC(C)[C@H](NC(=O)[C@H](CO)NC(=O)CN)C(O)=O ZLCLYFGMKFCDCN-XPUUQOCRSA-N 0.000 description 1
- FFJQHWKSGAWSTJ-BFHQHQDPSA-N Gly-Thr-Ala Chemical compound [H]NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C)C(O)=O FFJQHWKSGAWSTJ-BFHQHQDPSA-N 0.000 description 1
- YXTFLTJYLIAZQG-FJXKBIBVSA-N Gly-Thr-Arg Chemical compound NCC(=O)N[C@@H]([C@H](O)C)C(=O)N[C@H](C(O)=O)CCCN=C(N)N YXTFLTJYLIAZQG-FJXKBIBVSA-N 0.000 description 1
- CQMFNTVQVLQRLT-JHEQGTHGSA-N Gly-Thr-Gln Chemical compound [H]NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCC(N)=O)C(O)=O CQMFNTVQVLQRLT-JHEQGTHGSA-N 0.000 description 1
- KOYUSMBPJOVSOO-XEGUGMAKSA-N Gly-Tyr-Ile Chemical compound [H]NCC(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O KOYUSMBPJOVSOO-XEGUGMAKSA-N 0.000 description 1
- GWCJMBNBFYBQCV-XPUUQOCRSA-N Gly-Val-Ala Chemical compound NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C)C(O)=O GWCJMBNBFYBQCV-XPUUQOCRSA-N 0.000 description 1
- IZVICCORZOSGPT-JSGCOSHPSA-N Gly-Val-Tyr Chemical compound [H]NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O IZVICCORZOSGPT-JSGCOSHPSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 108010078321 Guanylate Cyclase Proteins 0.000 description 1
- 102000014469 Guanylate cyclase Human genes 0.000 description 1
- AAXMRLWFJFDYQO-GUBZILKMSA-N His-Asp-Gln Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O AAXMRLWFJFDYQO-GUBZILKMSA-N 0.000 description 1
- HVCRQRQPIIRNLY-IUCAKERBSA-N His-Gln-Gly Chemical compound C1=C(NC=N1)C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)NCC(=O)O)N HVCRQRQPIIRNLY-IUCAKERBSA-N 0.000 description 1
- IMPKSPYRPUXYAP-SZMVWBNQSA-N His-Gln-Trp Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CC3=CN=CN3)N IMPKSPYRPUXYAP-SZMVWBNQSA-N 0.000 description 1
- BQFGKVYHKCNEMF-DCAQKATOSA-N His-Glu-Gln Chemical compound NC(=O)CC[C@@H](C(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](N)CC1=CN=CN1 BQFGKVYHKCNEMF-DCAQKATOSA-N 0.000 description 1
- QPSCMXDWVKWVOW-BZSNNMDCSA-N His-His-Tyr Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O QPSCMXDWVKWVOW-BZSNNMDCSA-N 0.000 description 1
- YAALVYQFVJNXIV-KKUMJFAQSA-N His-Leu-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CC1=CN=CN1 YAALVYQFVJNXIV-KKUMJFAQSA-N 0.000 description 1
- FJCGVRRVBKYYOU-DCAQKATOSA-N His-Met-Ser Chemical compound CSCC[C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](CC1=CN=CN1)N FJCGVRRVBKYYOU-DCAQKATOSA-N 0.000 description 1
- PFOUFRJYHWZJKW-NKIYYHGXSA-N His-Thr-Gln Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](CC1=CN=CN1)N)O PFOUFRJYHWZJKW-NKIYYHGXSA-N 0.000 description 1
- FOCSWPCHUDVNLP-PMVMPFDFSA-N His-Trp-Tyr Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CC3=CC=C(C=C3)O)C(=O)O)NC(=O)[C@H](CC4=CN=CN4)N FOCSWPCHUDVNLP-PMVMPFDFSA-N 0.000 description 1
- DAKSMIWQZPHRIB-BZSNNMDCSA-N His-Tyr-Leu Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC(C)C)C(O)=O DAKSMIWQZPHRIB-BZSNNMDCSA-N 0.000 description 1
- CSTDQOOBZBAJKE-BWAGICSOSA-N His-Tyr-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)NC(=O)[C@H](CC2=CN=CN2)N)O CSTDQOOBZBAJKE-BWAGICSOSA-N 0.000 description 1
- SYPULFZAGBBIOM-GVXVVHGQSA-N His-Val-Glu Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)O)NC(=O)[C@H](CC1=CN=CN1)N SYPULFZAGBBIOM-GVXVVHGQSA-N 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 101000616698 Homo sapiens CMP-N-acetylneuraminate-poly-alpha-2,8-sialyltransferase Proteins 0.000 description 1
- 101000635799 Homo sapiens Run domain Beclin-1-interacting and cysteine-rich domain-containing protein Proteins 0.000 description 1
- 108091006905 Human Serum Albumin Proteins 0.000 description 1
- 102000008100 Human Serum Albumin Human genes 0.000 description 1
- 206010020772 Hypertension Diseases 0.000 description 1
- BOTVMTSMOUSDRW-GMOBBJLQSA-N Ile-Arg-Asn Chemical compound CC[C@H](C)[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC(N)=O)C(O)=O BOTVMTSMOUSDRW-GMOBBJLQSA-N 0.000 description 1
- QYZYJFXHXYUZMZ-UGYAYLCHSA-N Ile-Asn-Asn Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC(=O)N)C(=O)O)N QYZYJFXHXYUZMZ-UGYAYLCHSA-N 0.000 description 1
- DFJJAVZIHDFOGQ-MNXVOIDGSA-N Ile-Glu-Lys Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)O)N DFJJAVZIHDFOGQ-MNXVOIDGSA-N 0.000 description 1
- CDGLBYSAZFIIJO-RCOVLWMOSA-N Ile-Gly-Gly Chemical compound CC[C@H](C)[C@H]([NH3+])C(=O)NCC(=O)NCC([O-])=O CDGLBYSAZFIIJO-RCOVLWMOSA-N 0.000 description 1
- URWXDJAEEGBADB-TUBUOCAGSA-N Ile-His-Thr Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N[C@@H]([C@@H](C)O)C(=O)O)N URWXDJAEEGBADB-TUBUOCAGSA-N 0.000 description 1
- GVKKVHNRTUFCCE-BJDJZHNGSA-N Ile-Leu-Ser Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)O)N GVKKVHNRTUFCCE-BJDJZHNGSA-N 0.000 description 1
- NPAYJTAXWXJKLO-NAKRPEOUSA-N Ile-Met-Ser Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(=O)O)N NPAYJTAXWXJKLO-NAKRPEOUSA-N 0.000 description 1
- IVXJIMGDOYRLQU-XUXIUFHCSA-N Ile-Pro-Leu Chemical compound CC[C@H](C)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(O)=O IVXJIMGDOYRLQU-XUXIUFHCSA-N 0.000 description 1
- CAHCWMVNBZJVAW-NAKRPEOUSA-N Ile-Pro-Ser Chemical compound CC[C@H](C)[C@@H](C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)O)N CAHCWMVNBZJVAW-NAKRPEOUSA-N 0.000 description 1
- AKQFLPNANHNTLP-VKOGCVSHSA-N Ile-Pro-Trp Chemical compound CC[C@H](C)[C@@H](C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC2=CNC3=CC=CC=C32)C(=O)O)N AKQFLPNANHNTLP-VKOGCVSHSA-N 0.000 description 1
- JZNVOBUNTWNZPW-GHCJXIJMSA-N Ile-Ser-Asp Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(=O)O)C(=O)O)N JZNVOBUNTWNZPW-GHCJXIJMSA-N 0.000 description 1
- FBGXMKUWQFPHFB-JBDRJPRFSA-N Ile-Ser-Cys Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CS)C(=O)O)N FBGXMKUWQFPHFB-JBDRJPRFSA-N 0.000 description 1
- SAEWJTCJQVZQNZ-IUKAMOBKSA-N Ile-Thr-Asn Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(=O)N)C(=O)O)N SAEWJTCJQVZQNZ-IUKAMOBKSA-N 0.000 description 1
- WCNWGAUZWWSYDG-SVSWQMSJSA-N Ile-Thr-Ser Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)O)N WCNWGAUZWWSYDG-SVSWQMSJSA-N 0.000 description 1
- NURNJECQNNCRBK-FLBSBUHZSA-N Ile-Thr-Thr Chemical compound CC[C@H](C)[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O NURNJECQNNCRBK-FLBSBUHZSA-N 0.000 description 1
- REXAUQBGSGDEJY-IGISWZIWSA-N Ile-Tyr-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)O)N REXAUQBGSGDEJY-IGISWZIWSA-N 0.000 description 1
- ZGKVPOSSTGHJAF-HJPIBITLSA-N Ile-Tyr-Ser Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](CO)C(=O)O)N ZGKVPOSSTGHJAF-HJPIBITLSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 102000018071 Immunoglobulin Fc Fragments Human genes 0.000 description 1
- 102000012745 Immunoglobulin Subunits Human genes 0.000 description 1
- 108010079585 Immunoglobulin Subunits Proteins 0.000 description 1
- 108010067060 Immunoglobulin Variable Region Proteins 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- RCFDOSNHHZGBOY-UHFFFAOYSA-N L-isoleucyl-L-alanine Natural products CCC(C)C(N)C(=O)NC(C)C(O)=O RCFDOSNHHZGBOY-UHFFFAOYSA-N 0.000 description 1
- KFKWRHQBZQICHA-STQMWFEESA-N L-leucyl-L-phenylalanine Natural products CC(C)C[C@H](N)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 KFKWRHQBZQICHA-STQMWFEESA-N 0.000 description 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
- FBOZXECLQNJBKD-ZDUSSCGKSA-N L-methotrexate Chemical compound C=1N=C2N=C(N)N=C(N)C2=NC=1CN(C)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 FBOZXECLQNJBKD-ZDUSSCGKSA-N 0.000 description 1
- IBMVEYRWAWIOTN-RWMBFGLXSA-N Leu-Arg-Pro Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@@H]1C(O)=O IBMVEYRWAWIOTN-RWMBFGLXSA-N 0.000 description 1
- VPKIQULSKFVCSM-SRVKXCTJSA-N Leu-Gln-Arg Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O VPKIQULSKFVCSM-SRVKXCTJSA-N 0.000 description 1
- KUEVMUXNILMJTK-JYJNAYRXSA-N Leu-Gln-Tyr Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 KUEVMUXNILMJTK-JYJNAYRXSA-N 0.000 description 1
- PRZVBIAOPFGAQF-SRVKXCTJSA-N Leu-Glu-Met Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCSC)C(O)=O PRZVBIAOPFGAQF-SRVKXCTJSA-N 0.000 description 1
- VWHGTYCRDRBSFI-ZETCQYMHSA-N Leu-Gly-Gly Chemical compound CC(C)C[C@H](N)C(=O)NCC(=O)NCC(O)=O VWHGTYCRDRBSFI-ZETCQYMHSA-N 0.000 description 1
- VGPCJSXPPOQPBK-YUMQZZPRSA-N Leu-Gly-Ser Chemical compound CC(C)C[C@H](N)C(=O)NCC(=O)N[C@@H](CO)C(O)=O VGPCJSXPPOQPBK-YUMQZZPRSA-N 0.000 description 1
- BTNXKBVLWJBTNR-SRVKXCTJSA-N Leu-His-Asn Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC(N)=O)C(O)=O BTNXKBVLWJBTNR-SRVKXCTJSA-N 0.000 description 1
- BKTXKJMNTSMJDQ-AVGNSLFASA-N Leu-His-Gln Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N[C@@H](CCC(=O)N)C(=O)O)N BKTXKJMNTSMJDQ-AVGNSLFASA-N 0.000 description 1
- CSFVADKICPDRRF-KKUMJFAQSA-N Leu-His-Leu Chemical compound CC(C)C[C@H]([NH3+])C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C([O-])=O)CC1=CN=CN1 CSFVADKICPDRRF-KKUMJFAQSA-N 0.000 description 1
- LKXANTUNFMVCNF-IHPCNDPISA-N Leu-His-Trp Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O LKXANTUNFMVCNF-IHPCNDPISA-N 0.000 description 1
- HRTRLSRYZZKPCO-BJDJZHNGSA-N Leu-Ile-Ser Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(O)=O HRTRLSRYZZKPCO-BJDJZHNGSA-N 0.000 description 1
- IAJFFZORSWOZPQ-SRVKXCTJSA-N Leu-Leu-Asn Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(O)=O IAJFFZORSWOZPQ-SRVKXCTJSA-N 0.000 description 1
- QNBVTHNJGCOVFA-AVGNSLFASA-N Leu-Leu-Glu Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(O)=O)CCC(O)=O QNBVTHNJGCOVFA-AVGNSLFASA-N 0.000 description 1
- JLWZLIQRYCTYBD-IHRRRGAJSA-N Leu-Lys-Arg Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O JLWZLIQRYCTYBD-IHRRRGAJSA-N 0.000 description 1
- HDHQQEDVWQGBEE-DCAQKATOSA-N Leu-Met-Ser Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(O)=O HDHQQEDVWQGBEE-DCAQKATOSA-N 0.000 description 1
- ZAVCJRJOQKIOJW-KKUMJFAQSA-N Leu-Phe-Asp Chemical compound CC(C)C[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CC(O)=O)C(O)=O)CC1=CC=CC=C1 ZAVCJRJOQKIOJW-KKUMJFAQSA-N 0.000 description 1
- UHNQRAFSEBGZFZ-YESZJQIVSA-N Leu-Phe-Pro Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N2CCC[C@@H]2C(=O)O)N UHNQRAFSEBGZFZ-YESZJQIVSA-N 0.000 description 1
- DPURXCQCHSQPAN-AVGNSLFASA-N Leu-Pro-Pro Chemical compound CC(C)C[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1[C@H](C(O)=O)CCC1 DPURXCQCHSQPAN-AVGNSLFASA-N 0.000 description 1
- SBANPBVRHYIMRR-UHFFFAOYSA-N Leu-Ser-Pro Natural products CC(C)CC(N)C(=O)NC(CO)C(=O)N1CCCC1C(O)=O SBANPBVRHYIMRR-UHFFFAOYSA-N 0.000 description 1
- QWWPYKKLXWOITQ-VOAKCMCISA-N Leu-Thr-Leu Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@H](C(O)=O)CC(C)C QWWPYKKLXWOITQ-VOAKCMCISA-N 0.000 description 1
- KLSUAWUZBMAZCL-RHYQMDGZSA-N Leu-Thr-Pro Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1CCC[C@H]1C(O)=O KLSUAWUZBMAZCL-RHYQMDGZSA-N 0.000 description 1
- ILDSIMPXNFWKLH-KATARQTJSA-N Leu-Thr-Ser Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(O)=O ILDSIMPXNFWKLH-KATARQTJSA-N 0.000 description 1
- JGKHAFUAPZCCDU-BZSNNMDCSA-N Leu-Tyr-Leu Chemical compound CC(C)C[C@H]([NH3+])C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C([O-])=O)CC1=CC=C(O)C=C1 JGKHAFUAPZCCDU-BZSNNMDCSA-N 0.000 description 1
- YIRIDPUGZKHMHT-ACRUOGEOSA-N Leu-Tyr-Tyr Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O YIRIDPUGZKHMHT-ACRUOGEOSA-N 0.000 description 1
- TUIOUEWKFFVNLH-DCAQKATOSA-N Leu-Val-Cys Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CS)C(O)=O TUIOUEWKFFVNLH-DCAQKATOSA-N 0.000 description 1
- LMDVGHQPPPLYAR-IHRRRGAJSA-N Leu-Val-His Chemical compound N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC1=CNC=N1)C(=O)O LMDVGHQPPPLYAR-IHRRRGAJSA-N 0.000 description 1
- VKVDRTGWLVZJOM-DCAQKATOSA-N Leu-Val-Ser Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CO)C(O)=O VKVDRTGWLVZJOM-DCAQKATOSA-N 0.000 description 1
- FZIJIFCXUCZHOL-CIUDSAMLSA-N Lys-Ala-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCCCN FZIJIFCXUCZHOL-CIUDSAMLSA-N 0.000 description 1
- MPGHETGWWWUHPY-CIUDSAMLSA-N Lys-Ala-Asp Chemical compound OC(=O)C[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCCCN MPGHETGWWWUHPY-CIUDSAMLSA-N 0.000 description 1
- WSXTWLJHTLRFLW-SRVKXCTJSA-N Lys-Ala-Lys Chemical compound NCCCC[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(O)=O WSXTWLJHTLRFLW-SRVKXCTJSA-N 0.000 description 1
- KNKHAVVBVXKOGX-JXUBOQSCSA-N Lys-Ala-Thr Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O KNKHAVVBVXKOGX-JXUBOQSCSA-N 0.000 description 1
- YNNPKXBBRZVIRX-IHRRRGAJSA-N Lys-Arg-Leu Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(O)=O YNNPKXBBRZVIRX-IHRRRGAJSA-N 0.000 description 1
- NTSPQIONFJUMJV-AVGNSLFASA-N Lys-Arg-Val Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(O)=O NTSPQIONFJUMJV-AVGNSLFASA-N 0.000 description 1
- MWVUEPNEPWMFBD-SRVKXCTJSA-N Lys-Cys-Lys Chemical compound NCCCC[C@H](N)C(=O)N[C@@H](CS)C(=O)N[C@H](C(O)=O)CCCCN MWVUEPNEPWMFBD-SRVKXCTJSA-N 0.000 description 1
- OVAOHZIOUBEQCJ-IHRRRGAJSA-N Lys-Leu-Arg Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O OVAOHZIOUBEQCJ-IHRRRGAJSA-N 0.000 description 1
- WRODMZBHNNPRLN-SRVKXCTJSA-N Lys-Leu-Ser Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(O)=O WRODMZBHNNPRLN-SRVKXCTJSA-N 0.000 description 1
- LUTDBHBIHHREDC-IHRRRGAJSA-N Lys-Pro-Lys Chemical compound NCCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCCN)C(O)=O LUTDBHBIHHREDC-IHRRRGAJSA-N 0.000 description 1
- MGKFCQFVPKOWOL-CIUDSAMLSA-N Lys-Ser-Asp Chemical compound C(CCN)C[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(=O)O)C(=O)O)N MGKFCQFVPKOWOL-CIUDSAMLSA-N 0.000 description 1
- SBQDRNOLGSYHQA-YUMQZZPRSA-N Lys-Ser-Gly Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)NCC(O)=O SBQDRNOLGSYHQA-YUMQZZPRSA-N 0.000 description 1
- LKDXINHHSWFFJC-SRVKXCTJSA-N Lys-Ser-His Chemical compound C1=C(NC=N1)C[C@@H](C(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)N LKDXINHHSWFFJC-SRVKXCTJSA-N 0.000 description 1
- JOSAKOKSPXROGQ-BJDJZHNGSA-N Lys-Ser-Ile Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O JOSAKOKSPXROGQ-BJDJZHNGSA-N 0.000 description 1
- WZVSHTFTCYOFPL-GARJFASQSA-N Lys-Ser-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CO)NC(=O)[C@H](CCCCN)N)C(=O)O WZVSHTFTCYOFPL-GARJFASQSA-N 0.000 description 1
- DIBZLYZXTSVGLN-CIUDSAMLSA-N Lys-Ser-Ser Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O DIBZLYZXTSVGLN-CIUDSAMLSA-N 0.000 description 1
- PLOUVAYOMTYJRG-JXUBOQSCSA-N Lys-Thr-Ala Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C)C(O)=O PLOUVAYOMTYJRG-JXUBOQSCSA-N 0.000 description 1
- RPWTZTBIFGENIA-VOAKCMCISA-N Lys-Thr-Leu Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(O)=O RPWTZTBIFGENIA-VOAKCMCISA-N 0.000 description 1
- YKBSXQFZWFXFIB-VOAKCMCISA-N Lys-Thr-Lys Chemical compound NCCCC[C@H](N)C(=O)N[C@@H]([C@H](O)C)C(=O)N[C@@H](CCCCN)C(O)=O YKBSXQFZWFXFIB-VOAKCMCISA-N 0.000 description 1
- XABXVVSWUVCZST-GVXVVHGQSA-N Lys-Val-Gln Chemical compound NC(=O)CC[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)CCCCN XABXVVSWUVCZST-GVXVVHGQSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- VOOINLQYUZOREH-SRVKXCTJSA-N Met-Gln-Leu Chemical compound CC(C)C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CCSC)N VOOINLQYUZOREH-SRVKXCTJSA-N 0.000 description 1
- SJDQOYTYNGZZJX-SRVKXCTJSA-N Met-Glu-Leu Chemical compound CSCC[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(O)=O SJDQOYTYNGZZJX-SRVKXCTJSA-N 0.000 description 1
- RKIIYGUHIQJCBW-SRVKXCTJSA-N Met-His-Glu Chemical compound [H]N[C@@H](CCSC)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CCC(O)=O)C(O)=O RKIIYGUHIQJCBW-SRVKXCTJSA-N 0.000 description 1
- WXJXYMFUTRXRGO-UWVGGRQHSA-N Met-His-Gly Chemical compound CSCC[C@H](N)C(=O)N[C@H](C(=O)NCC(O)=O)CC1=CNC=N1 WXJXYMFUTRXRGO-UWVGGRQHSA-N 0.000 description 1
- JHDNAOVJJQSMMM-GMOBBJLQSA-N Met-Ile-Asp Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)O)NC(=O)[C@H](CCSC)N JHDNAOVJJQSMMM-GMOBBJLQSA-N 0.000 description 1
- FWAHLGXNBLWIKB-NAKRPEOUSA-N Met-Ile-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@@H](N)CCSC FWAHLGXNBLWIKB-NAKRPEOUSA-N 0.000 description 1
- UROWNMBTQGGTHB-DCAQKATOSA-N Met-Leu-Asp Chemical compound CSCC[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(O)=O)C(O)=O UROWNMBTQGGTHB-DCAQKATOSA-N 0.000 description 1
- WRXOPYNEKGZWAZ-FXQIFTODSA-N Met-Ser-Cys Chemical compound CSCC[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CS)C(O)=O WRXOPYNEKGZWAZ-FXQIFTODSA-N 0.000 description 1
- LHXFNWBNRBWMNV-DCAQKATOSA-N Met-Ser-His Chemical compound CSCC[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)N LHXFNWBNRBWMNV-DCAQKATOSA-N 0.000 description 1
- IHRFZLQEQVHXFA-RHYQMDGZSA-N Met-Thr-Lys Chemical compound CSCC[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@H](C(O)=O)CCCCN IHRFZLQEQVHXFA-RHYQMDGZSA-N 0.000 description 1
- ATBJCCFCJXCNGZ-UFYCRDLUSA-N Met-Tyr-Phe Chemical compound C([C@H](NC(=O)[C@@H](N)CCSC)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=C(O)C=C1 ATBJCCFCJXCNGZ-UFYCRDLUSA-N 0.000 description 1
- 101001077415 Mus musculus Potassium voltage-gated channel subfamily H member 8 Proteins 0.000 description 1
- 101100370002 Mus musculus Tnfsf14 gene Proteins 0.000 description 1
- WUGMRIBZSVSJNP-UHFFFAOYSA-N N-L-alanyl-L-tryptophan Natural products C1=CC=C2C(CC(NC(=O)C(N)C)C(O)=O)=CNC2=C1 WUGMRIBZSVSJNP-UHFFFAOYSA-N 0.000 description 1
- WYBVBIHNJWOLCJ-UHFFFAOYSA-N N-L-arginyl-L-leucine Natural products CC(C)CC(C(O)=O)NC(=O)C(N)CCCN=C(N)N WYBVBIHNJWOLCJ-UHFFFAOYSA-N 0.000 description 1
- XZFYRXDAULDNFX-UHFFFAOYSA-N N-L-cysteinyl-L-phenylalanine Natural products SCC(N)C(=O)NC(C(O)=O)CC1=CC=CC=C1 XZFYRXDAULDNFX-UHFFFAOYSA-N 0.000 description 1
- 108010002311 N-glycylglutamic acid Proteins 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 108700026244 Open Reading Frames Proteins 0.000 description 1
- HXSUFWQYLPKEHF-IHRRRGAJSA-N Phe-Asn-Arg Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)N HXSUFWQYLPKEHF-IHRRRGAJSA-N 0.000 description 1
- JOXIIFVCSATTDH-IHPCNDPISA-N Phe-Asn-Trp Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC2=CNC3=CC=CC=C32)C(=O)O)N JOXIIFVCSATTDH-IHPCNDPISA-N 0.000 description 1
- IUVYJBMTHARMIP-PCBIJLKTSA-N Phe-Asp-Ile Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O IUVYJBMTHARMIP-PCBIJLKTSA-N 0.000 description 1
- LXUJDHOKVUYHRC-KKUMJFAQSA-N Phe-Cys-Leu Chemical compound CC(C)C[C@@H](C(=O)O)NC(=O)[C@H](CS)NC(=O)[C@H](CC1=CC=CC=C1)N LXUJDHOKVUYHRC-KKUMJFAQSA-N 0.000 description 1
- LLGTYVHITPVGKR-RYUDHWBXSA-N Phe-Gln-Gly Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(O)=O LLGTYVHITPVGKR-RYUDHWBXSA-N 0.000 description 1
- YYKZDTVQHTUKDW-RYUDHWBXSA-N Phe-Gly-Gln Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)NCC(=O)N[C@@H](CCC(=O)N)C(=O)O)N YYKZDTVQHTUKDW-RYUDHWBXSA-N 0.000 description 1
- VJLLEKDQJSMHRU-STQMWFEESA-N Phe-Gly-Met Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)NCC(=O)N[C@@H](CCSC)C(O)=O VJLLEKDQJSMHRU-STQMWFEESA-N 0.000 description 1
- BWTKUQPNOMMKMA-FIRPJDEBSA-N Phe-Ile-Phe Chemical compound C([C@H](N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=CC=C1 BWTKUQPNOMMKMA-FIRPJDEBSA-N 0.000 description 1
- ZJPGOXWRFNKIQL-JYJNAYRXSA-N Phe-Pro-Pro Chemical compound C([C@H](N)C(=O)N1[C@@H](CCC1)C(=O)N1[C@@H](CCC1)C(O)=O)C1=CC=CC=C1 ZJPGOXWRFNKIQL-JYJNAYRXSA-N 0.000 description 1
- MSSXKZBDKZAHCX-UNQGMJICSA-N Phe-Thr-Val Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(O)=O MSSXKZBDKZAHCX-UNQGMJICSA-N 0.000 description 1
- ZVJGAXNBBKPYOE-HKUYNNGSSA-N Phe-Trp-Gly Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)NCC(O)=O)C1=CC=CC=C1 ZVJGAXNBBKPYOE-HKUYNNGSSA-N 0.000 description 1
- 208000004880 Polyuria Diseases 0.000 description 1
- 102220630778 Presenilin-1_L14H_mutation Human genes 0.000 description 1
- DBALDZKOTNSBFM-FXQIFTODSA-N Pro-Ala-Asn Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(O)=O DBALDZKOTNSBFM-FXQIFTODSA-N 0.000 description 1
- CYQQWUPHIZVCNY-GUBZILKMSA-N Pro-Arg-Ser Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(O)=O CYQQWUPHIZVCNY-GUBZILKMSA-N 0.000 description 1
- AMBLXEMWFARNNQ-DCAQKATOSA-N Pro-Asn-Leu Chemical compound CC(C)C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@@H]1CCCN1 AMBLXEMWFARNNQ-DCAQKATOSA-N 0.000 description 1
- GDXZRWYXJSGWIV-GMOBBJLQSA-N Pro-Asp-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H]1CCCN1 GDXZRWYXJSGWIV-GMOBBJLQSA-N 0.000 description 1
- SFECXGVELZFBFJ-VEVYYDQMSA-N Pro-Asp-Thr Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O SFECXGVELZFBFJ-VEVYYDQMSA-N 0.000 description 1
- PULPZRAHVFBVTO-DCAQKATOSA-N Pro-Glu-Arg Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O PULPZRAHVFBVTO-DCAQKATOSA-N 0.000 description 1
- KIPIKSXPPLABPN-CIUDSAMLSA-N Pro-Glu-Asn Chemical compound NC(=O)C[C@@H](C(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H]1CCCN1 KIPIKSXPPLABPN-CIUDSAMLSA-N 0.000 description 1
- MGDFPGCFVJFITQ-CIUDSAMLSA-N Pro-Glu-Asp Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(O)=O MGDFPGCFVJFITQ-CIUDSAMLSA-N 0.000 description 1
- UUHXBJHVTVGSKM-BQBZGAKWSA-N Pro-Gly-Asn Chemical compound [H]N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](CC(N)=O)C(O)=O UUHXBJHVTVGSKM-BQBZGAKWSA-N 0.000 description 1
- HAAQQNHQZBOWFO-LURJTMIESA-N Pro-Gly-Gly Chemical compound OC(=O)CNC(=O)CNC(=O)[C@@H]1CCCN1 HAAQQNHQZBOWFO-LURJTMIESA-N 0.000 description 1
- UIMCLYYSUCIUJM-UWVGGRQHSA-N Pro-Gly-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H]1CCCN1 UIMCLYYSUCIUJM-UWVGGRQHSA-N 0.000 description 1
- BRJGUPWVFXKBQI-XUXIUFHCSA-N Pro-Leu-Ile Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O BRJGUPWVFXKBQI-XUXIUFHCSA-N 0.000 description 1
- JUJCUYWRJMFJJF-AVGNSLFASA-N Pro-Lys-Arg Chemical compound NC(N)=NCCC[C@@H](C(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@@H]1CCCN1 JUJCUYWRJMFJJF-AVGNSLFASA-N 0.000 description 1
- ULWBBFKQBDNGOY-RWMBFGLXSA-N Pro-Lys-Pro Chemical compound C1C[C@H](NC1)C(=O)N[C@@H](CCCCN)C(=O)N2CCC[C@@H]2C(=O)O ULWBBFKQBDNGOY-RWMBFGLXSA-N 0.000 description 1
- WLJYLAQSUSIQNH-GUBZILKMSA-N Pro-Met-Ser Chemical compound CSCC[C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@@H]1CCCN1 WLJYLAQSUSIQNH-GUBZILKMSA-N 0.000 description 1
- SXJOPONICMGFCR-DCAQKATOSA-N Pro-Ser-Lys Chemical compound C1C[C@H](NC1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)O SXJOPONICMGFCR-DCAQKATOSA-N 0.000 description 1
- MKGIILKDUGDRRO-FXQIFTODSA-N Pro-Ser-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H]1CCCN1 MKGIILKDUGDRRO-FXQIFTODSA-N 0.000 description 1
- VVEQUISRWJDGMX-VKOGCVSHSA-N Pro-Trp-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CC1=CNC2=CC=CC=C21)NC(=O)[C@@H]3CCCN3 VVEQUISRWJDGMX-VKOGCVSHSA-N 0.000 description 1
- QKWYXRPICJEQAJ-KJEVXHAQSA-N Pro-Tyr-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)NC(=O)[C@@H]2CCCN2)O QKWYXRPICJEQAJ-KJEVXHAQSA-N 0.000 description 1
- XDKKMRPRRCOELJ-GUBZILKMSA-N Pro-Val-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C(C)C)NC(=O)[C@@H]1CCCN1 XDKKMRPRRCOELJ-GUBZILKMSA-N 0.000 description 1
- KHRLUIPIMIQFGT-AVGNSLFASA-N Pro-Val-Leu Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(O)=O KHRLUIPIMIQFGT-AVGNSLFASA-N 0.000 description 1
- 229940127314 Prostacyclin Receptor Agonists Drugs 0.000 description 1
- 102100030086 Receptor tyrosine-protein kinase erbB-2 Human genes 0.000 description 1
- 101710100968 Receptor tyrosine-protein kinase erbB-2 Proteins 0.000 description 1
- 108700005075 Regulator Genes Proteins 0.000 description 1
- 206010039163 Right ventricular failure Diseases 0.000 description 1
- UEJYSALTSUZXFV-SRVKXCTJSA-N Rigin Chemical compound NCC(=O)N[C@@H](CCC(N)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(O)=O UEJYSALTSUZXFV-SRVKXCTJSA-N 0.000 description 1
- 241000714474 Rous sarcoma virus Species 0.000 description 1
- 102100030852 Run domain Beclin-1-interacting and cysteine-rich domain-containing protein Human genes 0.000 description 1
- 229920002684 Sepharose Polymers 0.000 description 1
- WTWGOQRNRFHFQD-JBDRJPRFSA-N Ser-Ala-Ile Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O WTWGOQRNRFHFQD-JBDRJPRFSA-N 0.000 description 1
- YQHZVYJAGWMHES-ZLUOBGJFSA-N Ser-Ala-Ser Chemical compound OC[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(O)=O YQHZVYJAGWMHES-ZLUOBGJFSA-N 0.000 description 1
- JPIDMRXXNMIVKY-VZFHVOOUSA-N Ser-Ala-Thr Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O JPIDMRXXNMIVKY-VZFHVOOUSA-N 0.000 description 1
- HZWAHWQZPSXNCB-BPUTZDHNSA-N Ser-Arg-Trp Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O HZWAHWQZPSXNCB-BPUTZDHNSA-N 0.000 description 1
- BCKYYTVFBXHPOG-ACZMJKKPSA-N Ser-Asn-Gln Chemical compound C(CC(=O)N)[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CO)N BCKYYTVFBXHPOG-ACZMJKKPSA-N 0.000 description 1
- KAAPNMOKUUPKOE-SRVKXCTJSA-N Ser-Asn-Phe Chemical compound OC[C@H](N)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 KAAPNMOKUUPKOE-SRVKXCTJSA-N 0.000 description 1
- QPFJSHSJFIYDJZ-GHCJXIJMSA-N Ser-Asp-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H](N)CO QPFJSHSJFIYDJZ-GHCJXIJMSA-N 0.000 description 1
- OLIJLNWFEQEFDM-SRVKXCTJSA-N Ser-Asp-Phe Chemical compound OC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 OLIJLNWFEQEFDM-SRVKXCTJSA-N 0.000 description 1
- ULVMNZOKDBHKKI-ACZMJKKPSA-N Ser-Gln-Asp Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(O)=O ULVMNZOKDBHKKI-ACZMJKKPSA-N 0.000 description 1
- ZOHGLPQGEHSLPD-FXQIFTODSA-N Ser-Gln-Glu Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(O)=O ZOHGLPQGEHSLPD-FXQIFTODSA-N 0.000 description 1
- XWCYBVBLJRWOFR-WDSKDSINSA-N Ser-Gln-Gly Chemical compound OC[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(O)=O XWCYBVBLJRWOFR-WDSKDSINSA-N 0.000 description 1
- KJMOINFQVCCSDX-XKBZYTNZSA-N Ser-Gln-Thr Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O KJMOINFQVCCSDX-XKBZYTNZSA-N 0.000 description 1
- VDVYTKZBMFADQH-AVGNSLFASA-N Ser-Gln-Tyr Chemical compound OC[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 VDVYTKZBMFADQH-AVGNSLFASA-N 0.000 description 1
- SQBLRDDJTUJDMV-ACZMJKKPSA-N Ser-Glu-Asn Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O SQBLRDDJTUJDMV-ACZMJKKPSA-N 0.000 description 1
- HJEBZBMOTCQYDN-ACZMJKKPSA-N Ser-Glu-Asp Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(O)=O HJEBZBMOTCQYDN-ACZMJKKPSA-N 0.000 description 1
- WBINSDOPZHQPPM-AVGNSLFASA-N Ser-Glu-Tyr Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CO)N)O WBINSDOPZHQPPM-AVGNSLFASA-N 0.000 description 1
- BPMRXBZYPGYPJN-WHFBIAKZSA-N Ser-Gly-Asn Chemical compound [H]N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CC(N)=O)C(O)=O BPMRXBZYPGYPJN-WHFBIAKZSA-N 0.000 description 1
- SVWQEIRZHHNBIO-WHFBIAKZSA-N Ser-Gly-Cys Chemical compound [H]N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CS)C(O)=O SVWQEIRZHHNBIO-WHFBIAKZSA-N 0.000 description 1
- UAJAYRMZGNQILN-BQBZGAKWSA-N Ser-Gly-Met Chemical compound [H]N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CCSC)C(O)=O UAJAYRMZGNQILN-BQBZGAKWSA-N 0.000 description 1
- SFTZWNJFZYOLBD-ZDLURKLDSA-N Ser-Gly-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)CO SFTZWNJFZYOLBD-ZDLURKLDSA-N 0.000 description 1
- QBUWQRKEHJXTOP-DCAQKATOSA-N Ser-His-Arg Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O QBUWQRKEHJXTOP-DCAQKATOSA-N 0.000 description 1
- CLKKNZQUQMZDGD-SRVKXCTJSA-N Ser-His-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)CO)CC1=CN=CN1 CLKKNZQUQMZDGD-SRVKXCTJSA-N 0.000 description 1
- WEQAYODCJHZSJZ-KKUMJFAQSA-N Ser-His-Tyr Chemical compound C([C@H](NC(=O)[C@H](CO)N)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(O)=O)C1=CN=CN1 WEQAYODCJHZSJZ-KKUMJFAQSA-N 0.000 description 1
- LQESNKGTTNHZPZ-GHCJXIJMSA-N Ser-Ile-Asn Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(N)=O)C(O)=O LQESNKGTTNHZPZ-GHCJXIJMSA-N 0.000 description 1
- MOINZPRHJGTCHZ-MMWGEVLESA-N Ser-Ile-Pro Chemical compound CC[C@H](C)[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CO)N MOINZPRHJGTCHZ-MMWGEVLESA-N 0.000 description 1
- ZOPISOXXPQNOCO-SVSWQMSJSA-N Ser-Ile-Thr Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H]([C@@H](C)O)C(=O)O)NC(=O)[C@H](CO)N ZOPISOXXPQNOCO-SVSWQMSJSA-N 0.000 description 1
- NLOAIFSWUUFQFR-CIUDSAMLSA-N Ser-Leu-Asp Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(O)=O)C(O)=O NLOAIFSWUUFQFR-CIUDSAMLSA-N 0.000 description 1
- GJFYFGOEWLDQGW-GUBZILKMSA-N Ser-Leu-Gln Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](CO)N GJFYFGOEWLDQGW-GUBZILKMSA-N 0.000 description 1
- XNCUYZKGQOCOQH-YUMQZZPRSA-N Ser-Leu-Gly Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)NCC(O)=O XNCUYZKGQOCOQH-YUMQZZPRSA-N 0.000 description 1
- XUDRHBPSPAPDJP-SRVKXCTJSA-N Ser-Lys-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CO XUDRHBPSPAPDJP-SRVKXCTJSA-N 0.000 description 1
- QJKPECIAWNNKIT-KKUMJFAQSA-N Ser-Lys-Tyr Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O QJKPECIAWNNKIT-KKUMJFAQSA-N 0.000 description 1
- GDUZTEQRAOXYJS-SRVKXCTJSA-N Ser-Phe-Asn Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)[C@H](CO)N GDUZTEQRAOXYJS-SRVKXCTJSA-N 0.000 description 1
- KZPRPBLHYMZIMH-MXAVVETBSA-N Ser-Phe-Ile Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O KZPRPBLHYMZIMH-MXAVVETBSA-N 0.000 description 1
- RRVFEDGUXSYWOW-BZSNNMDCSA-N Ser-Phe-Phe Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O RRVFEDGUXSYWOW-BZSNNMDCSA-N 0.000 description 1
- AZWNCEBQZXELEZ-FXQIFTODSA-N Ser-Pro-Ser Chemical compound OC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(O)=O AZWNCEBQZXELEZ-FXQIFTODSA-N 0.000 description 1
- WLJPJRGQRNCIQS-ZLUOBGJFSA-N Ser-Ser-Asn Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(O)=O WLJPJRGQRNCIQS-ZLUOBGJFSA-N 0.000 description 1
- DYEGLQRVMBWQLD-IXOXFDKPSA-N Ser-Thr-Phe Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)NC(=O)[C@H](CO)N)O DYEGLQRVMBWQLD-IXOXFDKPSA-N 0.000 description 1
- UBTNVMGPMYDYIU-HJPIBITLSA-N Ser-Tyr-Ile Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O UBTNVMGPMYDYIU-HJPIBITLSA-N 0.000 description 1
- YXGCIEUDOHILKR-IHRRRGAJSA-N Ser-Tyr-Met Chemical compound CSCC[C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)NC(=O)[C@H](CO)N YXGCIEUDOHILKR-IHRRRGAJSA-N 0.000 description 1
- VVKVHAOOUGNDPJ-SRVKXCTJSA-N Ser-Tyr-Ser Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CO)C(O)=O VVKVHAOOUGNDPJ-SRVKXCTJSA-N 0.000 description 1
- IAOHCSQDQDWRQU-GUBZILKMSA-N Ser-Val-Arg Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O IAOHCSQDQDWRQU-GUBZILKMSA-N 0.000 description 1
- JGUWRQWULDWNCM-FXQIFTODSA-N Ser-Val-Ser Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CO)C(O)=O JGUWRQWULDWNCM-FXQIFTODSA-N 0.000 description 1
- SIEBDTCABMZCLF-XGEHTFHBSA-N Ser-Val-Thr Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O SIEBDTCABMZCLF-XGEHTFHBSA-N 0.000 description 1
- HSWXBJCBYSWBPT-GUBZILKMSA-N Ser-Val-Val Chemical compound CC(C)[C@H](NC(=O)[C@@H](NC(=O)[C@@H](N)CO)C(C)C)C(O)=O HSWXBJCBYSWBPT-GUBZILKMSA-N 0.000 description 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
- 108010003723 Single-Domain Antibodies Proteins 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 239000004098 Tetracycline Substances 0.000 description 1
- NJEMRSFGDNECGF-GCJQMDKQSA-N Thr-Ala-Asp Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@H](C(O)=O)CC(O)=O NJEMRSFGDNECGF-GCJQMDKQSA-N 0.000 description 1
- KEGBFULVYKYJRD-LFSVMHDDSA-N Thr-Ala-Phe Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 KEGBFULVYKYJRD-LFSVMHDDSA-N 0.000 description 1
- DWYAUVCQDTZIJI-VZFHVOOUSA-N Thr-Ala-Ser Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(O)=O DWYAUVCQDTZIJI-VZFHVOOUSA-N 0.000 description 1
- JNQZPAWOPBZGIX-RCWTZXSCSA-N Thr-Arg-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)[C@@H](C)O)CCCN=C(N)N JNQZPAWOPBZGIX-RCWTZXSCSA-N 0.000 description 1
- DCLBXIWHLVEPMQ-JRQIVUDYSA-N Thr-Asp-Tyr Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 DCLBXIWHLVEPMQ-JRQIVUDYSA-N 0.000 description 1
- LAFLAXHTDVNVEL-WDCWCFNPSA-N Thr-Gln-Lys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCCCN)C(=O)O)N)O LAFLAXHTDVNVEL-WDCWCFNPSA-N 0.000 description 1
- VOHWDZNIESHTFW-XKBZYTNZSA-N Thr-Glu-Cys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CS)C(=O)O)N)O VOHWDZNIESHTFW-XKBZYTNZSA-N 0.000 description 1
- GKWNLDNXMMLRMC-GLLZPBPUSA-N Thr-Glu-Gln Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)N)C(=O)O)N)O GKWNLDNXMMLRMC-GLLZPBPUSA-N 0.000 description 1
- OQCXTUQTKQFDCX-HTUGSXCWSA-N Thr-Glu-Phe Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)N)O OQCXTUQTKQFDCX-HTUGSXCWSA-N 0.000 description 1
- QQWNRERCGGZOKG-WEDXCCLWSA-N Thr-Gly-Leu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N[C@@H](CC(C)C)C(O)=O QQWNRERCGGZOKG-WEDXCCLWSA-N 0.000 description 1
- WPSDXXQRIVKBAY-NKIYYHGXSA-N Thr-His-Glu Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N[C@@H](CCC(=O)O)C(=O)O)N)O WPSDXXQRIVKBAY-NKIYYHGXSA-N 0.000 description 1
- BVOVIGCHYNFJBZ-JXUBOQSCSA-N Thr-Leu-Ala Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(O)=O BVOVIGCHYNFJBZ-JXUBOQSCSA-N 0.000 description 1
- HOVLHEKTGVIKAP-WDCWCFNPSA-N Thr-Leu-Gln Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O HOVLHEKTGVIKAP-WDCWCFNPSA-N 0.000 description 1
- PRNGXSILMXSWQQ-OEAJRASXSA-N Thr-Leu-Phe Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O PRNGXSILMXSWQQ-OEAJRASXSA-N 0.000 description 1
- JLNMFGCJODTXDH-WEDXCCLWSA-N Thr-Lys-Gly Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)NCC(O)=O JLNMFGCJODTXDH-WEDXCCLWSA-N 0.000 description 1
- QFEYTTHKPSOFLV-OSUNSFLBSA-N Thr-Met-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CCSC)NC(=O)[C@H]([C@@H](C)O)N QFEYTTHKPSOFLV-OSUNSFLBSA-N 0.000 description 1
- WRQLCVIALDUQEQ-UNQGMJICSA-N Thr-Phe-Arg Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O WRQLCVIALDUQEQ-UNQGMJICSA-N 0.000 description 1
- WYLAVUAWOUVUCA-XVSYOHENSA-N Thr-Phe-Asp Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC(O)=O)C(O)=O WYLAVUAWOUVUCA-XVSYOHENSA-N 0.000 description 1
- GYUUYCIXELGTJS-MEYUZBJRSA-N Thr-Phe-His Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC2=CN=CN2)C(=O)O)N)O GYUUYCIXELGTJS-MEYUZBJRSA-N 0.000 description 1
- XKWABWFMQXMUMT-HJGDQZAQSA-N Thr-Pro-Glu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(O)=O XKWABWFMQXMUMT-HJGDQZAQSA-N 0.000 description 1
- KERCOYANYUPLHJ-XGEHTFHBSA-N Thr-Pro-Ser Chemical compound C[C@@H](O)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(O)=O KERCOYANYUPLHJ-XGEHTFHBSA-N 0.000 description 1
- WPSKTVVMQCXPRO-BWBBJGPYSA-N Thr-Ser-Ser Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O WPSKTVVMQCXPRO-BWBBJGPYSA-N 0.000 description 1
- CSNBWOJOEOPYIJ-UVOCVTCTSA-N Thr-Thr-Lys Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(O)=O CSNBWOJOEOPYIJ-UVOCVTCTSA-N 0.000 description 1
- ZESGVALRVJIVLZ-VFCFLDTKSA-N Thr-Thr-Pro Chemical compound C[C@H]([C@@H](C(=O)N[C@@H]([C@@H](C)O)C(=O)N1CCC[C@@H]1C(=O)O)N)O ZESGVALRVJIVLZ-VFCFLDTKSA-N 0.000 description 1
- ZMYCLHFLHRVOEA-HEIBUPTGSA-N Thr-Thr-Ser Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(O)=O ZMYCLHFLHRVOEA-HEIBUPTGSA-N 0.000 description 1
- COYHRQWNJDJCNA-NUJDXYNKSA-N Thr-Thr-Thr Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O COYHRQWNJDJCNA-NUJDXYNKSA-N 0.000 description 1
- LECUEEHKUFYOOV-ZJDVBMNYSA-N Thr-Thr-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@@H](N)[C@@H](C)O LECUEEHKUFYOOV-ZJDVBMNYSA-N 0.000 description 1
- FYBFTPLPAXZBOY-KKHAAJSZSA-N Thr-Val-Asp Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(O)=O FYBFTPLPAXZBOY-KKHAAJSZSA-N 0.000 description 1
- KPMIQCXJDVKWKO-IFFSRLJSSA-N Thr-Val-Glu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O KPMIQCXJDVKWKO-IFFSRLJSSA-N 0.000 description 1
- KZTLZZQTJMCGIP-ZJDVBMNYSA-N Thr-Val-Thr Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O KZTLZZQTJMCGIP-ZJDVBMNYSA-N 0.000 description 1
- 208000007536 Thrombosis Diseases 0.000 description 1
- 102000004338 Transferrin Human genes 0.000 description 1
- 108090000901 Transferrin Proteins 0.000 description 1
- 229920004890 Triton X-100 Polymers 0.000 description 1
- 239000013504 Triton X-100 Substances 0.000 description 1
- WPSYJHFHZYJXMW-JSGCOSHPSA-N Trp-Gln-Gly Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(O)=O WPSYJHFHZYJXMW-JSGCOSHPSA-N 0.000 description 1
- UDCHKDYNMRJYMI-QEJZJMRPSA-N Trp-Glu-Ser Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(O)=O UDCHKDYNMRJYMI-QEJZJMRPSA-N 0.000 description 1
- GQHAIUPYZPTADF-FDARSICLSA-N Trp-Ile-Arg Chemical compound C1=CC=C2C(C[C@H](N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O)=CNC2=C1 GQHAIUPYZPTADF-FDARSICLSA-N 0.000 description 1
- ILDJYIDXESUBOE-HSCHXYMDSA-N Trp-Ile-Lys Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CC1=CNC2=CC=CC=C21)N ILDJYIDXESUBOE-HSCHXYMDSA-N 0.000 description 1
- XGFGVFMXDXALEV-XIRDDKMYSA-N Trp-Leu-Asn Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)[C@H](CC1=CNC2=CC=CC=C21)N XGFGVFMXDXALEV-XIRDDKMYSA-N 0.000 description 1
- NLLARHRWSFNEMH-NUTKFTJISA-N Trp-Lys-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC1=CNC2=CC=CC=C21)N NLLARHRWSFNEMH-NUTKFTJISA-N 0.000 description 1
- NLWCSMOXNKBRLC-WDSOQIARSA-N Trp-Lys-Val Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(O)=O NLWCSMOXNKBRLC-WDSOQIARSA-N 0.000 description 1
- ARKBYVBCEOWRNR-UBHSHLNASA-N Trp-Ser-Ser Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O ARKBYVBCEOWRNR-UBHSHLNASA-N 0.000 description 1
- GSCPHMSPGQSZJT-JYBASQMISA-N Trp-Ser-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC1=CNC2=CC=CC=C21)N)O GSCPHMSPGQSZJT-JYBASQMISA-N 0.000 description 1
- SSSDKJMQMZTMJP-BVSLBCMMSA-N Trp-Tyr-Val Chemical compound C([C@@H](C(=O)N[C@@H](C(C)C)C(O)=O)NC(=O)[C@@H](N)CC=1C2=CC=CC=C2NC=1)C1=CC=C(O)C=C1 SSSDKJMQMZTMJP-BVSLBCMMSA-N 0.000 description 1
- QJBWZNTWJSZUOY-UWJYBYFXSA-N Tyr-Ala-Cys Chemical compound C[C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)N QJBWZNTWJSZUOY-UWJYBYFXSA-N 0.000 description 1
- NOXKHHXSHQFSGJ-FQPOAREZSA-N Tyr-Ala-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 NOXKHHXSHQFSGJ-FQPOAREZSA-N 0.000 description 1
- IIJWXEUNETVJPV-IHRRRGAJSA-N Tyr-Arg-Ser Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CO)C(=O)O)N)O IIJWXEUNETVJPV-IHRRRGAJSA-N 0.000 description 1
- QYSBJAUCUKHSLU-JYJNAYRXSA-N Tyr-Arg-Val Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(O)=O QYSBJAUCUKHSLU-JYJNAYRXSA-N 0.000 description 1
- YGKVNUAKYPGORG-AVGNSLFASA-N Tyr-Asp-Glu Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(O)=O YGKVNUAKYPGORG-AVGNSLFASA-N 0.000 description 1
- QOEZFICGUZTRFX-IHRRRGAJSA-N Tyr-Cys-Val Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CS)C(=O)N[C@@H](C(C)C)C(O)=O QOEZFICGUZTRFX-IHRRRGAJSA-N 0.000 description 1
- SLCSPPCQWUHPPO-JYJNAYRXSA-N Tyr-Glu-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 SLCSPPCQWUHPPO-JYJNAYRXSA-N 0.000 description 1
- FNWGDMZVYBVAGJ-XEGUGMAKSA-N Tyr-Gly-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)CNC(=O)[C@H](CC1=CC=C(C=C1)O)N FNWGDMZVYBVAGJ-XEGUGMAKSA-N 0.000 description 1
- DZKFGCNKEVMXFA-JUKXBJQTSA-N Tyr-Ile-His Chemical compound CC[C@H](C)[C@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(O)=O DZKFGCNKEVMXFA-JUKXBJQTSA-N 0.000 description 1
- NSGZILIDHCIZAM-KKUMJFAQSA-N Tyr-Leu-Ser Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)N NSGZILIDHCIZAM-KKUMJFAQSA-N 0.000 description 1
- GZUIDWDVMWZSMI-KKUMJFAQSA-N Tyr-Lys-Cys Chemical compound NCCCC[C@@H](C(=O)N[C@@H](CS)C(O)=O)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 GZUIDWDVMWZSMI-KKUMJFAQSA-N 0.000 description 1
- VTCKHZJKWQENKX-KBPBESRZSA-N Tyr-Lys-Gly Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CCCCN)C(=O)NCC(O)=O VTCKHZJKWQENKX-KBPBESRZSA-N 0.000 description 1
- OGPKMBOPMDTEDM-IHRRRGAJSA-N Tyr-Met-Ser Chemical compound CSCC[C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)N OGPKMBOPMDTEDM-IHRRRGAJSA-N 0.000 description 1
- XOVDRAVPGHTYLP-JYJNAYRXSA-N Tyr-Pro-Met Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(O)=O XOVDRAVPGHTYLP-JYJNAYRXSA-N 0.000 description 1
- VYQQQIRHIFALGE-UWJYBYFXSA-N Tyr-Ser-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 VYQQQIRHIFALGE-UWJYBYFXSA-N 0.000 description 1
- HRHYJNLMIJWGLF-BZSNNMDCSA-N Tyr-Ser-Phe Chemical compound C([C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=C(O)C=C1 HRHYJNLMIJWGLF-BZSNNMDCSA-N 0.000 description 1
- PLVVHGFEMSDRET-IHPCNDPISA-N Tyr-Ser-Trp Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC3=CC=C(C=C3)O)N PLVVHGFEMSDRET-IHPCNDPISA-N 0.000 description 1
- WQOHKVRQDLNDIL-YJRXYDGGSA-N Tyr-Thr-Ser Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(O)=O WQOHKVRQDLNDIL-YJRXYDGGSA-N 0.000 description 1
- KLQPIEVIKOQRAW-IZPVPAKOSA-N Tyr-Thr-Thr Chemical compound C[C@H]([C@@H](C(=O)N[C@@H]([C@@H](C)O)C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)N)O KLQPIEVIKOQRAW-IZPVPAKOSA-N 0.000 description 1
- NUQZCPSZHGIYTA-HKUYNNGSSA-N Tyr-Trp-Gly Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)NCC(=O)O)NC(=O)[C@H](CC3=CC=C(C=C3)O)N NUQZCPSZHGIYTA-HKUYNNGSSA-N 0.000 description 1
- MWUYSCVVPVITMW-IGNZVWTISA-N Tyr-Tyr-Ala Chemical compound C([C@@H](C(=O)N[C@@H](C)C(O)=O)NC(=O)[C@@H](N)CC=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 MWUYSCVVPVITMW-IGNZVWTISA-N 0.000 description 1
- GPLTZEMVOCZVAV-UFYCRDLUSA-N Tyr-Tyr-Arg Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O)C1=CC=C(O)C=C1 GPLTZEMVOCZVAV-UFYCRDLUSA-N 0.000 description 1
- AGDDLOQMXUQPDY-BZSNNMDCSA-N Tyr-Tyr-Ser Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CO)C(O)=O AGDDLOQMXUQPDY-BZSNNMDCSA-N 0.000 description 1
- KSGKJSFPWSMJHK-JNPHEJMOSA-N Tyr-Tyr-Thr Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H]([C@@H](C)O)C(O)=O KSGKJSFPWSMJHK-JNPHEJMOSA-N 0.000 description 1
- SQUMHUZLJDUROQ-YDHLFZDLSA-N Tyr-Val-Asp Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(O)=O SQUMHUZLJDUROQ-YDHLFZDLSA-N 0.000 description 1
- ZLFHAAGHGQBQQN-AEJSXWLSSA-N Val-Ala-Pro Chemical compound C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](C(C)C)N ZLFHAAGHGQBQQN-AEJSXWLSSA-N 0.000 description 1
- ZLFHAAGHGQBQQN-GUBZILKMSA-N Val-Ala-Pro Natural products CC(C)[C@H](N)C(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(O)=O ZLFHAAGHGQBQQN-GUBZILKMSA-N 0.000 description 1
- CGGVNFJRZJUVAE-BYULHYEWSA-N Val-Asp-Asn Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)N)C(=O)O)N CGGVNFJRZJUVAE-BYULHYEWSA-N 0.000 description 1
- BMGOFDMKDVVGJG-NHCYSSNCSA-N Val-Asp-Lys Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)O)N BMGOFDMKDVVGJG-NHCYSSNCSA-N 0.000 description 1
- COSLEEOIYRPTHD-YDHLFZDLSA-N Val-Asp-Tyr Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 COSLEEOIYRPTHD-YDHLFZDLSA-N 0.000 description 1
- VCAWFLIWYNMHQP-UKJIMTQDSA-N Val-Glu-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C(C)C)N VCAWFLIWYNMHQP-UKJIMTQDSA-N 0.000 description 1
- OACSGBOREVRSME-NHCYSSNCSA-N Val-His-Asn Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(N)=O)C(O)=O OACSGBOREVRSME-NHCYSSNCSA-N 0.000 description 1
- WJVLTYSHNXRCLT-NHCYSSNCSA-N Val-His-Asp Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N[C@@H](CC(=O)O)C(=O)O)N WJVLTYSHNXRCLT-NHCYSSNCSA-N 0.000 description 1
- WDIWOIRFNMLNKO-ULQDDVLXSA-N Val-Leu-Tyr Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 WDIWOIRFNMLNKO-ULQDDVLXSA-N 0.000 description 1
- RWOGENDAOGMHLX-DCAQKATOSA-N Val-Lys-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C(C)C)N RWOGENDAOGMHLX-DCAQKATOSA-N 0.000 description 1
- FMQGYTMERWBMSI-HJWJTTGWSA-N Val-Phe-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)[C@H](C(C)C)N FMQGYTMERWBMSI-HJWJTTGWSA-N 0.000 description 1
- HJSLDXZAZGFPDK-ULQDDVLXSA-N Val-Phe-Leu Chemical compound CC(C)C[C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)[C@H](C(C)C)N HJSLDXZAZGFPDK-ULQDDVLXSA-N 0.000 description 1
- KISFXYYRKKNLOP-IHRRRGAJSA-N Val-Phe-Ser Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(=O)O)N KISFXYYRKKNLOP-IHRRRGAJSA-N 0.000 description 1
- BGXVHVMJZCSOCA-AVGNSLFASA-N Val-Pro-Lys Chemical compound CC(C)[C@@H](C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCCN)C(=O)O)N BGXVHVMJZCSOCA-AVGNSLFASA-N 0.000 description 1
- KSFXWENSJABBFI-ZKWXMUAHSA-N Val-Ser-Asn Chemical compound [H]N[C@@H](C(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(O)=O KSFXWENSJABBFI-ZKWXMUAHSA-N 0.000 description 1
- LTTQCQRTSHJPPL-ZKWXMUAHSA-N Val-Ser-Asp Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(=O)O)C(=O)O)N LTTQCQRTSHJPPL-ZKWXMUAHSA-N 0.000 description 1
- JQTYTBPCSOAZHI-FXQIFTODSA-N Val-Ser-Cys Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CS)C(=O)O)N JQTYTBPCSOAZHI-FXQIFTODSA-N 0.000 description 1
- KRAHMIJVUPUOTQ-DCAQKATOSA-N Val-Ser-His Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)N KRAHMIJVUPUOTQ-DCAQKATOSA-N 0.000 description 1
- GBIUHAYJGWVNLN-AEJSXWLSSA-N Val-Ser-Pro Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CO)C(=O)N1CCC[C@@H]1C(=O)O)N GBIUHAYJGWVNLN-AEJSXWLSSA-N 0.000 description 1
- GBIUHAYJGWVNLN-UHFFFAOYSA-N Val-Ser-Pro Natural products CC(C)C(N)C(=O)NC(CO)C(=O)N1CCCC1C(O)=O GBIUHAYJGWVNLN-UHFFFAOYSA-N 0.000 description 1
- NZYNRRGJJVSSTJ-GUBZILKMSA-N Val-Ser-Val Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(O)=O NZYNRRGJJVSSTJ-GUBZILKMSA-N 0.000 description 1
- BZDGLJPROOOUOZ-XGEHTFHBSA-N Val-Thr-Cys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](C(C)C)N)O BZDGLJPROOOUOZ-XGEHTFHBSA-N 0.000 description 1
- UVHFONIHVHLDDQ-IFFSRLJSSA-N Val-Thr-Glu Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)O)NC(=O)[C@H](C(C)C)N)O UVHFONIHVHLDDQ-IFFSRLJSSA-N 0.000 description 1
- TVGWMCTYUFBXAP-QTKMDUPCSA-N Val-Thr-His Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)[C@H](C(C)C)N)O TVGWMCTYUFBXAP-QTKMDUPCSA-N 0.000 description 1
- WUFHZIRMAZZWRS-OSUNSFLBSA-N Val-Thr-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](C(C)C)N WUFHZIRMAZZWRS-OSUNSFLBSA-N 0.000 description 1
- PGBMPFKFKXYROZ-UFYCRDLUSA-N Val-Tyr-Phe Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](CC2=CC=CC=C2)C(=O)O)N PGBMPFKFKXYROZ-UFYCRDLUSA-N 0.000 description 1
- BGTDGENDNWGMDQ-KJEVXHAQSA-N Val-Tyr-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)NC(=O)[C@H](C(C)C)N)O BGTDGENDNWGMDQ-KJEVXHAQSA-N 0.000 description 1
- ZHWZDZFWBXWPDW-GUBZILKMSA-N Val-Val-Cys Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CS)C(O)=O ZHWZDZFWBXWPDW-GUBZILKMSA-N 0.000 description 1
- NLNCNKIVJPEFBC-DLOVCJGASA-N Val-Val-Glu Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(O)=O)CCC(O)=O NLNCNKIVJPEFBC-DLOVCJGASA-N 0.000 description 1
- SSKKGOWRPNIVDW-AVGNSLFASA-N Val-Val-His Chemical compound CC(C)[C@@H](C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)N SSKKGOWRPNIVDW-AVGNSLFASA-N 0.000 description 1
- 206010072810 Vascular wall hypertrophy Diseases 0.000 description 1
- 206010047141 Vasodilatation Diseases 0.000 description 1
- 208000009982 Ventricular Dysfunction Diseases 0.000 description 1
- 241000251539 Vertebrata <Metazoa> Species 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- IXKSXJFAGXLQOQ-XISFHERQSA-N WHWLQLKPGQPMY Chemical compound C([C@@H](C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(O)=O)NC(=O)[C@@H](N)CC=1C2=CC=CC=C2NC=1)C1=CNC=N1 IXKSXJFAGXLQOQ-XISFHERQSA-N 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 101710185494 Zinc finger protein Proteins 0.000 description 1
- 102100023597 Zinc finger protein 816 Human genes 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 108010008685 alanyl-glutamyl-aspartic acid Proteins 0.000 description 1
- 108010069020 alanyl-prolyl-glycine Proteins 0.000 description 1
- 108010041407 alanylaspartic acid Proteins 0.000 description 1
- 108010005233 alanylglutamic acid Proteins 0.000 description 1
- KOSRFJWDECSPRO-UHFFFAOYSA-N alpha-L-glutamyl-L-glutamic acid Natural products OC(=O)CCC(N)C(=O)NC(CCC(O)=O)C(O)=O KOSRFJWDECSPRO-UHFFFAOYSA-N 0.000 description 1
- 108010050025 alpha-glutamyltryptophan Proteins 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 239000003392 amylase inhibitor Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 230000000692 anti-sense effect Effects 0.000 description 1
- 210000000628 antibody-producing cell Anatomy 0.000 description 1
- 102000025171 antigen binding proteins Human genes 0.000 description 1
- 108091000831 antigen binding proteins Proteins 0.000 description 1
- 230000000890 antigenic effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 108010029539 arginyl-prolyl-proline Proteins 0.000 description 1
- 108010060035 arginylproline Proteins 0.000 description 1
- 206010003119 arrhythmia Diseases 0.000 description 1
- 230000006793 arrhythmia Effects 0.000 description 1
- 210000001367 artery Anatomy 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 238000011190 asparagine deamidation Methods 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 210000003719 b-lymphocyte Anatomy 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 229920000249 biocompatible polymer Polymers 0.000 description 1
- 239000000090 biomarker Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- 210000005013 brain tissue Anatomy 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 239000000480 calcium channel blocker Substances 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 210000004413 cardiac myocyte Anatomy 0.000 description 1
- 239000013592 cell lysate Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000011260 co-administration Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000002648 combination therapy Methods 0.000 description 1
- 230000001447 compensatory effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- QPNKYNYIKKVVQB-UHFFFAOYSA-N crotaleschenine Natural products O1C(=O)C(C)C(C)C(C)(O)C(=O)OCC2=CCN3C2C1CC3 QPNKYNYIKKVVQB-UHFFFAOYSA-N 0.000 description 1
- 239000012228 culture supernatant Substances 0.000 description 1
- SUYVUBYJARFZHO-RRKCRQDMSA-N dATP Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@H]1C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O1 SUYVUBYJARFZHO-RRKCRQDMSA-N 0.000 description 1
- SUYVUBYJARFZHO-UHFFFAOYSA-N dATP Natural products C1=NC=2C(N)=NC=NC=2N1C1CC(O)C(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O1 SUYVUBYJARFZHO-UHFFFAOYSA-N 0.000 description 1
- 230000034994 death Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 108010060455 des-Tyr- beta-casomorphin Proteins 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 230000035487 diastolic blood pressure Effects 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 108020001096 dihydrofolate reductase Proteins 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- FSXRLASFHBWESK-UHFFFAOYSA-N dipeptide phenylalanyl-tyrosine Natural products C=1C=C(O)C=CC=1CC(C(O)=O)NC(=O)C(N)CC1=CC=CC=C1 FSXRLASFHBWESK-UHFFFAOYSA-N 0.000 description 1
- 230000005750 disease progression Effects 0.000 description 1
- 208000037765 diseases and disorders Diseases 0.000 description 1
- 230000035619 diuresis Effects 0.000 description 1
- 238000002651 drug therapy Methods 0.000 description 1
- 239000012636 effector Substances 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 239000012149 elution buffer Substances 0.000 description 1
- 239000002308 endothelin receptor antagonist Substances 0.000 description 1
- 210000003038 endothelium Anatomy 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003797 essential amino acid Substances 0.000 description 1
- 235000020776 essential amino acid Nutrition 0.000 description 1
- 239000013613 expression plasmid Substances 0.000 description 1
- 229950003499 fibrin Drugs 0.000 description 1
- 210000002950 fibroblast Anatomy 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 230000024924 glomerular filtration Effects 0.000 description 1
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 description 1
- 108010055341 glutamyl-glutamic acid Proteins 0.000 description 1
- 229960003180 glutathione Drugs 0.000 description 1
- 108010090037 glycyl-alanyl-isoleucine Proteins 0.000 description 1
- 108010027668 glycyl-alanyl-valine Proteins 0.000 description 1
- 108010062266 glycyl-glycyl-argininal Proteins 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 230000005986 heart dysfunction Effects 0.000 description 1
- 108010092114 histidylphenylalanine Proteins 0.000 description 1
- 239000000710 homodimer Substances 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 210000005260 human cell Anatomy 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000001077 hypotensive effect Effects 0.000 description 1
- 230000003053 immunization Effects 0.000 description 1
- 238000002649 immunization Methods 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 238000000099 in vitro assay Methods 0.000 description 1
- 210000003000 inclusion body Anatomy 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 230000031146 intracellular signal transduction Effects 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 239000007928 intraperitoneal injection Substances 0.000 description 1
- 238000004255 ion exchange chromatography Methods 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 210000004731 jugular vein Anatomy 0.000 description 1
- 229960004184 ketamine hydrochloride Drugs 0.000 description 1
- 230000003907 kidney function Effects 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 150000002614 leucines Chemical class 0.000 description 1
- 108010044311 leucyl-glycyl-glycine Proteins 0.000 description 1
- 108010044056 leucyl-phenylalanine Proteins 0.000 description 1
- 108010091871 leucylmethionine Proteins 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 238000011866 long-term treatment Methods 0.000 description 1
- 239000007937 lozenge Substances 0.000 description 1
- 239000008176 lyophilized powder Substances 0.000 description 1
- 108010025153 lysyl-alanyl-alanine Proteins 0.000 description 1
- 108010009298 lysylglutamic acid Proteins 0.000 description 1
- 238000010841 mRNA extraction Methods 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 108010005942 methionylglycine Proteins 0.000 description 1
- 229960000485 methotrexate Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 102000035118 modified proteins Human genes 0.000 description 1
- 108091005573 modified proteins Proteins 0.000 description 1
- 238000010369 molecular cloning Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- QVCMHGGNRFRMAD-XFGHUUIASA-N monocrotaline Chemical compound C1OC(=O)[C@](C)(O)[C@@](O)(C)[C@@H](C)C(=O)O[C@@H]2CCN3[C@@H]2C1=CC3 QVCMHGGNRFRMAD-XFGHUUIASA-N 0.000 description 1
- QVCMHGGNRFRMAD-UHFFFAOYSA-N monocrotaline Natural products C1OC(=O)C(C)(O)C(O)(C)C(C)C(=O)OC2CCN3C2C1=CC3 QVCMHGGNRFRMAD-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 208000031225 myocardial ischemia Diseases 0.000 description 1
- AEMBWNDIEFEPTH-UHFFFAOYSA-N n-tert-butyl-n-ethylnitrous amide Chemical compound CCN(N=O)C(C)(C)C AEMBWNDIEFEPTH-UHFFFAOYSA-N 0.000 description 1
- 229960001267 nesiritide Drugs 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000002777 nucleoside Substances 0.000 description 1
- 125000003835 nucleoside group Chemical group 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 238000010647 peptide synthesis reaction Methods 0.000 description 1
- 125000001151 peptidyl group Chemical group 0.000 description 1
- 230000036513 peripheral conductance Effects 0.000 description 1
- 230000036581 peripheral resistance Effects 0.000 description 1
- 210000003200 peritoneal cavity Anatomy 0.000 description 1
- 229940124531 pharmaceutical excipient Drugs 0.000 description 1
- 108010073101 phenylalanylleucine Proteins 0.000 description 1
- 230000026731 phosphorylation Effects 0.000 description 1
- 238000006366 phosphorylation reaction Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- BXRNXXXXHLBUKK-UHFFFAOYSA-N piperazine-2,5-dione Chemical compound O=C1CNC(=O)CN1 BXRNXXXXHLBUKK-UHFFFAOYSA-N 0.000 description 1
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 230000008488 polyadenylation Effects 0.000 description 1
- 229920002704 polyhistidine Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 210000004896 polypeptide structure Anatomy 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 235000020004 porter Nutrition 0.000 description 1
- 230000012495 positive regulation of renal sodium excretion Effects 0.000 description 1
- 230000001124 posttranscriptional effect Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 208000037821 progressive disease Diseases 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 238000001742 protein purification Methods 0.000 description 1
- 230000004088 pulmonary circulation Effects 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- 230000036454 renin-angiotensin system Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000010839 reverse transcription Methods 0.000 description 1
- 238000003757 reverse transcription PCR Methods 0.000 description 1
- 210000005245 right atrium Anatomy 0.000 description 1
- 230000003248 secreting effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000012163 sequencing technique Methods 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000012679 serum free medium Substances 0.000 description 1
- 108010048818 seryl-histidine Proteins 0.000 description 1
- 208000013220 shortness of breath Diseases 0.000 description 1
- 230000019491 signal transduction Effects 0.000 description 1
- 238000001542 size-exclusion chromatography Methods 0.000 description 1
- 210000000329 smooth muscle myocyte Anatomy 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 210000002325 somatostatin-secreting cell Anatomy 0.000 description 1
- 230000009870 specific binding Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 206010042772 syncope Diseases 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229930101283 tetracycline Natural products 0.000 description 1
- 229960002180 tetracycline Drugs 0.000 description 1
- 235000019364 tetracycline Nutrition 0.000 description 1
- 150000003522 tetracyclines Chemical class 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 108010061238 threonyl-glycine Proteins 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 239000012581 transferrin Substances 0.000 description 1
- 230000010474 transient expression Effects 0.000 description 1
- 238000005829 trimerization reaction Methods 0.000 description 1
- 239000012137 tryptone Substances 0.000 description 1
- 108010084932 tryptophyl-proline Proteins 0.000 description 1
- 108010079202 tyrosyl-alanyl-cysteine Proteins 0.000 description 1
- 108010035534 tyrosyl-leucyl-alanine Proteins 0.000 description 1
- 108010020532 tyrosyl-proline Proteins 0.000 description 1
- 108010071635 tyrosyl-prolyl-arginine Proteins 0.000 description 1
- 108010078580 tyrosylleucine Proteins 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 241000701161 unidentified adenovirus Species 0.000 description 1
- 241001430294 unidentified retrovirus Species 0.000 description 1
- 108010009962 valyltyrosine Proteins 0.000 description 1
- 210000004509 vascular smooth muscle cell Anatomy 0.000 description 1
- 229940124549 vasodilator Drugs 0.000 description 1
- 239000003071 vasodilator agent Substances 0.000 description 1
- 210000002620 vena cava superior Anatomy 0.000 description 1
- 230000006815 ventricular dysfunction Effects 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
- C07K14/58—Atrial natriuretic factor complex; Atriopeptin; Atrial natriuretic peptide [ANP]; Cardionatrin; Cardiodilatin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2869—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against hormone receptors
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K19/00—Hybrid peptides, i.e. peptides covalently bound to nucleic acids, or non-covalently bound protein-protein complexes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/62—DNA sequences coding for fusion proteins
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
- C07K2317/565—Complementarity determining region [CDR]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
- C07K2319/70—Fusion polypeptide containing domain for protein-protein interaction
- C07K2319/74—Fusion polypeptide containing domain for protein-protein interaction containing a fusion for binding to a cell surface receptor
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Cardiology (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Biomedical Technology (AREA)
- Biophysics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Biotechnology (AREA)
- Wood Science & Technology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Endocrinology (AREA)
- Hospice & Palliative Care (AREA)
- Physics & Mathematics (AREA)
- Epidemiology (AREA)
- Plant Pathology (AREA)
- Gastroenterology & Hepatology (AREA)
- Mycology (AREA)
- Pulmonology (AREA)
- Neurology (AREA)
- Toxicology (AREA)
- Peptides Or Proteins (AREA)
Abstract
本文提供了ETA抗体与BNP的融合蛋白质。本文还提供了ETA抗体与BNP融合蛋白质的药物组合物。本文进一步提供了ETA抗体与BNP融合蛋白质用于治疗、预防或改善肺动脉高压、肺高压、或心力衰竭的一种或多种症状方法。
Description
技术领域
本文提供了ETA抗体与BNP的融合蛋白质。本文还提供了ETA抗体 与BNP融合蛋白质的药物组合物。本文进一步提供了ETA抗体与BNP融 合蛋白质用于治疗、预防或改善肺动脉高压、肺高压、或心力衰竭的一种或 多种症状方法。
背景技术
肺动脉高压(Pulmonary Arterial Hypertension,PAH)是一种以肺动脉 血压明显升高为特征的罕见的、渐进性的疾病。肺动脉高压已成为威胁人类 健康的一个重要疾病,资料显示在全球范围内每年各类肺动脉高压发病率 约为2.4~7.6/100万,患病率约为每百万人口15~26人,已成为仅次于缺血 性心脏病和高血压的第3位常见的心血管疾病。肺动脉高压的致病原因人 们尚不完全清楚,因其起病隐匿,患者就诊时多已处于肺动脉高压心功能的 Ⅲ~Ⅳ级。肺动脉高压的伴随症状通常包括呼吸短促(特别是在运动时)、 胸部疼痛、间断性的昏厥等,另外,随着病情的延续,肺动脉持续的高压会 使得右心室向肺部供血的持续不畅,最终会导致右心室衰竭。心脏衰竭是肺 动脉高压患者最常见的死亡原因。
目前尚未有根治肺动脉高压的方法,而药物治疗是肺动脉高压维持治 疗的首选。经获FDA已批准用于肺动脉高压的治疗的药物均为血管舒张药 物,按机理可分为钙离子通道阻滞剂、前列环素受体激动剂、5型磷酸二酯 酶(PDE5)抑制剂、内皮素受体抑制剂等。
肺动脉高压由肺内或者与肺关联血管的不断束紧(vasoconstriction)引 起心脏对肺供血量不足后,心脏对肺供血压力补偿性增加而引起,其微观表 现有肺小动脉内膜增厚,血管紧缩,重构,僵硬或者血栓造成的局部闭塞, 进而血管对肺血液循环的阻力上升(Simonneau等,2004,J.Am.Coll. Cardiol.43:5S–12S;Barst等,2004,J.Am.Coll.Cardiol.43:40S–47S)。
内皮素受体(Endthelin Receptor A,ETA,或ETAR)抑制剂能够有效的 阻断由内皮素引起的血管压力增加来达到缓解肺动脉高压的症状,改善病 人的运动能力和血液动力学(Serasli等,2010,Recent Pat.Cardiovasc.Drug Discov.5:184-95)。
脑利钠肽(Brain Natriuretic Peptide,BNP),主要在心室表达,是由心 肌细胞合成的天然激素,同时也存在于脑组织中。血液BNP在心室功能障 碍时升高,并通过维持肾功能和钠平衡来保护机体免受容量超负荷的影响。 对肺高压患者的研究表明右心功能障碍时血液BNP相应升高。除了作为心 血管疾病的生物标记外,BNP还是急性心衰(ADHF)的治疗选择。“奈西 立肽”是人B型利钠肽的重组体,已在2001年被FDA批准治疗急性心衰。 BNP与血管平滑肌和内皮细胞上的鸟苷酸环化酶受体结合,引起细胞内第 二信使(secondmessager)环单磷酸鸟苷(cGMP)的水平升高,从而引发 一系列生理效应:(1)具有内皮非依赖性的血管舒张活性,扩张动静脉, 降低全身血管阻力、充盈压以及肺毛细血管嵌楔压,降低心脏前后负荷;(2) 提高肾小球滤过率,产生排钠利尿作用,降低体液负荷,提高心排血量,综 合性改善心脏功能;(3)在体内抑制肾素-血管紧张素-醛固酮系统(RAAS) 的激活,抑制由于扩血管效应引起的反射性心率增加,避免心律失常的发生; (4)抑制血管内皮细胞、平滑肌细胞及成纤维细胞的生长,对心肌肥厚有 抑制作用。
本文提供了ETA抗体与BNP的融合蛋白质。一方面,ETA抗体与BNP 的融合蛋白质可以抑制ETA信号通路和BNP信号通路在降低肺循环血管 阻力和外周血管阻力的联合作用,降低体液负荷,缓解肺动脉高压和心脏衰 竭的心脏重构,综合性的改善心脏功能。另一方面,ETA抗体与BNP的融 合蛋白质可以延长BNP的半衰期,从而达到延长药物有效时间、减少药物 副作用的目的。
发明内容
本文提供了ETA抗体与BNP的融合蛋白质。本文还提供了其用于治 疗、预防或改善肺动脉高压、肺高压以及心力衰竭的一种或多种症状方法。
本文提供了一种ETA抗体与BNP的融合蛋白质,其结构特征在于:所 述的融合蛋白质包含一个ETA抗体和一或多个BNP。
本文提供了一个ETA抗体与BNP的融合蛋白质,其结构特征在于: 所述的融合蛋白质包含一个ETA抗体、和一个,二个,三个,四个,五 个,六个,七个,或八个BNP;该融合蛋白质将一BNP的氨基端与所述 的ETA抗体轻链或重链的羧基端连接,或者该融合蛋白质将一BNP的羧 基端与所述的ETA抗体轻链或重链的氨基端连接。
本文提供了一个ETA抗体与BNP的融合蛋白质,其结构特征在于: 所述的融合蛋白质包含一个ETA抗体、和一个,二个,三个或四个 BNP;该融合蛋白质将一BNP的氨基端与所述的ETA抗体轻链或重链的 羧基端连接,或者该融合蛋白质将一BNP的羧基端与所述的ETA抗体轻 链或重链的氨基端连接。
本文提供了一个ETA抗体与BNP的融合蛋白质,其结构特征在于: 所述的融合蛋白质包含一个ETA抗体和二个BNP;该融合蛋白质将一 BNP的氨基端与所述的ETA抗体轻链或重链的羧基端连接,或者该融合 蛋白质将一BNP的羧基端与所述的ETA抗体轻链或重链的氨基端连接。
本文提供了一个ETA抗体与BNP的融合蛋白质,其结构特征在于: 所述的融合蛋白质包含一个ETA抗体和一个BNP;该融合蛋白质将所述 的BNP的氨基端与所述的ETA抗体轻链或重链的羧基端连接,或者该融 合蛋白质将所述的BNP的羧基端与所述的ETA抗体轻链或重链的氨基端 连接。
本文提供了一个ETA抗体与BNP的融合蛋白质,其结构特征在于: 所述的融合蛋白质包含一个ETA抗体、和一个,二个,三个,四个,五 个,六个,七个,或八个BNP和肽接头(Linker);该融合蛋白质通过一 肽接头序列(Linker)将一BNP的氨基端与所述的ETA抗体轻链或重链的羧 基端连接,或者该融合蛋白质通过一肽接头序列(Linker)将一BNP的羧基端与所述的ETA抗体轻链或重链的氨基端连接。
本文提供了一个ETA抗体与BNP的融合蛋白质,其结构特征在于: 所述的融合蛋白质包含一个ETA抗体、和一个,二个,三个或四个BNP 和肽接头(Linker);该融合蛋白质通过一肽接头序列(Linker)将一BNP 的氨基端与所述的ETA抗体轻链或重链的羧基端连接,或者该融合蛋白 质通过一肽接头序列(Linker)将一BNP的羧基端与所述的ETA抗体轻链或重链的氨基端连接。
本文提供了一个ETA抗体与BNP的融合蛋白质,其结构特征在于: 所述的融合蛋白质包含一个ETA抗体和二个BNP和二个肽接头 (Linker);该融合蛋白质通过一肽接头序列(Linker)将一BNP的氨基端 与所述的ETA抗体轻链或重链的羧基端连接,或者该融合蛋白质通过一 肽接头序列(Linker)将一BNP的羧基端与所述的ETA抗体轻链或重链的氨 基端连接。
本文提供了一个ETA抗体与BNP的融合蛋白质,其结构特征在于: 所述的融合蛋白质包含一个ETA抗体和一个BNP和一个肽接头 (Linker);该融合蛋白质通过所述的肽接头序列(Linker)将所述的BNP 的氨基端与所述的ETA抗体轻链或重链的羧基端连接,或者该融合蛋白 质通过所述的肽接头序列(Linker)将所述的BNP的羧基端与所述的ETA抗 体轻链或重链的氨基端连接。
本文提供了一个ETA抗体与BNP的融合蛋白质,其结构特征在于: 所述的ETA抗体、BNP和肽接头序列通过以下所述中一方式融合形成所 述的融合蛋白质:
(1)通过一个肽接头序列(Linker)将一BNP的氨基端和一ETA抗体重链 /轻链的羧基端连接:N'-R-Linker-BNP-C';及
(2)通过一肽接头序列(Linker)将一BNP的羧基端与一ETA抗体轻链或 重链的氨基端连接:N'-BNP-Linker-R-C';
其中:N'代表多肽链的氨基端,C'代表多肽链的羧基端,BNP代表一 BNP,R为一ETA抗体的轻链或者重链的氨基酸序列,及Linker代表一肽 接头。
本文提供了一个多核苷酸,其编码本文中所述的一个ETA抗体和BNP 的融合蛋白质。
本文提供了一个载体,其包含编码本文中所述的一个ETA抗体和BNP 的融合蛋白质的多核苷酸。
本文提供了一个宿主细胞,其包含本文中所述的一个载体。
本文提供了一个药用组合物,其包含本文所述的一个ETA抗体和BNP 的融合蛋白质,和一个药用可接受载体。
本文提供了本文所述的一个ETA抗体与BNP的融合蛋白质在制备用于 治疗、预防或改善肺动脉高压以及肺动脉高压相关病症的药物中的用途。
本文提供了本文所述的一个ETA抗体与BNP的融合蛋白质在制备用于 治疗、预防或改善肺高压以及肺高压相关病症的药物中的用途。
本文提供了本文所述的一个ETA抗体与BNP的融合蛋白质在制备用于 减肥或者治疗、预防或改善心力衰竭以及心力衰竭相关病症的药物中的用 途。
本文提供了本文所述的一个ETA抗体与BNP的融合蛋白质在制备用于 同时治疗、预防或改善肺动脉高压、肺高压或者心力衰竭二种及二种以上病 症的药物中的用途。
本文提供了治疗、预防或改善肺动脉高压以及肺动脉高压相关病症的一 种或多种症状方法,其包括给予受试者治疗有效量的本文所述的一个ETA 抗体与BNP的融合蛋白质。
本文提供了治疗、预防或改善肺高压以及肺高压相关病症的一种或多种 症状方法,其包括给予受试者治疗有效量的本文所述的一个ETA抗体与BNP的融合蛋白质。
本文提供了治疗、预防或改善心力衰竭以及心力衰竭相关病症的一种或 多种症状方法,其包括给予受试者治疗有效量的本文所述的一个ETA抗体 与BNP的融合蛋白质。
本文提供了治疗、预防或改善肺动脉高压、肺高压或者心力衰竭的二种 及二种以上病症方法,其包括给予受试者治疗有效量的本文所述的一个 ETA抗体与BNP的融合蛋白质。
附图说明:
图1:显示了ETA抗体与BNP的融合蛋白质h15F3-(G4S)2-BNP(其包含 SEQ ID NO:162,SEQ ID NO:190,SEQ ID NO:218,及SEQ ID NO:205)、 h15F3-BNP(3-29)(其包含SEQID NO:162,SEQ ID NO:190,及SEQ ID NO:210)和h15F3-BNP(9-32)(其包含SEQ ID NO:162,SEQ ID NO:190, 及SEQ ID NO:209)抑制人ETA介导的Ca2+变化的结果。
图2:显示了ETA抗体与BNP的融合蛋白质h15F3-(G4S)2-BNP、h15F3- BNP(3-29)和h15F3-BNP(9-32)在给药后15分钟后降低正常小鼠动脉压的效 果。
图3:显示了ETA抗体与BNP的融合蛋白质h15F3-(G4S)2-BNP不同剂量 在MCT大鼠上降低右心室压力的效果。
图4:显示了ETA抗体与BNP的融合蛋白质h15F3-(G4S)2-BNP、h15F3- BNP(3-29)和h15F3-BNP(9-32)在给药后10分钟降低健康猴子动脉压的效果。
图5:显示了ETA抗体与BNP的融合蛋白质h15F3-(G4S)2-BNP、h15F3- BNP(3-29)和h15F3-BNP(9-32)在给药后60分钟降低健康猴子动脉压的效果。
图6:显示了ETA抗体与BNP的融合蛋白质h15F3-(G4S)2-BNP在健康猴 子上的药代动力学结果。
图7:显示了ETA抗体与BNP的融合蛋白质h15F3-BNP(9-32)在健康猴子 上的药代动力学结果。
具体实施方式定义
除非本文另外定义,与本文相关的科学和技术术语应具有本领域普通 技术人员所理解的含义。通常,与本文所述药物学、生物学、生物化学、细 胞和组织培养学、生物学、分子生物学、免疫学、微生物学、遗传学和蛋白 质核酸化学以及杂交相关的命名法和技术为本领域熟知和经常使用的。
本文使用标准的单字母或三字母缩写表明多聚核苷酸和多肽序列。除 非另外指明,多肽序列的氨基端在左而它们的羧基端在右,单链核酸序列和 双链核酸序列的上游链的5’端在左而它们的3’端在右。多肽的具体部分可 由氨基酸残基编号表示,例如氨基酸80至130,或由该位点的实际残基表 示例如Lys80至Lys130。也可通过解释其与参比序列的差异描述具体的多 肽或多聚核苷酸序列。
术语“肽”、“多肽”、和“蛋白”均指包含两个或多个通过肽健相互连接的 氨基酸的分子。这些术语涵盖例如天然和人工蛋白、蛋白片段和蛋白序列的 多肽类似物(例如突变蛋白、变异体和融合蛋白)以及转录后或否则为共价 或非共价修饰的蛋白。肽、多肽或蛋白可为单体或多聚体。
术语“多肽片段”指与对应的全长蛋白相比具有氨基端和/或羧基端缺失 的多肽。片段长度可为例如至少5、6、7、8、9、10、11、12、13、14、15、 20、50、70、80、90、100、150或200个氨基酸。片段长度可为例如最多 1000、750、500、250、200、175、150、125、100、90、80、70、60、50、 40、30、20、15、14、13、12、11或10个氨基酸。片段可在其一端或两端 进一步包含一个或多个附加氨基酸,例如,来自不同天然蛋白质的氨基酸序 列(例如,Fc或亮氨酸拉链结构域)或人工氨基酸序列(例如,人工接头 序列)。
本文的多肽包括以任何原因和经任何方法修饰的多肽,例如,以:(1) 降低蛋白水解敏感性,(2)降低氧化敏感性,(3)改变形成蛋白复合物的 亲和性,(4)改变结合亲和性以及(4)赋予或修饰其它物理化学或功能性 质。类似物包含多肽的突变蛋白。例如,可在天然序列(例如在形成分子内 接触的结构域之外的多肽部分)中进行单个或多个氨基酸替换(例如,保守 氨基酸替换)。“保守氨基酸替换”为不显著改变母体序列结构特性者(例如,替换氨基酸不应破坏母体序列中出现的螺旋或干扰其它赋予母体序列特性 或对其功能是必须的二级结构类型)。
多肽的“变异体”包含相对于另一多肽序列在氨基酸序列中插入、缺失和 /或替换了一个或多个氨基酸残基的氨基酸序列。本文的变异体包括融合蛋 白。
多肽的“衍生物”为经化学修饰的多肽,例如通过与其它化学部分例如聚 乙二醇、白蛋白(例如人血清白蛋白)结合、磷酸化和糖基化。
除非另外说明,术语“抗体”包括除包含两个全长重链和两个全长轻链的 抗体外的其衍生物,变异体、片段和突变蛋白,其实例见下文。
术语“抗体”为包含与抗原结合部分并任选为允许抗原结合部分采取促 进该抗体与该抗原结合的构象的支架或框架部分的蛋白。抗体的实例包括 完整抗体、抗体片段(例如抗体的抗原结合部分)、抗体衍生物、和抗体类 似物。该抗体可包含例如可选择的蛋白支架或具有移植CDRs或CDRs衍 生物的人工支架。该支架包括但不限于包含被引入的例如以稳定化该抗体 的三维结构的抗体衍生支架以及包含例如生物相容性多聚体的全合成支架。 参见,例如,Korndorfer等,2003,Proteins:Structure,Function andBioinformatics 53:121-129;Roque等,2004,Biotechnol.Prog.20:639-654。 此外,可使用模拟肽抗体(“PAMs”)以及基于模拟抗体的支架,其如支架 一样利用纤维蛋白连接素。
抗体可具有例如天然免疫球蛋白的结构。“免疫球蛋白”为四聚体分子。 在天然的免疫球蛋白中,各四聚体由两个相同的多肽链对组成,各对具有一 个“轻”(约25kDa)和一个“重”链(约50-70kDa)。各链的氨基端包括约100 至110或更多氨基酸的可变结构域,主要与抗原识别相关。各链的羧基端 部分确定了主要与效应器作用相关的恒定区。人的轻链分为κ和λ轻链。 重链分为μ、δ、α或ε,并确定了抗原的同种型,例如分别为IgM、IgD、 IgG、IgA和IgE。在轻链和重链中,可变和恒定区由约12或更多个氨基酸 的“J”区连接,重链也包括约10多个氨基酸的“D”区。参见,Fundamental Immunology Ch.7(Paul编辑,第2版,RavenPress,1989)(其完整内容 以参考形式并于本文用于任何目的)。各轻/重链对的可变区形成抗体结合 位点,这样一个完整的免疫球蛋白具有两个结合位点。
天然免疫球蛋白链显示出由三个高度可变区连接的相对保守骨架区 (FR)的相同基本结构,也被称作互补决定区或CDRs。从N端到C端, 轻和重链均包含结构域FR1、CDR1、FR2、CDR2、FR3、CDR3和FR4。 各结构域氨基酸的分配与Kabat等在Sequences of Proteinsof Immunological Interest,第5版,US Dept.of Health and Human Services,PHS,NIH,NIH Publication No.91-3242,1991中的定义一致。
除非另外指明,“抗体”指完整的免疫球蛋白或其可与完整抗体竞争特异 性结合的抗原结合部分。可由重组DNA技术或通过酶或化学裂解完整抗体 生产抗原结合部分。抗原结合部分包括,尤其是,Fab、Fab’、F(ab’)2、Fv、 结构域抗体(dAbs),包括互补决定区(CDRs)的片段、单链抗体(scFv)、 嵌合抗体、双链抗体(diabodies)、三链抗体(triabodies)、四链抗体(tetrabodies) 和至少包含足以赋予多肽特异抗原结合的免疫球蛋白的一部分的多肽。
Fab片段为具有VL、VH、CL和CH1结构域的单价片段;F(ab’)2片段为 具有两个在铰链区由二硫键连接的Fab片段的二价片段;Fd片段具有VH或VL结构域;dAb片段具有VH结构域、VL结构域,或VH或VL结构域的 抗原结合片段(美国专利号US6,846,634、US6,696,245,美国专利申请公开 号US2005/0202512、US2004/0202995、US2004/0038291、US2004/0009507、US2003/0039958,Ward等,1989,Nature 341:544-546.)。
单链抗体(scFv)为其中的VL扣VH区由接头(例如,合成的氨基酸残基 序列)连接以形成连续蛋白质的抗体,其中该接头足够长以允许该蛋白链折 叠回自身并形成单价抗原结合位点(参见,例如,Bird等,1988,Science 242:423-26and Huston等,1988,Proc.Natl.Acad.Sci.USA 85:5879-83)。
双链抗体为包含两个多肽链的二价抗体,其中各多肽链包含由接头连 接的VH和VL结构域,该接头很短以致于不允许两个结构域在相同链上的 配对,因此允许各结构域与另一多肽链上的互补结构域配对(参见,例如, Holliger等,1993,Proc.Natl.Acad.Sci.USA90:6444-48,和Poljak等, 1994,Structure 2:1121-23)。如果双链抗体的两个多肽链是相同的,那么由 它们配对得到的双链抗体将具有相同的抗原结合位点。具有不同序列的多肽链可用于制备具有不同抗原结合位点的双链抗体。相似地,三链抗体和四 链抗体分别为包含三个和四个多肽链的抗体并分别形成三个和四个抗原结 合位点,其可相同或不同。
可使用Kabat等在Sequences of Proteins of Immunological Interest,第 5版,US Dept.of Health and Human Services,PHS,NIH,NIH Publication No. 91-3242,1991中描述的方法鉴定给定抗体的互补决定区(CDRs)和框架 区(FR)。可向分子中共价或非共价并入一个或多个CDRs使其成为抗体。 抗体可以较大多肽链并入CDR(s)。可将CDR(s)共价连接至另一乡肽链, 或非共价并入CDR(s)。CDRs允许抗体与具体的相关抗原特异性结合。
抗体可有一个或多个结合位点。如果多于一个结合位点,该结合位点可 与另一个相同或不同。例如,天然人免疫球蛋白通常具有两个相同的结合位 点,而“双特异性”或“双功能”抗体具有两个不同的结合位点。
术语“鼠源抗体”包括具有一个或多个来源于小鼠免疫球蛋白序列的可 变区和恒定区的所有抗体。
术语“人源化抗体”是将小鼠抗体分子的互补决定区序列移植到人抗体 可变区框架中而制成的抗体。
术语“抗原结合结构域”、“抗原结合区”或“抗原结合位点”为包含与抗原 相互作用的氨基酸残基(或其它部分)并有助于抗体对抗原的特异性和亲和 力的抗体的部分。对与其抗原特异性结合的抗体而言,这将包括至少部分的 至少一个其CDR结构域。
术语“表位”为与抗体(例如,通过抗体)结合的分子部分。表位可包含 分子的非连续部分(例如,在多肽中,在多肽的一级序列中不连续的氨基酸 残基在该多肽的三级和四级结构中相互足够接近以致于被一个抗体结合)。
两个多聚核苷酸或两个多肽序列的“相同百分比”由使用GAP计算机程 序(GCGWisconsin Package;version 10.3(Accelrys,San Diego,CA)的一 部分)使用其默认参数比较序列测定。
术语“多聚核苷酸”、“寡聚核苷酸”和“核酸”可在全文中交替使用并包括 DNA分子(例如,cDNA或基因组DNA)、RNA分子(例如mRNA)、 使用核苷酸类似物(例如,肽核酸和非天然核苷酸类似物)生成的DNA或 RNA类似物及其杂交体。核酸分子可为单链或双链。在一个实施方案中, 本文的核酸分子包含编码本文提供抗体或其片段、衍生物、突变蛋白或变异体连续的开放阅读框。
如果它们的序列可反向平行排列则两个单链多聚核苷酸是相互“互补 的”,这样一个多聚核苷酸中的各核苷酸与另一多聚核苷酸中的互补核苷酸 相反,不会引入空隙并且各序列的5’或3’端没有未配对的核苷酸。如果两 个多聚核苷酸可在中等严格条件下相互杂交那么一个多聚核苷酸与另一多 聚核苷酸“互补”。因此,一个多聚核苷酸可与另一多聚核苷酸互补,但并不 是它的互补序列。
术语“载体”为可用于将与其相连的另一核酸引入细胞的核酸。载体的一 种类型为“质粒”,其指可连接附加核酸区段的线性或环状双链DNA分子。 载体的另一类型为病毒载体(例如,复制缺陷逆转录病毒、腺病毒和腺病毒 伴随病毒),其中可将附加DNA区段引入病毒基因组。某些载体可在它们 被引入的宿主细胞中自主复制(例如,包含细菌复制起点的细菌载体以及游 离型哺乳动物载体)。其它载体(例如,非游离型哺乳动物载体)在引入宿 主细胞时整合入宿主细胞的基因组中并因此与宿主基因组一起复制。
“表达载体”为可引导所选多聚核苷酸表达的载体类型。
如果调控序列影响核苷酸序列的表达(例如,表达水平、时间或位点) 那么核苷酸序列与调控序列“可操作地相连”。“调控序列”为可影响与其可操 作相连的核酸的表达(例如,表达水平、时间或位点)的核酸。调控基因, 例如,直接对受调控核酸发挥作用或通过一个或多个其它分子(例如,与调 控序列和/或核酸结合的多聚核苷酸)的作用。调控序列的实例包括启动子、 增强子和其它表达控制元件(例如,多腺苷酸化信号)。调控序列的进一步 实例描述于例如Goeddel,1990,Gene Expression Technology:Methods inEnzymology,Volume 185,Academic Press,San Diego,CA and Baron等,1995, NucleicAcids Res.23:3605-06。
术语“宿主细胞”为用于表达核酸例如本文提供核酸的细胞。宿主细胞可 为原核生物,例如大肠杆菌,或者其可为真核生物,例如单细胞真核生物(例 如,酵母或其它真菌)、植物细胞(例如烟草或番茄植物细胞)、动物细胞(例如,人细胞、猴细胞、仓鼠细胞、大鼠细胞、小鼠细胞或昆虫细胞)或 杂交瘤。通常,宿主细胞为可用多肽编码核酸转化或转染的培养细胞,其可 接着在宿主细胞中表达。短语“重组宿主细胞”可用于表述用预期表达的核酸 转化或转染的宿主细胞。宿主细胞也可为包含该核酸但是不以期望水平表 达的细胞,除非向该宿主细胞引入了调控序列这样其与核酸可操作地相连。 应理解的是术语宿主细胞不仅指具体的受试者细胞也指该细胞的子代或可 能的子代。由于例如突变或环境影响后续世代会出现某些修饰,该子代事实 上可能与母体细胞不同但是仍然属于本文使用的术语范围。
内皮素受体
内皮素受体(ETA)属于7-跨膜受体家族的A亚家族,其通过异源三 聚体鸟嘌呤核苷酸结合蛋白(G蛋白)与一个或多个胞内信号传导途径偶 联(Jelinek等,1993,Science259:1614-1616,Segre等,1993,Trends Endocrinol.Metab.4:309-314)。如本文所使用“内皮素受体”和“ETA”或 “ETAR”可交替使用。
在一个实施方案中,可选择本文所述的抗体结合表达于细胞上的膜结 合内皮素受体并通过内皮素受体抑制或阻断内皮素信号传导。在一个实施 方案中,本文所述的抗体与人内皮素受体特异性结合。在进一步的实施方案 中,与人内皮素受体结合的抗体也可与其它物种的内皮素受体结合,例如大 鼠。下文中的实施例提供生成与人膜结合内皮素受体结合的鼠源抗体,在 进一步的实施方案中与其它物种的内皮素受体结合。
已知数个物种的内皮素受体的多聚核苷酸和多肽序列。SEQ ID NO:1- SEQ IDNO:6显示了人、猴子和大鼠的序列。序列数据来源于美国国立生 物技术信息中心的GeneBank数据库。
内皮素受体A(ETA)如下:
人(Homo sapiens)多聚核苷酸(SEQ ID NO:1);登录号:S63938。
人(Homo sapiens)氨基酸(SEQ ID NO:2);登录号:AAB20278。
猴子(Cynomolgus monkey)多聚核苷酸(SEQ ID NO:3);登录号:JV635771。
猴子(Cynomolgus monkey)氨基酸(SEQ ID NO:4);登录号:AFJ71111。
大鼠(Rattus norvegicus)多聚核苷酸(SEQ ID NO:5);登录号:M60786。
大鼠(Rattus norvegicus)氨基酸(SEQ ID NO:6);登录号:AAA41114。
内皮素受体A(ETA)抗体
在一个实施方式中,本文所述的ETA抗体包含一个、两个、三个、四 个、五个、或六个氨基酸序列,其中每个氨基酸序列独立地选自于以下所列 氨基酸序列:
a.轻链CDR1氨基酸序列:SEQ ID NO:8、SEQ ID NO:10、SEQ ID NO: 12、SEQ IDNO:14、SEQ ID NO:16、SEQ ID NO:18、SEQ ID NO:20、 SEQ ID NO:22、SEQ ID NO:24、SEQID NO:26、SEQ ID NO:28、及 SEQ ID NO:30;
b.轻链CDR2氨基酸序列:SEQ ID NO:32、SEQ ID NO:34、SEQ ID NO:36、 SEQ IDNO:38、SEQ ID NO:40、SEQ ID NO:42、SEQ ID NO:44、SEQ ID NO:46、及SEQ ID NO:48;
c.轻链CDR3氨基酸序列:SEQ ID NO:50、SEQ ID NO:52、SEQ ID NO:54、 SEQ IDNO:56、SEQ ID NO:58、SEQ ID NO:60、SEQ ID NO:62、SEQ ID NO:64、SEQ ID NO:66、SEQ IDNO:68,及SEQ ID NO:220;
d.重链CDR1氨基酸序列:SEQ ID NO:70、SEQ ID NO:72、SEQ ID NO: 74、SEQ IDNO:76、SEQ ID NO:78、SEQ ID NO:80、SEQ ID NO:82、 SEQ ID NO:84、SEQ ID NO:86、SEQID NO:88、及SEQ ID NO:90;
e.重链CDR2氨基酸序列:SEQ ID NO:92、SEQ ID NO:94、SEQ ID NO:96、 SEQ IDNO:98、SEQ ID NO:100、SEQ ID NO:102、SEQ ID NO:104、 SEQ ID NO:106、SEQ ID NO:108、SEQ ID NO:110、SEQ ID NO:112、 及SEQ ID NO:114;及
f.重链CDR3氨基酸序列:SEQ ID NO:116、SEQ ID NO:118、SEQ ID NO:120、SEQ IDNO:122、SEQ ID NO:124、SEQ ID NO:126、SEQ ID NO:128、SEQ ID NO:130、SEQ ID NO:132、SEQ ID NO:134、及SEQ ID NO:136。
表一列出本文所述的ETA抗体的轻链CDRs的氨基酸序列,以及其 相应的多聚核苷酸编码序列。表二列出本文所述的ETA抗体的重链CDRs 的氨基酸序列,以及其相应的多聚核苷酸编码序列。
表一:轻链CDRs的氨基酸序列及其多聚核苷酸编码序列
表二:重链CDRs的氨基酸序列及其多聚核苷酸编码序列
在一个实施方案中,本文所述的抗体包含与表1和表2中的CDR氨基 酸序列各相差5、4、3、2、或1个单氨基酸添加、替换和/或缺失的序列。 在另一个实施方案中,本文所述的抗体包含与表1和表2中的CDR氨基酸 序列各相差4、3、2、或1个单氨基酸添加、替换和/或缺失的序列。在另一 个实施方案中,本文所述的抗体包含与表1和表2中的CDR氨基酸序列各相差3、2、或1个单氨基酸添加、替换和/或缺失的序列。在另一个实施方 案中,本文所述的抗体包含与表1和表2中的CDR氨基酸序列各相差2或 1个单氨基酸添加、替换和/或缺失的序列。在另一个实施方案中,本文所述 的抗体包含与表1和表2中的CDR氨基酸序列各相差1个单氨基酸添加、 替换和/或缺失的序列。
在另一个实施方式中,本文所述的ETA抗体(ETA-1抗体),其包含一 个或两个氨基酸序列,其中每个氨基酸序列独立地选自于以下所列氨基酸 序列:
a.轻链CDR1氨基酸序列:SEQ ID NO:8、SEQ ID NO:10、SEQ ID NO: 12、SEQ IDNO:14、SEQ ID NO:16、SEQ ID NO:18、SEQ ID NO:20、SEQ ID NO:22、SEQ ID NO:24、SEQ IDNO:26、SEQ ID NO:28、及SEQ ID NO:30;和
b.重链CDR1氨基酸序列:SEQ ID NO:70、SEQ ID NO:72、SEQ ID NO: 74、SEQ IDNO:76、SEQ ID NO:78、SEQ ID NO:80、SEQ ID NO:82、SEQ ID NO:84、SEQ ID NO:86、SEQ IDNO:88、及SEQ ID NO:90。
一方面,ETA-1抗体还包含一个或两个氨基酸序列,其中每个氨基酸 序列独立地选自于以下所列氨基酸序列:
a.轻链CDR2氨基酸序列:SEQ ID NO:32、SEQ ID NO:34、SEQ ID NO:36、 SEQ IDNO:38、SEQ ID NO:40、SEQ ID NO:42、SEQ ID NO:44、SEQ ID NO:46、及SEQ ID NO:48;和
b.重链CDR2氨基酸序列:SEQ ID NO:92、SEQ ID NO:94、SEQ ID NO:96、 SEQ IDNO:98、SEQ ID NO:100、SEQ ID NO:102、SEQ ID NO:104、SEQ ID NO:106、SEQ ID NO:108、SEQ ID NO:110、SEQ ID NO:112、及SEQ ID NO:114。
另一方面,ETA-1抗体还包含一个或两个氨基酸序列,其中每个氨基 酸序列独立地选自于以下所列氨基酸序列:
a.轻链CDR3氨基酸序列:SEQ ID NO:50、SEQ ID NO:52、SEQ ID NO:54、 SEQ IDNO:56、SEQ ID NO:58、SEQ ID NO:60、SEQ ID NO:62、SEQ ID NO:64、SEQ ID NO:66、SEQ IDNO:68,及SEQ ID NO:220;和
b.重链CDR3氨基酸序列:SEQ ID NO:116、SEQ ID NO:118、SEQ ID NO:120、SEQ IDNO:122、SEQ ID NO:124、SEQ ID NO:126、SEQ ID NO: 128、SEQ ID NO:130、SEQ ID NO:132、SEQ ID NO:134、及SEQ ID NO: 136。
在另一个实施方式中,本文所述的ETA抗体(ETA-2抗体),其包含一 个或两个氨基酸序列,其中每个氨基酸序列独立地选自于以下所列氨基酸 序列:
a.轻链CDR2氨基酸序列:SEQ ID NO:32、SEQ ID NO:34、SEQ ID NO:36、 SEQ IDNO:38、SEQ ID NO:40、SEQ ID NO:42、SEQ ID NO:44、SEQ ID NO:46、及SEQ ID NO:48;和
b.重链CDR2氨基酸序列:SEQ ID NO:92、SEQ ID NO:94、SEQ ID NO:96、 SEQ IDNO:98、SEQ ID NO:100、SEQ ID NO:102、SEQ ID NO:104、SEQ ID NO:106、SEQ ID NO:108、SEQ ID NO:110、SEQ ID NO:112、及SEQ ID NO:114。
一方面,ETA-2抗体还包含一个或两个氨基酸序列,其中每个氨基酸 序列独立地选自于以下所列氨基酸序列:
a.轻链CDR1氨基酸序列:SEQ ID NO:8、SEQ ID NO:10、SEQ ID NO: 12、SEQ IDNO:14、SEQ ID NO:16、SEQ ID NO:18、SEQ ID NO:20、SEQ ID NO:22、SEQ ID NO:24、SEQ IDNO:26、SEQ ID NO:28、及SEQ ID NO:30;和
b.重链CDR1氨基酸序列:SEQ ID NO:70、SEQ ID NO:72、SEQ ID NO:74、 SEQ IDNO:76、SEQ ID NO:78、SEQ ID NO:80、SEQ ID NO:82、SEQ ID NO:84、SEQ ID NO:86、SEQ IDNO:88、及SEQ ID NO:90。
另一方面,ETA-2抗体还包含一个或两个氨基酸序列,其中每个氨基 酸序列独立地选自于以下所列氨基酸序列:
a.轻链CDR3氨基酸序列:SEQ ID NO:50、SEQ ID NO:52、SEQ ID NO:54、 SEQ IDNO:56、SEQ ID NO:58、SEQ ID NO:60、SEQ ID NO:62、SEQ ID NO:64、SEQ ID NO:66、SEQ IDNO:68,及SEQ ID NO:220;和
b.重链CDR3氨基酸序列:SEQ ID NO:116、SEQ ID NO:118、SEQ ID NO:120、SEQ IDNO:122、SEQ ID NO:124、SEQ ID NO:126、SEQ ID NO: 128、SEQ ID NO:130、SEQ ID NO:132、SEQ ID NO:134、及SEQ ID NO: 136。
在另一个实施方式中,本文所述的ETA抗体(ETA-3抗体),其包含一 个或两个氨基酸序列,其中每个氨基酸序列独立地选自于以下所列氨基酸 序列:
a.轻链CDR3氨基酸序列:SEQ ID NO:50、SEQ ID NO:52、SEQ ID NO:54、 SEQ IDNO:56、SEQ ID NO:58、SEQ ID NO:60、SEQ ID NO:62、SEQ ID NO:64、SEQ ID NO:66、SEQ IDNO:68,及SEQ ID NO:220;和
b.重链CDR3氨基酸序列:SEQ ID NO:116、SEQ ID NO:118、SEQ ID NO:120、SEQ IDNO:122、SEQ ID NO:124、SEQ ID NO:126、SEQ ID NO: 128、SEQ ID NO:130、SEQ ID NO:132、SEQ ID NO:134、及SEQ ID NO: 136。
一方面,ETA-3抗体还包含一个或两个氨基酸序列,其中每个氨基酸 序列独立地选自于以下所列氨基酸序列:
a.轻链CDR1氨基酸序列:SEQ ID NO:8、SEQ ID NO:10、SEQ ID NO: 12、SEQ IDNO:14、SEQ ID NO:16、SEQ ID NO:18、SEQ ID NO:20、SEQ ID NO:22、SEQ ID NO:24、SEQ IDNO:26、SEQ ID NO:28、及SEQ ID NO:30;和
b.重链CDR1氨基酸序列:SEQ ID NO:70、SEQ ID NO:72、SEQ ID NO:74、 SEQ IDNO:76、SEQ ID NO:78、SEQ ID NO:80、SEQ ID NO:82、SEQ ID NO:84、SEQ ID NO:86、SEQ IDNO:88、及SEQ ID NO:90。
另一方面,ETA-3抗体还包含一个或两个氨基酸序列,其中每个氨基 酸序列独立地选自于以下所列氨基酸序列:
a.轻链CDR2氨基酸序列:SEQ ID NO:32、SEQ ID NO:34、SEQ ID NO:36、 SEQ IDNO:38、SEQ ID NO:40、SEQ ID NO:42、SEQ ID NO:44、SEQ ID NO:46、及SEQ ID NO:48;和
b.重链CDR2氨基酸序列:SEQ ID NO:92、SEQ ID NO:94、SEQ ID NO:96、 SEQ IDNO:98、SEQ ID NO:100、SEQ ID NO:102、SEQ ID NO:104、SEQ ID NO:106、SEQ ID NO:108、SEQ ID NO:110、SEQ ID NO:112、及SEQ ID NO:114。
在一个实施方式中,本文所述的ETA抗体包含:a.一个独立地选自 于以下所列的轻链CDR1氨基酸序列:SEQ ID NO:8、SEQ ID NO:10、 SEQ ID NO:12、SEQ ID NO:14、SEQ IDNO:16、SEQ ID NO:18、SEQ ID NO:20、SEQ ID NO:22、SEQ ID NO:24、SEQ ID NO:26、SEQ IDNO:28、 及SEQ ID NO:30;
b.一个独立地选自于以下所列的轻链CDR2氨基酸序列:SEQ ID NO:32、 SEQ IDNO:34、SEQ ID NO:36、SEQ ID NO:38、SEQ ID NO:40、SEQ ID NO:42、SEQ ID NO:44、SEQ IDNO:46、及SEQ ID NO:48;
c.一个独立地选自于以下所列的轻链CDR3氨基酸序列:SEQ ID NO:50、 SEQ IDNO:52、SEQ ID NO:54、SEQ ID NO:56、SEQ ID NO:58、SEQ ID NO:60、SEQ ID NO:62、SEQ IDNO:64、SEQ ID NO:66、及SEQ ID NO:68;
d.一个独立地选自于以下所列的重链CDR1氨基酸序列:SEQ ID NO:70、 SEQ IDNO:72、SEQ ID NO:74、SEQ ID NO:76、SEQ ID NO:78、SEQ ID NO:80、SEQ ID NO:82、SEQ IDNO:84、SEQ ID NO:86、SEQ ID NO:88、 及SEQ ID NO:90;
e.一个独立地选自于以下所列的重链CDR2氨基酸序列:SEQ ID NO:92、 SEQ IDNO:94、SEQ ID NO:96、SEQ ID NO:98、SEQ ID NO:100、SEQ ID NO:102、SEQ ID NO:104、SEQID NO:106、SEQ ID NO:108、SEQ ID NO:110、SEQ ID NO:112、及SEQ ID NO:114;及
f.一个独立地选自于以下所列的重链CDR3氨基酸序列:SEQ ID NO:116、 SEQ IDNO:118、SEQ ID NO:120、SEQ ID NO:122、SEQ ID NO:124、SEQ ID NO:126、SEQ ID NO:128、SEQ ID NO:130、SEQ ID NO:132、SEQ ID NO:134、及SEQ ID NO:136。
在一个实施方式中,本文所述的ETA抗体包含一个独立地选自于以 下所列的轻链CDR3氨基酸序列:SEQ ID NO:50、SEQ ID NO:52、SEQ ID NO:54、SEQ ID NO:56、SEQ ID NO:58、SEQ ID NO:60、SEQ ID NO: 62、SEQID NO:64、SEQ ID NO:66、SEQ ID NO:68,及SEQ IDNO:220。 在另一个实施方式中,本文所述的ETA抗体包含一个独立地选自于以下 所列的重链CDR3氨基酸序列:SEQ ID NO:116、SEQ ID NO:118、SEQ ID NO:120、SEQ ID NO:122、SEQID NO:124、SEQ ID NO:126、SEQ ID NO:128、SEQ ID NO:130、SEQID NO:132、SEQ ID NO:134、及SEQ ID NO:136。
在另一个实施方式中,本文所述的ETA抗体包含一个独立地选自于 以下所列的轻链与重链CDR3氨基酸序列的组合:SEQ ID NO:50与SEQ ID NO:116、SEQ ID NO:50与SEQ IDNO:220、SEQ ID NO:62与SEQ ID NO:128、SEQ ID NO:62与SEQ ID NO:130、SEQ ID NO:64与SEQ ID NO:132、SEQ ID NO:66与SEQ ID NO:134、及SEQ ID NO:68与SEQ ID NO:136。
在一个实施方式中,本文所述的ETA抗体包含:
(a)轻链CDR1氨基酸序列:SEQ ID NO:8;
轻链CDR2氨基酸序列:SEQ ID NO:32;
轻链CDR3氨基酸序列:SEQ ID NO:50或SEQ ID NO:220;
重链CDR1氨基酸序列:SEQ ID NO:70;
重链CDR2氨基酸序列:SEQ ID NO:92;及
重链CDR3氨基酸序列:SEQ ID NO:116;
(b)轻链CDR1氨基酸序列:SEQ ID NO:10;
轻链CDR2氨基酸序列:SEQ ID NO:34;
轻链CDR3氨基酸序列:SEQ ID NO:52;
重链CDR1氨基酸序列:SEQ ID NO:72;
重链CDR2氨基酸序列:SEQ ID NO:94;及
重链CDR3氨基酸序列:SEQ ID NO:118;
(c)轻链CDR1氨基酸序列:SEQ ID NO:12;
轻链CDR2氨基酸序列:SEQ ID NO:36;
轻链CDR3氨基酸序列:SEQ ID NO:54;
重链CDR1氨基酸序列:SEQ ID NO:74;
重链CDR2氨基酸序列:SEQ ID NO:96;及
重链CDR3氨基酸序列:SEQ ID NO:120;
(d)轻链CDR1氨基酸序列:SEQ ID NO:14;
轻链CDR2氨基酸序列:SEQ ID NO:38;
轻链CDR3氨基酸序列:SEQ ID NO:56;
重链CDR1氨基酸序列:SEQ ID NO:76;
重链CDR2氨基酸序列:SEQ ID NO:98;及
重链CDR3氨基酸序列:SEQ ID NO:122;
(e)轻链CDR1氨基酸序列:SEQ ID NO:16;
轻链CDR2氨基酸序列:SEQ ID NO:40;
轻链CDR3氨基酸序列:SEQ ID NO:58;
重链CDR1氨基酸序列:SEQ ID NO:78;
重链CDR2氨基酸序列:SEQ ID NO:100;及
重链CDR3氨基酸序列:SEQ ID NO:124;
(f)轻链CDR1氨基酸序列:SEQ ID NO:18;
轻链CDR2氨基酸序列:SEQ ID NO:42;
轻链CDR3氨基酸序列:SEQ ID NO:60;
重链CDR1氨基酸序列:SEQ ID NO:80;
重链CDR2氨基酸序列:SEQ ID NO:102;及
重链CDR3氨基酸序列:SEQ ID NO:126;
(g)轻链CDR1氨基酸序列:SEQ ID NO:20或22;
轻链CDR2氨基酸序列:SEQ ID NO:44;
轻链CDR3氨基酸序列:SEQ ID NO:62;
重链CDR1氨基酸序列:SEQ ID NO:82;
重链CDR2氨基酸序列:SEQ ID NO:104或106;及
重链CDR3氨基酸序列:SEQ ID NO:128;
(h)轻链CDR1氨基酸序列:SEQ ID NO:24;
轻链CDR2氨基酸序列:SEQ ID NO:44;
轻链CDR3氨基酸序列:SEQ ID NO:62;
重链CDR1氨基酸序列:SEQ ID NO:84;
重链CDR2氨基酸序列:SEQ ID NO:108;及
重链CDR3氨基酸序列:SEQ ID NO:130;
(i)轻链CDR1氨基酸序列:SEQ ID NO:26;
轻链CDR2氨基酸序列:SEQ ID NO:46;
轻链CDR3氨基酸序列:SEQ ID NO:64;
重链CDR1氨基酸序列:SEQ ID NO:86;
重链CDR2氨基酸序列:SEQ ID NO:110;及
重链CDR3氨基酸序列:SEQ ID NO:132;
(j)轻链CDR1氨基酸序列:SEQ ID NO:28;
轻链CDR2氨基酸序列:SEQ ID NO:46;
轻链CDR3氨基酸序列:SEQ ID NO:66;
重链CDR1氨基酸序列:SEQ ID NO:88;
重链CDR2氨基酸序列:SEQ ID NO:112;及
重链CDR3氨基酸序列:SEQ ID NO:134;或
(k)轻链CDR1氨基酸序列:SEQ ID NO:30;
轻链CDR2氨基酸序列:SEQ ID NO:48;
轻链CDR3氨基酸序列:SEQ ID NO:68;
重链CDR1氨基酸序列:SEQ ID NO:90;
重链CDR2氨基酸序列:SEQ ID NO:114;及
重链CDR3氨基酸序列:SEQ ID NO:136。
在另一个实施方式中,本文所述的ETA抗体包含:
轻链CDR1氨基酸序列:SEQ ID NO:28;
轻链CDR2氨基酸序列:SEQ ID NO:46;
轻链CDR3氨基酸序列:SEQ ID NO:66;
重链CDR1氨基酸序列:SEQ ID NO:88;
重链CDR2氨基酸序列:SEQ ID NO:112;及
重链CDR3氨基酸序列:SEQ ID NO:134。
在另一个实施方式中,本文所述的ETA抗体,其包含一个或两个氨基 酸序列,其中每个氨基酸序列独立地选自于以下所列氨基酸序列:
a.轻链可变结构域氨基酸序列:SEQ ID NO:138(L1)、SEQ ID NO:140 (L2)、SEQID NO:142(L3)、SEQ ID NO:144(L4)、SEQ ID NO:146 (L5)、SEQ ID NO:148(L6)、SEQ IDNO:150(L7)、SEQ ID NO:152 (L8)、SEQ ID NO:154(L9)、SEQ ID NO:156(L10)、SEQ ID NO:158 (L11)、SEQ ID NO:160(L12)、SEQ ID NO:162(L13)、及SEQ ID NO:164(L14)、及与其有至少80%、至少85%、至少90%、或至少95% 相同的氨基酸序列;及
b.重链可变结构域氨基酸序列:SEQ ID NO:166(H1)、SEQ ID NO:168 (H2)、SEQID NO:170(H3)、SEQ ID NO:172(H4)、SEQ ID NO:174 (H5)、SEQ ID NO:176(H6)、SEQ IDNO:178(H7)、SEQ ID NO:180 (H8)、SEQ ID NO:182(H9)、SEQ ID NO:184(H10)、SEQ ID NO:186(H11)、SEQ ID NO:188(H12)、SEQ ID NO:190(H13)、及SEQ ID NO:192(H14)、及与其有至少80%、至少85%、至少90%、或至少 95%相同的氨基酸序列。
在另一个实施方式中,本文所述的ETA抗体的多聚核苷酸编码序列 包含一个或两个多聚核苷酸序列,其中每个多聚核苷酸列独立地选自于以 下所列多聚核苷酸序列:
a.轻链可变结构域的多聚核苷酸编码序列:SEQ ID NO:137、SEQ ID NO:139、 SEQID NO:141、SEQ ID NO:143、SEQ ID NO:145、SEQ ID NO:147、SEQ ID NO:149、SEQ ID NO:151、SEQ ID NO:153、SEQ ID NO:155、SEQ ID NO:157、SEQ ID NO:159、SEQ ID NO:161、及SEQ ID NO:163、及与其 有至少80%、至少85%、至少90%、或至少95%相同的多聚核苷酸序列; 及
b.重链可变结构域的多聚核苷酸编码序列:SEQ ID NO:165、SEQ ID NO:167、 SEQID NO:169、SEQ ID NO:171、SEQ ID NO:173、SEQ ID NO:175、SEQ ID NO:177、SEQ ID NO:179、SEQ ID NO:181、SEQ ID NO:183、SEQ ID NO:185、SEQ ID NO:187、SEQ ID NO:189、及SEQ ID NO:191、及与其 有至少80%、至少85%、至少90%、或至少95%相同的多聚核苷酸序列。
在另一个实施方式中,本文所述的ETA抗体,其包含:
a.一个独立地选自于以下所列的轻链可变结构域氨基酸序列:SEQ ID NO:138(L1)、SEQ ID NO:140(L2)、SEQ ID NO:142(L3)、SEQ ID NO:144(L4)、SEQ ID NO:146(L5)、SEQ ID NO:148(L6)、SEQ ID NO:150(L7)、SEQ ID NO:152(L8)、SEQ ID NO:154(L9)、SEQID NO:156(L10)、SEQ ID NO:158(L11)、SEQ ID NO:160(L12)、SEQ ID NO:162(L13)、及SEQID NO:164(L14)及与其有至少80%、至少 85%、至少90%、或至少95%相同的氨基酸序列;及
b.一个独立地选自于以下所列的重链可变结构域氨基酸序列:SEQ ID NO:166(H1)、SEQ ID NO:168(H2)、SEQ ID NO:170(H3)、SEQ ID NO:172(H4)、SEQ ID NO:174(H5)、SEQ ID NO:176(H6)、SEQ ID NO:178(H7)、SEQ ID NO:180(H8)、SEQ ID NO:182(H9)、SEQID NO:184(H10)、SEQ ID NO:186(H11)、SEQ ID NO:188(H12)、SEQ ID NO:190(H13)、及SEQID NO:192(H14)、及与其有至少80%、至 少85%、至少90%、或至少95%相同的氨基酸序列。
在另一个实施方式中,本文所述的ETA抗体,其包含:
a.一个独立地选自于以下所列的轻链可变结构域氨基酸序列:SEQ ID NO:138(L1)、SEQ ID NO:140(L2)、SEQ ID NO:142(L3)、SEQ ID NO:144(L4)、SEQ ID NO:146(L5)、SEQ ID NO:148(L6)、SEQ ID NO:150(L7)、SEQ ID NO:152(L8)、SEQ ID NO:154(L9)、SEQID NO:156(L10)、SEQ ID NO:158(L11)、SEQ ID NO:160(L12)、SEQ ID NO:162(L13)、及SEQID NO:164(L14);及
b.一个独立地选自于以下所列的重链可变结构域氨基酸序列:SEQ ID NO:166(H1)、SEQ ID NO:168(H2)、SEQ ID NO:170(H3)、SEQ ID NO:172(H4)、SEQ ID NO:174(H5)、SEQ ID NO:176(H6)、SEQ ID NO:178(H7)、SEQ ID NO:180(H8)、SEQ ID NO:182(H9)、SEQID NO:184(H10)、SEQ ID NO:186(H11)、SEQ ID NO:188(H12)、SEQ ID NO:190(H13)、及SEQID NO:192(H14)。
在另一个实施方式中,本文所述的ETA抗体包含一个独立地选自于 以下所列的轻链与重链可变结构域氨基酸序列的组合:SEQ ID NO:138和 SEQ ID NO:166(L1H1)、SEQ IDNO:140和SEQ ID NO:168(L2H2)、 SEQ ID NO:142和SEQ ID NO:170(L3H3)、SEQ ID NO:144和SEQ ID NO:172(L4H4)、SEQ ID NO:146和SEQ ID NO:174(L5H5)、SEQ ID NO:148和SEQID NO:176(L6H6)、SEQ ID NO:150和SEQ ID NO:178 (L7H7)、SEQ ID NO:152和SEQ ID NO:180(L8H8)、SEQ ID NO:154 和SEQ ID NO:182(L9H9)、SEQ ID NO:156和SEQ ID NO:184(L10H10)、 SEQ ID NO:158和SEQ ID NO:186(L11H11)、SEQ ID NO:160和SEQ ID NO:188(L12H12)、SEQ ID NO:162和SEQ ID NO:190(L13H13)、 及SEQ ID NO:164和SEQ ID NO:192(L14H14)。在另一个实施方式中, 本文所述的ETA抗体包含一轻链与重链可变结构域氨基酸序列的组合: SEQ ID NO:162和SEQ ID NO:190(L13H13)。
本文也可用“LxHy”符号来表示本文所述的ETA抗体,其中“x”对应于 轻链可变区并且“y”对应于重链可变区。例如,L2H1指具有包含SEQ ID NO:140(L2)氨基酸序列的轻链可变区和包含SEQ ID NO:166(H1)氨 基酸序列的重链可变区的抗体。
在另一个实施方式中,本文所述的ETA抗体包含选自L1-L14的轻 链可变区或选自H1-H14的重链可变区及其片段、衍生物、突变蛋白、或 变异体的抗体。
在另一个实施方式中,本文所述的ETA抗体包含一个独立地选自于 以下所列的轻链与重链CDR3氨基酸序列的组合:SEQ ID NO:138与SEQ ID NO:166、SEQ ID NO:150与SEQID NO:178、SEQ ID NO:152与SEQ ID NO:180、SEQ ID NO:154与SEQ ID NO:182、SEQ IDNO:156与SEQ ID NO:184、SEQ ID NO:158与SEQ ID NO:186、SEQ ID NO:160与SEQ ID NO:188、SEQ ID NO:162与SEQ ID NO:190、及SEQ ID NO:164与 SEQ ID NO:192。
在一个实施方式中,本文所述的ETA抗体包含SEQ ID NO:138轻链 可变结构域氨基酸序列或SEQ ID NO:166重链可变结构域氨基酸序列。 在另一个实施方式中,本文所述的ETA抗体包含SEQ ID NO:138轻链可 变结构域氨基酸序列和SEQ ID NO:166的重链可变结构域氨基酸序列的 组合。在另一个实施方式中,本文所述的ETA抗体还包含恒定氨基酸序列, 其中每个恒定氨基酸序列独立地选自于以下所列的氨基酸序列:a.轻链恒 定氨基酸序列:SEQ ID NO:194及SEQ ID NO:196;及b.重链恒定氨基酸 序列:SEQ ID NO:198及SEQ ID NO:221。
在另一个实施方式中,本文所述的ETA抗体还包含恒定氨基酸序列, 其中每个恒定氨基酸序列独立地选自于以下所列的轻链和重链恒定氨基酸 序列的组合:
a.轻链恒定氨基酸序列SEQ ID NO:194和重链恒定氨基酸序列SEQ ID NO:198的组合;
b.轻链恒定氨基酸序列SEQ ID NO:194和重链恒定氨基酸序列SEQ ID NO:221的组合;
c.轻链恒定氨基酸序列SEQ ID NO:196和重链恒定氨基酸序列SEQ ID NO:198的组合;
d.轻链恒定氨基酸序列SEQ ID NO:196和重链恒定氨基酸序列SEQ ID NO:221的组合。
在另一个实施方式中,本文所述ETA抗体的轻链和重链的氨基酸序 列分别为SEQID NO:222和SEQ ID NO:236。
在一个实施方案中,本文所述的抗体包含本文所列轻链及重链CDRs 和FRs(框架)的氨基酸序列。在一个实施方案中,该抗体包含本文所列的 轻链CDR1序列。在另一个实施方案中,该抗体包含本文所列的轻链 CDR2序列。在另一个实施方案中,该抗体包含本文所列的轻链CDR3序 列。在另一个实施方案中,该抗体包含本文所列的重链CDR1序列。在另 一个实施方案中,该抗体包含本文所列的重链CDR2序列。在另一个实施 方案中,该抗体包含本文所列的重链CDR3序列。在另一个实施方案中, 该抗体包含本文所列的轻链FR1序列。在另一个实施方案中,该抗体包含 本文所列的轻链FR2序列。在另一个实施方案中,该抗体包含本文所列轻 链的FR3序列。在另一个实施方案中,该抗体包含本文所列的轻链FR4 序列。在另一个实施方案中,该抗体包含本文所列的重链FR1序列。在另 一个实施方案中,该抗体包含本文所列重链的FR2序列。在另一个实施方 案中,该抗体包含本文所列的重链FR3厚列。在另一个实施方案中,该抗 体包含本文所列的重链FR4序列。
在一个实施方案中,该抗体的CDR3序列与本文所列轻重链CDR3 氨基酸序列SEQID NO:50与SEQ ID NO:116的组合相差最多不超过6、 5、4、3、2、或1个单氨基酸添加、替换和/或缺失。在另一个实施方案中, 该抗体的轻链CDR3序列与本文所列轻链CDR3氨基酸序列SEQ ID NO: 50相差不得超过6、5、4、3、2、或1个单氨基酸添加、替换和/或缺失。 在另一个实施方案中,该抗体的轻链CDR3序列与本文所列轻链CDR3 氨基酸序列SEQ ID NO:50相差不得超过6、5、4、3、2、或1个单氨基 酸添加、替换和/或缺失,并且该抗体的重链CDR3序列与本文所列重链 CDR3氨基酸序列SEQ ID NO:116或SEQ ID NO:118相差最多不超过6、 5、4、3、2、或1个单氨基酸添加、替换和/或缺失。在另一个实施方案中, 该抗体进一步包含1、2、3、4、5、或6个本文所列轻重链CDR轻重链 序列组合。在另一个实施方案中,该抗体进一步包含1、2、3、4、5、或6 个CDR轻重链序列组合,各序列独自与本文所列轻重链轻重链CDR3氨基酸序列SEQ ID NO:50与SEQ ID NO:116的组合相差最多不超过6、 5、4、3、2、或1个单氨基酸。在另一个实施方案中,该抗体包含本文所 列轻链可变区的CDRs和重链可变区的CDRs。在另一实施方案中,该抗 体包含本文所列的1、2、3、4、5、和/或6个CDR轻重链序列组合。
在一个实施方案中,该抗体(例如抗体或抗体片段)包含本文所列L1 轻链可变结构域序列。在一个实施方案中,该轻链可变结构域包含与L1的 轻链可变结构域序列存在15、14、13、12、11、10、9、8、7、6、5、4、 3、2、或1个氨基酸差异的氨基酸序列,其中各该序列的差异独立为一个 氨基酸残基的缺失、插入或替换。在另一个实施方案中,该轻链可变结构域 包含与L1的轻链可变结构域序列有至少70%、至少75%、至少80%、至 少85%、至少90%、至少95%、至少97%、或至少99%相同的氨基酸序 列。在另一个实施方案中,该轻链可变结构域多聚核苷酸编码序列包含与 L1多聚核苷酸编码序列有至少70%、至少75%、至少80%、至少85%、 至少90%、至少95%、至少97%、或至少99%相同的核苷酸编码序列。在另一个实施方案中,该轻链可变结构域多聚核苷酸编码序列包含在中等 条件下与L1的轻链可变结构域的多聚核苷酸编码序列互补序列杂交的多 聚核苷酸序列。在另一个实施方棠中,该轻链可变结构域多聚核苷酸编码序 列包含在严格条件下与L1的轻链可变结构域的多聚核苷酸编码序列互补 序列杂交的多聚核苷酸序列。
在一个实施方案中,该抗体(例如抗体或抗体片段)包含本文所列H1 重链可变结构域序列。在另一个实施方案中,该可变结构域包含选与H1的 重链可变结构域序列存在15、14、13、12、11、10、9、8、7、6、5、4、 3、2、或1个氨基酸差异的氨基酸序列,其中各该序列的差异独立为一个 氨基酸残基的缺失、插入或替换。在另一个实施方案中,该重链可变结构域 包含与H1的重链可变结构域序列有至少70%、至少75%、至少80%、 至少85%、至少90%、至少95%、至少97%、或至少99%相同的氨基酸 序列。在另一个实施方案中,该重链可变结构域多聚核苷酸编码序列包含与 H1多聚核苷酸编码序列有至少70%、至少75%、至少80%、至少85%、 至少90%、至少95%、至少97%、或至少99%相同的核苷酸编码序列。在另一个实施方案中,该重链可变结构域多聚核苷酸编码序列包含在中等 严格条件下与H1的重链可变结构域的多聚核苷酸编码序列互补序列杂交 的多聚核苷酸序列。在一个实施方案中,该重链可变结构域多聚核苷酸编码 序列包含在严格条件下与H1的重链可变结构域的多聚核苷酸编码序列互 补序列杂交的多聚核苷酸序列。
在一个实施方案中,本文所述的抗体包括包含组合L1H1、L2H2、L3H3、 L4H4、L5H5、L6H6、L7H7、L8H8、L9H9、L10H10、L11H11、L12H12、 L13H13、或L14H14的抗体,或其期望表型(例如,IgA、IgG1、IgG2a、 IgG2b、IgG3、IgM、IgE和IgD),或其Fab或F(ab')2片段。
在一个实施方案中,本文所述的抗体包括包含组合L1H1的抗体,或 其类转换的抗体(例如,IgA、IgG1、IgG2a、IgG2b、IgG3、IgM、IgE和 IgD),或其Fab或F(ab')2片段。
本文所述的抗体(例如,抗体、抗体片段、和抗体衍生物)可包含本领 域已知的恒定区中任何一个。轻链恒定区可为例如κ或λ型轻链恒定区, 例如小鼠κ或λ型轻链恒定区。重链恒定区可为例如α、δ、ε、γ、或μ 型重链恒定区,例如小鼠α、δ、ε、γ、或μ型重链恒定区。在一个实施方 案中,该轻链或重链恒定区为天然恒定区的片段、衍生物、变异体、或突变蛋白。
在一个实施方案中,本文所述的抗体进一步包含恒定轻链κ或λ结 构域或这些的片段。轻链恒定区序列和它们的多聚核苷酸提编码序列供如 下:多聚核苷酸(κ),(SEQ IDNO:193);氨基酸(κ),(SEQ ID NO:194); 多聚核苷酸(λ),(SEQ ID NO:195);氨基酸(λ),(SEQ ID NO:196)。
在另一个实施方案中,本文所述的抗体进一步包含重链恒定结构域或 其片段。重链恒定区序列和它的多聚核苷酸编码序列提供如下:多聚核苷酸 (IgG4),(SEQ ID NO:197);氨基酸(IgG4),(SEQ ID NO:198)。
在一个实施方式中,本文所述的ETA抗体选自鼠源抗体、人源化抗体、 嵌合抗体、单克隆抗体、多克隆抗体、重组抗体、抗原结合抗体片段、单链 抗体、双链抗体、三链抗体、四链抗体、Fab片段、F(ab’)x片段、结构域 抗体、IgD抗体、IgE抗体、IgM抗体、IgGl抗体、IgG2抗体、IgG3抗 体、和IgG4抗体。在另一个实施方式中,本文所述的ETA抗体为ETA 单克隆抗体。在另一个实施方式中,本文所述的ETA抗体为自鼠源ETA 抗体。本文所述的ETA抗体为人源化ETA抗体。
在一个实施方式中,本文所述的ETA抗体为单克隆抗体A-1(其包含 SEQ ID NO:138与SEQ ID NO:166)、A-7(其包含SEQ ID NO:150与 SEQ ID NO:178)、A-8(其包含SEQ IDNO:152与SEQ ID NO:180)、 A-9(其包含SEQ ID NO:154与SEQ ID NO:182)、A-10(其包含SEQ ID NO:156与SEQ ID NO:184)、A-11(其包含SEQ ID NO:158与SEQ ID NO:186)、A-12(其包含SEQ ID NO:160与SEQ ID NO:188)、A-13 (其包含SEQ ID NO:162与SEQ ID NO:190)、或A-14(其包含SEQ ID NO:164与SEQ ID NO:192)。
抗体和抗体片段
在一个实施方案中,本文所述的抗体为完整抗体(包括具有全长重和/ 或轻链的多克隆、单克隆、嵌合、人源化或人类抗体)。在另一个实施方案 中,本文所述的抗体为抗体片段,列如F(ab’)2、Fab、Fab’、Fv、Fc、或Fd 片段,并可整合入单结构域抗体、单链抗体、最大抗体(maxibodies)、微 抗体(minibodies)、内抗体(intrabodies)、二链抗体、三链抗体、四链抗 体、v-NAR和bis-scFv(参见,例如Hollinger and Hudson,2005,NatureBiotechnology 23:1126-1136)。在另一个实施方案中,本文所述的抗体也包 括抗体多肽例如美国专利号US6,703,199中所公开的那些,包括纤维结合素 多肽单抗体。在另一个实施方案中,本文所述的抗体也包括其它抗体多肽公 开于美国专利申请公开号US2005/0238646,其为单链多肽。
在一个实施方案中,使用核苷酸引物扩增在杂交瘤中表达相关单克隆 抗体的基因的可变区。这些引物可由本领域普通技术人员合成或从商业来 源购买(参见,例如Stratagene,La Jolla,California),这些厂商销售鼠和 人可变区引物包括VHa、VHb、VHc、VHd、CH1、VL和CL区的引物。这些引 物可用于扩增重链或轻链可变区,然后将其分别插入载体例如 IMMUNOZAPTMH或ILLLFFLUNOZAPTML(Stratagene)中。然后将这 些载体引入大肠杆菌、酵母或哺乳动物为基础的表达系统。可使用这些方法 生产大量包含VH和VL结构域融合的单链蛋白(参见Bird等,1988,Science 242:423-426)。
一旦使用上述任何免疫和其它技术获得了根据本文生产抗体的细胞, 可根据本文所述标准方法通过分离并从其扩增DNA或mRNA将特异抗体 基因克隆。测序从其生产的抗体并鉴定CDRs,可如之前所述对编码CDRs 的DNA进行操作以生成根据本文所述的其它抗体。
本文所述的抗体优选在本文描述的基于细胞的测定法中和/或本文描述 的体内测定法中调节内皮素信号传导和/或交叉阻断本申请所述抗体之一的 结合和/或经本申请所述抗体之一被结合ETA交叉阻断。因此可使用本文所 述测定法鉴定该类结合剂。
在一些实施方案中,通过首先鉴定在本文描述的基于细胞的和/或体内 测定法中与过表达ETA的细胞结合和/或中和和/或交叉阻断本申请描述的 抗体和/或经本申请描述的抗体之一被结合ETA交叉阻断的抗体以生成抗 体。
本领域技术人员应理解的是一些蛋白质,例如抗体,可能进行可多种转 录后修饰。这些修饰的类型和程度取决于用于表达该蛋白的宿主细胞系以 及培养条件。该类修饰包括糖基化作用、甲硫氨酸氧化、二酮哌嗪形成、天 冬氨酸异构化和天冬酰胺脱酰胺作用的变化。由于羧肽酶的作用频繁修饰 导致羧端碱性残基(例如赖氨酸或精氨酸)的丢失(如Harris,1995,Journal of Chromatography 705:129-134中所述)。
生产鼠单克隆抗体的可选择方法为将杂交瘤细胞注入同系基因小鼠的 腹膜腔,例如经处理(例如姥鲛烷初次免疫)促进形成包含单克隆抗体的腹 水的小鼠。可通过多种已确立的技术分离和纯化单克隆抗体。该类分离技术 包括使用蛋白A-琼脂糖的亲和色谱法、分子排阻色谱法和离子交换色谱法, 参见,例如,Coligan第2.7.1-2.7.12页和第2.9.1-2.9.3页;Baines等, “Purification of Immunoglobulin G(IgG),”Methods inMolecular Biology,第 10卷,第79-104页(The Humana Press,Inc.,1992)。可使用基于抗体的 特殊性质(例如,重链或轻链同种型、结合特异性等)筛选的适当配基通过 亲和色谱法纯化单克隆抗体。固定化于固体载体的适当配基的实例包括蛋 白A、蛋白G、抗恒定区(轻链或重链)抗体、抗独特型抗体以及TGF-p结 合蛋白或其片段或变异体。
可使用抗体结合位点中央的互补决定区(CDRs)的分子进化分离亲和 性增加的抗体,例如对c-erbB-2亲和性增加的抗体,如Schier等,1996, J.Mol.Biol.263:551-567所述。因此,该类技术可用于制备人内皮素受体 的抗体。例如可在检测是否存在内皮素受体的体外或体内测定法中使用针 对人内皮素受体的抗体。
也可通过任何传统技术制备抗体。例如,可从天然表达这些抗体的细胞 将其纯化(例如,可从生产抗体的杂交瘤将其纯化)或使用本领域任何已知 的技术在重组表达系统中生产。参见,例如,Monoclonal Antibodies, Hybridomas:A New DimensioninBiological Analyses,Kennet等编辑,Plenum Press(1980);和Antibodies:A LaboratoryManual,Harlowand Land编辑, Cold Spring Harbor Laboratory Press(1988)。这在下文的核酸部分讨论。
可通过任何已知技术制备抗体并筛选期望性质。一些技术涉及分离编 码相关抗体(例如,抗内皮素受体抗体)的多肽链(或其部分)的核酸,并 通过重组DNA技术操作核酸。该核酸可与另一相关核酸融合或经修饰(例 如通过诱变或其它传统技术)以添加、缺失或替换一个或多个氨基酸残基。
当需要提高根据本文包含一个或多个上述CDRs的抗体的亲和性时, 可通过多种亲和成熟方案包括维持CDRs(Yang等,1995,J.Mol.Biol. 254:392-403)、链替换(Marks等,1992,Bio/Technology 10:779-783)、 使用大肠杆菌的突变株(Low等,1996,J.Mol.Biol.250:350-368)DNA 重排(Patten等,1997,Curr.Opin.Biotechnol.8:724-733)、噬菌体展示 (Thompson等,1996,J.Mol.Biol.256:7-88)以及其它PCR技术(Crameri等,1998,Nature 391:28 8-291)。所有这些亲和力成熟方法讨论于Vaughan 等,1998,Nature Biotechnology 16:535-539中。
在一个实施方案中,本文所述的抗体为抗内皮素受体片段。该片段可完 全由抗体衍生序列组成或可包含附加序列。抗原结合片段的实例包括Fab、 F(ab’)2、单链抗体、双链抗体、三链抗体、四链抗体和结构域抗体,其它实 例提供于Lunde等,2002,Biochem.Soc.Trans.30:500-06。
可经氨基酸桥(短肽接头)连接重链和轻链可变结构域(Fv区)形成 单链抗体,从而得到单多肽链。已通过将编码肽接头的DNA融合在编码两 个可变结构域多肽(VL和VH)的DNAs之间制备该单链Fvs(scFvs)。所得多 肽可折叠回自身形成抗原结合单体,或它们可形成多聚体(例如,二聚体、 三聚体或四聚体),取决于两个可变结构域之间的柔性接头的长度(Kortt 等,1997,Prot.Eng.10:423;Kortt等2001,Biomol.Eng.18:95-108)。通 过组合包含多肽的不同VL和VH,可形成与不同表型结合的多体scFvs (Kriangkum等,2001,Biomol.Eng.18:31-40)。已研发的用于生产单链抗 体的技术包括美国专利号US4,946,778;Bird,1988,Science 242:423;Huston 等,1988,PNAS USA 85:5879-5883;Ward等,1989,Nature 334:544-546; deGraaf等,2002,Methods Mol.Biol.178:379-87申描述的那些。来源于本 文所述的抗体的单链抗体包括但不限于包含可变结构域组合L1H1的scFvs,均涵盖于本文。
也可通过抗体的蛋白水解作用例如根据传统方法用胃蛋白酶或木瓜蛋 白酶消化完整的抗体获得来源于抗体的抗原结合片段。举例而言,可用胃蛋 白酶酶裂解抗体提供称作F(ab’)2的SS片段生产抗体片段。可使用巯基还 原剂进一步裂解这一片段产生3.5SFab’单价片段。可选择的方案有,使用 巯基保护基团进行该裂解反应得到二硫键的裂解;另外还可以使用木瓜蛋 白酶的酶裂解直接产生两个单价Fab片段和一个Fc片段。这些方法描述于 例如Goldenberg,美国专利号US4,331,647,Nisonoff等,1960,Arch.Biochem.Biophys.89:230;Porter,1959,Biochem.J.73:119;Edelman等,Methods in Enzymologyl:422(Academic Press,1967);以及Andrews和Titus,J.A. Current Protocols inImmunology(Coligan等编辑,John Wiley&Sons,2003), 第2.8,1-2.8.10页和第2.10A.1-2.10A.5页。其它裂解抗体的方法,例如制备 重链以形成单价重、轻链片段(Fd),进一步裂解片段或也可使用其它酶、化 学或基因技术,只要片段与可被该完整抗体识别的抗原结合。
另一种形式的抗体片段为包含一个或多个抗体互补决定区(CDRs)的 肽。可通过构建编码相关CDR的多肽获得CDRs。例如可通过使用聚合酶 链式反应用抗体生成细胞的mRNA作为模板合成可变区制备该类多肽,参 见,例如,Larrick等,1991,Methods:ACompanion to Methods in Enzymology 2:106;Courtenay-Luck,“Genetic Manipulationof Monoclonal Antibodies,” Monoclonal Antibodies:Production,Engineering andClinical Application,Ritter 等编辑,166页(Cambridge University Press,1995);和Ward等,“Genetic Manipulation and Expression of Antibodies,”MonoclonalAntibodies:Principles and Applications,Birch等编辑,137页(Wiley-Liss,Inc.,1995)。该抗体 片段可进一步包含本文所述抗体的至少一个可变结构域。因此,例如,V区结构域可为单体并且是VH或VL结构域,其可以如下文所述的至少等于 1x10-7M或更低的亲和度独立与内皮素受体结合。
该可变区结构域可为任何天然可变结构域或其基因工程形式。基因工 程形式指使用重组DNA工程技术生产的可变区结构域。该基因工程形式包 括例如通过向特异抗体的氨基酸序列插入、缺失或改变从特异抗体可变区 产生的。具体实例包括包含只含一个CDR以及任选来自一个抗体的一个或 多个框架氨基酸和来自另一抗体的可变区结构域剩余部分,并由基因工程 组装成的可变区结构域。
可变区结构域可与至少一个其它抗体结构域或其片段在C端氨基酸共 价连接。因此,举例而言,存在于可变区结构域的VH结构域可与免疫球蛋 白CH1结构域或其片段相连。相似地,VL结构域可与CK结构域或其片段相 连。以这种方式,例如,该抗体可为Fab片段,其中抗原结合结构域包含它 们的C端分别与CH1和CK结构域共价连接的联合VH和VL结构域。可用其 它氨基酸延长CH1结构域,例如以提供铰链区或如Fab’片段中的部分铰链 结构域或提供其它结构域,例如抗体CH2和CH3结构域。
抗体的衍生物和变异体
例如可通过随机诱变或通过定点诱变(例如寡聚核苷酸诱导的定点诱 变)改变编码对应于氨基酸序列A-1的核苷酸序列L1和H1以产生与未突 变多聚核苷酸相比包含一个或多个具体核苷酸替换、缺失或插入的经改变 的多聚核苷酸。用于产生该类改变的技术实例描述于Walder等,1986,Gene 42:133;Bauer等,1985,Gene 37:73;Craik,1985,BioTechniques,3:12-19; Smith等,1981,Genetic Engineering:Principles andMethods,Plenum Press; 以及美国专利号US4,518,584和US4,737,462。这些和其它方法可用于产生 例如与未衍生化抗体相比具有期望性质例如亲和性、亲和力或对内皮素受 体的特异性增强、体内或体外活性或稳定性增强或体内副作用降低的抗内 皮素受体抗体的衍生物。
本文领域的其它抗内皮素受体抗体衍生物包括抗内皮素受体抗体或其 片段与它蛋白或多肽的共价或聚集结合物,例如通过表达包含与抗内皮素 受体抗体多肽的N端或C端融合的异源多肽的重组融合蛋白。例如,该结 合肽可为异源信号(或引导)多肽,例如酵母α因子前导肽或例如表位标签 的肽。包含融合蛋白的抗体可包含被添加以辅助抗体的纯化或鉴定的肽(例 如多聚组氨酸)。抗体也可与FLAG肽连接,如Hopp等,1988,Bio/Technology 6:1204和美国专利号US5,011,912所述。FLAG肽具有高抗原性并提供被特 异单克隆抗体(mAb)可逆结合的表位,允许已表达重组蛋白的快速检测和 方便纯化。可商业购买(Sigma-Aldrich,St.Louis,MO)用于制备其中FLAG 肽与给定多肽融合的融合蛋白的试剂,在另一个实施方案中,包含一个或多 个抗体的寡聚体可用作内皮素受体拮抗剂或用更高级的寡聚体。寡聚体可 以是共价连接的或非共价连接的二聚体、三聚体或更高的寡聚体形式。可使 用包含两个或更多个抗体的寡具体,其中一个实例为同型二聚体。其它寡聚体包括异二聚体、同型三聚体、异三聚体、同型四聚体、杂四聚体等。
一个实施方案是针对包含多个抗体的寡聚体,它们通过与抗体融合的 肽部分之间的共价或非共价相互作用连接。该类肽可为肽接头(spacers)或 具有促进寡聚化作用性质的肽。亮氨酸拉链和某些来源于抗体的多肽为可 促进抗体寡聚化的肽,如下文详细描述。
在具体的实施方案中,寡聚体包含两个至四个抗体。寡聚体的抗体可为 任何形式,如上文所述任何形式,例如变异体或片段。优选地,该寡聚体包 含具有内皮素受体结合活性的抗体。
在一个实施方案中,使用来源于免疫球蛋白的多肽制备寡聚体。制备包 含一些与抗体衍生多肽(包括Fc结构域)的不同部位融合的异源多肽已描 述于例如Ashkenazi等,1991,PNAS USA 88:10535;Byrn等,1990,Nature 344:677;和Hollenbaugh等,Construction of Immunoglobulin Fusion Proteins, Current Protocols inImmunology,Suppl.4,第10.19.1-10.19.11页。本文的 一个实施方案是针对包含两个由融合抗内皮素受体抗体的内皮素结合片段 与抗体的Fc区产生的融合蛋白的二聚体。可通过以下方式制备二聚体:例 如在适当的表达载体中插入编码融合蛋白的基因融合,在用重组表达载体 转化的宿主细胞中表达该融合基因并允许已表达融合蛋白像抗体分子一样 组装,其中Fc部分之间的链间二硫键形成二聚体。
如本文所使用术语“Fc多肽”包括来源于抗体Fc区的天然和突变蛋白形 式的多肽。也包括包含促进二聚体化的铰链区的该类多肽的截短形式。包含 Fc部分(以及由其形成的寡聚体)的融合蛋白提供了在蛋白A或蛋白G柱 子上进行亲和层析法方便纯化的优势。
PCT申请W093/10151(以参考形式并于本文)中一种适当的Fc多肽 为从N端铰链区延伸至人IgG1抗体的Fc区的天然C端的单链多肽。另一 种可用的Fc多肽为美国专利号US5,457,035和Baum等,1994,EMBO J.13:3992-4001中描述的Fc突变蛋白。该突变蛋白的氨基酸序列与 W093/10151中所示天然Fc序列的氨基酸序列相同,除了氨基酸19从亮氨 酸变为丙氨酸,氨基酸20从亮氨酸变为谷氨酰胺以及氨基酸22从甘氨酸 变为丙氨酸。该突变蛋白表现出对Fc受体的亲和力降低。在其它实施方案 中,抗内皮素受体抗体的重链和/或轻链可被取代为抗体重链和/或轻链的可 变部分。
或者,该寡聚体为包含多个抗体的融合蛋白,包含或不包含接头肽 (spacerpeptides)。这些适当的接头肽描述于美国专利号US4,751,180和 US4,935,233。
制备寡聚抗体的另一种方法涉及使用亮氨酸拉链。亮氨酸拉链结构域 为促进它们所存在的蛋白寡聚化作用的肽。最初发现亮氨酸拉链存在于数 种DNA结合蛋白中(Landschulz等,1988,Science 240:1759),此后发现 存在于各种不同蛋白中。在已知的亮氨酸拉链中为可二聚体化或三聚体化 的天然肽或其衍生物。适用于生产可溶寡聚蛋白的亮氨酸拉链结构域的实 例描述于PCT申请W094/10308,来源于肺表面活性蛋白D(SPD)的亮氨酸 拉链描述于Hoppe筝,1994,FEBS Letters 344:191,以参考形式并于本文。 允许与其融合的异源蛋白稳定三聚体化的经修饰的亮氨酸拉链的使用描述 于Fanslow等,1994,Semin.Immunol.6:267-78。在一种方法中,在适当的 宿主细胞中表达包含与亮氨酸拉链肽融合的抗内皮素受体抗体片段或衍生 物的重组融合蛋白,从培养物上清中收集可溶寡聚抗内皮素受体抗体片段 或其衍生物。
在另一个实施方案中,该抗体衍生物可包含至少本文公开的CDRs之 一。举例而言,可将一个或多个CDR整合入已知的抗体骨架区(IgG1,IgG2 等)或与适当的载体结合以增强其半衰期。适当载体包括但不限于Fc、白 蛋白、转铁蛋及类似物质。这些和其它适当的载体为本领域已知。该结合 CDR肽可为单体、二聚体、四聚体或其它形式。在一个实施方案中,一个 或多个水溶性多聚体在结合剂的一个或多个特异位点结合,例如在氨基端。 在一个实例中,抗体衍生物包含一个或多个水溶性多聚体附着物包括但不 限于聚乙二醇、聚氧乙烯二醇或聚丙二醇。参见,例如,美国专利号 US4,640,835、US4,496,689、US4,301,144、US4,670,417、US4,791,192和 US4,179,337,在一些实施方案中,衍生物包含一个或多个一甲氧基.聚乙 二醇、葡聚糖、纤维素或其它基于碳水化合物的聚合物,聚(N-乙烯基吡咯酮)。聚乙二醇、聚氧乙烯多元醇(例如甘油)和聚乙烯醇,以及该类聚合 物的混合物。在一些实施方案中,一个或多个水溶性聚合物与一个或多个侧 链随机结合。在一些实施方案中。PEG可提高结合剂例如抗体的治疗作用。 一些该类方法描述于例如美国专利号US6,133,426,其以参考形式以任何目 的并于本文。
应当理解的是本文所述的抗体可具有至少一个氨基酸替换,只要该抗 体保留了结合特异性。因此,抗体结构的修饰包含于本文范畴。这些可包括 不破坏抗体内皮素受体结合能力的氨基酸替换,其可为保守或非保守的。保 守氨基酸替换可包括非天然氨基酸残基,其通常经化学肽合成整合而不是 生物系统合成。这些包括拟肽和其它反向或倒转形式的氨基酸部分。保守氨 基酸替换也可涉及用非天然残基替换天然氨基酸残基这样对该位点氨基酸 残基的极性或电荷作用很小或没有作用。非保守替换可涉及一类氨基酸或 氨基酸类似物的一个成员与具有不同物理性质(例如,体积、极性、疏水性、 电荷)的另一类氨基酸的成员交换。
而且,本领域技术人员可生成在各期望氨基酸残基上包含氨基酸替换 的待测变异体。可使用本领域技术人员已知的活性测定法筛选该类变异体。 该类变异体可用于收集关于适当变异体的信息。举例而言,如果发现某一氨 基酸残基可引起活性破坏、非期望的降低或不当的活性,可避免具有该类变 化的变异体。换言之,基于从这些常规试验收集的信息,本领域技术人员可 轻松确定应避免进一步替换(单独或与其它突变组合)的氨基酸。
技术人员可使用已知技术确定如本文所列的多肽的适当变异体。在一 些实施方案中,本领域技术人员可通过靶向对于活性不重要的区域鉴定经 改变后不会破坏活性的分子适当区域。在一些实施方案中,可鉴定在相似多 肽中保守的残基或分子部分。在一些实施方案中,甚至可保守替换对于生物 活性或结构重要的区域而不破坏生物活性或不会有不利作用于多肽结构。 此外,本领域技术人员可考察结构.功能研究鉴定对活性或结构重要的相似 多肽中的残基。鉴于这一对比,可预测对应于在相似蛋白中对活性或结构重要的氨基酸残基的蛋白质中氨基酸残基的重要性。本领域技术人员可为这 些经预测重要的氨基酸残基选择化学相似氨基酸替换。
本领域技术人员也可分析与相似多肽的结构相关的三维结构和氨基酸 序列。鉴于该类信息,本领域技术人员可预测就三维结构而言抗体的氨基酸 残基比对。在一些实施方案中,本领域技术人员可选择不对经预测在蛋白质 表面的氨基酸残基进行显著改变,因为该类残基可能参与与其它分子的重 要相互作用。许多科学出版物致力于二级结构的预测。参见,Moult,1996, Curr.Op.Biotech.7:422-427,Chou等,1974,Biochemistry 13:222-245;Chou 等,1974,Biochemistry 113:211-222;Chou等,1978,Adv.Enzymol.Relat.Areas Mol.Biol.47:45-148;Chou等,1979,Ann.Rev.Biochem.47:251-276 和Chou等,Biophys.J.26:367-384。此外,目前可使用计算机程序辅助预 测二级结构。举例而言,序列同一性大于30%或相似性大于40%的两个多 肽或蛋白质通常具有相似的高级结构。近期蛋白结构数据库(PDB)的增长 增强了二级结构的可预测性,包括多肽或蛋白结构中潜在的折叠数量。参见, Holm等,1999,Nucl.Acid.Res.27:244-247。已表明(Brenner等,1997,Curr.Op.Struct.Biol.7:369-376)在给定多肽或蛋白质中存在有限数量的折 叠并且一旦确定了临界数量的结构,结构预测将变得显著更加精确。预测二 级结构的其它方法包括“穿接(threading)”(Jones,1997,Curr.Opin.Struct. Biol.,7:377-87;Sippl等,1996,Structure 4:15-19;“图谱分析(profile analysis)” (Bowie等,1991,Science 253:164-170;Gribskov等,1990,Meth.Enzym. 183:146-159;Gribskov等,1987,PNAS USA 84:4355-4358和“进化联系 (evolutionary linkage)”(参见Holm,supra(1999),and Brenner,supra (1997))。在一些实施方案中,抗体变异体包括糖基化变异体,其中与母 体多肽的氨基酸序列相比改变了糖基化位点的数量和/或类型。在一些实施 方案中,变异体与天然蛋白质相比具有更多或更少数量的N连接糖基化位 点。或者,去除该序列的替换可移除现有的N连接糖链。也提供了N连接 糖链的重排,其中去除了一个或多个N连接糖链位点(通常为天然存在的 那些)并创造了一个或多个新的N连接位点。其它优选抗体变异体包括半 胱氨酸变异体,与母体氨基酸序列相比其中缺失或由另一氨基酸(例如丝氨 酸)替换一个或多个半胱氨酸残基。当抗体必须折叠成生物活性构象时(例 如在分离可溶包涵体之后)可用半胱氨酸变异体。半胱氨酸变异体通常比天 然蛋白质具有较少的半胱氨酸残基,并通常具有偶数个半胱氨酸以最小化 未配对半胱氨酸引起的相互作用。
本领域技术人员可在需要该类替换时确定期望的氨基酸替换(保守或 非保守)。在一些实施方案中,氨基酸替换可用于鉴定人内皮素受体抗体的 重要残基或者增加或降低本文所述人内皮素受体抗体的亲和力。根据一些 实施方案,优选的氨基酸替换为以下:(1)降低蛋白质水解敏感性,(2) 降低氧化敏感性,(3)改变形成蛋白质复合物的结合亲和力,(4)改变结 合亲和力和/或(4)赋予或修饰该类多肽上的其它物理化学或功能性质。根据一些实施方案,可在天然存在序列中(在一些实施方案中,在形成分子间 接触的结构域之外的多肽部分)进行单个或多个氨基酸替换(在一些实施方 案中为保守氨基酸替换)。在一些实施方案中,保守氨基酸替换通常不会本 质上改变母体序列的结构特性(例如,替换氨基酸不应破解存在于母体序列 中的螺旋或干扰特征化母体序列的其它类型二级结构)。本领域认可的多肽 二级和三级结构的实例描述于Proteins,Structures and MolecularPrinciples, Creighton编辑,W.H.Freeman and Company(1984);Introduction toProtein Structure,Branden and Tooze编辑,Garl and Publishing(1991);以及Thornton 等,1991,Nature 354:105,其以参考形式并于本文。
在一些实施方案中,本文所述的抗体可与多聚体、脂类或其它部分 (moieties)化学键合。抗原结合试剂可包含至少一个本文描述的CDRs,其掺 入生物相容性骨架结构中。在一个实例中,该生物相容性骨架结构包含足以 形成构象稳定结构支持或骨架或支架的多肽或其部分,其可在局限的表面 区域展示可与抗原结合的一个或多个氨基酸序列(例如,CDRs、可变区等)。 该类结构可为天然存在多肽或多肽“折叠”(结构基序),或相对与天然多肽 或折叠可具有一个或多个修饰,例如氨基酸添加、缺失或替换。这些支架可 来源于任何物种(或多于一个物种)的多肽,例如,人类、其它哺乳动物、 其它脊椎动物、无脊椎动物、细菌或病毒。生物可溶性骨架结构通常是基于 蛋白质支架或骨架而不是免疫球蛋白结构域。举例而言,可使用基于纤维结 合素、锚蛋白、脂质运载蛋白(lipocalin)、新抑癌蛋白、细胞色素b、CP1 锌指蛋白、PST1、卷曲螺旋、LACI-D1、Z结构域和淀粉酶抑肽结构域(参见,例如,Nygren和Uhlen,1997,Current Opinionin Structural Biology 7:463- 469)。
此外,本领域技术人员可认识到适当的结合剂包括这些抗体的部分,例 如一个或多个重链CDR1、CDR2、CDR3,轻链CDR1、CDR2和CDR3, 如本文所具体公开。至少一个重链CDR1、CDR2、CDR3、CDR1,CDR2和 CDR3区具有至少一个氨基酸替换,只要该抗体保留了非替换CDR的结合 特异性。该抗体的非CDR部分可为非蛋白分子,其中该结合剂交叉阻断本 文公开的抗体与人ETA的结合和/或抑制经该受体的内皮素信号传导。该抗 体的非CDR部分可为非蛋白质分子,其中该抗体在竞争结合测定法中显示 出与至少抗体A-1/A-2之一所显示相似的与人ETA肽的结合类型,和/或中 和内皮素的活性。抗体的非CDR部分可由氨基酸组成,其中该抗体为重组 结合蛋白或合成肽,并且该重组结合蛋白交叉阻断本文公开的抗体与人 ETA的结合和/或中和体内或体外内皮素活性。抗体的非CDR部分可由氨 基酸组成,其中该抗体为重组抗体,并且该重组抗体在竞争结合测定法中显 示出与至少抗体A-1/A-2之一所显示相似的与人ETA肽的结合类型,和/或 中和内皮素信号传导。
核酸
一方面,本文提供分离的核酸分子。该核酸分子包含例如编码全部或部 分抗体的多聚核苷酸,例如本文抗体的一条链或两条链,或其片段、衍生物、 突变蛋白或变异体;足以用作杂交探针的多聚核苷酸;PCR引物或用于鉴 定、分析、突变或扩增编码多肽的多聚核苷酸的测序引物;用于抑制多聚核 苷酸表达的反义核酸以及其互补序列。该核酸可为任何长度。例如它们的长 度可为5、10、15、20、25、30、35、40、45、50、75、100、125、150、 175、200、250、300、350、400、450、500、750、1000、1500、3000、5000 或更多个核苷酸,和/或包含一个或多个附加序列,例如调控序列,和/或是 较大核酸例如载体的一部分。该核酸可为单链或双链并包含RNA和/或 DNA核苷酸以及其人工变异体(例如,肽核酸)。
可从经ETA抗原免疫的小鼠B细胞中分离编码抗体多肽(例如,重链 或轻链、仅可变结构域或全长)的核酸。可通过常规方法例如聚合酶链式反 应(PCR)分离该核酸。
编码重链和轻链可变区的核酸序列如上文所示。熟练的技术人员可理 解由于遗传密码的简并性,本文公开的各多肽序列可由更多数量的其他核 酸序列编码。本文提供编码本文所述的抗体的各简并核苷酸序列。
本文进一步提供在具体杂交条件下与其他核酸(例如,包含任何A-1/A- 2的核苷酸序列的核酸)杂交的核酸。杂交核酸的方法为本领域熟知。参见, 例如,CurrentProtocols in Molecular Biology,John Wiley&Son(1989), 6.3.1-6.3.6。如本文定义,例如,中等严格条件使用包含5x氯化钠/柠檬酸 钠(SSC)的预洗溶液、0.5%SDS、1.0mMEDTA(pH8.0)、约50%甲酰胺 的杂交缓冲液、6xSSC和55℃的杂交温度(或其他相似的杂交溶液,例如 包含绚50%甲酰胺的,以42℃杂交),并且洗脱条件为60℃,使用0.5xSSC、0.1%SDS。严格杂交条件在6xSSC中于45℃杂交,然后于68℃在0.1xSSC、 0.2%SDS中洗涤一次或多次。此外,本领域技术人员可操作杂交和/或洗涤 条件以增加或降低杂交严格度这样包含相互之间至少65、70、75、80、85、 90、95、98或99%同源的核苷酸序列的核酸通常仍可以相互杂交。影响杂 交条件选择的基本参数和设计适当条件的指导列于例如Sambrook,Fritsch 和Maniatis,1989,Molecular Cloning:A Laboratory Manual,ColdSpring Harbor Laboratory Press,第9和11章;Current Protocols in MolecularBiology,1995, Ausubel等编辑,John Wiley&Sons,Inc.,第2.10和6.3-6.4节)并可由具有本领域普通技术的人员基于例如DNA的长度和/或碱基组成轻松确定。 可通过突变在核酸中引入变化,藉此导致其编码的多肽(例如,抗原结合蛋 白)氨基酸序列的变化。可使用本领域已知的任何技术引入突变。在一个实 施方案中,使用例如定点诱变方案改变一个或多个具体氨基酸残基。在另一 个实施方案中,使用例如随机诱变方案改变一个或多个随机选择的残基。无 论其如何生成,可表达突变多肽并筛选期望性质。
可将突变引入核酸而不显著改变其编码多肽的生物学活性。例如,可进 行引起非必需氨基酸残基处氨基酸替换的核苷酸替换。在一个实施方案中, 突变本文为L-1至L-2和H-1至H-2提供的核苷酸序列或其片段、变异体 或衍生物这样其编码包含本文所示L-1至L-2和H-1至H-2的氨基酸残基 的一个或多个缺失或替换,成为两个或多个序列相异的残基。在另一个实施 方案中,诱变作用在本文所示L-1至L-2和H-1至H-2的一个或多个氨基 酸残基附近插入一个氨基酸成为两个或多个序列相异的残基。或者,可将一 个或多个突变引入核酸以选择性改变其编码多肽的生物学活性(例如,与 ETA结合)。例如,该突变可在数量上或性质上改变生物学活性。量变的 实例包括增加、降低或消除该活性。质变的实例包括改变抗体的抗原特异性。
在另一方面,本文提供适于用做引物或检测本文核酸序列的杂交探针 的核酸分子。本文的核酸分子可仅包含编码本文全长多肽的核酸序列的一 部分,例如,可用作探针或引物或编码本文多肽活性部分的片段(例如,ETA 结合部分)的片段。基于本文核酸序列的探针可用于检测该核酸或相似核酸, 例如编码本文多肽的转录物。该探针可包含标记基团,例如放射性同位素、 荧光化合物、酶或酶辅因子。该类探针可用于鉴定表达该多肽的细胞。
在另一方面本文提供包含编码本文多肽或其部分的核酸的载体。载体 的实例包括但是不限于质粒、病毒载体、非游离基因哺乳动物载体和表达载 体,例如重组表达载体。本文的重组表达载体可包含适于该核酸在宿主细胞 中表达的形式的本文核酸。该重组表达载体包括一个或多个调控序列,基于 用于表达的宿主细胞进行筛选,其与该预表达的核酸序列可操作性相连。调 控序列包括引导核苷酸序列在多个种类宿主细胞中组成型表达的(例如, SV40早期基因增强剂、劳斯氏肉瘤病毒启动子和细胞巨化病毒启动子), 引导仅在某些宿主细胞中核苷酸序列的表达的(例如,组织特异调控序列, 参见Voss等,1986,Trends Biochem.Sci.11:287,Maniatis等,1987,Science 236:1237,其完整内容以参考形式并于本文)以及引导核苷酸序列响应具体 处理或条件的诱导型表达的(例如,哺乳动物细胞中的金属硫堇启动子和原 核和真核系统二者中的四环霉素反应(tet-sesponsive)启动子和/或链霉素反 应启动子(同前))。本领域技术人员应理解表达载体的设计取决于例如用 于转化的宿主细胞的选择、所需蛋白表达水平等因素。本文的表达载体可引 入宿主细胞,藉此生产由本文所述核酸编码的蛋白或肽,包括融合蛋白或肽。
另一方面,本文提供可引入本文表达载体的宿主细胞。宿主细胞可为任 何原核或真核细胞。原核宿主细胞包括革兰氏阴性或革兰氏阳性生物体,例 如大肠杆菌或杆菌。更高级的真核细胞包括昆虫细胞、酵母细胞以及哺乳动 物源的确立细胞系。适当哺乳动物宿主细胞系的实例包括中国仓鼠卵巢 (CHO)细胞或它们的衍生物例如Veggie CHO和在无血清培养基中生长 的相关细胞系(参见Rasmussen等,1998,Cytotechnology 28:31)或CHO株DXB-11,其缺失DHFR(参见Urlaub等,1980,PNAS USA77:4216-20)。 其它CHO细胞系包括CHO-K1(ATCC#CCL-61)、EM9(ATCC#CRL-1861), 和UV20(ATCC#CRL-1862),其它宿主细胞包括猴肾细胞的COS-7系 (ATCC#CRL-1651)(参见Gluzman等,1981,Cell23:175)、L细胞、C127细胞、3T3细胞(ATCCCCL-163),AM-1/D细胞(描述于美国专利号 US6,210,924)、HeLa细胞、BHK(ATCCCRL-10)细胞系、来源于非洲绿 猴肾细胞系CV1的CV1/EBNA细胞系(ATCCCCL-70)(参见McMahan 等,1991,EMBO J.10:2821)、人胚肾细胞例如293,293EBNA或MSR293、 人上皮A431细胞、人C010205细胞、其它经转化灵长动物细胞系、正常二 倍体细胞、来源于初生组织体外培养物的细胞株、初移植体、HL-60、U937、 HaK或Jurkat细胞。用于细菌、真菌、酵母和哺乳细胞宿主的适当克隆和 表达载体描述于Pouwels等(Cloning Vectors:ALaboratory Manual,Elsevier, 1985)。
可通过传统转化或转染技术将载体DNA引入原核或真核细胞中。对于 稳定的哺乳动物转染而言,取决于使用的表达载体和转染技术,已知只有一 小部分细胞可将外源DNA鏊合入它们的基因组中。为了鉴定和筛选这些整 合子,通常将编码筛选标记(例如抗生素抗性)的基因与所关注基因一起引 入宿主细胞。优选的筛选标记包括可赋予药物(如G418、潮霉素和甲氨喋 呤)抗性的那些。在其它方法中可通过药物筛选鉴别包含被引入核酸的稳定 转染细胞(例如,整合了筛选基因的细胞可存活,而其它细胞则死亡)。
可在提高多肽表达的条件下培养已转化细胞,可通过常规蛋白纯化方 法回收多肽。一种该纯化方法描述于下文实施例。预用于本文的多肽包括基 本同源的重组哺乳动物抗内皮素受体抗体多肽,其基本不含污染性内源材 料。
抗体的活性
在一个实施方案中,本文所述的抗体与内皮素受体特异性结合,抑制信 号传导并显示出治疗性生物作用,例如降低动物模型的肺动脉高压。在另一 个实施方案中,本文所述的抗体是能与人内皮素受体特异性结合的鼠源抗 体或人源化抗体。该类抗体包括可减少或中和内皮素信号传导的拮抗或中 和抗体。
在一个实施方案中,本文所述的抗体与人内皮素受体ETA结合时的Kd大约为0.01nM至1000nM、0.1nM至500nM、0.5nM至200nM、1nM 至200nM、或10nM至100nM。在另一个实施方案中,本文所述的抗体与 人内皮素受体ETA结合时的Kd大约为1nM至200nM。在另一个实施方 案中,本文所述的抗体与人内皮素受体ETA结合时的Kd大约为10nM至 100nM。在另一个实施方案中,本文所述的抗体与人内皮素受体ETA结合 时的Kd大约为1nM、2nM、5nM、10nM、20nM、30nM、40nM、50nM、 60nM、70nM、80nM、90nM、或100nM。
在一个实施方案中,本文所述的抗体在降低人内皮素信号传导的IC50值大约为0.01nM至500nM、0.1nM至200nM、0.5nM至200nM、1nM 至200nM、或10nM至100nM。在另一个实施方案中,本文所述的抗体在 降低人内皮素信号传导的IC50值大约为1nM至200nM。在另一个实施方 案中,本文所述的抗体在降低人内皮素信号传导的IC50值大约为10nM至 100nM。在另一个实施方案中,本文所述的抗体在降低人内皮素信号传导 的IC50值大约为1nM、2nM、5nM、10nM、20nM、30nM、40nM、50 nM、60nM、70nM、80nM、90nM、或100nM。
在一个实施方式中,本文所述的ETA抗体具有一个或多个以下所列的 性质:
a.当与人内皮素受体ETA结合时,其Kd与所述参比抗体相同或更优;
b.当抑制人内皮素受体ETA的内皮素激活时,其IC50与所述参比抗体相 同或更优;和
c.该ETA抗体在人内皮素受体ETA上与所述参比抗体交叉竞争结合。
在另一个实施方式中,本文所述的ETA抗体是一抗体具有一个或多个 以下所列的性质:
a.当与人内皮素受体ETA结合时,其Kd与一参比ETA抗体相同或更优;
b.当抑制人内皮素受体ETA的内皮素激活时,其IC50与一参比ETA抗体 相同或更优;和
c.该ETA抗体在人内皮素受体ETA上,与一参比ETA抗体交叉竞争结 合。
在一方面,所述参比抗体包含轻链可变结构域氨基酸序列SEQ ID NO: 138和重链可变结构域氨基酸序列SEQ ID NO:166的组合。在另一方面,所 述参比抗体为单克隆抗体A-1、A-2、A-7、A-9、或A-12。在本文中,术语 “基本相似”意为与参比抗体的IC50或Kd可比或大约是参比抗体的IC50或Kd值的200%、180%、160%、150%、140%、120%、110%、100%、99%、98%、 97%、95%、90%、85%、80%、75%、70%、65%、或50%。在一个实施方 案中,参比抗体包括,例如,具有重链和轻链组合L1H1或L2H2的抗体。 在另一个实施方案中,参比抗体包括ETA抗体A-1。在一个实施方案中, 本文所述的ETA抗体可与人内皮素受体特异性结合,并能降低动物模型的 肺动脉高压。在一个实施方案中,与未处理动物相比肺动脉高压降低2%。 在另一个实施方案中,与未处理动物相比肺动脉高压降低约5%。在另一个 实施方案中,与未处理动物相比肺动脉高压降低约10%。在另一个实施方 案中,与未处理动物相比肺动脉高压降低约15%。在另一个实施方案中,与 未处理动物相比肺动脉高压降低约20%,在另一个实施方案中,与未处理 动物相比肺动脉高压降低约25%。肺动脉高压降低量由剂量控制,对于动 物或人类患者而言,治疗有效剂量是为将肺动脉高压降低至正常范围的剂 量。
BNP
在一个实施方案中,本文所述的BNP是一可以激活NPRA的功能的 肽。在另一个实施方案中,本文所述的BNP在激活NPRA的功能上比自 然的BNP(SEQ ID NO:205)要弱上十到一千倍。
在一个实施方案中,本文所述的BNP包含各独立地选自于以下之一 的氨基酸序列:SEQ ID NO:205、SEQ ID NO:206、SEQ ID NO:207、 SEQ ID NO:208、SEQ ID NO:209、SEQID NO:210、SEQ ID NO:211、SEQ ID NO:212、SEQ ID NO:213、SEQ ID NO:214、SEQ ID NO:215、 及SEQ ID NO:216。
在一个实施方案中,本文所述的BNP的氨基酸序列为:SEQ ID NO: 205。在另一个实施方案中,本文所述的BNP的氨基酸序列为:SEQ ID NO:206。在另一个实施方案中,本文所述的BNP的氨基酸序列为:SEQ ID NO:207。在另一个实施方案中,本文所述的BNP的氨基酸序列为: SEQ ID NO:208。在另一个实施方案中,本文所述的BNP的氨基酸序列 为:SEQID NO:209。在另一个实施方案中,本文所述的BNP的氨基酸序 列为:SEQ ID NO:210。在另一个实施方案中,本文所述的BNP的氨基酸 序列为:SEQ ID NO:211。在另一个实施方案中,本文所述的BNP的氨基 酸序列为:SEQ ID NO:212。在另一个实施方案中,本文所述的BNP的氨 基酸序列为:SEQ ID NO:213。在另一个实施方案中,本文所述的BNP的 氨基酸序列为:SEQ ID NO:214。在另一个实施方案中,本文所述的BNP 的氨基酸序列为:SEQ ID NO:215。在另一个实施方案中,本文所述的 BNP的氨基酸序列为:SEQ ID NO:216。
肽接头(Linker)
在一个实施方案中,本文所述的肽接头(Linker)包含各独立地选自于以 下之一的氨基酸序列:SEQ ID NO:217、SEQ ID NO:218、及SEQ ID NO: 219。
在一个实施方案中,本文所述的肽接头的氨基酸序列为:SEQ ID NO: 217。在另一个实施方案中,本文所述的肽接头的氨基酸序列为:SEQ ID NO:218。在另一个实施方案中,本文所述的肽接头的氨基酸序列为:SEQ ID NO:219。
ETA抗体与BNP的融合蛋白质
在一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质包 含一个本文所述的ETA抗体和一或多个BNP。
在一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质包 含一个本文所述的ETA抗体和一、两、三、四、五、六,七,或八个 BNP。在另一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白 质包含一个本文所述的ETA抗体和一个BNP。另一个实施方案中,本文 所提供的ETA抗体与BNP的融合蛋白质包含一个本文所述的ETA抗体和 两个BNP。另一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋 白质包含一个本文所述的ETA抗体和三个BNP。另一个实施方案中,本 文所提供的ETA抗体与BNP的融合蛋白质包含一个本文所述的ETA抗体 和四个BNP。另一个实施方案中,本文所提供的ETA抗体与BNP的融合 蛋白质包含一个本文所述的ETA抗体和五个BNP。另一个实施方案中, 本文所提供的ETA抗体与BNP的融合蛋白质包含一个本文所述的ETA抗 体和六个BNP。另一个实施方案中,本文所提供的ETA抗体与BNP的融 合蛋白质包含一个本文所述的ETA抗体和七个BNP。另一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质包含一个本文所述的 ETA抗体和八个BNP。
在一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质包 含一个ETA抗体、和一个,二个,三个,四个,五个,六个,七个,或 八个BNP;该融合蛋白质将一BNP的氨基端与本文所述的ETA抗体的轻 链或重链的羧基端连接,或者该融合蛋白质将一BNP的羧基端与本文所 述的ETA抗体的轻链或重链的氨基端连接。
在另一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质 包含一个ETA抗体、和一个,二个,三个,或四个BNP;该融合蛋白质 将一BNP的氨基端与本文所述的ETA抗体的轻链或重链的羧基端连接, 或者该融合蛋白质将一BNP的羧基端与本文所述的ETA抗体的轻链或重 链的氨基端连接。
在另一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质 包含一个ETA抗体、和一个或二个BNP;该融合蛋白质将一BNP的氨基 端与本文所述的ETA抗体的轻链或重链的羧基端连接,或者该融合蛋白 质将一BNP的羧基端与本文所述的ETA抗体的轻链或重链的氨基端连 接。
在另一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质 包含一个ETA抗体、和二个BNP;该融合蛋白质将一BNP的氨基端与本 文所述的ETA抗体的轻链或重链的羧基端连接,或者该融合蛋白质将一 BNP的羧基端与本文所述的ETA抗体的轻链或重链的氨基端连接。
在一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质将 一BNP的氨基端与本文所述的ETA抗体的轻链或重链的羧基端连接。在 另一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质将一 BNP的氨基端与本文所述的ETA抗体的轻链的羧基端连接。在另一个实 施方案中,本文所提供的ETA抗体与BNP的融合蛋白质将一BNP的氨基 端与本文所述的ETA抗体的重链的羧基端连接。
在一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质包 含氨基酸序列:SEQ ID NO:162和SEQ ID NO:190,以及SEQ ID NO: 209或SEQ ID NO:210。在另一个实施方案中,本文所提供的ETA抗体与 BNP的融合蛋白质包含氨基酸序列:SEQ ID NO:162,SEQ IDNO:190, 及SEQ ID NO:209。在另一个实施方案中,本文所提供的ETA抗体与 BNP的融合蛋白质包含氨基酸序列:SEQ ID NO:162,SEQ ID NO:190, 及SEQ ID NO:210。
在一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质包 含一个ETA抗体、和一个,二个,三个,四个,五个,六个,七个,或 八个BNP已及同样数量的肽接头(Linker);该融合蛋白质通过一肽接头 序列将一BNP的氨基端与本文所述的ETA抗体的轻链或重链的羧基端连 接,或者该融合蛋白质通过一肽接头序列将一BNP的羧基端与本文所述 的ETA抗体的轻链或重链的氨基端连接。
在另一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质 包含一个ETA抗体、和一个,二个,三个,或四个BNP已及同样数量的 肽接头(Linker);该融合蛋白质通过一肽接头序列将一BNP的氨基端与 本文所述的ETA抗体的轻链或重链的羧基端连接,或者该融合蛋白质通 过一肽接头序列将一BNP的羧基端与本文所述的ETA抗体的轻链或重链 的氨基端连接。
在另一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质 包含一个ETA抗体、和一个或二个BNP已及经同样数量的肽接头 (Linker);该融合蛋白质通过一肽接头序列将一BNP的氨基端与本文所 述的ETA抗体的轻链或重链的羧基端连接,或者该融合蛋白质通过一肽 接头序列将一BNP的羧基端与本文所述的ETA抗体的轻链或重链的氨基 端连接。
在另一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质 包含一个ETA抗体、和二个BNP及二个肽接头(Linker);该融合蛋白 质通过一肽接头序列将一BNP的氨基端与本文所述的ETA抗体的轻链或 重链的羧基端连接,或者该融合蛋白质通过一肽接头序列将一BNP的羧 基端与本文所述的ETA抗体的轻链或重链的氨基端连接。
在一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质通 过一肽接头序列将一BNP的氨基端与所述ETA抗体的轻链或重链的羧基 端连接。在另一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋 白质通过一肽接头序列将一BNP的氨基端与所述ETA抗体的轻链的羧基 端连接。在另一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋 白质通过一肽接头序列将一BNP的氨基端与所述ETA抗体的重链的羧基 端连接。
在一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质包 含氨基酸序列:SEQ ID NO:162,SEQ ID NO:190,SEQ ID NO:205,和 SEQ ID NO:218。
在一个实施方案中,本文所提供的ETA抗体与BNP的融合蛋白质,其 中所述的ETA抗体、BNP和肽接头序列通过以下所述中一方式融合形成 所述的融合蛋白质:
(3)通过一个肽接头序列将一BNP的氨基端和所述ETA抗体的重链/ 轻链的羧基端连接:N'-R-Linker-BNP-C';及
(4)通过一肽接头序列将一BNP的羧基端与所述ETA抗体的轻链或重 链的氨基端连接:N'-BNP-Linker-R-C';
其中:N'代表多肽链的氨基端,C'代表多肽链的羧基端,BNP代表一BNP, R为所述的ETA抗体的轻链或者重链的氨基酸序列,及Linker代表一肽接 头。
在一个实施方式中,本文所提供的ETA抗体与BNP的融合蛋白质含 有两个相同的轻链,其氨基酸序列为SEQ ID NO:222;及两个相同的重 链,其氨基酸序列为以下所列的序列之一:SEQ ID NO:223、SEQ ID NO: 224、SEQ ID NO:225、SEQ ID NO:226、SEQ ID NO:227、SEQ ID NO: 228、SEQ ID NO:229、SEQ ID NO:230、SEQ ID NO:231、SEQ ID NO: 232、SEQ ID NO:233、SEQ ID NO:234、及SEQ ID NO:235,其中一 BNP的氨基端与一ETA抗体重链(SEQ ID NO:235)的羧基端连接或者 通过一肽接头序列与一ETA抗体重链的羧基端连接。
ETA抗体与BNP的融合蛋白质的生物学活性
ETA抗体与BNP的融合蛋白质的生物学活性包含BNP的生物学活性 和ETA抗体活性。ETA的抗体抑制剂能够有效地阻断由内皮素引起的血管 压力增加来达到缓解肺动脉高压的症状,改善病人的运动能力和血液动力 学。“BNP生物学活性”指ETA抗体与BNP的融合蛋白质在体内结合并激 活NPRA受体并引起细胞应激反应,并显示出治疗作用的生物学活性,例 如肺动脉高压、肺高压和心力衰竭的其它相关症状。前述细胞应激反应包括 但是不限于降低肺动脉压、降低主动脉压,以及相关的心脏和肺血管重构变 化。综合了BNP和ETA抗体的生物学活性,本文所述的BNP融合蛋白质 可以用于治疗多种与NPRA和ETA相关联的疾病和病症。该融合蛋白质通 过作用于NPRA和/或ETA发挥其生物学作用,因此可以用本文所述的BNP 融合蛋白质治疗对“增加NPRA刺激”或对“降低ETA刺激”做出有利应答的 疾病和病症的受试者。这些受试者称为“需要NPRA刺激治疗”或“需要降低ETA刺激”的受试者。包括肺动脉高压、肺高压和心脏和肺血管重构的其它 相关症状。
在一个实施方案中,ETA抗体或BNP融合蛋白质的生物学活性变化是 用钙流实验和直接cGMP检测方法来检测的,量化ETA抗体或BNP融合 蛋白质在体外抑制ETA和激活NPRA的功能。
药物组合物
在一个实施方案中,本文提供了一药物组合物,其包括本文提供的一个 ETA抗体与BNP的融合蛋白质,与一种或多种可药用载体。
在一个实施方案中,本文所述的药用组合物是用于静脉或皮下注射。
本文所使用的术语“载体”包括载体、药用辅料或者在使用的剂量和浓度 下将细胞或哺乳动物暴露于其中无害的稳定剂。
治疗方法
在一个实施方案中,本文提供了本文所述的ETA抗体与BNP的融合 蛋白质在制备用于治疗、预防或改善肺动脉高压以及肺动脉高压相关病症 的药物中的用途。
在另一个实施方案中,本文提供了本文所述的ETA抗体与BNP的融 合蛋白质在制备用于治疗、预防或改善肺高压以及肺高压相关病症的药物 中的用途。
在另一个实施方案中,本文提供了本文所述的ETA抗体与BNP的融 合蛋白质在制备用于治疗、预防或改善心力衰竭以及心力衰竭相关病症的 药物中的用途。
在进一步的实施方案中,本文提供了本文所述的ETA抗体与BNP的 融合蛋白质在制备用于同时治疗、预防或改善肺动脉高压、肺高压或者心力 衰竭二种及二种以上病症的药物中的用途。
本文中,术语“受试者”指哺乳动物,包括人类,可与术语“患者”交替使 用。
术语“治疗”包括减轻至少一种症状或病症的其它方面,或者减轻疾病严 重性。本文提供的ETA抗体与BNP的融合蛋白质不需要产生完全治愈的 效果,或根除疾病的所有症状或表现,即可构成有效治疗剂。如相关领域所 公认,作为治疗剂的药物可减少给定疾病状态的严重程度,但不需消除疾病 的所有表现即可被认为是有效的治疗剂。相似地,预防给药治疗不需在预防 症状出现上完全有效即可构成有效预防剂。只减少疾病的影响(例如,通过 减少其症状的数量或严重度,或通过提高另一治疗效果,或通过产生另一有 效作用),或者减少受试者中疾病发生或加重的可能性就已经足够。本文的 一个实施方案涉及包含以足以诱导反应具体病症严重性的指示剂高于基线 水平的持续改善的量和时间给予患者ETA抗体与BNP融合蛋白质的方法。
ETA抗体与BNP的融合蛋白质药物组合物可采用任意适当技术包括但 不限于肠道外、局部或吸入给药。如果是注射,可通过例如关节内、静脉内、 肌肉内、损伤区内、腹膜内或皮下途径,以快速注射或连续输注给予药用组 合物。可考虑例如在疾病或损伤部位局部给药,如透皮给药和埋植剂持续释 放给药。吸入给药包括例如鼻腔或口腔吸入、采用喷雾剂、以气雾剂形式吸 入抗体等等。其它选择包括口腔制剂包括片剂、糖浆剂或锭剂。
以包含一个或更多其它组分例如生理学可接受载体、辅料或稀释剂的 组合物形式给予本文提供的ETA抗体与BNP的融合蛋白质是有利的。组 合物可任选额外包含一个或更多如下所述的生理学活性剂。在多个具体实 施方案中,组合物包含除一个或更多本文提供的抗体(例如鼠源抗体或人源 化抗体)与BNP融合蛋白质之外的一个、两个、三个、四个、五个或六个 生理学活性剂。
在一个实施方案中,药物组合物包含本文提供的鼠源抗体或人源化抗 体与BNP的融合蛋白质以及一个或更多选自以下的物质:pH适合于抗体 与BNP的融合蛋白质的缓冲液、抗氧化剂例如抗坏血酸、低分子量多肽(例 如含少于10个氨基酸的多肽)、蛋白质、氨基酸、糖例如糊精、络合物例 如EDTA、谷胱甘肽、稳定剂和辅料。根据适当工业标准,也可加入防腐剂。 可使用适当辅料溶液作为稀释剂将组合物配制成冻干粉末。适当组分在所 用剂量和浓度下对受者无毒。可用于药物处方组分的进一步实例见 Remington'sPharmaceutical Sciences,第16版(1980)和20版(2000),Mack Publishing Company提供医学从业者使用的试剂盒,其包括一种或更多本文 提供的抗体与BNP的融合蛋白质以及治疗本文讨论任何病症的标签或其它 说明。在一个实施方案中,试剂盒包括以上述组合物形式装在一个或多个管 型瓶中的一种或多种抗体与BNP的融合蛋白质的无菌制剂。
给药剂量和频率可根据以下因素而改变:给药途径、所用具体抗体与 BNP的融合蛋白质、所治疾病的性质和严重度、症状为急性还是慢性以及 患者的体积和总体症状。可通过本领域熟知的方法确定适当剂量,例如在临 床试验中包括剂量放大研究。
本文提供的抗体与BNP的融合蛋白质可在例如一段时间内按规律间隔 给药一次或多次。在具体实施方案中,在至少一个月或更长时间给药一次给 予鼠源抗体或人源化抗体与BNP的融合蛋白质,例如一个、两个或三个月 或者甚至不确定。对于治疗慢性症状,长期治疗通常最有效。但是,对于治 疗急性症状,短期给药例如从一周至六周就已足够。通常,给予人类抗体直 至患者表现出所选体征或指示剂高于基线水平的医学相关改善度为止。
本文提供的治疗方案的一个实例包括以适当剂量一周一次或者更长的 皮下注射抗体与BNP的融合蛋白质治疗肺动脉高压、肺高压和心力衰竭的 症状。可持续每周或每月给予抗体与BNP的融合蛋白质直到达到所需结果 例如病人症状消退。可按需要重新治疗,或者,可选择地,给予维持剂量。
可在使用抗体与BNP的融合蛋白质治疗之前、进行中和/或之后监测病 人肺动脉压,以检测其压力的任何变化。对于某些病症,肺动脉压的变化可 随例如疾病进程等因素而变化。可用已知技术测定肺动脉压。
本文提供的方法和组合物的具体实施方案涉及使用例如抗体与BNP的 融合蛋白质和一个或多个内皮素拮抗剂、两个或更多本文提供的抗体与 BNP的融合蛋白质,或者本文提供的抗体与BNP的融合蛋白质和一个或更 多其它内皮素拮抗剂。在进一步的实施方案中,单独或与其它用于治疗使患 者痛苦的症状的药剂组合给予本文提供的抗体与BNP的融合蛋白质。这些 药剂的实例包括蛋白质以及非蛋白质药物。当联合给予多种药物时,如本领 域所熟知其剂量应相应调整。“联合给药”组合疗法不限于同时给药,也包括 在涉及给予患者至少一种其它治疗剂的疗程中至少给予一次抗原和蛋白的 治疗方案。
另一方面,本文提供制备治疗肺动脉高压、肺高压和心力衰竭症状的方 法,其包含本文提供的抗体与BNP的融合蛋白质与药学可接受辅料中的混 合物,用于治疗上述疾病的相关病症。药剂制备方法如上所述。
本文进一步提供可特异性结合与人ETA的抗体与BNP的融合蛋白质 相关的组合物、试剂盒和方法。也提供了核酸分子及其衍生物和片段,其包 含编码与ETA结合的多肽与BNP的融合蛋白质的全部或部分的多聚核苷 酸,例如编码全部或部分抗ETA抗体、抗体片段、抗体衍生物与BNP的融 合蛋白质的核酸。本文进一步提供包含该类核酸的载体和质粒以及包含该 类核酸和/或载体和质粒的细胞和细胞系。所提供方法包括,例如,制备、 鉴定或分离与人ETA结合的抗体与BNP的融合蛋白质例如抗ETA抗体与 BNP的融合蛋白质的方法,测定该抗体与BNP的融合蛋白质是否与ETA 结合的方法、以及将与ETA结合的抗体与BNP的融合蛋白质给予动物模 型的方法。
下面通过具体实例,对本文的技术方案作进一步的说明。
本文中,若非特指,所采用的原料和设备等均可从市场购得或是本领域 常用的。下述实例中的方法,如无特别说明,均为本领域的常规方法。
1.抗体基因的克隆及亚克隆
收集分泌抗体的杂交瘤细胞,按照QIAGEN的mRNA抽提试剂盒操作 规程,提取杂交瘤细胞的mRNA。然后将提取后的mRNA反转录成cDNA, 逆转录引物为小鼠轻、重链恒定区的特异性引物,重链逆转录引物为(5’- TTTGGRGGGAAGATGAAGAC-3’)(SEQ ID NO:199),轻链逆转录引 物为(5’-TTAACACTCTCCCCTGTTGAA-3’)(SEQ ID NO:200)和(5’-TTAACACTCATTCCTGTTGAA-3’)(SEQ ID NO:201)。RT-PCR的反应 条件为:25℃5min(minutes);50℃60min;70℃15min。将反转录的 cDNA用0.1mM的TE稀释至500μL,加入到超滤离心管(Amicon Ultra- 0.5)中,2000g离心10min;弃滤液,再加500μL的0.1mM的TE,2000g离心10min;弃滤液,将制备管倒置到新的离心管中,2000g离心10min, 得到纯化后的cDNA;取10μL的纯化后的cDNA作为模板,加入4μL的 5xtailing buffer(Promega,市售),4μL的dATP(1mM)和10U的末端 转移酶(Promega,市售)后混匀,37℃孵育5min后65℃5min;然后以 加上PolyA尾的cDNA为模板,PCR扩增抗体的轻、重链可变区基因。上 游引物均为OligodT,重链下游引物为(5’- TGGACAGGGATCCAGAGTTCC-3’)(SEQ ID NO:202)和(5’-TGGACAGGGCTCCATAGTTCC-3’)(SEQ ID NO:203),轻链下游引物 为(5’-ACTCGTCCTTGGTCAACGTG-3’)(SEQ ID NO:204)。PCR反应 条件:95℃5min;95℃30s(seconds),56℃30s,72℃1min 40cycles; 72℃7min;PCR产物连接到PMD 18-T载体(Takara Bio,市售)后进行 测序。克隆的抗体的CDR序列见表一和表二。
基于已测序得到的抗体的DNA序列设计PCR引物,从而将完整轻链、 重链信号肽和可变域以及小鼠IgG1恒定区与表达载体pTM5相连。
2.抗体融合蛋白基因表达质粒的制备
人BNP(hBNP)基因序列与抗ETA抗体通过overlapping PCR的方法, 将hBNP基因融合于重链抗体C端。通过PCR引物将融合蛋白重链可变区 5’端带入Nhe1酶切位点,融合蛋白3’端带入Not1酶切位点,从而将完整 的重链与hBNP融合蛋白基因装入表达载体pTM5;同样,将轻链可变区5’ 端带入Nhe1酶切位点,3’端带入Bsiw1酶切位点,从而将完整的轻链可变 区序列与已装入轻链恒定区的表达载体pTM5相连。
3.抗体融合蛋白的瞬时表达
接种5×105/mL的悬浮HEK293或者CHO表达细胞系至转瓶中,经过 24h(hours)37℃,5%CO2旋转培养后,密度达到1×106/mL后被用于转 染。转染过程中使用polyethylenimine(PEI)作为转染介质,将其与的DNA (DNA用量为每1×106个细胞0.5μg,其中抗体轻链和重链的比重为3:2) 混合,PEI和DNA的质量混合优选配比为3:1。两者混合物在静置孵育15 分钟后被加入到细胞培养中。细胞在接受PEI与DNA混合物后继续37℃,5%CO2旋转培养24h后,向细胞培养液中加入0.5%的胰蛋白胨作为表达 需要的添加物,最后在表达完成后(96h以上)收集细胞上清用于抗体的纯 化分离。
4.抗体融合蛋白的纯化分离
收集的细胞上清经过高速(8000rpm,15min)离心去除细胞以及细胞 碎片后,再用0.45μm滤膜过滤澄清,澄清后的上清被用于纯化。纯化过程 由层析仪完成。上清首先流过蛋白G亲和层析柱,上清中包含的抗体在此 期间与蛋白G亲和层析柱的配基相结合后被滞留于柱内,然后低pH值(小 于等于3.0)的洗脱缓冲液灌洗层析柱解离与层析柱结合的抗体,收集到的 抗体洗脱液的低pH值用1M的Tris-HCl迅速中和以保护抗体不变性失活。 得到的抗体融合蛋白洗脱液经过16h的透析后置换成PBS缓冲体系。
5.钙流实验检测抗ETA抗体与BNP的融合蛋白在体外阻断ETA的生物学 活性
以每孔25000个接种共表达hETA-Aequorin的CHO-DHFR细胞至黑色 96孔细胞培养板,37℃培养过夜。第二天除去细胞上清,加入50μL底物 coelenterazine h(Promega,市售)避光孵育2h,再加入50μl杂交瘤细胞 上清或纯化后的抗体继续孵育30分钟。在Molecular Devices的SpectraMax L酶标仪上采用自动进样器灌注endothelin 1,在40s内检测瞬间钙流变化, 记录出峰时间和峰值。如图1所示,不同构建的ETA抗体与BNP的融合蛋白显示出不同的抑制细胞内人ETA介导的Ca2+变化的结果。
6.cGMP实验检测ETA抗体与BNP的融合蛋白在体外激活NPRA的生物 学活性
以每孔5.5×104接种表达人/鼠NPRA的HEK 293细胞至96孔细胞培 养板,置于37℃,5%CO2培养箱中过夜。第二天除去细胞上清,加入梯度 稀释的ETA抗体与BNP融合蛋白或突变体90μL/孔,置于37℃,5%CO2培养箱中孵育30min,再加10μL/孔的10%Triton X-100,室温裂解,用排 枪混合均匀。采用cGMP试剂盒(CisBio)检测实验中产生的cGMP。取上述10μL/孔细胞裂解液于白色384孔板中,加入5μL/孔1:20稀释的cGMP- d2,最后加5μL/孔1:20稀释的Anti-cGMP-Eu3-cryptate,室温孵育1h。在 Envision 2103酶标仪上读取时间分辨荧光665nm/620nm信号比值,然后 采用Prism5.0计算EC50值。表三显示了直接cGMP实验检测ETA抗体与 BNP的融合蛋白激活人/鼠NPRA信号通路的EC50,其中h15F3代表一人 源化ETA抗体包含SEQ ID NO:162和SEQ ID NO:190;其中BNP(如BNP,BNP(1-28),BNP(1-29NSF),BNP(3-28),BNP(3-29NSF),BNP (3-32),BNP(7-29),BNP(7-32),BNP(9-29),及BNP(9-32))的氨基端直接或通过一肽接头(Linker)(如G4S及(G4S)2)与h15F3抗体 重链的羧基端相连。
表三.cGMP实验检测ETA抗体与BNP的融合蛋白的生物学活性
7.单次尾静脉给药对正常C57小鼠降主动脉压的体内活性
动物根据体重随机进行分组,用鼠网将小鼠固定在鼠袋中,然后放于保 温筒内,将加压传感器置于尾根处,传感器标志的尖端与尾巴尖端的方向保 持一致,鼠尾插入传感器后,通过Softron智能无创血压计鼠仪(BP-2010) 检测小鼠血压。连续记录5次,取平均值,作为基础值;按照动物体重尾静 脉注射生理盐水或者药物,注射后15分钟开始测量血压,连续记录5次取 平均值。通过Softron智能无创血压计鼠仪检测h15F3-BNP(3-29)、h15F3- (G4S)2-BNP和h15F3-BNP(9-32)在静脉注射给药前后对正常C57BL/6小鼠 的动脉压的影响。h15F3-(G4S)2-BNP、h15F3-BNP(3-29)和h15F3-BNP(9-32) 这3个受试物均按照10mg/kg的剂量给药。如图2所示,结果显示h15F3- (G4S)2-BNP和h15F3-BNP(9-32)组在给药后15min能降低小鼠的血压。
8.连续多次尾静脉给药对野百合碱诱发SD大鼠肺动脉高压的体内活性
动物按照体重进行随机分组,造模大鼠颈背部皮下按照50mg/kg的剂 量一次性注射MCT溶液,正常对照组大鼠注射等体积的生理盐水,造模后 一天根据体重以10mg/kg的剂量给药开始尾静脉给药。给药结束后,大鼠 用25%乌拉坦(4mL/kg)腹腔注射麻醉,固定于操作台,用预先连接生理 记录仪的脐血管导管插入颈外静脉,经上腔静脉、右心房,进入右心室。动 物放置3~5min,待血压稳定后,记录心率、右心室收缩压和舒张压。如图 3所示,正常组、模型组、h15F3-(G4S)2-BNP低、高剂量组,各组的右心室 收缩压分别为38.46±2.56、55.20±8.59、47.95±2.52和45.79±7.36mmHg,与 模型组相比,统计学P值分别为0.000、0.038、和0.034,给药组相对模型 组的右心室收缩压抑制率分别为43.27%和56.19%。
9.单次静脉注射给药对健康恒河猴血压的体内活性
此次实验委托普莱美生物科技有限公司开展,研究分别按2mg/kg的剂 量单次静脉注射给予h15F3-(G4S)2-BNP、h15F3-BNP(3-29)和h15F3-BNP(9- 32)对健康恒河猴血压的影响。猴子按体重进行随机分组,麻醉前禁食14-16 h,使用10mg/kg盐酸氯胺酮肌肉注射麻醉动物,观察动物手臂的大小选取 正确袖带,将袖带绑于动物左上臂,进行血压检测。共检测4次,分别为给 药前2次,在给药前48-72h进行,麻醉后10min和麻醉后1h测定;给药 后10min和给药后1h测定;给药前后血压测量尽量保证在当天同一时间 段进行。其中,麻醉后开始每隔1min进行1次血压测量,当有3次结果 (不需要连续)的SBP/DBP/MBP差距均小于10mmHg时,检测结束。考 察动物给药后血压的抑制情况(△P=给药后平均血压-给药前平均血压)。 如图4和图5所示,实验结果显示,h15F3-(G4S)2-BNP和h15F3-BNP(9-32) 组在给药后10min均能降低猴子的血压,且h15F3-(G4S)2-BNP在给药后60 min还能降压。
10.ETA抗体与BNP的融合蛋白在健康食蟹猴上的药代动力学实验
给予雌雄各半共6只食蟹猴皮下单次人ETA抗体与BNP的融合蛋白 注射,剂量为2mg/kg,并在给药前0h,给药后立即(2min之内),给药 后0.5h、2h、8h、24h、2d(days)、3d、4d、7d各1次进行给药侧肢 静脉取全血0.6mL置于离心管中在冰上待其自然凝固后离心提取血清,超 低温保存(-80℃)至检测为止。血清样品中的人ETA抗体与BNP的融合 蛋白的BNP部分是用ELISA方法对其进行定量,并通过软件分析确定其在 食蟹猴体内的半衰期。
PK研究显示,上述二个BNP的融合蛋白质的BNP部分半衰期T1/2分 别为44.0和29.5小时左右。各组猴子的PK曲线及参数见图6和图7和表 四。
表四:ETA抗体与BNP融合蛋白质的药代动力学结果
以上所述的实施例只是本发明的一种较佳的方案,并非对本发明作任 何形式上的限制,在不超出权利要求所记载的技术方案的前提下还有其它 的变体及改型。
序列表
<110> 鸿运华宁(杭州)生物医药有限公司
<120> ETA抗体与BNP的融合蛋白质,及其药物组合物和应用
<130> 2019
<160> 236
<170> PatentIn version 3.5
<210> 1
<211> 1868
<212> DNA
<213> 智人
<400> 1
gaattcggga aaaagtgaag gtgtaaaagc agcacaagtg caataagaga tatttcctca 60
aatttgcctc aagatggaaa ccctttgcct cagggcatcc ttttggctgg cactggttgg 120
atgtgtaatc agtgataatc ctgagagata cagcacaaat ctaagcaatc atgtggatga 180
tttcaccact tttcgtggca cagagctcag cttcctggtt accactcatc aacccactaa 240
tttggtccta cccagcaatg gctcaatgca caactattgc ccacagcaga ctaaaattac 300
ttcagctttc aaatacatta acactgtgat atcttgtact attttcatcg tgggaatggt 360
ggggaatgca actctgctca ggatcattta ccagaacaaa tgtatgagga atggccccaa 420
cgcgctgata gccagtcttg cccttggaga ccttatctat gtggtcattg atctccctat 480
caatgtattt aagctgctgg ctgggcgctg gccttttgat cacaatgact ttggcgtatt 540
tctttgcaag ctgttcccct ttttgcagaa gtcctcggtg gggatcaccg tcctcaacct 600
ctgcgctctt agtgttgaca ggtacagagc agttgcctcc tggagtcgtg ttcagggaat 660
tgggattcct ttggtaactg ccattgaaat tgtctccatc tggatcctgt cctttatcct 720
ggccattcct gaagcgattg gcttcgtcat ggtacccttt gaatataggg gtgaacagca 780
taaaacctgt atgctcaatg ccacatcaaa attcatggag ttctaccaag atgtaaagga 840
ctggtggctc ttcgggttct atttctgtat gcccttggtg tgcactgcga tcttctacac 900
cctcatgact tgtgagatgt tgaacagaag gaatggcagc ttgagaattg ccctcagtga 960
acatcttaag cagcgtcgag aagtggcaaa aacagttttc tgcttggttg taatttttgc 1020
tctttgctgg ttccctcttc atttaagccg tatattgaag aaaactgtgt ataacgagat 1080
ggacaagaac cgatgtgaat tacttagttt cttactgctc atggattaca tcggtattaa 1140
cttggcaacc atgaattcat gtataaaccc catagctctg tattttgtga gcaagaaatt 1200
taaaaattgt ttccagtcat gcctctgctg ctgctgttac cagtccaaaa gtctgatgac 1260
ctcggtcccc atgaacggaa caagcatcca gtggaagaac cacgatcaaa acaaccacaa 1320
cacagaccgg agcagccata aggacagcat gaactgacca cccttagaag cactcctcgg 1380
tactcccata atcctctcgg agaaaaaaat cacaaggcaa ctgtgagtcc gggaatctct 1440
tctctgatcc ttcttcctta attcactccc acacccaaga agaaatgctt tccaaaaccg 1500
caagggtaga ctggtttatc cacccacaac atctacgaat cgtacttctt taattgatct 1560
aatttacata ttctgcgtgt tgtattcagc actaaaaaat ggtgggagct gggggagaat 1620
gaagactgtt aaatgaaacc agaaggatat ttactacttt tgcatgaaaa tagagctttc 1680
aagtacatgg ctagctttta tggcagttct ggtgaatgtt caatgggaac tggtcaccat 1740
gaaactttag agattaacga caagattttc tacttttttt aagtgatttt tttgtccttc 1800
agccaaacac aatatgggct caagtcactt ttatttgaaa tgtcatttgg tgccagtatc 1860
ccgaattc 1868
<210> 2
<211> 427
<212> PRT
<213> 智人
<400> 2
Met Glu Thr Leu Cys Leu Arg Ala Ser Phe Trp Leu Ala Leu Val Gly
1 5 10 15
Cys Val Ile Ser Asp Asn Pro Glu Arg Tyr Ser Thr Asn Leu Ser Asn
20 25 30
His Val Asp Asp Phe Thr Thr Phe Arg Gly Thr Glu Leu Ser Phe Leu
35 40 45
Val Thr Thr His Gln Pro Thr Asn Leu Val Leu Pro Ser Asn Gly Ser
50 55 60
Met His Asn Tyr Cys Pro Gln Gln Thr Lys Ile Thr Ser Ala Phe Lys
65 70 75 80
Tyr Ile Asn Thr Val Ile Ser Cys Thr Ile Phe Ile Val Gly Met Val
85 90 95
Gly Asn Ala Thr Leu Leu Arg Ile Ile Tyr Gln Asn Lys Cys Met Arg
100 105 110
Asn Gly Pro Asn Ala Leu Ile Ala Ser Leu Ala Leu Gly Asp Leu Ile
115 120 125
Tyr Val Val Ile Asp Leu Pro Ile Asn Val Phe Lys Leu Leu Ala Gly
130 135 140
Arg Trp Pro Phe Asp His Asn Asp Phe Gly Val Phe Leu Cys Lys Leu
145 150 155 160
Phe Pro Phe Leu Gln Lys Ser Ser Val Gly Ile Thr Val Leu Asn Leu
165 170 175
Cys Ala Leu Ser Val Asp Arg Tyr Arg Ala Val Ala Ser Trp Ser Arg
180 185 190
Val Gln Gly Ile Gly Ile Pro Leu Val Thr Ala Ile Glu Ile Val Ser
195 200 205
Ile Trp Ile Leu Ser Phe Ile Leu Ala Ile Pro Glu Ala Ile Gly Phe
210 215 220
Val Met Val Pro Phe Glu Tyr Arg Gly Glu Gln His Lys Thr Cys Met
225 230 235 240
Leu Asn Ala Thr Ser Lys Phe Met Glu Phe Tyr Gln Asp Val Lys Asp
245 250 255
Trp Trp Leu Phe Gly Phe Tyr Phe Cys Met Pro Leu Val Cys Thr Ala
260 265 270
Ile Phe Tyr Thr Leu Met Thr Cys Glu Met Leu Asn Arg Arg Asn Gly
275 280 285
Ser Leu Arg Ile Ala Leu Ser Glu His Leu Lys Gln Arg Arg Glu Val
290 295 300
Ala Lys Thr Val Phe Cys Leu Val Val Ile Phe Ala Leu Cys Trp Phe
305 310 315 320
Pro Leu His Leu Ser Arg Ile Leu Lys Lys Thr Val Tyr Asn Glu Met
325 330 335
Asp Lys Asn Arg Cys Glu Leu Leu Ser Phe Leu Leu Leu Met Asp Tyr
340 345 350
Ile Gly Ile Asn Leu Ala Thr Met Asn Ser Cys Ile Asn Pro Ile Ala
355 360 365
Leu Tyr Phe Val Ser Lys Lys Phe Lys Asn Cys Phe Gln Ser Cys Leu
370 375 380
Cys Cys Cys Cys Tyr Gln Ser Lys Ser Leu Met Thr Ser Val Pro Met
385 390 395 400
Asn Gly Thr Ser Ile Gln Trp Lys Asn His Asp Gln Asn Asn His Asn
405 410 415
Thr Asp Arg Ser Ser His Lys Asp Ser Met Asn
420 425
<210> 3
<211> 2493
<212> DNA
<213> 食蟹猴
<400> 3
cgggggtggc tgtgtcccag gatagctgga aggttaggac gctcttgcgg tcccagagtg 60
gagtggaagt tctggagctt tgggaggaga cggggaggac agactggagg cgtgttcctc 120
cggagttttc ttttccgtgc gagccctcgc gcgcgcgtac agtcatcccg ctggtctgac 180
gattgtggag aggaggtgga gaggcttcat ccatcccacc cggtcgtcgc ggggaattgg 240
ggtcccagcg agacctcccc cggagaagca gtgcccagga agttttctga agccggggta 300
gctgtgcagc cggagccgcc gccgcgccgg agcccgggac accggccacc ctccgcgcca 360
cccacccttg ccggctccgg cttcctctgg cccaggcgcc tcgcggaccc ggcagctgtc 420
tgcgcccgcc gagctccacg gtgaaaaaaa tagtgaaggt gtaaaagcag cacaagtgca 480
ataagagata tttcctcaaa tttgcctcaa gatggaaacc gtttgcctca gggcatcctt 540
ttggctggca ctggttggat gtgtaatcag tgataatgct gagagataca gcacaaatct 600
aagcaatcat gtggatgatt tcaccacttt tcatggcaca gagctcagcc tcctggttac 660
cactcatcaa cccactaact tggtcctacc cagcaatggc tcaatgcaca actattgccc 720
acagcagact aaaattactt cagcttttaa atacattaac actgtgatat cttgtactat 780
tttcatcgtg ggaatggtgg ggaatgcaac tctgctcagg atcatttacc agaacaaatg 840
tatgaggaat ggccccaacg cgctgatagc cagccttgcc cttggagacc ttatctatgt 900
ggtcattgat ctccctatca atgtatttaa gctgctggct gggcgctggc cttttgatca 960
caatgacttt ggcgtatttc tttgcaagct gttccccttt ttgcagaagt cctcagtggg 1020
gatcaccgtc ctcaacctct gcgctcttag tgttgacagg tacagagcag ttgcctcctg 1080
gagtcgtgtt cagggaattg ggattccttt ggtaactgcc attgaaattg tctccatctg 1140
gatcctgtcc ttcatcctgg ccattcctga agcgattggc ttcgtcatgg taccctttga 1200
atataggggt gaacagcata aaacctgtat gctcaatgct acgtcaaaat tcatggagtt 1260
ctaccaagat gtaaaggact ggtggctctt tgggttctat ttctgtatgc ccttggtgtg 1320
cactgcgatc ttctacaccc tcatgacttg tgagatgttg aacagaagga atggcagctt 1380
gagaattgcc ctcagtgaac atcttaagca gcgtcgagaa gtggcaaaaa cagttttctg 1440
cttggtcgta atttttgctc tgtgctggtt ccctcttcat ttaagccgta tattgaagaa 1500
aaccgtgtat aatgagatgg acaagaaccg atgtgaatta cttagtttct tgctgctcat 1560
ggattacatc ggtattaact tggcaaccat gaattcatgt ataaacccca tagctctgta 1620
ttttgtgagc aagaaattta aaaattgttt ccagtcatgc ctctgctgct gctgttacca 1680
gtccaaaagt ctgatgacct cggtccccat gaacggaaca agcatccagt ggaagaacca 1740
cgaacaaaac aaccacaaca cagaccggag cagccacaag gacagcatga actgaccacc 1800
ctgcgaagca ctcctgggta ctcccataat cctctgggag aaaaaaatca caaggcaact 1860
gtgactccgg aaatctcttc tctgatcctt cttccttaac tcactcccac acccaagaag 1920
aaatgctttc caaaaccgca agggtagacc ggtttagcca cccacgacat ctaccaatcg 1980
tacttcttta attaatctga tttacatatt ccgcgtgttg tattcagcac taaaaaatgg 2040
tgggagctgg gagagaatga agactgttca atgaaaccag aaggatattt actacttttg 2100
catgaaaata gagctttcaa gtacatgggt agcttttatg gcagttctgg tgaatgttca 2160
gtgggaactg gtcaccatga aactttagag attatgacaa gattttctac tttttttaac 2220
tgattttttg tccttcagcc aaacacaata tgggctcaag ttacttttat ttgaaatgtc 2280
atttggtgcc agtatttttt aactgcataa tagcctaaca tgactatttg aacttattta 2340
cacatagttt gcaaaaaaaa aaagacaaaa atagtattca ggtgagcaat taggttagta 2400
ttttctatgt cactgtttat ttttttaaaa cacaaattct aaagctacaa caaatactac 2460
aggcccttaa aacacagtct gatgatacat ttg 2493
<210> 4
<211> 427
<212> PRT
<213> 食蟹猴
<400> 4
Met Glu Thr Val Cys Leu Arg Ala Ser Phe Trp Leu Ala Leu Val Gly
1 5 10 15
Cys Val Ile Ser Asp Asn Ala Glu Arg Tyr Ser Thr Asn Leu Ser Asn
20 25 30
His Val Asp Asp Phe Thr Thr Phe His Gly Thr Glu Leu Ser Leu Leu
35 40 45
Val Thr Thr His Gln Pro Thr Asn Leu Val Leu Pro Ser Asn Gly Ser
50 55 60
Met His Asn Tyr Cys Pro Gln Gln Thr Lys Ile Thr Ser Ala Phe Lys
65 70 75 80
Tyr Ile Asn Thr Val Ile Ser Cys Thr Ile Phe Ile Val Gly Met Val
85 90 95
Gly Asn Ala Thr Leu Leu Arg Ile Ile Tyr Gln Asn Lys Cys Met Arg
100 105 110
Asn Gly Pro Asn Ala Leu Ile Ala Ser Leu Ala Leu Gly Asp Leu Ile
115 120 125
Tyr Val Val Ile Asp Leu Pro Ile Asn Val Phe Lys Leu Leu Ala Gly
130 135 140
Arg Trp Pro Phe Asp His Asn Asp Phe Gly Val Phe Leu Cys Lys Leu
145 150 155 160
Phe Pro Phe Leu Gln Lys Ser Ser Val Gly Ile Thr Val Leu Asn Leu
165 170 175
Cys Ala Leu Ser Val Asp Arg Tyr Arg Ala Val Ala Ser Trp Ser Arg
180 185 190
Val Gln Gly Ile Gly Ile Pro Leu Val Thr Ala Ile Glu Ile Val Ser
195 200 205
Ile Trp Ile Leu Ser Phe Ile Leu Ala Ile Pro Glu Ala Ile Gly Phe
210 215 220
Val Met Val Pro Phe Glu Tyr Arg Gly Glu Gln His Lys Thr Cys Met
225 230 235 240
Leu Asn Ala Thr Ser Lys Phe Met Glu Phe Tyr Gln Asp Val Lys Asp
245 250 255
Trp Trp Leu Phe Gly Phe Tyr Phe Cys Met Pro Leu Val Cys Thr Ala
260 265 270
Ile Phe Tyr Thr Leu Met Thr Cys Glu Met Leu Asn Arg Arg Asn Gly
275 280 285
Ser Leu Arg Ile Ala Leu Ser Glu His Leu Lys Gln Arg Arg Glu Val
290 295 300
Ala Lys Thr Val Phe Cys Leu Val Val Ile Phe Ala Leu Cys Trp Phe
305 310 315 320
Pro Leu His Leu Ser Arg Ile Leu Lys Lys Thr Val Tyr Asn Glu Met
325 330 335
Asp Lys Asn Arg Cys Glu Leu Leu Ser Phe Leu Leu Leu Met Asp Tyr
340 345 350
Ile Gly Ile Asn Leu Ala Thr Met Asn Ser Cys Ile Asn Pro Ile Ala
355 360 365
Leu Tyr Phe Val Ser Lys Lys Phe Lys Asn Cys Phe Gln Ser Cys Leu
370 375 380
Cys Cys Cys Cys Tyr Gln Ser Lys Ser Leu Met Thr Ser Val Pro Met
385 390 395 400
Asn Gly Thr Ser Ile Gln Trp Lys Asn His Glu Gln Asn Asn His Asn
405 410 415
Thr Asp Arg Ser Ser His Lys Asp Ser Met Asn
420 425
<210> 5
<211> 1436
<212> DNA
<213> 褐家鼠
<400> 5
gtgagaccaa cataacagga cgtttcttca gatccacatt aagatgggtg tcctttgctt 60
tctggcgtcc ttttggctgg ccctggtggg aggcgcaatc gctgacaatg ctgagagata 120
cagtgctaat ctaagcagcc acgtggagga cttcacccct tttccaggga cagagttcga 180
ctttctgggc accacccttc gaccccctaa tttggccctg cctagcaatg gctcaatgca 240
tggctattgc ccacagcaga caaaaatcac gacggctttc aaatatatca acactgtgat 300
atcctgtacc attttcatcg tgggaatggt ggggaacgcc actctcctaa gaatcattta 360
ccaaaacaag tgtatgagga acggccccaa tgcgctcata gccagcctgg cccttggaga 420
ccttatctac gtggtcattg atctccccat caatgtgttt aagctgttgg cggggcgctg 480
gccttttgac cacaatgatt ttggagtgtt tctctgcaag ctgttcccct ttttgcagaa 540
gtcgtccgtg ggcatcactg tcctgaatct ctgcgctctc agtgtggaca ggtacagagc 600
agtggcttcc tggagccggg ttcaaggaat cgggatcccc ttgattaccg ccattgaaat 660
tgtctccatc tggatccttt cctttatctt ggccatccca gaagcaatcg gcttcgtcat 720
ggtacccttc gaatacaagg gcgagcagca caggacctgc atgctcaacg ccacgaccaa 780
gttcatggag ttttaccaag acgtgaagga ctggtggctc tttggattct acttctgcat 840
gcccttggtg tgcacagcaa tcttctatac cctcatgacc tgtgagatgc tcaacagaag 900
gaatgggagc ttgcggattg ccctcagcga acacctcaag cagcgtcgag aggtggcaaa 960
gaccgtcttc tgcttggttg tcatcttcgc cctgtgctgg ttccctcttc acttaagccg 1020
aattttgaag aaaaccgtct atgatgagat ggataagaac cggtgtgaac tgctcagctt 1080
cttgctgctc atggattaca ttggcattaa cctggcaacc atgaactctt gcataaaccc 1140
aatagctctg tattttgtga gcaagaaatt caaaaattgt tttcagtcat gcctctgttg 1200
ctgttgtcac cagtccaaaa gcctcatgac ctcggtcccc atgaatggaa cgagtatcca 1260
gtggaagaac caggagcaga accacaacac agaacggagc agccacaagg acagcatgaa 1320
ctaaccctgt gcagaagcac cgagcagtgt gccttcgagt cccaggatga aacggtcacg 1380
cagcagctgc gctcccaaaa cctcccaggt ctctcccctg ctttttgtct aagctt 1436
<210> 6
<211> 426
<212> PRT
<213> 褐家鼠
<400> 6
Met Gly Val Leu Cys Phe Leu Ala Ser Phe Trp Leu Ala Leu Val Gly
1 5 10 15
Gly Ala Ile Ala Asp Asn Ala Glu Arg Tyr Ser Ala Asn Leu Ser Ser
20 25 30
His Val Glu Asp Phe Thr Pro Phe Pro Gly Thr Glu Phe Asp Phe Leu
35 40 45
Gly Thr Thr Leu Arg Pro Pro Asn Leu Ala Leu Pro Ser Asn Gly Ser
50 55 60
Met His Gly Tyr Cys Pro Gln Gln Thr Lys Ile Thr Thr Ala Phe Lys
65 70 75 80
Tyr Ile Asn Thr Val Ile Ser Cys Thr Ile Phe Ile Val Gly Met Val
85 90 95
Gly Asn Ala Thr Leu Leu Arg Ile Ile Tyr Gln Asn Lys Cys Met Arg
100 105 110
Asn Gly Pro Asn Ala Leu Ile Ala Ser Leu Ala Leu Gly Asp Leu Ile
115 120 125
Tyr Val Val Ile Asp Leu Pro Ile Asn Val Phe Lys Leu Leu Ala Gly
130 135 140
Arg Trp Pro Phe Asp His Asn Asp Phe Gly Val Phe Leu Cys Lys Leu
145 150 155 160
Phe Pro Phe Leu Gln Lys Ser Ser Val Gly Ile Thr Val Leu Asn Leu
165 170 175
Cys Ala Leu Ser Val Asp Arg Tyr Arg Ala Val Ala Ser Trp Ser Arg
180 185 190
Val Gln Gly Ile Gly Ile Pro Leu Ile Thr Ala Ile Glu Ile Val Ser
195 200 205
Ile Trp Ile Leu Ser Phe Ile Leu Ala Ile Pro Glu Ala Ile Gly Phe
210 215 220
Val Met Val Pro Phe Glu Tyr Lys Gly Glu Gln His Arg Thr Cys Met
225 230 235 240
Leu Asn Ala Thr Thr Lys Phe Met Glu Phe Tyr Gln Asp Val Lys Asp
245 250 255
Trp Trp Leu Phe Gly Phe Tyr Phe Cys Met Pro Leu Val Cys Thr Ala
260 265 270
Ile Phe Tyr Thr Leu Met Thr Cys Glu Met Leu Asn Arg Arg Asn Gly
275 280 285
Ser Leu Arg Ile Ala Leu Ser Glu His Leu Lys Gln Arg Arg Glu Val
290 295 300
Ala Lys Thr Val Phe Cys Leu Val Val Ile Phe Ala Leu Cys Trp Phe
305 310 315 320
Pro Leu His Leu Ser Arg Ile Leu Lys Lys Thr Val Tyr Asp Glu Met
325 330 335
Asp Lys Asn Arg Cys Glu Leu Leu Ser Phe Leu Leu Leu Met Asp Tyr
340 345 350
Ile Gly Ile Asn Leu Ala Thr Met Asn Ser Cys Ile Asn Pro Ile Ala
355 360 365
Leu Tyr Phe Val Ser Lys Lys Phe Lys Asn Cys Phe Gln Ser Cys Leu
370 375 380
Cys Cys Cys Cys His Gln Ser Lys Ser Leu Met Thr Ser Val Pro Met
385 390 395 400
Asn Gly Thr Ser Ile Gln Trp Lys Asn Gln Glu Gln Asn His Asn Thr
405 410 415
Glu Arg Ser Ser His Lys Asp Ser Met Asn
420 425
<210> 7
<211> 33
<212> DNA
<213> 小家鼠
<400> 7
agggccagtc agaacattgg cacaagcata cac 33
<210> 8
<211> 11
<212> PRT
<213> 小家鼠
<400> 8
Arg Ala Ser Gln Asn Ile Gly Thr Ser Ile His
1 5 10
<210> 9
<211> 33
<212> DNA
<213> 小家鼠
<400> 9
cgagcaagtg aaaatattta cagttattta gca 33
<210> 10
<211> 11
<212> PRT
<213> 小家鼠
<400> 10
Arg Ala Ser Glu Asn Ile Tyr Ser Tyr Leu Ala
1 5 10
<210> 11
<211> 39
<212> DNA
<213> 小家鼠
<400> 11
cagagcctct ttgatattga tggaaagaca tatttgaat 39
<210> 12
<211> 13
<212> PRT
<213> 小家鼠
<400> 12
Gln Ser Leu Phe Asp Ile Asp Gly Lys Thr Tyr Leu Asn
1 5 10
<210> 13
<211> 33
<212> DNA
<213> 小家鼠
<400> 13
cgggcaagtc aggacattgg tggtagctta aac 33
<210> 14
<211> 11
<212> PRT
<213> 小家鼠
<400> 14
Arg Ala Ser Gln Asp Ile Gly Gly Ser Leu Asn
1 5 10
<210> 15
<211> 33
<212> DNA
<213> 小家鼠
<400> 15
agggccagcc agactattag cgacttctta cac 33
<210> 16
<211> 11
<212> PRT
<213> 小家鼠
<400> 16
Arg Ala Ser Gln Thr Ile Ser Asp Phe Leu His
1 5 10
<210> 17
<211> 33
<212> DNA
<213> 小家鼠
<400> 17
agggcaagtg aggacataca cactcaatta gcc 33
<210> 18
<211> 11
<212> PRT
<213> 小家鼠
<400> 18
Arg Ala Ser Glu Asp Ile His Thr Gln Leu Ala
1 5 10
<210> 19
<211> 48
<212> DNA
<213> 小家鼠
<400> 19
agatctagtc agtacattgt tcatagtact ggaaccacct atttagaa 48
<210> 20
<211> 16
<212> PRT
<213> 小家鼠
<400> 20
Arg Ser Ser Gln Tyr Ile Val His Ser Thr Gly Thr Thr Tyr Leu Glu
1 5 10 15
<210> 21
<211> 48
<212> DNA
<213> 小家鼠
<400> 21
agatctagtc attaccttgt tcatgataac ggaaacacct atgttgaa 48
<210> 22
<211> 16
<212> PRT
<213> 小家鼠
<400> 22
Arg Ser Ser His Tyr Leu Val His Asp Asn Gly Asn Thr Tyr Val Glu
1 5 10 15
<210> 23
<211> 48
<212> DNA
<213> 小家鼠
<400> 23
agatctagtc agaacattgt ccatagtact ggaaacacct atttagaa 48
<210> 24
<211> 16
<212> PRT
<213> 小家鼠
<400> 24
Arg Ser Ser Gln Asn Ile Val His Ser Thr Gly Asn Thr Tyr Leu Glu
1 5 10 15
<210> 25
<211> 30
<212> DNA
<213> 小家鼠
<400> 25
agtgtcagct caagtgtaag ttacatacac 30
<210> 26
<211> 10
<212> PRT
<213> 小家鼠
<400> 26
Ser Val Ser Ser Ser Val Ser Tyr Ile His
1 5 10
<210> 27
<211> 30
<212> DNA
<213> 小家鼠
<400> 27
agtgccagct caagtgtaag ttacatgtgc 30
<210> 28
<211> 10
<212> PRT
<213> 小家鼠
<400> 28
Ser Ala Ser Ser Ser Val Ser Tyr Met Cys
1 5 10
<210> 29
<211> 18
<212> DNA
<213> 小家鼠
<400> 29
cagggcatta acaattat 18
<210> 30
<211> 6
<212> PRT
<213> 小家鼠
<400> 30
Gln Gly Ile Asn Asn Tyr
1 5
<210> 31
<211> 21
<212> DNA
<213> 小家鼠
<400> 31
tatgcttcta agtctatatc t 21
<210> 32
<211> 7
<212> PRT
<213> 小家鼠
<400> 32
Tyr Ala Ser Lys Ser Ile Ser
1 5
<210> 33
<211> 21
<212> DNA
<213> 小家鼠
<400> 33
aatgcaaaaa ccttagcaga a 21
<210> 34
<211> 7
<212> PRT
<213> 小家鼠
<400> 34
Asn Ala Lys Thr Leu Ala Glu
1 5
<210> 35
<211> 21
<212> DNA
<213> 小家鼠
<400> 35
ctggtgtctg aattggactc t 21
<210> 36
<211> 7
<212> PRT
<213> 小家鼠
<400> 36
Leu Val Ser Glu Leu Asp Ser
1 5
<210> 37
<211> 21
<212> DNA
<213> 小家鼠
<400> 37
gccacatcca gcttagattc t 21
<210> 38
<211> 7
<212> PRT
<213> 小家鼠
<400> 38
Ala Thr Ser Ser Leu Asp Ser
1 5
<210> 39
<211> 21
<212> DNA
<213> 小家鼠
<400> 39
tatgcttccc aatccatctc t 21
<210> 40
<211> 7
<212> PRT
<213> 小家鼠
<400> 40
Tyr Ala Ser Gln Ser Ile Ser
1 5
<210> 41
<211> 21
<212> DNA
<213> 小家鼠
<400> 41
ggtgcagcca gtttgaaaag t 21
<210> 42
<211> 7
<212> PRT
<213> 小家鼠
<400> 42
Gly Ala Ala Ser Leu Lys Ser
1 5
<210> 43
<211> 21
<212> DNA
<213> 小家鼠
<400> 43
aaagtttcca accgattttc t 21
<210> 44
<211> 7
<212> PRT
<213> 小家鼠
<400> 44
Lys Val Ser Asn Arg Phe Ser
1 5
<210> 45
<211> 21
<212> DNA
<213> 小家鼠
<400> 45
gacacatcca aactggcttc t 21
<210> 46
<211> 7
<212> PRT
<213> 小家鼠
<400> 46
Asp Thr Ser Lys Leu Ala Ser
1 5
<210> 47
<211> 21
<212> DNA
<213> 小家鼠
<400> 47
tatacatcaa ctttacagtc a 21
<210> 48
<211> 7
<212> PRT
<213> 小家鼠
<400> 48
Tyr Thr Ser Thr Leu Gln Ser
1 5
<210> 49
<211> 27
<212> DNA
<213> 小家鼠
<400> 49
caacatagtt atagcttccc gtggacg 27
<210> 50
<211> 9
<212> PRT
<213> 小家鼠
<400> 50
Gln His Ser Tyr Ser Phe Pro Trp Thr
1 5
<210> 51
<211> 27
<212> DNA
<213> 小家鼠
<400> 51
cagcatcatt atggtattcc gttcacg 27
<210> 52
<211> 9
<212> PRT
<213> 小家鼠
<400> 52
Gln His His Tyr Gly Ile Pro Phe Thr
1 5
<210> 53
<211> 27
<212> DNA
<213> 小家鼠
<400> 53
tggcaaggta cacattttcc gctcacg 27
<210> 54
<211> 9
<212> PRT
<213> 小家鼠
<400> 54
Trp Gln Gly Thr His Phe Pro Leu Thr
1 5
<210> 55
<211> 27
<212> DNA
<213> 小家鼠
<400> 55
ctacaatatg ctagttctcc gtatacg 27
<210> 56
<211> 9
<212> PRT
<213> 小家鼠
<400> 56
Leu Gln Tyr Ala Ser Ser Pro Tyr Thr
1 5
<210> 57
<211> 27
<212> DNA
<213> 小家鼠
<400> 57
caaagtggta acacctttcc gtggacg 27
<210> 58
<211> 9
<212> PRT
<213> 小家鼠
<400> 58
Gln Ser Gly Asn Thr Phe Pro Trp Thr
1 5
<210> 59
<211> 27
<212> DNA
<213> 小家鼠
<400> 59
caacagtata ggagtattcc gtggacg 27
<210> 60
<211> 9
<212> PRT
<213> 小家鼠
<400> 60
Gln Gln Tyr Arg Ser Ile Pro Trp Thr
1 5
<210> 61
<211> 27
<212> DNA
<213> 小家鼠
<400> 61
tttcaaggtt cacattttcc attcacg 27
<210> 62
<211> 9
<212> PRT
<213> 小家鼠
<400> 62
Phe Gln Gly Ser His Phe Pro Phe Thr
1 5
<210> 63
<211> 27
<212> DNA
<213> 小家鼠
<400> 63
tttcaaggtt cacatttccc attcacg 27
<210> 64
<211> 9
<212> PRT
<213> 小家鼠
<400> 64
His Gln Trp Ser Thr Asn Pro Pro Thr
1 5
<210> 65
<211> 27
<212> DNA
<213> 小家鼠
<400> 65
cagcagtgga gtagtaaccc acccacg 27
<210> 66
<211> 9
<212> PRT
<213> 小家鼠
<400> 66
Gln Gln Trp Ser Ser Asn Pro Pro Thr
1 5
<210> 67
<211> 24
<212> DNA
<213> 小家鼠
<400> 67
cagcagttta gtaaacttcg gaca 24
<210> 68
<211> 8
<212> PRT
<213> 小家鼠
<400> 68
Gln Gln Phe Ser Lys Leu Arg Thr
1 5
<210> 69
<211> 36
<212> DNA
<213> 小家鼠
<400> 69
gggttctcac tgaccacttc tggcttgggt gttgcc 36
<210> 70
<211> 12
<212> PRT
<213> 小家鼠
<400> 70
Gly Phe Ser Leu Thr Thr Ser Gly Leu Gly Val Ala
1 5 10
<210> 71
<211> 30
<212> DNA
<213> 小家鼠
<400> 71
ggctacacct ttactagcta ctggatacac 30
<210> 72
<211> 10
<212> PRT
<213> 小家鼠
<400> 72
Gly Tyr Thr Phe Thr Ser Tyr Trp Ile His
1 5 10
<210> 73
<211> 30
<212> DNA
<213> 小家鼠
<400> 73
ggcctcaaca ttaaagacat ctatattcac 30
<210> 74
<211> 10
<212> PRT
<213> 小家鼠
<400> 74
Gly Leu Asn Ile Lys Asp Ile Tyr Ile His
1 5 10
<210> 75
<211> 30
<212> DNA
<213> 小家鼠
<400> 75
ggttactcat tcaccaacta ctggatacac 30
<210> 76
<211> 10
<212> PRT
<213> 小家鼠
<400> 76
Gly Tyr Ser Phe Thr Asn Tyr Trp Ile His
1 5 10
<210> 77
<211> 30
<212> DNA
<213> 小家鼠
<400> 77
ggattcactt tcagtgacta tcccatgtct 30
<210> 78
<211> 10
<212> PRT
<213> 小家鼠
<400> 78
Gly Phe Thr Phe Ser Asp Tyr Pro Met Ser
1 5 10
<210> 79
<211> 30
<212> DNA
<213> 小家鼠
<400> 79
ggattcactt tcagtagctt tggcatgtct 30
<210> 80
<211> 10
<212> PRT
<213> 小家鼠
<400> 80
Gly Phe Thr Phe Ser Ser Phe Gly Met Ser
1 5 10
<210> 81
<211> 30
<212> DNA
<213> 小家鼠
<400> 81
ggattcactt tcagtaccta tggcatgtct 30
<210> 82
<211> 10
<212> PRT
<213> 小家鼠
<400> 82
Gly Phe Thr Phe Ser Thr Tyr Gly Met Ser
1 5 10
<210> 83
<211> 30
<212> DNA
<213> 小家鼠
<400> 83
ggattcactt tcagtagtta tggcatgtct 30
<210> 84
<211> 10
<212> PRT
<213> 小家鼠
<400> 84
Gly Phe Thr Phe Ser Ser Tyr Gly Met Ser
1 5 10
<210> 85
<211> 36
<212> DNA
<213> 小家鼠
<400> 85
gggttttcac tgaccacttc tggtatgggt gtaggc 36
<210> 86
<211> 12
<212> PRT
<213> 小家鼠
<400> 86
Gly Phe Ser Leu Thr Thr Ser Gly Met Gly Val Gly
1 5 10
<210> 87
<211> 36
<212> DNA
<213> 小家鼠
<400> 87
ggattttcac tgagcacttc tggtttgggt gtaggc 36
<210> 88
<211> 12
<212> PRT
<213> 小家鼠
<400> 88
Gly Phe Ser Leu Ser Thr Ser Gly Leu Gly Val Gly
1 5 10
<210> 89
<211> 24
<212> DNA
<213> 小家鼠
<400> 89
ggattcacct tcagtgatta ttac 24
<210> 90
<211> 8
<212> PRT
<213> 小家鼠
<400> 90
Gly Phe Thr Phe Ser Asp Tyr Tyr
1 5
<210> 91
<211> 48
<212> DNA
<213> 小家鼠
<400> 91
cacatttggt cggatggtga cacgcgctat tacccagccc tgaagaac 48
<210> 92
<211> 16
<212> PRT
<213> 小家鼠
<400> 92
His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala Leu Lys Asn
1 5 10 15
<210> 93
<211> 36
<212> DNA
<213> 小家鼠
<400> 93
tacattaatc ctgacactga ttatagtgag tacaat 36
<210> 94
<211> 12
<212> PRT
<213> 小家鼠
<400> 94
Tyr Ile Asn Pro Asp Thr Asp Tyr Ser Glu Tyr Asn
1 5 10
<210> 95
<211> 36
<212> DNA
<213> 小家鼠
<400> 95
aggattgatc ctgcgaacgg taagactgca tatgac 36
<210> 96
<211> 12
<212> PRT
<213> 小家鼠
<400> 96
Arg Ile Asp Pro Ala Asn Gly Lys Thr Ala Tyr Asp
1 5 10
<210> 97
<211> 36
<212> DNA
<213> 小家鼠
<400> 97
atgattgatc cttccgatgc tgaaactggg ttaaat 36
<210> 98
<211> 12
<212> PRT
<213> 小家鼠
<400> 98
Met Ile Asp Pro Ser Asp Ala Glu Thr Gly Leu Asn
1 5 10
<210> 99
<211> 24
<212> DNA
<213> 小家鼠
<400> 99
gttagtgatg gtggtggttc cacc 24
<210> 100
<211> 8
<212> PRT
<213> 小家鼠
<400> 100
Val Ser Asp Gly Gly Gly Ser Thr
1 5
<210> 101
<211> 24
<212> DNA
<213> 小家鼠
<400> 101
attagtagtg ctggtagttt cacc 24
<210> 102
<211> 8
<212> PRT
<213> 小家鼠
<400> 102
Ile Ser Ser Ala Gly Ser Phe Thr
1 5
<210> 103
<211> 51
<212> DNA
<213> 小家鼠
<400> 103
accattaata ctaatggtgg taccacctat tatcgagaca gtgtgaaggg c 51
<210> 104
<211> 17
<212> PRT
<213> 小家鼠
<400> 104
Thr Ile Asn Thr Asn Gly Gly Thr Thr Tyr Tyr Arg Asp Ser Val Lys
1 5 10 15
Gly
<210> 105
<211> 51
<212> DNA
<213> 小家鼠
<400> 105
accataaata ctaatggtgg taacacctat tattcagaca atgtgaaggg c 51
<210> 106
<211> 17
<212> PRT
<213> 小家鼠
<400> 106
Thr Ile Asn Thr Asn Gly Gly Asn Thr Tyr Tyr Ser Asp Asn Val Lys
1 5 10 15
Gly
<210> 107
<211> 51
<212> DNA
<213> 小家鼠
<400> 107
accattagta ctaatggtgc caccgccaat tatccagaca gtgtgaaggg c 51
<210> 108
<211> 17
<212> PRT
<213> 小家鼠
<400> 108
Thr Ile Ser Thr Asn Gly Ala Thr Ala Asn Tyr Pro Asp Ser Val Lys
1 5 10 15
Gly
<210> 109
<211> 48
<212> DNA
<213> 小家鼠
<400> 109
cacatttggt gggatgatga taagtactat aatccatccc tgaagagc 48
<210> 110
<211> 16
<212> PRT
<213> 小家鼠
<400> 110
His Ile Trp Trp Asp Asp Asp Lys Tyr Tyr Asn Pro Ser Leu Lys Ser
1 5 10 15
<210> 111
<211> 48
<212> DNA
<213> 小家鼠
<400> 111
cacatttggt gggatgatga taagtactat aatccatccc ttaagaga 48
<210> 112
<211> 16
<212> PRT
<213> 小家鼠
<400> 112
His Ile Trp Trp Asp Asp Asp Lys Tyr Tyr Asn Pro Ser Leu Lys Arg
1 5 10 15
<210> 113
<211> 30
<212> DNA
<213> 小家鼠
<400> 113
attagaaatc gggctaatgg ttacacaaca 30
<210> 114
<211> 10
<212> PRT
<213> 小家鼠
<400> 114
Ile Arg Asn Arg Ala Asn Gly Tyr Thr Thr
1 5 10
<210> 115
<211> 30
<212> DNA
<213> 小家鼠
<400> 115
atgaaggatg atagtcttta ctttgacaac 30
<210> 116
<211> 10
<212> PRT
<213> 小家鼠
<400> 116
Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn
1 5 10
<210> 117
<211> 30
<212> DNA
<213> 小家鼠
<400> 117
gcaagtgctg gttattattt ttttgacttc 30
<210> 118
<211> 10
<212> PRT
<213> 小家鼠
<400> 118
Ala Ser Ala Gly Tyr Tyr Phe Phe Asp Phe
1 5 10
<210> 119
<211> 15
<212> DNA
<213> 小家鼠
<400> 119
ggtagggggg cccac 15
<210> 120
<211> 5
<212> PRT
<213> 小家鼠
<400> 120
Gly Arg Gly Ala His
1 5
<210> 121
<211> 33
<212> DNA
<213> 小家鼠
<400> 121
gcaagaattg gcgattacta taatatggac tac 33
<210> 122
<211> 11
<212> PRT
<213> 小家鼠
<400> 122
Ala Arg Ile Gly Asp Tyr Tyr Asn Met Asp Tyr
1 5 10
<210> 123
<211> 45
<212> DNA
<213> 小家鼠
<400> 123
acaagacatg cttcctacta tagctacgac cattctatgg actac 45
<210> 124
<211> 15
<212> PRT
<213> 小家鼠
<400> 124
Thr Arg His Ala Ser Tyr Tyr Ser Tyr Asp His Ser Met Asp Tyr
1 5 10 15
<210> 125
<211> 36
<212> DNA
<213> 小家鼠
<400> 125
gcaagacggg ggtacgacgt tgggtgcttt gaccac 36
<210> 126
<211> 12
<212> PRT
<213> 小家鼠
<400> 126
Ala Arg Arg Gly Tyr Asp Val Gly Cys Phe Asp His
1 5 10
<210> 127
<211> 27
<212> DNA
<213> 小家鼠
<400> 127
gcaagagact acggggctat ggactac 27
<210> 128
<211> 9
<212> PRT
<213> 小家鼠
<400> 128
Ala Arg Asp Tyr Gly Ala Met Asp Tyr
1 5
<210> 129
<211> 27
<212> DNA
<213> 小家鼠
<400> 129
gcaactgaaa agggagctat gggctac 27
<210> 130
<211> 9
<212> PRT
<213> 小家鼠
<400> 130
Ala Thr Glu Lys Gly Ala Met Gly Tyr
1 5
<210> 131
<211> 57
<212> DNA
<213> 小家鼠
<400> 131
gctcgaagaa ctgagactat gattacgaca gtgctatatt actatgctat ggactac 57
<210> 132
<211> 19
<212> PRT
<213> 小家鼠
<400> 132
Ala Arg Arg Thr Glu Thr Met Ile Thr Thr Val Leu Tyr Tyr Tyr Ala
1 5 10 15
Met Asp Tyr
<210> 133
<211> 54
<212> DNA
<213> 小家鼠
<400> 133
gctcgaagga gggaagttaa cttcggtatt aactattact attctatgga ctac 54
<210> 134
<211> 18
<212> PRT
<213> 小家鼠
<400> 134
Ala Arg Arg Arg Glu Val Asn Phe Gly Ile Asn Tyr Tyr Tyr Ser Met
1 5 10 15
Asp Tyr
<210> 135
<211> 36
<212> DNA
<213> 小家鼠
<400> 135
gtaagagatt cctatcacta cgggtacttc gatgtc 36
<210> 136
<211> 12
<212> PRT
<213> 小家鼠
<400> 136
Val Arg Asp Ser Tyr His Tyr Gly Tyr Phe Asp Val
1 5 10
<210> 137
<211> 324
<212> DNA
<213> 小家鼠
<400> 137
gacatcttgc tgactcagtc tccagccatc ctgtctgtga gtccaggaaa aagagtcagt 60
ttctcctgca gggccagtca gaacattggc acaagcatac actggtatca gcaaagaaca 120
aatggttctc caaggcttct cataaagtat gcttctaagt ctatatctgg gatttcttcc 180
aggtttagtg gcagtggctc agggacagat tttactctta gtatcaacag tgtggagtct 240
gaagatattg cagcttatta ctgtcaacat agttatagct tcccgtggac gttcggtgga 300
ggcaccaagc tggaaatcaa acgg 324
<210> 138
<211> 108
<212> PRT
<213> 小家鼠
<400> 138
Asp Ile Leu Leu Thr Gln Ser Pro Ala Ile Leu Ser Val Ser Pro Gly
1 5 10 15
Lys Arg Val Ser Phe Ser Cys Arg Ala Ser Gln Asn Ile Gly Thr Ser
20 25 30
Ile His Trp Tyr Gln Gln Arg Thr Asn Gly Ser Pro Arg Leu Leu Ile
35 40 45
Lys Tyr Ala Ser Lys Ser Ile Ser Gly Ile Ser Ser Arg Phe Ser Gly
50 55 60
Ser Gly Ser Gly Thr Asp Phe Thr Leu Ser Ile Asn Ser Val Glu Ser
65 70 75 80
Glu Asp Ile Ala Ala Tyr Tyr Cys Gln His Ser Tyr Ser Phe Pro Trp
85 90 95
Thr Phe Gly Gly Gly Thr Lys Leu Glu Ile Lys Arg
100 105
<210> 139
<211> 324
<212> DNA
<213> 小家鼠
<400> 139
gacatccaga tgactcagtc tccagcctcc ctatctacat ctgtgggaga aactgtcacc 60
atcacatgtc gagcaagtga aaatatttac agttatttag catggtatca gcagagacag 120
ggaaaatctc ctcacctcct ggtcaataat gcaaaaacct tagcagaagg tgtgccatca 180
aggttcagtg gcagtggatc aggcacacat ttttctctga ggatcagcgg cctgcagcct 240
gaagattttg ggagttatta ctgtcagcat cattatggta ttccgttcac gttcggaggg 300
gggaccaagt tgtcaataaa acgg 324
<210> 140
<211> 108
<212> PRT
<213> 小家鼠
<400> 140
Asp Ile Gln Met Thr Gln Ser Pro Ala Ser Leu Ser Thr Ser Val Gly
1 5 10 15
Glu Thr Val Thr Ile Thr Cys Arg Ala Ser Glu Asn Ile Tyr Ser Tyr
20 25 30
Leu Ala Trp Tyr Gln Gln Arg Gln Gly Lys Ser Pro His Leu Leu Val
35 40 45
Asn Asn Ala Lys Thr Leu Ala Glu Gly Val Pro Ser Arg Phe Ser Gly
50 55 60
Ser Gly Ser Gly Thr His Phe Ser Leu Arg Ile Ser Gly Leu Gln Pro
65 70 75 80
Glu Asp Phe Gly Ser Tyr Tyr Cys Gln His His Tyr Gly Ile Pro Phe
85 90 95
Thr Phe Gly Gly Gly Thr Lys Leu Ser Ile Lys Arg
100 105
<210> 141
<211> 339
<212> DNA
<213> 小家鼠
<400> 141
gatgttgtga tgacccagat tccactcact ttgtcggtta ccattggaca accagcctcc 60
atctcttgca agtcaagtca gagcctcttt gatattgatg gaaagacata tttgaattgg 120
ttgttacaga ggccaggcca gtctccaaag cgcctaatct atctggtgtc tgaattggac 180
tctggagtcc ctgacaggtt cactggcagt ggatcaggga cagatttcac actgaaaatc 240
agcagagtgg aggctgagga tttgggagtt tactattgtt ggcaaggtac acattttccg 300
ctcacgttcg gtgctgggac caagctggag ctgaaacgg 339
<210> 142
<211> 113
<212> PRT
<213> 小家鼠
<400> 142
Asp Val Val Met Thr Gln Ile Pro Leu Thr Leu Ser Val Thr Ile Gly
1 5 10 15
Gln Pro Ala Ser Ile Ser Cys Lys Ser Ser Gln Ser Leu Phe Asp Ile
20 25 30
Asp Gly Lys Thr Tyr Leu Asn Trp Leu Leu Gln Arg Pro Gly Gln Ser
35 40 45
Pro Lys Arg Leu Ile Tyr Leu Val Ser Glu Leu Asp Ser Gly Val Pro
50 55 60
Asp Arg Phe Thr Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Lys Ile
65 70 75 80
Ser Arg Val Glu Ala Glu Asp Leu Gly Val Tyr Tyr Cys Trp Gln Gly
85 90 95
Thr His Phe Pro Leu Thr Phe Gly Ala Gly Thr Lys Leu Glu Leu Lys
100 105 110
Arg
<210> 143
<211> 324
<212> DNA
<213> 小家鼠
<400> 143
gacatccaga tgacccagtc tccatcctcc ttatctgcct ctctgggaga aagagtcagt 60
ctcacttgtc gggcaagtca ggacattggt ggtagcttaa actggcttca gcagaaacca 120
gatggaacta ttaaacgcct gatctacgcc acatccagct tagattctgg tgtccccaaa 180
aggttcagtg gcagtaggtc tgggtcagtt ttttctctca ccatcaccag ccttgagtct 240
gaagattttg tagactattt ctgtctacaa tatgctagtt ctccgtatac gttcggaggg 300
gggaccaagc tggaaataaa acgg 324
<210> 144
<211> 108
<212> PRT
<213> 小家鼠
<400> 144
Asp Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Leu Gly
1 5 10 15
Glu Arg Val Ser Leu Thr Cys Arg Ala Ser Gln Asp Ile Gly Gly Ser
20 25 30
Leu Asn Trp Leu Gln Gln Lys Pro Asp Gly Thr Ile Lys Arg Leu Ile
35 40 45
Tyr Ala Thr Ser Ser Leu Asp Ser Gly Val Pro Lys Arg Phe Ser Gly
50 55 60
Ser Arg Ser Gly Ser Val Phe Ser Leu Thr Ile Thr Ser Leu Glu Ser
65 70 75 80
Glu Asp Phe Val Asp Tyr Phe Cys Leu Gln Tyr Ala Ser Ser Pro Tyr
85 90 95
Thr Phe Gly Gly Gly Thr Lys Leu Glu Ile Lys Arg
100 105
<210> 145
<211> 324
<212> DNA
<213> 小家鼠
<400> 145
gacattgtga tgactcagtc tccagccacc ctgtctgtga ctccaggaga tagagtctct 60
ctttcctgca gggccagcca gactattagc gacttcttac actggtatca acaaaaatca 120
catgagtctc caaggcttct catcaaatat gcttcccaat ccatctctgg gatcccctcc 180
aggttcagtg gcactggatc agggtcagat ttcactctca ctatcaacag tgtggaacct 240
gaagatgttg gagtgtatta ctgtcaaagt ggtaacacct ttccgtggac gttcggtgga 300
ggcaccaagc tggaaatcaa acgg 324
<210> 146
<211> 108
<212> PRT
<213> 小家鼠
<400> 146
Asp Ile Val Met Thr Gln Ser Pro Ala Thr Leu Ser Val Thr Pro Gly
1 5 10 15
Asp Arg Val Ser Leu Ser Cys Arg Ala Ser Gln Thr Ile Ser Asp Phe
20 25 30
Leu His Trp Tyr Gln Gln Lys Ser His Glu Ser Pro Arg Leu Leu Ile
35 40 45
Lys Tyr Ala Ser Gln Ser Ile Ser Gly Ile Pro Ser Arg Phe Ser Gly
50 55 60
Thr Gly Ser Gly Ser Asp Phe Thr Leu Thr Ile Asn Ser Val Glu Pro
65 70 75 80
Glu Asp Val Gly Val Tyr Tyr Cys Gln Ser Gly Asn Thr Phe Pro Trp
85 90 95
Thr Phe Gly Gly Gly Thr Lys Leu Glu Ile Lys Arg
100 105
<210> 147
<211> 324
<212> DNA
<213> 小家鼠
<400> 147
gacatccaga tgacacaatc ttcatcctcc ttttctggat ttctaggaga cagagtcacc 60
attacttgca gggcaagtga ggacatacac actcaattag cctggtatca gcagaaacca 120
ggaaatgctc ctaggctctt aatatctggt gcagccagtt tgaaaagtgg ggttccttca 180
agattcagtg gcactggatc tggaaaggat tacactctca gcattaccag tcttcagact 240
gaagatgttg ctacatatta ctgtcaacag tataggagta ttccgtggac gttcggtgga 300
ggcaccaagc tggaaatcaa acgg 324
<210> 148
<211> 108
<212> PRT
<213> 小家鼠
<400> 148
Asp Ile Gln Met Thr Gln Ser Ser Ser Ser Phe Ser Gly Phe Leu Gly
1 5 10 15
Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Glu Asp Ile His Thr Gln
20 25 30
Leu Ala Trp Tyr Gln Gln Lys Pro Gly Asn Ala Pro Arg Leu Leu Ile
35 40 45
Ser Gly Ala Ala Ser Leu Lys Ser Gly Val Pro Ser Arg Phe Ser Gly
50 55 60
Thr Gly Ser Gly Lys Asp Tyr Thr Leu Ser Ile Thr Ser Leu Gln Thr
65 70 75 80
Glu Asp Val Ala Thr Tyr Tyr Cys Gln Gln Tyr Arg Ser Ile Pro Trp
85 90 95
Thr Phe Gly Gly Gly Thr Lys Leu Glu Ile Lys Arg
100 105
<210> 149
<211> 339
<212> DNA
<213> 小家鼠
<400> 149
gatgttttga tgacccaaac tccgctctcc ctgcctgtca gtcttggaga tcacgcctcc 60
atctcttgca gatctagtca gtacattgtt catagtactg gaaccaccta tttagaatgg 120
tacctacaga aaccaggcca gtctccacag ctcctgatct acaaagtttc caaccgattt 180
tctggggtcc cagacaggtt cactggcagt ggatcaggga cagatttcac actcaggatc 240
agcagagtgg aggctgagga tctgggagtt tatttctgct ttcaaggttc acattttcca 300
ttcacgttcg gctcggggac aaagttggaa ataaaacgg 339
<210> 150
<211> 113
<212> PRT
<213> 小家鼠
<400> 150
Asp Val Leu Met Thr Gln Thr Pro Leu Ser Leu Pro Val Ser Leu Gly
1 5 10 15
Asp His Ala Ser Ile Ser Cys Arg Ser Ser Gln Tyr Ile Val His Ser
20 25 30
Thr Gly Thr Thr Tyr Leu Glu Trp Tyr Leu Gln Lys Pro Gly Gln Ser
35 40 45
Pro Gln Leu Leu Ile Tyr Lys Val Ser Asn Arg Phe Ser Gly Val Pro
50 55 60
Asp Arg Phe Thr Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Arg Ile
65 70 75 80
Ser Arg Val Glu Ala Glu Asp Leu Gly Val Tyr Phe Cys Phe Gln Gly
85 90 95
Ser His Phe Pro Phe Thr Phe Gly Ser Gly Thr Lys Leu Glu Ile Lys
100 105 110
Arg
<210> 151
<211> 339
<212> DNA
<213> 小家鼠
<400> 151
gaagttgtga tgacccaaac tccactctcc ttgcctgtca gtcttggaga tcaagcctcc 60
atctcttgca gatctagtca ttaccttgtt catgataacg gaaacaccta tgttgaatgg 120
tacctgcaga agccaggcca gtctccaaag ctcctgatct acaaggtttc caaccgattt 180
tctggagtcc cagacaggtt tactggcagt ggttcaggga cagatttcac actcaagatc 240
agcagagtgg agtctgagga tctgggaatt tattactgct ttcaaggttc acatttccca 300
ttcacgttcg gctcggggac agagttggaa ataaaacgg 339
<210> 152
<211> 113
<212> PRT
<213> 小家鼠
<400> 152
Glu Val Val Met Thr Gln Thr Pro Leu Ser Leu Pro Val Ser Leu Gly
1 5 10 15
Asp Gln Ala Ser Ile Ser Cys Arg Ser Ser His Tyr Leu Val His Asp
20 25 30
Asn Gly Asn Thr Tyr Val Glu Trp Tyr Leu Gln Lys Pro Gly Gln Ser
35 40 45
Pro Lys Leu Leu Ile Tyr Lys Val Ser Asn Arg Phe Ser Gly Val Pro
50 55 60
Asp Arg Phe Thr Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Lys Ile
65 70 75 80
Ser Arg Val Glu Ser Glu Asp Leu Gly Ile Tyr Tyr Cys Phe Gln Gly
85 90 95
Ser His Phe Pro Phe Thr Phe Gly Ser Gly Thr Glu Leu Glu Ile Lys
100 105 110
Arg
<210> 153
<211> 339
<212> DNA
<213> 小家鼠
<400> 153
gatgttttga tgacccaaac tccactctcc ctgcctgtca gtcttggaga tcaagcctcc 60
atctcttgca gatctagtca gaacattgtc catagtactg gaaacaccta tttagaatgg 120
tacctgcaga aaccaggcca gtctccaaag ctcctgattt ataaagtttc caaccgattt 180
tctggggtcc caaacaggtt ccgtggcagt ggatcaggga cagatttcac actcaagatc 240
accagagtgg aggctgagga tctgggaatt tattactgct ttcaaggttc acattttcca 300
ttcacgttcg gctcggggac aaagttggaa ataaaacgg 339
<210> 154
<211> 113
<212> PRT
<213> 小家鼠
<400> 154
Asp Val Leu Met Thr Gln Thr Pro Leu Ser Leu Pro Val Ser Leu Gly
1 5 10 15
Asp Gln Ala Ser Ile Ser Cys Arg Ser Ser Gln Asn Ile Val His Ser
20 25 30
Thr Gly Asn Thr Tyr Leu Glu Trp Tyr Leu Gln Lys Pro Gly Gln Ser
35 40 45
Pro Lys Leu Leu Ile Tyr Lys Val Ser Asn Arg Phe Ser Gly Val Pro
50 55 60
Asn Arg Phe Arg Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Lys Ile
65 70 75 80
Thr Arg Val Glu Ala Glu Asp Leu Gly Ile Tyr Tyr Cys Phe Gln Gly
85 90 95
Ser His Phe Pro Phe Thr Phe Gly Ser Gly Thr Lys Leu Glu Ile Lys
100 105 110
Arg
<210> 155
<211> 321
<212> DNA
<213> 小家鼠
<400> 155
caaattgttc tcacccagtc tccagcaatc atgtctgcat ctccagggga gaaggtcacc 60
atgacctgca gtgtcagctc aagtgtaagt tacatacact ggtaccaaca gaagtcaggc 120
acctccccca aaagatggat ttatgacaca tccaaactgg cttctggagt ccctgctcgc 180
ttcagtggca gtgggtctgg gacctcttac tctctcacaa tcagcagcat ggaggctgaa 240
gatgctgcca cttattactg ccaccagtgg agtactaacc cacccacgtt cggagggggg 300
accaagctgg aaataagacg g 321
<210> 156
<211> 107
<212> PRT
<213> 小家鼠
<400> 156
Gln Ile Val Leu Thr Gln Ser Pro Ala Ile Met Ser Ala Ser Pro Gly
1 5 10 15
Glu Lys Val Thr Met Thr Cys Ser Val Ser Ser Ser Val Ser Tyr Ile
20 25 30
His Trp Tyr Gln Gln Lys Ser Gly Thr Ser Pro Lys Arg Trp Ile Tyr
35 40 45
Asp Thr Ser Lys Leu Ala Ser Gly Val Pro Ala Arg Phe Ser Gly Ser
50 55 60
Gly Ser Gly Thr Ser Tyr Ser Leu Thr Ile Ser Ser Met Glu Ala Glu
65 70 75 80
Asp Ala Ala Thr Tyr Tyr Cys His Gln Trp Ser Thr Asn Pro Pro Thr
85 90 95
Phe Gly Gly Gly Thr Lys Leu Glu Ile Arg Arg
100 105
<210> 157
<211> 321
<212> DNA
<213> 小家鼠
<400> 157
caaattgttc tcacccagtc tccagcactc atgtctgcat ctccagggga gaaggtcacc 60
atgacctgca gtgccagctc aagtgtaagt tacatgtgct ggtaccagca gaagccaaga 120
tcctccccca aaccctggat ttatctcaca tccaacctgg cttctggagt ccctgctcgc 180
ttcagtggca gtgggtctgg gacctcttac tctctcacaa tcagtagcat ggaggctgaa 240
gatgctgcca cttattactg ccagcagtgg agtagtaacc cacccacgtt cggtgctggg 300
accaagctgg agctgaaacg g 321
<210> 158
<211> 107
<212> PRT
<213> 小家鼠
<400> 158
Gln Ile Val Leu Thr Gln Ser Pro Ala Leu Met Ser Ala Ser Pro Gly
1 5 10 15
Glu Lys Val Thr Met Thr Cys Ser Ala Ser Ser Ser Val Ser Tyr Met
20 25 30
Cys Trp Tyr Gln Gln Lys Pro Arg Ser Ser Pro Lys Pro Trp Ile Tyr
35 40 45
Leu Thr Ser Asn Leu Ala Ser Gly Val Pro Ala Arg Phe Ser Gly Ser
50 55 60
Gly Ser Gly Thr Ser Tyr Ser Leu Thr Ile Ser Ser Met Glu Ala Glu
65 70 75 80
Asp Ala Ala Thr Tyr Tyr Cys Gln Gln Trp Ser Ser Asn Pro Pro Thr
85 90 95
Phe Gly Ala Gly Thr Lys Leu Glu Leu Lys Arg
100 105
<210> 159
<211> 321
<212> DNA
<213> 小家鼠
<400> 159
gaaatccaga tgacacagac tccatcctcc ctgtctgcct ctctgggaga cagagtcacc 60
atcacttgca gtgcaagtca gggcattaac aattatttga actggtatca gcagaaacca 120
ggtggaaaga ctagactcct catctattat acatcaactt tacagtcagg agtcccatca 180
aggttcagtg gcagtgggtc tgggacacat tattctctca ccatcagcaa tctggaacct 240
gaagatattg ccacttacta ttgtcagcag tttagtaaac ttcggacatt cggtggaggc 300
accaggctgg aaatcaaacg g 321
<210> 160
<211> 107
<212> PRT
<213> 小家鼠
<400> 160
Glu Ile Gln Met Thr Gln Thr Pro Ser Ser Leu Ser Ala Ser Leu Gly
1 5 10 15
Asp Arg Val Thr Ile Thr Cys Ser Ala Ser Gln Gly Ile Asn Asn Tyr
20 25 30
Leu Asn Trp Tyr Gln Gln Lys Pro Gly Gly Lys Thr Arg Leu Leu Ile
35 40 45
Tyr Tyr Thr Ser Thr Leu Gln Ser Gly Val Pro Ser Arg Phe Ser Gly
50 55 60
Ser Gly Ser Gly Thr His Tyr Ser Leu Thr Ile Ser Asn Leu Glu Pro
65 70 75 80
Glu Asp Ile Ala Thr Tyr Tyr Cys Gln Gln Phe Ser Lys Leu Arg Thr
85 90 95
Phe Gly Gly Gly Thr Arg Leu Glu Ile Lys Arg
100 105
<210> 161
<211> 324
<212> DNA
<213> 智人
<400> 161
gagattgtgc tgactcagag tccagacttc cagtcagtga cccccaagga gaaagtcacc 60
atcacatgcc gggcaagcca gaacatcggc acaagcattc actggtacca gcagaagccc 120
gatcagtccc ctaagctgct gatcaaatat gcctctaaga gtatttcagg ggtgccctct 180
agattcagcg gctccgggtc tggaacagac tttactctga ccattaactc cctggaggct 240
gaagatgccg ctacttacta ttgtcagcat agctactcat tcccttggac attcgggcag 300
gggaccaaag tggaaatcaa acgt 324
<210> 162
<211> 108
<212> PRT
<213> 智人
<400> 162
Glu Ile Val Leu Thr Gln Ser Pro Asp Phe Gln Ser Val Thr Pro Lys
1 5 10 15
Glu Lys Val Thr Ile Thr Cys Arg Ala Ser Gln Asn Ile Gly Thr Ser
20 25 30
Ile His Trp Tyr Gln Gln Lys Pro Asp Gln Ser Pro Lys Leu Leu Ile
35 40 45
Lys Tyr Ala Ser Lys Ser Ile Ser Gly Val Pro Ser Arg Phe Ser Gly
50 55 60
Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Asn Ser Leu Glu Ala
65 70 75 80
Glu Asp Ala Ala Thr Tyr Tyr Cys Gln His Ser Tyr Ser Phe Pro Trp
85 90 95
Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys Arg
100 105
<210> 163
<211> 339
<212> DNA
<213> 智人
<400> 163
gatattgtga tgacccaaac tccgctctcc ctgtccgtca cccctggaca gccggcctcc 60
atctcttgca gatctagtca gaacattgtt catagtactg gaaacaccta tttagaatgg 120
tacctacaga aaccaggcca gtctccacag ctcctgatct acaaagtttc caaccgattt 180
tctggggtcc cagacaggtt cagtggcagt ggatcaggga cagatttcac actcaaaatc 240
agcagagtgg aggctgagga tgttggagtt tattactgct ttcaaggttc acattttcca 300
ttcacgttcg gccaagggac caaggtggaa atcaaacgt 339
<210> 164
<211> 113
<212> PRT
<213> 智人
<400> 164
Asp Ile Val Met Thr Gln Thr Pro Leu Ser Leu Ser Val Thr Pro Gly
1 5 10 15
Gln Pro Ala Ser Ile Ser Cys Arg Ser Ser Gln Asn Ile Val His Ser
20 25 30
Thr Gly Asn Thr Tyr Leu Glu Trp Tyr Leu Gln Lys Pro Gly Gln Ser
35 40 45
Pro Gln Leu Leu Ile Tyr Lys Val Ser Asn Arg Phe Ser Gly Val Pro
50 55 60
Asp Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Lys Ile
65 70 75 80
Ser Arg Val Glu Ala Glu Asp Val Gly Val Tyr Tyr Cys Phe Gln Gly
85 90 95
Ser His Phe Pro Phe Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys
100 105 110
Arg
<210> 165
<211> 360
<212> DNA
<213> 小家鼠
<400> 165
caggttactc tgaaagagtc tggccctggg atattgcagc cctcccagac cctcagtctg 60
acttgttctt tctctgggtt ctcactgacc acttctggct tgggtgttgc ctggattcgt 120
cagccttcag ggaagggtct ggagtggctg gcacacattt ggtcggatgg tgacacgcgc 180
tattacccag ccctgaagaa ccgactgaca atctccaagg attcctccag caaccaggtc 240
ttcctcaaga tcgcccgtgt ggacactgca gatactgcca catactactg tgctcgaatg 300
aaggatgata gtctttactt tgacaactgg ggccaaggca ctattttcac agtctcctca 360
<210> 166
<211> 120
<212> PRT
<213> 小家鼠
<400> 166
Gln Val Thr Leu Lys Glu Ser Gly Pro Gly Ile Leu Gln Pro Ser Gln
1 5 10 15
Thr Leu Ser Leu Thr Cys Ser Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Ser Gly Lys Gly Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Ser Lys Asp Ser Ser Ser Asn Gln Val
65 70 75 80
Phe Leu Lys Ile Ala Arg Val Asp Thr Ala Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala Arg Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Ile Phe Thr Val Ser Ser
115 120
<210> 167
<211> 351
<212> DNA
<213> 小家鼠
<400> 167
cagatccagt tggtgcagtc tggggctgaa ctggcaaaac ctggggcctc agtgaggatg 60
tcctgcgaga cttctggcta cacctttact agctactgga tacactggat aaaagagagg 120
cctggacagg gtctggaatg gattggatac attaatcctg acactgatta tagtgagtac 180
aatcagaaat tcaaggacaa ggccagattg actgcagaca aatcctccac cacagcctac 240
atggagctga acagcctgac atttgatgat tctgcagtct attactgtgc aagtgctggt 300
tattattttt ttgacttctg gggccaaggc accactctca cagtctcctc a 351
<210> 168
<211> 117
<212> PRT
<213> 小家鼠
<400> 168
Gln Ile Gln Leu Val Gln Ser Gly Ala Glu Leu Ala Lys Pro Gly Ala
1 5 10 15
Ser Val Arg Met Ser Cys Glu Thr Ser Gly Tyr Thr Phe Thr Ser Tyr
20 25 30
Trp Ile His Trp Ile Lys Glu Arg Pro Gly Gln Gly Leu Glu Trp Ile
35 40 45
Gly Tyr Ile Asn Pro Asp Thr Asp Tyr Ser Glu Tyr Asn Gln Lys Phe
50 55 60
Lys Asp Lys Ala Arg Leu Thr Ala Asp Lys Ser Ser Thr Thr Ala Tyr
65 70 75 80
Met Glu Leu Asn Ser Leu Thr Phe Asp Asp Ser Ala Val Tyr Tyr Cys
85 90 95
Ala Ser Ala Gly Tyr Tyr Phe Phe Asp Phe Trp Gly Gln Gly Thr Thr
100 105 110
Leu Thr Val Ser Ser
115
<210> 169
<211> 336
<212> DNA
<213> 小家鼠
<400> 169
gaggttcagc tgcagcagtc tggggcagaa cttgtgaaac caggggcctc agtcaagttg 60
tcctgtacaa cttctggcct caacattaaa gacatctata ttcactgggt gaagcagagg 120
cctgaacagg gcctggagtg gattgggagg attgatcctg cgaacggtaa gactgcatat 180
gacctgaagt tccaggccaa ggccactata acagcagaca catcttccaa aacagcctac 240
ctgcacctca gcagcctgac atctgaggac actgccgtct attactgtgg taggggggcc 300
cactggggcc aaggcaccac tctcacagtc tcctca 336
<210> 170
<211> 112
<212> PRT
<213> 小家鼠
<400> 170
Glu Val Gln Leu Gln Gln Ser Gly Ala Glu Leu Val Lys Pro Gly Ala
1 5 10 15
Ser Val Lys Leu Ser Cys Thr Thr Ser Gly Leu Asn Ile Lys Asp Ile
20 25 30
Tyr Ile His Trp Val Lys Gln Arg Pro Glu Gln Gly Leu Glu Trp Ile
35 40 45
Gly Arg Ile Asp Pro Ala Asn Gly Lys Thr Ala Tyr Asp Leu Lys Phe
50 55 60
Gln Ala Lys Ala Thr Ile Thr Ala Asp Thr Ser Ser Lys Thr Ala Tyr
65 70 75 80
Leu His Leu Ser Ser Leu Thr Ser Glu Asp Thr Ala Val Tyr Tyr Cys
85 90 95
Gly Arg Gly Ala His Trp Gly Gln Gly Thr Thr Leu Thr Val Ser Ser
100 105 110
<210> 171
<211> 354
<212> DNA
<213> 小家鼠
<400> 171
cagatccagt tggtgcagtc tgggcctcag ctggttaggc ctggggcttc agtgaagata 60
tcctgcgagg cttctggtta ctcattcacc aactactgga tacactgggt gaagcagagg 120
cctggacagg gtcttgagtg gattggcatg attgatcctt ccgatgctga aactgggtta 180
aatcagaagt tcaaggacaa ggccacattg actgtagaca aatcctccag cacagcctac 240
atgcaactca gcagcccgac atctgaagac tctgcggtct attactgtgc aagaattggc 300
gattactata atatggacta ctggggtcaa ggaacctcag tcaccgtctc ctca 354
<210> 172
<211> 118
<212> PRT
<213> 小家鼠
<400> 172
Gln Ile Gln Leu Val Gln Ser Gly Pro Gln Leu Val Arg Pro Gly Ala
1 5 10 15
Ser Val Lys Ile Ser Cys Glu Ala Ser Gly Tyr Ser Phe Thr Asn Tyr
20 25 30
Trp Ile His Trp Val Lys Gln Arg Pro Gly Gln Gly Leu Glu Trp Ile
35 40 45
Gly Met Ile Asp Pro Ser Asp Ala Glu Thr Gly Leu Asn Gln Lys Phe
50 55 60
Lys Asp Lys Ala Thr Leu Thr Val Asp Lys Ser Ser Ser Thr Ala Tyr
65 70 75 80
Met Gln Leu Ser Ser Pro Thr Ser Glu Asp Ser Ala Val Tyr Tyr Cys
85 90 95
Ala Arg Ile Gly Asp Tyr Tyr Asn Met Asp Tyr Trp Gly Gln Gly Thr
100 105 110
Ser Val Thr Val Ser Ser
115
<210> 173
<211> 366
<212> DNA
<213> 小家鼠
<400> 173
gaagtgaagg tggtggagtc tgggggaggt ttagtgcagc ctggagggtc cctgaaactc 60
tcctgtgcag cctctggatt cactttcagt gactatccca tgtcttgggt tcgccagact 120
ccagagaaga gactggagtg ggtcgcatac gttagtgatg gtggtggttc cacctactat 180
ccagacattg taaagggccg attcaccatc tcccgagaca atgccaagaa caccctgtac 240
cttcaaatga gcagtctgaa gtctgaggac acggccatgt atttctgtac aagacatgct 300
tcctactata gctacgacca ttctatggac tactggggtc agggaacctc agtcaccgtc 360
tcatca 366
<210> 174
<211> 122
<212> PRT
<213> 小家鼠
<400> 174
Glu Val Lys Val Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly
1 5 10 15
Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Asp Tyr
20 25 30
Pro Met Ser Trp Val Arg Gln Thr Pro Glu Lys Arg Leu Glu Trp Val
35 40 45
Ala Tyr Val Ser Asp Gly Gly Gly Ser Thr Tyr Tyr Pro Asp Ile Val
50 55 60
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr
65 70 75 80
Leu Gln Met Ser Ser Leu Lys Ser Glu Asp Thr Ala Met Tyr Phe Cys
85 90 95
Thr Arg His Ala Ser Tyr Tyr Ser Tyr Asp His Ser Met Asp Tyr Trp
100 105 110
Gly Gln Gly Thr Ser Val Thr Val Ser Ser
115 120
<210> 175
<211> 357
<212> DNA
<213> 小家鼠
<400> 175
cagatccagt tggtgcagtc tgggggagac ttagtgaggc ctggagggtc cctgaaactc 60
tcctgtgcag cctctggatt cactttcagt agctttggca tgtcttggat tcgccagact 120
ccagacaaga ggctggagtg ggtcgcaacc attagtagtg ctggtagttt cacctactat 180
ccagacagtg tgaagggccg attcaccatc tccagagaca atgccaggaa caccctgtat 240
ctacaaatga acagtctgaa gtctgaggac tcagccatgt attactgtgc aagacggggg 300
tacgacgttg ggtgctttga ccactggggc cgaggcacca ctctcacagt ctcctca 357
<210> 176
<211> 119
<212> PRT
<213> 小家鼠
<400> 176
Gln Ile Gln Leu Val Gln Ser Gly Gly Asp Leu Val Arg Pro Gly Gly
1 5 10 15
Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Ser Phe
20 25 30
Gly Met Ser Trp Ile Arg Gln Thr Pro Asp Lys Arg Leu Glu Trp Val
35 40 45
Ala Thr Ile Ser Ser Ala Gly Ser Phe Thr Tyr Tyr Pro Asp Ser Val
50 55 60
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Arg Asn Thr Leu Tyr
65 70 75 80
Leu Gln Met Asn Ser Leu Lys Ser Glu Asp Ser Ala Met Tyr Tyr Cys
85 90 95
Ala Arg Arg Gly Tyr Asp Val Gly Cys Phe Asp His Trp Gly Arg Gly
100 105 110
Thr Thr Leu Thr Val Ser Ser
115
<210> 177
<211> 348
<212> DNA
<213> 小家鼠
<400> 177
gaggtgcacc tggtggagtc tgggggaggc ttagtgcagc ctggagggtc cctgaaactc 60
tcctgtgcag cctctggatt cactttcagt acctatggca tgtcttgggt tcgccagact 120
ccagacaaga ggctggagtt ggtcgcgacc attaatacta atggtggtac cacctattat 180
cgagacagtg tgaagggccg attcaccatc tccagagaca atgccaagaa caccctgtac 240
ctgcaaatga gcagtctgaa gtctgatgac acagccatgt attactgtgc aagagactac 300
ggggctatgg actactgggg tcaaggaacc tcagtcaccg tctcctca 348
<210> 178
<211> 116
<212> PRT
<213> 小家鼠
<400> 178
Glu Val His Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly
1 5 10 15
Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Thr Tyr
20 25 30
Gly Met Ser Trp Val Arg Gln Thr Pro Asp Lys Arg Leu Glu Leu Val
35 40 45
Ala Thr Ile Asn Thr Asn Gly Gly Thr Thr Tyr Tyr Arg Asp Ser Val
50 55 60
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr
65 70 75 80
Leu Gln Met Ser Ser Leu Lys Ser Asp Asp Thr Ala Met Tyr Tyr Cys
85 90 95
Ala Arg Asp Tyr Gly Ala Met Asp Tyr Trp Gly Gln Gly Thr Ser Val
100 105 110
Thr Val Ser Ser
115
<210> 179
<211> 345
<212> DNA
<213> 小家鼠
<400> 179
gatgtgcacc tggtggagtc tgggggaggc ttagtgcagc ctggagggtc cctgacagtc 60
tcctgcgcag cctctggatt cactttcagt acctatggca tgtcttgggt tcgccagact 120
cgagacaaga ggctggagtt ggtcgcaacc ataaatacta atggtggtaa cacctattat 180
tcagacaatg tgaagggccg attcaccatt tccagagaca atgccaagaa caccctgtat 240
ttggaaatga gaggtctgag gtctggggac acagccatgt attactgtgc aagagactac 300
ggggctatgg actactgggg tcaaggaacc tcagtcaccg tctct 345
<210> 180
<211> 115
<212> PRT
<213> 小家鼠
<400> 180
Asp Val His Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly
1 5 10 15
Ser Leu Thr Val Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Thr Tyr
20 25 30
Gly Met Ser Trp Val Arg Gln Thr Arg Asp Lys Arg Leu Glu Leu Val
35 40 45
Ala Thr Ile Asn Thr Asn Gly Gly Asn Thr Tyr Tyr Ser Asp Asn Val
50 55 60
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr
65 70 75 80
Leu Glu Met Arg Gly Leu Arg Ser Gly Asp Thr Ala Met Tyr Tyr Cys
85 90 95
Ala Arg Asp Tyr Gly Ala Met Asp Tyr Trp Gly Gln Gly Thr Ser Val
100 105 110
Thr Val Ser
115
<210> 181
<211> 348
<212> DNA
<213> 小家鼠
<400> 181
gaggtgcagc tgcagcagcc tgggggaggc ttagtacagc ctggagggtc cctgacactc 60
tcctgtgcaa cctctggatt cactttcagt agttatggca tgtcttgggt tcgccagact 120
ccagccaaga ggctggagtt ggtcgcaacc attagtacta atggtgccac cgccaattat 180
ccagacagtg tgaagggccg attcaccatc tccagagaca atgccaagag caccctgtac 240
ctacaaatgc gcagtctgaa gtctgaggac acagccatgt attactgtgc aactgaaaag 300
ggagctatgg gctactgggg tcaaggaacc tcagtcaccg tctcctca 348
<210> 182
<211> 116
<212> PRT
<213> 小家鼠
<400> 182
Glu Val Gln Leu Gln Gln Pro Gly Gly Gly Leu Val Gln Pro Gly Gly
1 5 10 15
Ser Leu Thr Leu Ser Cys Ala Thr Ser Gly Phe Thr Phe Ser Ser Tyr
20 25 30
Gly Met Ser Trp Val Arg Gln Thr Pro Ala Lys Arg Leu Glu Leu Val
35 40 45
Ala Thr Ile Ser Thr Asn Gly Ala Thr Ala Asn Tyr Pro Asp Ser Val
50 55 60
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Ser Thr Leu Tyr
65 70 75 80
Leu Gln Met Arg Ser Leu Lys Ser Glu Asp Thr Ala Met Tyr Tyr Cys
85 90 95
Ala Thr Glu Lys Gly Ala Met Gly Tyr Trp Gly Gln Gly Thr Ser Val
100 105 110
Thr Val Ser Ser
115
<210> 183
<211> 381
<212> DNA
<213> 小家鼠
<400> 183
caagttactc taaaagagtc tggccctggg atattgaagc cctcacagac cctcagtctg 60
acttgttctt tctctgggtt ttcactgacc acttctggta tgggtgtagg ctggattcgt 120
cagccttcag ggaagggtct ggagtggctg gcacacattt ggtgggatga tgataagtac 180
tataatccat ccctgaagag ccaggtcaca atctccaagg acacctccag aaaccaggta 240
ttcctcaaga tcaccagtgt ggacactgca gatactgcca cttactactg tgctcgaaga 300
actgagacta tgattacgac agtgctatat tactatgcta tggactactg gggtcaagga 360
acctcagtca ccgtctcctc a 381
<210> 184
<211> 127
<212> PRT
<213> 小家鼠
<400> 184
Gln Val Thr Leu Lys Glu Ser Gly Pro Gly Ile Leu Lys Pro Ser Gln
1 5 10 15
Thr Leu Ser Leu Thr Cys Ser Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Met Gly Val Gly Trp Ile Arg Gln Pro Ser Gly Lys Gly Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Trp Asp Asp Asp Lys Tyr Tyr Asn Pro Ser
50 55 60
Leu Lys Ser Gln Val Thr Ile Ser Lys Asp Thr Ser Arg Asn Gln Val
65 70 75 80
Phe Leu Lys Ile Thr Ser Val Asp Thr Ala Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala Arg Arg Thr Glu Thr Met Ile Thr Thr Val Leu Tyr Tyr Tyr
100 105 110
Ala Met Asp Tyr Trp Gly Gln Gly Thr Ser Val Thr Val Ser Ser
115 120 125
<210> 185
<211> 378
<212> DNA
<213> 小家鼠
<400> 185
caagttactc taaaagagtc tggccctggg atattgaagc cctcacagac cctcagtctg 60
acttgttctt tctctggatt ttcactgagc acttctggtt tgggtgtagg ctggattcgt 120
cagccttcag ggaagggtct ggagtggctg gcacacattt ggtgggatga tgataagtac 180
tataatccat cccttaagag acagatcaca atctccaagg attcctccag aaaccaggta 240
ttcctcaaga tcaccaatgt ggacactgca gatactgcca cttactactg tgctcgaagg 300
agggaagtta acttcggtat taactattac tattctatgg actactgggg tcaaggaacc 360
tcagtcaccg tctcctca 378
<210> 186
<211> 126
<212> PRT
<213> 小家鼠
<400> 186
Gln Val Thr Leu Lys Glu Ser Gly Pro Gly Ile Leu Lys Pro Ser Gln
1 5 10 15
Thr Leu Ser Leu Thr Cys Ser Phe Ser Gly Phe Ser Leu Ser Thr Ser
20 25 30
Gly Leu Gly Val Gly Trp Ile Arg Gln Pro Ser Gly Lys Gly Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Trp Asp Asp Asp Lys Tyr Tyr Asn Pro Ser
50 55 60
Leu Lys Arg Gln Ile Thr Ile Ser Lys Asp Ser Ser Arg Asn Gln Val
65 70 75 80
Phe Leu Lys Ile Thr Asn Val Asp Thr Ala Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala Arg Arg Arg Glu Val Asn Phe Gly Ile Asn Tyr Tyr Tyr Ser
100 105 110
Met Asp Tyr Trp Gly Gln Gly Thr Ser Val Thr Val Ser Ser
115 120 125
<210> 187
<211> 363
<212> DNA
<213> 小家鼠
<400> 187
gaggtgaagc tggtggagtc tggaggacgc ttggtacagc ctgggaattc tctgagactc 60
tcctgtgcaa cttctggatt caccttcagt gattattaca tgagttgggt ccgccagact 120
ccaggaaggg cacttgagtg gttgagtttt attagaaatc gggctaatgg ttacacaaca 180
gagtacagtg catctgtgaa gggtcgattc accatctcca gagataattc ccaaagcatc 240
ctctatcttc acatgagcac cctgagacct gaggacagtg ccacttatta ctgtgtaaga 300
gattcctatc actacgggta cttcgatgtc tggggcgcag ggaccacggt caccgtctcc 360
tca 363
<210> 188
<211> 121
<212> PRT
<213> 小家鼠
<400> 188
Glu Val Lys Leu Val Glu Ser Gly Gly Arg Leu Val Gln Pro Gly Asn
1 5 10 15
Ser Leu Arg Leu Ser Cys Ala Thr Ser Gly Phe Thr Phe Ser Asp Tyr
20 25 30
Tyr Met Ser Trp Val Arg Gln Thr Pro Gly Arg Ala Leu Glu Trp Leu
35 40 45
Ser Phe Ile Arg Asn Arg Ala Asn Gly Tyr Thr Thr Glu Tyr Ser Ala
50 55 60
Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Gln Ser Ile
65 70 75 80
Leu Tyr Leu His Met Ser Thr Leu Arg Pro Glu Asp Ser Ala Thr Tyr
85 90 95
Tyr Cys Val Arg Asp Ser Tyr His Tyr Gly Tyr Phe Asp Val Trp Gly
100 105 110
Ala Gly Thr Thr Val Thr Val Ser Ser
115 120
<210> 189
<211> 360
<212> DNA
<213> 智人
<400> 189
caggtgaccc tgaaggaatc cgggcctact ctggtgaaac ctacccagac tctgactctg 60
acttgtactt ttagcggctt ctcactgacc acatctggac tgggagtggc ttggatcaga 120
cagcctcctg gaaaggccct ggagtggctg gctcacattt ggagcgacgg cgatactcgg 180
tactatccag ccctgaaaaa cagactgact atcaccaagg acacatccaa aaaccaggtg 240
gtcctgacaa tgactaatat ggaccccgtc gataccgcaa catactattg cgcccatatg 300
aaggatgact ctctgtactt tgataactgg gggcagggaa ctctggtgac cgtgagcagc 360
<210> 190
<211> 120
<212> PRT
<213> 智人
<400> 190
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser
115 120
<210> 191
<211> 348
<212> DNA
<213> 智人
<400> 191
gaggtgcagc tgctggaatc tgggggggga ctggtgcagc ctggaggaag cctgagactg 60
agttgtgccg caagtgggtt tacatttagc tcctacggaa tgagctgggt gaggcaggct 120
ccaggcaagg gactggagtg ggtctctgca atcagtacca acggagccac agcttactat 180
gccgactccg tgaagggccg gttcactatc tcaagagata acagcaagaa caccctgtat 240
ctgcagatga attctctgcg ggcagaagac acagccgtct actattgcgc tactgagaaa 300
ggggcaatga gccactgggg acagggcaca ctggtgaccg tgagttcc 348
<210> 192
<211> 116
<212> PRT
<213> 智人
<400> 192
Glu Val Gln Leu Leu Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly
1 5 10 15
Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Ser Tyr
20 25 30
Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val
35 40 45
Ser Ala Ile Ser Thr Asn Gly Ala Thr Ala Tyr Tyr Ala Asp Ser Val
50 55 60
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr
65 70 75 80
Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys
85 90 95
Ala Thr Glu Lys Gly Ala Met Ser His Trp Gly Gln Gly Thr Leu Val
100 105 110
Thr Val Ser Ser
115
<210> 193
<211> 318
<212> DNA
<213> 智人
<400> 193
accgtggccg ccccctccgt gttcatcttc cccccctccg acgagcagct gaagtccggc 60
accgcctccg tggtgtgcct gctgaacaac ttctacccca gggaggccaa ggtgcagtgg 120
aaggtggaca acgccctgca gtccggcaac tcccaggagt ccgtgaccga gcaggactcc 180
aaggactcca cctactccct gtcctccacc ctgaccctgt ccaaggccga ctacgagaag 240
cacaaggtgt acgcctgcga ggtgacccac cagggcctgt cctcccccgt gaccaagtcc 300
ttcaacaggg gcgagtgc 318
<210> 194
<211> 106
<212> PRT
<213> 智人
<400> 194
Thr Val Ala Ala Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Glu Gln
1 5 10 15
Leu Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe Tyr
20 25 30
Pro Arg Glu Ala Lys Val Gln Trp Lys Val Asp Asn Ala Leu Gln Ser
35 40 45
Gly Asn Ser Gln Glu Ser Val Thr Glu Gln Asp Ser Lys Asp Ser Thr
50 55 60
Tyr Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys
65 70 75 80
His Lys Val Tyr Ala Cys Glu Val Thr His Gln Gly Leu Ser Ser Pro
85 90 95
Val Thr Lys Ser Phe Asn Arg Gly Glu Cys
100 105
<210> 195
<211> 318
<212> DNA
<213> 智人
<400> 195
ggacagccaa aggcagcacc atctgtgacc ctgttcccac ctagctccga ggagctgcag 60
gccaacaagg ccaccctggt gtgcctgatc tccgactttt acccaggagc agtgacagtg 120
gcatggaagg ccgattctag ccctgtgaag gccggcgtgg agaccacaac cccatctaag 180
cagagcaaca ataagtacgc cgcctcctct tatctgtccc tgacccccga gcagtggaag 240
tctcaccgga gctattcctg ccaggtgaca cacgagggca gcacagtgga gaagaccgtg 300
gcccctacag agtgttcc 318
<210> 196
<211> 106
<212> PRT
<213> 智人
<400> 196
Gly Gln Pro Lys Ala Ala Pro Ser Val Thr Leu Phe Pro Pro Ser Ser
1 5 10 15
Glu Glu Leu Gln Ala Asn Lys Ala Thr Leu Val Cys Leu Ile Ser Asp
20 25 30
Phe Tyr Pro Gly Ala Val Thr Val Ala Trp Lys Ala Asp Ser Ser Pro
35 40 45
Val Lys Ala Gly Val Glu Thr Thr Thr Pro Ser Lys Gln Ser Asn Asn
50 55 60
Lys Tyr Ala Ala Ser Ser Tyr Leu Ser Leu Thr Pro Glu Gln Trp Lys
65 70 75 80
Ser His Arg Ser Tyr Ser Cys Gln Val Thr His Glu Gly Ser Thr Val
85 90 95
Glu Lys Thr Val Ala Pro Thr Glu Cys Ser
100 105
<210> 197
<211> 978
<212> DNA
<213> 智人
<400> 197
gcctccacca agggcccctc cgtgttcccc ctggccccct gctccaggtc cacctccgag 60
tccaccgccg ccctgggctg cctggtgaag gactacttcc ccgagcccgt gaccgtgtcc 120
tggaactccg gcgccctgac ctccggcgtg cacaccttcc ccgccgtgct gcagtcctcc 180
ggcctgtact ccctgtcctc cgtggtgacc gtgccctcct cctccctggg caccaagacc 240
tacacctgca acgtggacca caagccctcc aacaccaagg tggacaagag ggtggagtcc 300
aagtacggcc ccccctgccc cccctgcccc gcccccgagg ccgccggcgg cccctccgtg 360
ttcctgttcc cccccaagcc caaggacacc ctgatgatct ccaggacccc cgaggtgacc 420
tgcgtggtgg tggacgtgtc ccaggaggac cccgaggtgc agttcaactg gtacgtggac 480
ggcgtggagg tgcacaacgc caagaccaag cccagggagg agcagttcaa ctccacctac 540
agggtggtgt ccgtgctgac cgtgctgcac caggactggc tgaacggcaa ggagtacaag 600
tgcaaggtgt ccaacaaggg cctgccctcc tccatcgaga agaccatctc caaggccaag 660
ggccagccca gggagcccca ggtgtacacc ctgcccccct cccaggagga gatgaccaag 720
aaccaggtgt ccctgacctg cctggtgaag ggcttctacc cctccgacat cgccgtggag 780
tgggagtcca acggccagcc cgagaacaac tacaagacca ccccccccgt gctggactcc 840
gacggctcct tcttcctgta ctccaggctg accgtggaca agtccaggtg gcaggagggc 900
aacgtgttct cctgctccgt gatgcacgag gccctgcaca accactacac ccagaagtcc 960
ctgtccctgt ccctgggc 978
<210> 198
<211> 326
<212> PRT
<213> 智人
<400> 198
Ala Ser Thr Lys Gly Pro Ser Val Phe Pro Leu Ala Pro Cys Ser Arg
1 5 10 15
Ser Thr Ser Glu Ser Thr Ala Ala Leu Gly Cys Leu Val Lys Asp Tyr
20 25 30
Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser
35 40 45
Gly Val His Thr Phe Pro Ala Val Leu Gln Ser Ser Gly Leu Tyr Ser
50 55 60
Leu Ser Ser Val Val Thr Val Pro Ser Ser Ser Leu Gly Thr Lys Thr
65 70 75 80
Tyr Thr Cys Asn Val Asp His Lys Pro Ser Asn Thr Lys Val Asp Lys
85 90 95
Arg Val Glu Ser Lys Tyr Gly Pro Pro Cys Pro Pro Cys Pro Ala Pro
100 105 110
Glu Ala Ala Gly Gly Pro Ser Val Phe Leu Phe Pro Pro Lys Pro Lys
115 120 125
Asp Thr Leu Met Ile Ser Arg Thr Pro Glu Val Thr Cys Val Val Val
130 135 140
Asp Val Ser Gln Glu Asp Pro Glu Val Gln Phe Asn Trp Tyr Val Asp
145 150 155 160
Gly Val Glu Val His Asn Ala Lys Thr Lys Pro Arg Glu Glu Gln Phe
165 170 175
Asn Ser Thr Tyr Arg Val Val Ser Val Leu Thr Val Leu His Gln Asp
180 185 190
Trp Leu Asn Gly Lys Glu Tyr Lys Cys Lys Val Ser Asn Lys Gly Leu
195 200 205
Pro Ser Ser Ile Glu Lys Thr Ile Ser Lys Ala Lys Gly Gln Pro Arg
210 215 220
Glu Pro Gln Val Tyr Thr Leu Pro Pro Ser Gln Glu Glu Met Thr Lys
225 230 235 240
Asn Gln Val Ser Leu Thr Cys Leu Val Lys Gly Phe Tyr Pro Ser Asp
245 250 255
Ile Ala Val Glu Trp Glu Ser Asn Gly Gln Pro Glu Asn Asn Tyr Lys
260 265 270
Thr Thr Pro Pro Val Leu Asp Ser Asp Gly Ser Phe Phe Leu Tyr Ser
275 280 285
Arg Leu Thr Val Asp Lys Ser Arg Trp Gln Glu Gly Asn Val Phe Ser
290 295 300
Cys Ser Val Met His Glu Ala Leu His Asn His Tyr Thr Gln Lys Ser
305 310 315 320
Leu Ser Leu Ser Leu Gly
325
<210> 199
<211> 20
<212> DNA
<213> 人工序列
<220>
<223> 合成构建体
<400> 199
tttggrggga agatgaagac 20
<210> 200
<211> 21
<212> DNA
<213> 人工序列
<220>
<223> 合成构建体
<400> 200
ttaacactct cccctgttga a 21
<210> 201
<211> 21
<212> DNA
<213> 人工序列
<220>
<223> 合成构建体
<400> 201
ttaacactca ttcctgttga a 21
<210> 202
<211> 21
<212> DNA
<213> 人工序列
<220>
<223> 合成构建体
<400> 202
tggacaggga tccagagttc c 21
<210> 203
<211> 21
<212> DNA
<213> 人工序列
<220>
<223> 合成构建体
<400> 203
tggacagggc tccatagttc c 21
<210> 204
<211> 20
<212> DNA
<213> 人工序列
<220>
<223> 合成构建体
<400> 204
actcgtcctt ggtcaacgtg 20
<210> 205
<211> 32
<212> PRT
<213> 智人
<400> 205
Ser Pro Lys Met Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp
1 5 10 15
Arg Ile Ser Ser Ser Ser Gly Leu Gly Cys Lys Val Leu Arg Arg His
20 25 30
<210> 206
<211> 30
<212> PRT
<213> 智人
<400> 206
Lys Met Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile
1 5 10 15
Ser Ser Ser Ser Gly Leu Gly Cys Lys Val Leu Arg Arg His
20 25 30
<210> 207
<211> 28
<212> PRT
<213> 智人
<400> 207
Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile Ser Ser
1 5 10 15
Ser Ser Gly Leu Gly Cys Lys Val Leu Arg Arg His
20 25
<210> 208
<211> 26
<212> PRT
<213> 智人
<400> 208
Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile Ser Ser Ser Ser
1 5 10 15
Gly Leu Gly Cys Lys Val Leu Arg Arg His
20 25
<210> 209
<211> 24
<212> PRT
<213> 智人
<400> 209
Gly Cys Phe Gly Arg Lys Met Asp Arg Ile Ser Ser Ser Ser Gly Leu
1 5 10 15
Gly Cys Lys Val Leu Arg Arg His
20
<210> 210
<211> 27
<212> PRT
<213> 智人
<400> 210
Lys Met Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile
1 5 10 15
Ser Ser Ser Ser Gly Leu Gly Cys Lys Val Leu
20 25
<210> 211
<211> 26
<212> PRT
<213> 智人
<400> 211
Lys Met Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile
1 5 10 15
Ser Ser Ser Ser Gly Leu Gly Cys Lys Val
20 25
<210> 212
<211> 27
<212> PRT
<213> 智人
<400> 212
Lys Met Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile
1 5 10 15
Ser Ser Ser Ser Gly Leu Gly Cys Asn Ser Phe
20 25
<210> 213
<211> 28
<212> PRT
<213> 智人
<400> 213
Ser Pro Lys Met Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp
1 5 10 15
Arg Ile Ser Ser Ser Ser Gly Leu Gly Cys Lys Val
20 25
<210> 214
<211> 29
<212> PRT
<213> 智人
<400> 214
Ser Pro Lys Met Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp
1 5 10 15
Arg Ile Ser Ser Ser Ser Gly Leu Gly Cys Asn Ser Phe
20 25
<210> 215
<211> 23
<212> PRT
<213> 智人
<400> 215
Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile Ser Ser Ser Ser
1 5 10 15
Gly Leu Gly Cys Lys Val Leu
20
<210> 216
<211> 21
<212> PRT
<213> 智人
<400> 216
Gly Cys Phe Gly Arg Lys Met Asp Arg Ile Ser Ser Ser Ser Gly Leu
1 5 10 15
Gly Cys Lys Val Leu
20
<210> 217
<211> 5
<212> PRT
<213> 人工序列
<220>
<223> 合成构建体
<400> 217
Gly Gly Gly Gly Ser
1 5
<210> 218
<211> 10
<212> PRT
<213> 人工序列
<220>
<223> 合成构建体
<400> 218
Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser
1 5 10
<210> 219
<211> 15
<212> PRT
<213> 人工序列
<220>
<223> 合成构建体
<400> 219
Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser
1 5 10 15
<210> 220
<211> 9
<212> PRT
<213> 小家鼠
<400> 220
Gln His Ser Tyr Ser Trp Pro Trp Thr
1 5
<210> 221
<211> 326
<212> PRT
<213> 智人
<400> 221
Ala Ser Thr Lys Gly Pro Ser Val Phe Pro Leu Ala Pro Cys Ser Arg
1 5 10 15
Ser Thr Ser Glu Ser Thr Ala Ala Leu Gly Cys Leu Val Lys Asp Tyr
20 25 30
Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser
35 40 45
Gly Val His Thr Phe Pro Ala Val Leu Gln Ser Ser Gly Leu Tyr Ser
50 55 60
Leu Ser Ser Val Val Thr Val Pro Ser Ser Asn Phe Gly Thr Gln Thr
65 70 75 80
Tyr Thr Cys Asn Val Asp His Lys Pro Ser Asn Thr Lys Val Asp Lys
85 90 95
Thr Val Glu Arg Lys Cys Cys Val Glu Cys Pro Pro Cys Pro Ala Pro
100 105 110
Pro Val Ala Gly Pro Ser Val Phe Leu Phe Pro Pro Lys Pro Lys Asp
115 120 125
Thr Leu Met Ile Ser Arg Thr Pro Glu Val Thr Cys Val Val Val Asp
130 135 140
Val Ser His Glu Asp Pro Glu Val Gln Phe Asn Trp Tyr Val Asp Gly
145 150 155 160
Val Glu Val His Asn Ala Lys Thr Lys Pro Arg Glu Glu Gln Phe Asn
165 170 175
Ser Thr Phe Arg Val Val Ser Val Leu Thr Val Val His Gln Asp Trp
180 185 190
Leu Asn Gly Lys Glu Tyr Lys Cys Lys Val Ser Asn Lys Gly Leu Pro
195 200 205
Ala Pro Ile Glu Lys Thr Ile Ser Lys Thr Lys Gly Gln Pro Arg Glu
210 215 220
Pro Gln Val Tyr Thr Leu Pro Pro Ser Arg Glu Glu Met Thr Lys Asn
225 230 235 240
Gln Val Ser Leu Thr Cys Leu Val Lys Gly Phe Tyr Pro Ser Asp Ile
245 250 255
Ser Val Glu Trp Glu Ser Asn Gly Gln Pro Glu Asn Asn Tyr Lys Thr
260 265 270
Thr Pro Pro Met Leu Asp Ser Asp Gly Ser Phe Phe Leu Tyr Ser Lys
275 280 285
Leu Thr Val Asp Lys Ser Arg Trp Gln Gln Gly Asn Val Phe Ser Cys
290 295 300
Ser Val Met His Glu Ala Leu His Asn His Tyr Thr Gln Lys Ser Leu
305 310 315 320
Ser Leu Ser Pro Gly Lys
325
<210> 222
<211> 214
<212> PRT
<213> 智人
<400> 222
Glu Ile Val Leu Thr Gln Ser Pro Asp Phe Gln Ser Val Thr Pro Lys
1 5 10 15
Glu Lys Val Thr Ile Thr Cys Arg Ala Ser Gln Asn Ile Gly Thr Ser
20 25 30
Ile His Trp Tyr Gln Gln Lys Pro Asp Gln Tyr Pro Lys Leu Leu Ile
35 40 45
Lys Tyr Ala Ser Lys Ser Ile Ser Gly Val Pro Ser Arg Phe Ser Gly
50 55 60
Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Asn Ser Leu Glu Ala
65 70 75 80
Glu Asp Ala Ala Thr Tyr Tyr Cys Gln His Ser Tyr Ser Phe Pro Trp
85 90 95
Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys Arg Thr Val Ala Ala
100 105 110
Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Glu Gln Leu Lys Ser Gly
115 120 125
Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe Tyr Pro Arg Glu Ala
130 135 140
Lys Val Gln Trp Lys Val Asp Asn Ala Leu Gln Ser Gly Asn Ser Gln
145 150 155 160
Glu Ser Val Thr Glu Gln Asp Ser Lys Asp Ser Thr Tyr Ser Leu Ser
165 170 175
Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys His Lys Val Tyr
180 185 190
Ala Cys Glu Val Thr His Gln Gly Leu Ser Ser Pro Val Thr Lys Ser
195 200 205
Phe Asn Arg Gly Glu Cys
210
<210> 223
<211> 470
<212> PRT
<213> 智人
<400> 223
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Gly Cys
435 440 445
Phe Gly Arg Lys Met Asp Arg Ile Ser Ser Ser Ser Gly Leu Gly Cys
450 455 460
Lys Val Leu Arg Arg His
465 470
<210> 224
<211> 488
<212> PRT
<213> 智人
<400> 224
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Gly Gly
435 440 445
Gly Gly Ser Gly Gly Gly Gly Ser Ser Pro Lys Met Val Gln Gly Ser
450 455 460
Gly Cys Phe Gly Arg Lys Met Asp Arg Ile Ser Ser Ser Ser Gly Leu
465 470 475 480
Gly Cys Lys Val Leu Arg Arg His
485
<210> 225
<211> 483
<212> PRT
<213> 智人
<400> 225
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Gly Gly
435 440 445
Gly Gly Ser Ser Pro Lys Met Val Gln Gly Ser Gly Cys Phe Gly Arg
450 455 460
Lys Met Asp Arg Ile Ser Ser Ser Ser Gly Leu Gly Cys Lys Val Leu
465 470 475 480
Arg Arg His
<210> 226
<211> 478
<212> PRT
<213> 智人
<400> 226
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Ser Pro
435 440 445
Lys Met Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile
450 455 460
Ser Ser Ser Ser Gly Leu Gly Cys Lys Val Leu Arg Arg His
465 470 475
<210> 227
<211> 476
<212> PRT
<213> 智人
<400> 227
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Lys Met
435 440 445
Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile Ser Ser
450 455 460
Ser Ser Gly Leu Gly Cys Lys Val Leu Arg Arg His
465 470 475
<210> 228
<211> 472
<212> PRT
<213> 智人
<400> 228
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Gly Ser
435 440 445
Gly Cys Phe Gly Arg Lys Met Asp Arg Ile Ser Ser Ser Ser Gly Leu
450 455 460
Gly Cys Lys Val Leu Arg Arg His
465 470
<210> 229
<211> 474
<212> PRT
<213> 智人
<400> 229
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Ser Pro
435 440 445
Lys Met Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile
450 455 460
Ser Ser Ser Ser Gly Leu Gly Cys Lys Val
465 470
<210> 230
<211> 472
<212> PRT
<213> 智人
<400> 230
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Lys Met
435 440 445
Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile Ser Ser
450 455 460
Ser Ser Gly Leu Gly Cys Lys Val
465 470
<210> 231
<211> 478
<212> PRT
<213> 智人
<400> 231
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Ser Pro
435 440 445
Lys Met Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile
450 455 460
Ser Ser Ser Ser Gly Leu Gly Cys Lys Val Leu Asn Ser Phe
465 470 475
<210> 232
<211> 473
<212> PRT
<213> 智人
<400> 232
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Lys Met
435 440 445
Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile Ser Ser
450 455 460
Ser Ser Gly Leu Gly Cys Lys Val Leu
465 470
<210> 233
<211> 476
<212> PRT
<213> 智人
<400> 233
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Lys Met
435 440 445
Val Gln Gly Ser Gly Cys Phe Gly Arg Lys Met Asp Arg Ile Ser Ser
450 455 460
Ser Ser Gly Leu Gly Cys Lys Val Leu Asn Ser Phe
465 470 475
<210> 234
<211> 469
<212> PRT
<213> 智人
<400> 234
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Gly Ser
435 440 445
Gly Cys Phe Gly Arg Lys Met Asp Arg Ile Ser Ser Ser Ser Gly Leu
450 455 460
Gly Cys Lys Val Leu
465
<210> 235
<211> 467
<212> PRT
<213> 智人
<400> 235
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly Gly Cys
435 440 445
Phe Gly Arg Lys Met Asp Arg Ile Ser Ser Ser Ser Gly Leu Gly Cys
450 455 460
Lys Val Leu
465
<210> 236
<211> 446
<212> PRT
<213> 智人
<400> 236
Gln Val Thr Leu Lys Glu Ser Gly Pro Thr Leu Val Lys Pro Thr Gln
1 5 10 15
Thr Leu Thr Leu Thr Cys Thr Phe Ser Gly Phe Ser Leu Thr Thr Ser
20 25 30
Gly Leu Gly Val Ala Trp Ile Arg Gln Pro Pro Gly Lys Ala Leu Glu
35 40 45
Trp Leu Ala His Ile Trp Ser Asp Gly Asp Thr Arg Tyr Tyr Pro Ala
50 55 60
Leu Lys Asn Arg Leu Thr Ile Thr Lys Asp Thr Ser Lys Asn Gln Val
65 70 75 80
Val Leu Thr Met Thr Asn Met Asp Pro Val Asp Thr Ala Thr Tyr Tyr
85 90 95
Cys Ala His Met Lys Asp Asp Ser Leu Tyr Phe Asp Asn Trp Gly Gln
100 105 110
Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val
115 120 125
Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala
130 135 140
Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser
145 150 155 160
Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val
165 170 175
Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro
180 185 190
Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys
195 200 205
Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro
210 215 220
Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val
225 230 235 240
Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
245 250 255
Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro Glu
260 265 270
Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
275 280 285
Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser
290 295 300
Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
305 310 315 320
Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile
325 330 335
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
340 345 350
Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu
355 360 365
Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
370 375 380
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser
385 390 395 400
Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg
405 410 415
Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
420 425 430
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly
435 440 445
Claims (56)
1.一种ETA抗体与BNP的融合蛋白质,其结构特征在于:所述的融合蛋白质包含一个ETA抗体和一或多个BNP。
2.权利要求1所述的融合蛋白质,其中所述的ETA抗体包含一、两、三、四、五、或六个氨基酸序列,其中每个氨基酸序列独立地选自以下所列的氨基酸序列:
a.轻链CDR1氨基酸序列:SEQ ID NO:8、SEQ ID NO:10、SEQ ID NO:12、SEQ ID NO:14、SEQ ID NO:16、SEQ ID NO:18、SEQ ID NO:20、SEQ ID NO:22、SEQ ID NO:24、SEQ ID NO:26、SEQ ID NO:28、及SEQ ID NO:30;
b.轻链CDR2氨基酸序列:SEQ ID NO:32、SEQ ID NO:34、SEQ ID NO:36、SEQ ID NO:38、SEQ ID NO:40、SEQ ID NO:42、SEQ ID NO:44、SEQ ID NO:46、及SEQ ID NO:48;
c.轻链CDR3氨基酸序列:SEQ ID NO:50、SEQ ID NO:52、SEQ ID NO:54、SEQ ID NO:56、SEQ ID NO:58、SEQ ID NO:60、SEQ ID NO:62、SEQ ID NO:64、SEQ ID NO:66、SEQ ID NO:68,及SEQ ID NO:220;
d.重链CDR1氨基酸序列:SEQ ID NO:70、SEQ ID NO:72、SEQ ID NO:74、SEQ ID NO:76、SEQ ID NO:78、SEQ ID NO:80、SEQ ID NO:82、SEQ ID NO:84、SEQ ID NO:86、SEQ ID NO:88、及SEQ ID NO:90;
e.重链CDR2氨基酸序列:SEQ ID NO:92、SEQ ID NO:94、SEQ ID NO:96、SEQ ID NO:98、SEQ ID NO:100、SEQ ID NO:102、SEQ ID NO:104、SEQ ID NO:106、SEQ ID NO:108、SEQ IDNO:110、SEQ ID NO:112、及SEQ ID NO:114;及
f.重链CDR3氨基酸序列:SEQ ID NO:116、SEQ ID NO:118、SEQ ID NO:120、SEQ ID NO:122、SEQ ID NO:124、SEQ ID NO:126、SEQ ID NO:128、SEQ ID NO:130、SEQ ID NO:132、SEQID NO:134、及SEQ ID NO:136。
3.权利要求1或2所述的融合蛋白质,其中所述的ETA抗体包含一或两个氨基酸序列,其中每个氨基酸序列独立地选自以下所列的氨基酸序列:
a.轻链CDR1氨基酸序列:SEQ ID NO:8、SEQ ID NO:10、SEQ ID NO:12、SEQ ID NO:14、SEQ ID NO:16、SEQ ID NO:18、SEQ ID NO:20、SEQ ID NO:22、SEQ ID NO:24、SEQ ID NO:26、SEQ ID NO:28、及SEQ ID NO:30;及
b.重链CDR1氨基酸序列:SEQ ID NO:70、SEQ ID NO:72、SEQ ID NO:74、SEQ ID NO:76、SEQ ID NO:78、SEQ ID NO:80、SEQ ID NO:82、SEQ ID NO:84、SEQ ID NO:86、SEQ ID NO:88、及SEQ ID NO:90。
4.权利要求1至3中任一项所述的融合蛋白质,其中所述的ETA抗体包含一或两个氨基酸序列,其中每个氨基酸序列独立地选自于以下所列的氨基酸序列:
a.轻链CDR2氨基酸序列:SEQ ID NO:32、SEQ ID NO:34、SEQ ID NO:36、SEQ ID NO:38、SEQ ID NO:40、SEQ ID NO:42、SEQ ID NO:44、SEQ ID NO:46、及SEQ ID NO:48;及
b.重链CDR2氨基酸序列:SEQ ID NO:92、SEQ ID NO:94、SEQ ID NO:96、SEQ ID NO:98、SEQ ID NO:100、SEQ ID NO:102、SEQ ID NO:104、SEQ ID NO:106、SEQ ID NO:108、SEQ IDNO:110、SEQ ID NO:112、及SEQ ID NO:114。
5.权利要求1至4中任一项所述的融合蛋白质,其中所述的ETA抗体包含一或两个氨基酸序列,其中每个氨基酸序列独立地选自于以下所列的氨基酸序列:
a.轻链CDR3氨基酸序列:SEQ ID NO:50、SEQ ID NO:52、SEQ ID NO:54、SEQ ID NO:56、SEQ ID NO:58、SEQ ID NO:60、SEQ ID NO:62、SEQ ID NO:64、SEQ ID NO:66、SEQ ID NO:68,及SEQ ID NO:220;及
b.重链CDR3氨基酸序列:SEQ ID NO:116、SEQ ID NO:118、SEQ ID NO:120、SEQ ID NO:122、SEQ ID NO:124、SEQ ID NO:126、SEQ ID NO:128、SEQ ID NO:130、SEQ ID NO:132、SEQID NO:134、及SEQ ID NO:136。
6.权利要求1至5中任一项所述的融合蛋白质,其中所述的ETA抗体包含一或两个氨基酸序列,其中每个氨基酸序列独立地选自于以下所列的氨基酸序列:SEQ ID NO:8、SEQ IDNO:20、SEQ ID NO:22、SEQ ID NO:24、SEQ ID NO:26、SEQ ID NO:28、SEQ ID NO:30、SEQ IDNO:32、SEQ ID NO:44、SEQ ID NO:46、SEQ ID NO:48、SEQ ID NO:50、SEQ ID NO:62、SEQ IDNO:64、SEQ ID NO:66、SEQ ID NO:68,及SEQ ID NO:220。
7.权利要求1至6中任一项所述的融合蛋白质,其中所述的ETA抗体包含一或两个氨基酸序列,其中每个氨基酸序列独立地选自于以下所列的氨基酸序列:SEQ ID NO:70、SEQ IDNO:82、SEQ ID NO:84、SEQ ID NO:86、SEQ ID NO:88、SEQ ID NO:90、SEQ ID NO:92、SEQ IDNO:104、SEQ ID NO:106、SEQ ID NO:108、SEQ ID NO:110、SEQ ID NO:112、SEQ ID NO:114、SEQ ID NO:116、SEQ ID NO:128、SEQ ID NO:130、SEQ ID NO:132、SEQ ID NO:134、及SEQID NO:136。
8.权利要求1至7中任一项所述的融合蛋白质,其中所述的ETA抗体包含一个独立地选自于以下所列的轻链与重链CDR3氨基酸序列的组合:SEQ ID NO:50与SEQ ID NO:116、SEQID NO:50与SEQ ID NO:220、SEQ ID NO:62与SEQ ID NO:128、SEQ ID NO:62与SEQ ID NO:130、SEQ ID NO:64与SEQ ID NO:132、SEQ ID NO:66与SEQ ID NO:134、及SEQ ID NO:68与SEQ ID NO:136。
9.权利要求1至8中任一项所述的融合蛋白质,其中所述的ETA抗体包含
(a)轻链CDR1氨基酸序列:SEQ ID NO:8;
轻链CDR2氨基酸序列:SEQ ID NO:32;
轻链CDR3氨基酸序列:SEQ ID NO:50或SEQ ID NO:220;
重链CDR1氨基酸序列:SEQ ID NO:70;
重链CDR2氨基酸序列:SEQ ID NO:92;及
重链CDR3氨基酸序列:SEQ ID NO:116;
(b)轻链CDR1氨基酸序列:SEQ ID NO:10;
轻链CDR2氨基酸序列:SEQ ID NO:34;
轻链CDR3氨基酸序列:SEQ ID NO:52;
重链CDR1氨基酸序列:SEQ ID NO:72;
重链CDR2氨基酸序列:SEQ ID NO:94;及
重链CDR3氨基酸序列:SEQ ID NO:118;
(c)轻链CDR1氨基酸序列:SEQ ID NO:12;
轻链CDR2氨基酸序列:SEQ ID NO:36;
轻链CDR3氨基酸序列:SEQ ID NO:54;
重链CDR1氨基酸序列:SEQ ID NO:74;
重链CDR2氨基酸序列:SEQ ID NO:96;及
重链CDR3氨基酸序列:SEQ ID NO:120;
(d)轻链CDR1氨基酸序列:SEQ ID NO:14;
轻链CDR2氨基酸序列:SEQ ID NO:38;
轻链CDR3氨基酸序列:SEQ ID NO:56;
重链CDR1氨基酸序列:SEQ ID NO:76;
重链CDR2氨基酸序列:SEQ ID NO:98;及
重链CDR3氨基酸序列:SEQ ID NO:122;
(e)轻链CDR1氨基酸序列:SEQ ID NO:16;
轻链CDR2氨基酸序列:SEQ ID NO:40;
轻链CDR3氨基酸序列:SEQ ID NO:58;
重链CDR1氨基酸序列:SEQ ID NO:78;
重链CDR2氨基酸序列:SEQ ID NO:100;及
重链CDR3氨基酸序列:SEQ ID NO:124;
(f)轻链CDR1氨基酸序列:SEQ ID NO:18;
轻链CDR2氨基酸序列:SEQ ID NO:42;
轻链CDR3氨基酸序列:SEQ ID NO:60;
重链CDR1氨基酸序列:SEQ ID NO:80;
重链CDR2氨基酸序列:SEQ ID NO:102;及
重链CDR3氨基酸序列:SEQ ID NO:126;
(g)轻链CDR1氨基酸序列:SEQ ID NO:20或22;
轻链CDR2氨基酸序列:SEQ ID NO:44;
轻链CDR3氨基酸序列:SEQ ID NO:62;
重链CDR1氨基酸序列:SEQ ID NO:82;
重链CDR2氨基酸序列:SEQ ID NO:104或106;及
重链CDR3氨基酸序列:SEQ ID NO:128;
(h)轻链CDR1氨基酸序列:SEQ ID NO:24;
轻链CDR2氨基酸序列:SEQ ID NO:44;
轻链CDR3氨基酸序列:SEQ ID NO:62;
重链CDR1氨基酸序列:SEQ ID NO:84;
重链CDR2氨基酸序列:SEQ ID NO:108;及
重链CDR3氨基酸序列:SEQ ID NO:130;
(i)轻链CDR1氨基酸序列:SEQ ID NO:26;
轻链CDR2氨基酸序列:SEQ ID NO:46;
轻链CDR3氨基酸序列:SEQ ID NO:64;
重链CDR1氨基酸序列:SEQ ID NO:86;
重链CDR2氨基酸序列:SEQ ID NO:110;及
重链CDR3氨基酸序列:SEQ ID NO:132;
(j)轻链CDR1氨基酸序列:SEQ ID NO:28;
轻链CDR2氨基酸序列:SEQ ID NO:46;
轻链CDR3氨基酸序列:SEQ ID NO:66;
重链CDR1氨基酸序列:SEQ ID NO:88;
重链CDR2氨基酸序列:SEQ ID NO:112;及
重链CDR3氨基酸序列:SEQ ID NO:134;或
(k)轻链CDR1氨基酸序列:SEQ ID NO:30;
轻链CDR2氨基酸序列:SEQ ID NO:48;
轻链CDR3氨基酸序列:SEQ ID NO:68;
重链CDR1氨基酸序列:SEQ ID NO:90;
重链CDR2氨基酸序列:SEQ ID NO:114;及
重链CDR3氨基酸序列:SEQ ID NO:136。
10.权利要求9所述的融合蛋白质,其中所述的ETA抗体包含
轻链CDR1氨基酸序列:SEQ ID NO:28;
轻链CDR2氨基酸序列:SEQ ID NO:46;
轻链CDR3氨基酸序列:SEQ ID NO:66;
重链CDR1氨基酸序列:SEQ ID NO:88;
重链CDR2氨基酸序列:SEQ ID NO:112;及
重链CDR3氨基酸序列:SEQ ID NO:134。
11.权利要求1至10中任一项所述的融合蛋白质,其中所述的ETA抗体包含一或两个氨基酸序列,其中每个氨基酸序列独立地选自于以下所列的氨基酸序列:
a.轻链可变结构域氨基酸序列:SEQ ID NO:138、SEQ ID NO:140、SEQ ID NO:142、SEQID NO:144、SEQ ID NO:146、SEQ ID NO:148、SEQ ID NO:150、SEQ ID NO:152、SEQ ID NO:154、SEQ ID NO:156、SEQ ID NO:158、SEQ ID NO:160、SEQ ID NO:162、及SEQ ID NO:164;及
b.重链可变结构域氨基酸序列:SEQ ID NO:166、SEQ ID NO:168、SEQ ID NO:170、SEQID NO:172、SEQ ID NO:174、SEQ ID NO:176、SEQ ID NO:178、SEQ ID NO:180、SEQ ID NO:182、SEQ ID NO:184、SEQ ID NO:186、SEQ ID NO:188、SEQ ID NO:190、及SEQ ID NO:192。
12.权利要求1至11中任一项所述的融合蛋白质,其中所述的ETA抗体的多聚核苷酸编码序列包含一或两个多聚核苷酸序列,其中每个多聚核苷酸列独立地选自于以下所列多聚核苷酸序列:
a.轻链可变结构域多聚核苷酸编码序列:SEQ ID NO:137、SEQ ID NO:139、SEQ ID NO:141、SEQ ID NO:143、SEQ ID NO:145、SEQ ID NO:147、SEQ ID NO:149、SEQ ID NO:151、SEQID NO:153、SEQ ID NO:155、SEQ ID NO:157、SEQ ID NO:159、SEQ ID NO:161、及SEQ IDNO:163;
b.重链可变结构域多聚核苷酸编码序列:SEQ ID NO:165、SEQ ID NO:167、SEQ ID NO:169、SEQ ID NO:171、SEQ ID NO:173、SEQ ID NO:175、SEQ ID NO:177、SEQ ID NO:179、SEQID NO:181、SEQ ID NO:183、SEQ ID NO:185、SEQ ID NO:187、SEQ ID NO:189、及SEQ IDNO:191。
13.权利要求1至12中任一项所述的融合蛋白质,其中所述的ETA抗体包含一个独立地选自于以下所列的氨基酸序列的组合:SEQ ID NO:138和SEQ ID NO:166、SEQ ID NO:140和SEQ ID NO:168、SEQ ID NO:142和SEQ ID NO:170、SEQ ID NO:144和SEQ ID NO:172、SEQID NO:146和SEQ ID NO:174、SEQ ID NO:148和SEQ ID NO:176、SEQ ID NO:150和SEQ IDNO:178、SEQ ID NO:152和SEQ ID NO:180、SEQ ID NO:154和SEQ ID NO:182、SEQ ID NO:156和SEQ ID NO:184、SEQ ID NO:158和SEQ ID NO:186、SEQ ID NO:160和SEQ ID NO:188、SEQ ID NO:162和SEQ ID NO:190、及SEQ ID NO:164和SEQ ID NO:192。
14.权利要求1至13中任一项所述的融合蛋白质,其中所述的ETA抗体包含一个独立地选自于以下所列的氨基酸序列:SEQ ID NO:138、SEQ ID NO:150、SEQ ID NO:152、SEQ IDNO:154、SEQ ID NO:156、SEQ ID NO:158、SEQ ID NO:160、SEQ ID NO:162、及SEQ ID NO:164。
15.权利要求1至14中任一项所述的融合蛋白质,其中所述的ETA抗体包含一个独立地选自于以下所列的氨基酸序列:SEQ ID NO:166、SEQ ID NO:178、SEQ ID NO:180、SEQ IDNO:182、SEQ ID NO:184、SEQ ID NO:186、SEQ ID NO:188、SEQ ID NO:190、及SEQ ID NO:192。
16.权利要求1至15中任一项所述的融合蛋白质,其中所述的ETA抗体包含一个独立地选自于以下所列的轻链与重链可变区氨基酸序列的组合:SEQ ID NO:138与SEQ ID NO:166、SEQ ID NO:150与SEQ ID NO:178、SEQ ID NO:152与SEQ ID NO:180、SEQ ID NO:154与SEQ ID NO:182、SEQ ID NO:156与SEQ ID NO:184、SEQ ID NO:158与SEQ ID NO:186、SEQID NO:160与SEQ ID NO:188、SEQ ID NO:162与SEQ ID NO:190、及SEQ ID NO:164与SEQ IDNO:192。
17.权利要求16所述的融合蛋白质,其中所述的ETA抗体包含氨基酸序列SEQ ID NO:138或SEQ ID NO:166。
18.权利要求16所述的融合蛋白质,其中所述的ETA抗体包含的SEQ ID NO:138和SEQID NO:166氨基酸序列的组合。
19.权利要求16所述的融合蛋白质,其中所述的ETA抗体包含氨基酸序列SEQ ID NO:162或SEQ ID NO:190。
20.权利要求16所述的融合蛋白质,其中所述的ETA抗体包含的SEQ ID NO:162和SEQID NO:190氨基酸序列的组合。
21.权利要求1至20中任一项所述的融合蛋白质,其中所述的ETA抗体包含一或两个氨基酸序列,其中每个氨基酸序列独立地选自于以下所列的氨基酸序列:
a.轻链恒定氨基酸序列:SEQ ID NO:194及SEQ ID NO:196;
b.重链恒定氨基酸序列:SEQ ID NO:198及SEQ ID NO:221。
22.权利要求1所述的融合蛋白质,其中所述的ETA抗体具有一个或多个以下所列的性质:
a.当与人内皮素受体ETA结合时,其Kd与一参比ETA抗体相同或更优;
b.当抑制人内皮素受体ETA的内皮素激活时,其IC50与一参比ETA抗体相同或更优;和
c.该ETA抗体在人内皮素受体ETA上与一参比ETA抗体交叉竞争结合。
23.权利要求22所述的融合蛋白质,其中所述的ETA抗体在人内皮素受体ETA上与所述的参比ETA抗体交叉竞争结合。
24.权利要求22或23所述的融合蛋白质,其中所述的参比ETA抗体包含权利要求1至21中任一项所述的抗体。
25.权利要求24所述的融合蛋白质,其中所述的参比ETA抗体包含轻链可变结构域氨基酸序列SEQ ID NO:138和重链可变结构域氨基酸序列SEQ ID NO:166的组合或轻链可变结构域氨基酸序列SEQ ID NO:162和重链可变结构域氨基酸序列SEQ ID NO:190的组合。
26.权利要求1至25中任一项所述的融合蛋白质,其中所述的ETA抗体包含鼠源ETA抗体或人源化ETA抗体。
27.权利要求1至26中任一项所述的融合蛋白质,其中所述的ETA抗体包含ETA单克隆抗体。
28.权利要求1至27中任一项所述的融合蛋白质,其中所述的ETA抗体的降低人内皮素信号传导的IC50值大约为1nM至200nM或10nM至100nM。
29.权利要求1至28中任一项所述的融合蛋白质,其中所述的融合蛋白质包含一个ETA抗体、和一个,二个,三个,四个,五个,六个,七个,或八个BNP;该融合蛋白质将一BNP的氨基端与所述ETA抗体的轻链或重链的羧基端连接,或者该融合蛋白质将一BNP的羧基端与所述ETA抗体的轻链或重链的氨基端连接。
30.权利要求29所述的融合蛋白质,其中所述的融合蛋白质包含一个ETA抗体、和一个,二个,三个,或四个BNP。
31.权利要求29所述的融合蛋白质,其中所述的融合蛋白质包含一个ETA抗体、和一个或二个BNP。
32.权利要求29所述的融合蛋白质,其中所述的融合蛋白质包含一个ETA抗体和二个BNP。
33.权利要求29至32中任一项所述的融合蛋白质,其中所述的融合蛋白质将一BNP的氨基端与所述ETA抗体的轻链或重链的羧基端连接。
34.权利要求29至33中任一项所述的融合蛋白质,其中所述的融合蛋白质将一BNP的氨基端与所述ETA抗体的重链的羧基端连接。
35.权利要求1至34中任一项所述的融合蛋白质,其中所述的融合蛋白质包含氨基酸序列:SEQ ID NO:162和SEQ ID NO:190,以及SEQ ID NO:209或SEQ ID NO:210。
36.权利要求1至28中任一项所述的融合蛋白质,其中所述的融合蛋白质包含一个ETA抗体、和一个,二个,三个,四个,五个,六个,七个,或八个BNP和肽接头(Linker);该融合蛋白质通过一肽接头序列将一BNP的氨基端与所述ETA抗体的轻链或重链的羧基端连接,或者该融合蛋白质通过一肽接头序列将一BNP的羧基端与所述ETA抗体的轻链或重链的氨基端连接。
37.权利要求36的融合蛋白质,其中所述的融合蛋白质包含一个ETA抗体、和一个,二个,三个,或四个BNP和肽接头(Linker)。
38.权利要求36的融合蛋白质,其中所述的融合蛋白质包含一个ETA抗体和二个BNP和二个肽接头(Linker)。
39.权利要求36的融合蛋白质,其中所述的融合蛋白质包含一个ETA抗体,一个BNP和一个肽接头(Linker)。
40.权利要求36至39中任一项所述的融合蛋白质,其中所述的融合蛋白质通过一肽接头序列将一BNP的氨基端与所述ETA抗体的轻链或重链的羧基端连接。
41.权利要求36至40中任一项所述的融合蛋白质,其中所述的融合蛋白质通过一肽接头序列将一BNP的氨基端与所述ETA抗体的重链的羧基端连接。
42.权利要求36至41中任一项所述的融合蛋白质,其中所述的融合蛋白质包含氨基酸序列:SEQ ID NO:162,SEQ ID NO:190,SEQ ID NO:205,和SEQ ID NO:218。
43.权利要求36至42中任一项的融合蛋白质,其中所述的ETA抗体、BNP和肽接头序列通过以下所述中一方式融合形成所述的融合蛋白质:
(1)通过一个肽接头序列将一BNP的氨基端和所述ETA抗体的重链/轻链的羧基端连接:N'-R-Linker-BNP-C';及
(2)通过一肽接头序列将一BNP的羧基端与所述ETA抗体的轻链或重链的氨基端连接:N'-BNP-Linker-R-C';
其中:N'代表多肽链的氨基端,C'代表多肽链的羧基端,BNP代表一BNP,R为所述的ETA抗体的轻链或者重链的氨基酸序列,及Linker代表一肽接头。
44.权利要求1至43中任一项的融合蛋白质,其中所述的BNP各独立地包含选自于以下之一的氨基酸序列:SEQ ID NO:205、SEQ ID NO:206、SEQ ID NO:207、SEQ ID NO:208、SEQID NO:209、SEQ ID NO:210、SEQ ID NO:211、SEQ ID NO:212、SEQ ID NO:213、SEQ ID NO:214、SEQ ID NO:215、及SEQ ID NO:216。
45.权利要求44的融合蛋白质,其中所述的BNP各独立地选自于以下之一的氨基酸序列:SEQ ID NO:205、SEQ ID NO:209、及SEQ ID NO:210。
46.权利要求36至45中任一项的融合蛋白质,其中所述的肽接头(Linker)的序列各自独立地包含以下之一的氨基酸序列:SEQ ID NO:217、SEQ ID NO:218、及SEQ ID NO:219。
47.权利要求46的融合蛋白质,其中所述的肽接头(Linker)的序列为SEQ ID NO:218。
48.一种多核苷酸,其编码权利要求1至47中任一项所述的融合蛋白质。
49.一种载体,其包含权利要求48中所述的一多核苷酸。
50.一种宿主细胞,其包含权利要求49中所述的一载体。
51.一种药用组合物,其包含权利要求1至47中任一项所述的融合蛋白质和一药用可接受的载体。
52.一种包含权利要求1至47中任一项所述的融合蛋白质在制备用于预防、改善、或治疗肺动脉高压的药物中的用途。
53.一种包含权利要求1至47中任一项所述的融合蛋白质在制备用于预防、改善、或治疗肺高压的药物中的用途。
54.一种包含权利要求1至47中任一项所述的融合蛋白质在制备用于预防、改善、或治疗心力衰竭的药物中的用途。
55.一种包含权利要求1至47中任一项所述的融合蛋白质在制备用于预防、改善、或治疗肺动脉高压,肺高压或者心力衰竭二种及二种以上病症的药物中的用途。
56.根据权利要求52至55中任一项所述的用途,其所述的药物是用于静脉或皮下注射。
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910496142.4A CN112062857B (zh) | 2019-06-10 | 2019-06-10 | Eta抗体与bnp的融合蛋白质,及其药物组合物和应用 |
PCT/CN2020/095062 WO2020248967A1 (zh) | 2019-06-10 | 2020-06-09 | Eta抗体与bnp的融合蛋白质,以及其药物组合物和应用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910496142.4A CN112062857B (zh) | 2019-06-10 | 2019-06-10 | Eta抗体与bnp的融合蛋白质,及其药物组合物和应用 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN112062857A true CN112062857A (zh) | 2020-12-11 |
CN112062857B CN112062857B (zh) | 2024-08-09 |
Family
ID=73658711
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201910496142.4A Active CN112062857B (zh) | 2019-06-10 | 2019-06-10 | Eta抗体与bnp的融合蛋白质,及其药物组合物和应用 |
Country Status (2)
Country | Link |
---|---|
CN (1) | CN112062857B (zh) |
WO (1) | WO2020248967A1 (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2022206857A1 (zh) * | 2021-03-31 | 2022-10-06 | 鸿运华宁(杭州)生物医药有限公司 | 一种能与人内皮素受体特异性结合的抗体及其在糖尿病肾病和慢性肾病治疗中的应用 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102510719A (zh) * | 2009-08-10 | 2012-06-20 | 得克萨斯大学体系董事会 | 用与细胞毒性化学治疗剂组合的内皮素受体抑制剂治疗脑转移 |
CN107987162A (zh) * | 2016-10-27 | 2018-05-04 | 鸿运华宁(杭州)生物医药有限公司 | Etar抗体,其药物组合物及其应用 |
US20190022165A1 (en) * | 2016-03-02 | 2019-01-24 | Stealth Biotherapeutics Corp | Methods and compositions for the treatment and prevention of pulmonary arterial hypertension |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2173773A4 (en) * | 2007-07-06 | 2010-07-07 | Theratechnologies Inc | BIFUNCTIONAL FUSION PROTEINS OF ALPHA-MELANOCYTE STIMULATION HORMONE (ALPHA-MSH) AND AURICULAR NATRIURETIC PROTEIN (ANP), AND USES THEREOF IN HYPERTENSION AND ACUTE RENAL INJURY |
CN105669863B (zh) * | 2014-12-05 | 2019-09-13 | 鸿运华宁(杭州)生物医药有限公司 | 一种能与人内皮素受体特异性结合的抗体及其应用 |
-
2019
- 2019-06-10 CN CN201910496142.4A patent/CN112062857B/zh active Active
-
2020
- 2020-06-09 WO PCT/CN2020/095062 patent/WO2020248967A1/zh active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102510719A (zh) * | 2009-08-10 | 2012-06-20 | 得克萨斯大学体系董事会 | 用与细胞毒性化学治疗剂组合的内皮素受体抑制剂治疗脑转移 |
US20190022165A1 (en) * | 2016-03-02 | 2019-01-24 | Stealth Biotherapeutics Corp | Methods and compositions for the treatment and prevention of pulmonary arterial hypertension |
CN107987162A (zh) * | 2016-10-27 | 2018-05-04 | 鸿运华宁(杭州)生物医药有限公司 | Etar抗体,其药物组合物及其应用 |
Non-Patent Citations (2)
Title |
---|
CARMINE DARIO VIZZA 等: "Venous endotelin-1 (ET-1) and brain natriuretic peptide (BNP) plasma levels during 6-month bosentan treatment for pulmonary arterial hypertension", REGUL PEPT, vol. 151, no. 1, pages 48 - 53, XP025680337, DOI: 10.1016/j.regpep.2008.08.002 * |
JARKKO PIUHOLA 等: "Direct cardiac actions of erythropoietin (EPO): effects on cardiac contractility, BNP secretion and ischaemia/reperfusion injury", CLIN SCI (LOND), vol. 114, no. 4, pages 293 - 304 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2022206857A1 (zh) * | 2021-03-31 | 2022-10-06 | 鸿运华宁(杭州)生物医药有限公司 | 一种能与人内皮素受体特异性结合的抗体及其在糖尿病肾病和慢性肾病治疗中的应用 |
Also Published As
Publication number | Publication date |
---|---|
WO2020248967A1 (zh) | 2020-12-17 |
CN112062857B (zh) | 2024-08-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN111018987B (zh) | 一种能与人内皮素受体特异性结合的抗体及其应用 | |
CN112239507A (zh) | ETA抗体与TGF-β Trap的融合蛋白质,以及其药物组合物和应用 | |
AU2020350715A1 (en) | GIPR antibody and fusion protein between same and GLP-1, and pharmaceutical composition and application thereof | |
KR20200133365A (ko) | Gipr 항체 및 이와 glp-1의 융합 단백질, 및 그의 약학 조성물 및 적용 | |
CN107987162A (zh) | Etar抗体,其药物组合物及其应用 | |
KR102669444B1 (ko) | Etar 항체 및 이의 약학 조성물 및 용도 | |
CN112062857B (zh) | Eta抗体与bnp的融合蛋白质,及其药物组合物和应用 | |
WO2019196603A1 (zh) | Gcgr抗体及其与glp-1的融合蛋白质,以及其药物组合物和应用 | |
KR20210019535A (ko) | Apj 항체 및 이와 엘라벨라의 융합 단백질, 및 그의 약학 조성물 및 적용 | |
AU2016272399B2 (en) | Therapeutic agent and therapeutic method for pulmonary hypertension | |
RU2800370C2 (ru) | Антитело к gipr и его слитый с glp-1 белок, а также фармацевтическая композиция на его основе и его применение | |
CN112442127A (zh) | 针对tfpi的单克隆抗体 | |
TW202304982A (zh) | 一種能與人內皮素受體特異性結合的抗體及其在糖尿病腎病及慢性腎病治療中的應用 | |
KR20240022546A (ko) | 항il-36r 항체 및 그의 사용 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
REG | Reference to a national code |
Ref country code: HK Ref legal event code: DE Ref document number: 40036359 Country of ref document: HK |
|
GR01 | Patent grant | ||
GR01 | Patent grant |