TW202246341A - 針對NKp46的抗體及其應用 - Google Patents
針對NKp46的抗體及其應用 Download PDFInfo
- Publication number
- TW202246341A TW202246341A TW111107983A TW111107983A TW202246341A TW 202246341 A TW202246341 A TW 202246341A TW 111107983 A TW111107983 A TW 111107983A TW 111107983 A TW111107983 A TW 111107983A TW 202246341 A TW202246341 A TW 202246341A
- Authority
- TW
- Taiwan
- Prior art keywords
- cdata
- seq
- ser
- gly
- ala
- Prior art date
Links
- 230000027455 binding Effects 0.000 claims abstract description 101
- 239000000427 antigen Substances 0.000 claims abstract description 94
- 108091007433 antigens Proteins 0.000 claims abstract description 94
- 102000036639 antigens Human genes 0.000 claims abstract description 94
- 108010004217 Natural Cytotoxicity Triggering Receptor 1 Proteins 0.000 claims abstract description 76
- 239000012634 fragment Substances 0.000 claims abstract description 72
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 22
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 12
- 210000004027 cell Anatomy 0.000 claims description 125
- 102100032870 Natural cytotoxicity triggering receptor 1 Human genes 0.000 claims description 72
- 210000000822 natural killer cell Anatomy 0.000 claims description 33
- 241001416177 Vicugna pacos Species 0.000 claims description 22
- 230000014509 gene expression Effects 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 18
- 150000007523 nucleic acids Chemical class 0.000 claims description 16
- 239000013598 vector Substances 0.000 claims description 16
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 15
- 238000001514 detection method Methods 0.000 claims description 14
- 201000010099 disease Diseases 0.000 claims description 13
- 108020004707 nucleic acids Proteins 0.000 claims description 13
- 102000039446 nucleic acids Human genes 0.000 claims description 13
- 239000000872 buffer Substances 0.000 claims description 12
- 239000003814 drug Substances 0.000 claims description 11
- 238000002360 preparation method Methods 0.000 claims description 11
- 239000000126 substance Substances 0.000 claims description 8
- 239000000611 antibody drug conjugate Substances 0.000 claims description 6
- 229940049595 antibody-drug conjugate Drugs 0.000 claims description 6
- 201000011510 cancer Diseases 0.000 claims description 6
- 206010008342 Cervix carcinoma Diseases 0.000 claims description 5
- 108010019670 Chimeric Antigen Receptors Proteins 0.000 claims description 5
- 206010025323 Lymphomas Diseases 0.000 claims description 5
- 208000006105 Uterine Cervical Neoplasms Diseases 0.000 claims description 5
- 201000010881 cervical cancer Diseases 0.000 claims description 5
- 229940079593 drug Drugs 0.000 claims description 5
- 229940124597 therapeutic agent Drugs 0.000 claims description 5
- 238000011282 treatment Methods 0.000 claims description 5
- 208000023275 Autoimmune disease Diseases 0.000 claims description 4
- 208000032612 Glial tumor Diseases 0.000 claims description 4
- 206010018338 Glioma Diseases 0.000 claims description 4
- 208000008839 Kidney Neoplasms Diseases 0.000 claims description 4
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 4
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims description 4
- 206010038389 Renal cancer Diseases 0.000 claims description 4
- 239000002246 antineoplastic agent Substances 0.000 claims description 4
- 239000003153 chemical reaction reagent Substances 0.000 claims description 4
- 229940127089 cytotoxic agent Drugs 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 4
- 201000010982 kidney cancer Diseases 0.000 claims description 4
- 208000032839 leukemia Diseases 0.000 claims description 4
- 201000005202 lung cancer Diseases 0.000 claims description 4
- 208000020816 lung neoplasm Diseases 0.000 claims description 4
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims description 4
- 201000002528 pancreatic cancer Diseases 0.000 claims description 4
- 208000008443 pancreatic carcinoma Diseases 0.000 claims description 4
- 208000035473 Communicable disease Diseases 0.000 claims description 3
- 208000005718 Stomach Neoplasms Diseases 0.000 claims description 3
- 239000000562 conjugate Substances 0.000 claims description 3
- 206010017758 gastric cancer Diseases 0.000 claims description 3
- 208000027866 inflammatory disease Diseases 0.000 claims description 3
- 230000002757 inflammatory effect Effects 0.000 claims description 3
- 201000007270 liver cancer Diseases 0.000 claims description 3
- 208000014018 liver neoplasm Diseases 0.000 claims description 3
- 201000011549 stomach cancer Diseases 0.000 claims description 3
- 108090000695 Cytokines Proteins 0.000 claims description 2
- 102000004127 Cytokines Human genes 0.000 claims description 2
- 108090000790 Enzymes Proteins 0.000 claims description 2
- 102000004190 Enzymes Human genes 0.000 claims description 2
- 208000015914 Non-Hodgkin lymphomas Diseases 0.000 claims description 2
- 208000015634 Rectal Neoplasms Diseases 0.000 claims description 2
- 239000004037 angiogenesis inhibitor Substances 0.000 claims description 2
- 239000002257 antimetastatic agent Substances 0.000 claims description 2
- 239000012472 biological sample Substances 0.000 claims description 2
- 229940022399 cancer vaccine Drugs 0.000 claims description 2
- 238000009566 cancer vaccine Methods 0.000 claims description 2
- 239000003638 chemical reducing agent Substances 0.000 claims description 2
- 239000002254 cytotoxic agent Substances 0.000 claims description 2
- 231100000599 cytotoxic agent Toxicity 0.000 claims description 2
- 201000010536 head and neck cancer Diseases 0.000 claims description 2
- 208000014829 head and neck neoplasm Diseases 0.000 claims description 2
- 239000005556 hormone Substances 0.000 claims description 2
- 229940088597 hormone Drugs 0.000 claims description 2
- 239000000367 immunologic factor Substances 0.000 claims description 2
- 208000015181 infectious disease Diseases 0.000 claims description 2
- 230000002265 prevention Effects 0.000 claims description 2
- 206010038038 rectal cancer Diseases 0.000 claims description 2
- 201000001275 rectum cancer Diseases 0.000 claims description 2
- 230000008685 targeting Effects 0.000 claims description 2
- 239000003053 toxin Substances 0.000 claims description 2
- 230000002001 anti-metastasis Effects 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 230000008878 coupling Effects 0.000 claims 1
- 238000010168 coupling process Methods 0.000 claims 1
- 238000005859 coupling reaction Methods 0.000 claims 1
- 239000002955 immunomodulating agent Substances 0.000 claims 1
- 230000003439 radiotherapeutic effect Effects 0.000 claims 1
- 102000002755 Natural Cytotoxicity Triggering Receptor 1 Human genes 0.000 abstract description 4
- 108090000623 proteins and genes Proteins 0.000 description 172
- 102000004169 proteins and genes Human genes 0.000 description 157
- 235000018102 proteins Nutrition 0.000 description 156
- XKUKSGPZAADMRA-UHFFFAOYSA-N glycyl-glycyl-glycine Natural products NCC(=O)NCC(=O)NCC(O)=O XKUKSGPZAADMRA-UHFFFAOYSA-N 0.000 description 52
- 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 50
- 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 49
- 108010067216 glycyl-glycyl-glycine Proteins 0.000 description 48
- 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 47
- 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 45
- 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 43
- 108010008355 arginyl-glutamine Proteins 0.000 description 43
- 108010069020 alanyl-prolyl-glycine Proteins 0.000 description 42
- 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 41
- 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 41
- 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 39
- 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 39
- 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 39
- 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 36
- SLOYNOMYOAOUCX-BVSLBCMMSA-N Trp-Phe-Arg Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O SLOYNOMYOAOUCX-BVSLBCMMSA-N 0.000 description 35
- 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 31
- 108010086434 alanyl-seryl-glycine Proteins 0.000 description 31
- 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 30
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 30
- AJHCSUXXECOXOY-UHFFFAOYSA-N N-glycyl-L-tryptophan Natural products C1=CC=C2C(CC(NC(=O)CN)C(O)=O)=CNC2=C1 AJHCSUXXECOXOY-UHFFFAOYSA-N 0.000 description 30
- 235000001014 amino acid Nutrition 0.000 description 30
- 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 29
- 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 29
- 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 29
- DTPOVRRYXPJJAZ-FJXKBIBVSA-N Gly-Arg-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)CN)CCCN=C(N)N DTPOVRRYXPJJAZ-FJXKBIBVSA-N 0.000 description 28
- 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 28
- 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 27
- 101000589301 Homo sapiens Natural cytotoxicity triggering receptor 1 Proteins 0.000 description 26
- 108010073969 valyllysine Proteins 0.000 description 26
- 150000001413 amino acids Chemical class 0.000 description 25
- 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 24
- 229940024606 amino acid Drugs 0.000 description 24
- 102100035360 Cerebellar degeneration-related antigen 1 Human genes 0.000 description 23
- 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 23
- 241000880493 Leptailurus serval Species 0.000 description 23
- 102000050738 human NCR1 Human genes 0.000 description 23
- 108010090333 leucyl-lysyl-proline Proteins 0.000 description 23
- 101710117290 Aldo-keto reductase family 1 member C4 Proteins 0.000 description 22
- 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 22
- HHWQMFIGMMOVFK-WDSKDSINSA-N Gln-Ala-Gly Chemical compound OC(=O)CNC(=O)[C@H](C)NC(=O)[C@@H](N)CCC(N)=O HHWQMFIGMMOVFK-WDSKDSINSA-N 0.000 description 22
- 108010063718 gamma-glutamylaspartic acid Proteins 0.000 description 22
- VNYMOTCMNHJGTG-JBDRJPRFSA-N Ala-Ile-Ser Chemical compound [H]N[C@@H](C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(O)=O VNYMOTCMNHJGTG-JBDRJPRFSA-N 0.000 description 21
- 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 21
- 108010076324 alanyl-glycyl-glycine Proteins 0.000 description 21
- 239000006228 supernatant Substances 0.000 description 21
- ZFBBMCKQSNJZSN-AUTRQRHGSA-N Gln-Val-Gln Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O ZFBBMCKQSNJZSN-AUTRQRHGSA-N 0.000 description 19
- 108010020755 prolyl-glycyl-glycine Proteins 0.000 description 19
- 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 18
- 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 18
- 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 18
- 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 18
- 108010008685 alanyl-glutamyl-aspartic acid Proteins 0.000 description 18
- 108010005942 methionylglycine Proteins 0.000 description 18
- 239000000523 sample Substances 0.000 description 18
- 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 17
- 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 17
- CNGOEHJCLVCJHN-SRVKXCTJSA-N Lys-Pro-Glu Chemical compound NCCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(O)=O CNGOEHJCLVCJHN-SRVKXCTJSA-N 0.000 description 17
- 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 17
- 108010059459 arginyl-threonyl-phenylalanine Proteins 0.000 description 17
- 108020004414 DNA Proteins 0.000 description 16
- QESXLSQLQHHTIX-RHYQMDGZSA-N Leu-Val-Thr Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O QESXLSQLQHHTIX-RHYQMDGZSA-N 0.000 description 16
- 241000282567 Macaca fascicularis Species 0.000 description 16
- 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 16
- 125000003275 alpha amino acid group Chemical group 0.000 description 16
- 108010068265 aspartyltyrosine Proteins 0.000 description 16
- 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 15
- 101000589304 Macaca fascicularis Natural cytotoxicity triggering receptor 1 Proteins 0.000 description 15
- 108010045350 alanyl-tyrosyl-alanine Proteins 0.000 description 14
- SKTGPBFTMNLIHQ-KKUMJFAQSA-N Arg-Glu-Phe Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O SKTGPBFTMNLIHQ-KKUMJFAQSA-N 0.000 description 13
- 210000004602 germ cell Anatomy 0.000 description 13
- 102000005962 receptors Human genes 0.000 description 13
- 108020003175 receptors Proteins 0.000 description 13
- WEDZFLRYSIDIRX-IHRRRGAJSA-N Phe-Ser-Arg Chemical compound NC(=N)NCCC[C@@H](C(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC1=CC=CC=C1 WEDZFLRYSIDIRX-IHRRRGAJSA-N 0.000 description 12
- VEUACYMXJKXALX-IHRRRGAJSA-N Pro-Tyr-Ser Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CO)C(O)=O VEUACYMXJKXALX-IHRRRGAJSA-N 0.000 description 12
- 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 12
- 108010044374 isoleucyl-tyrosine Proteins 0.000 description 12
- 108090000765 processed proteins & peptides Proteins 0.000 description 12
- 238000006467 substitution reaction Methods 0.000 description 12
- 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 11
- 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 11
- MFDPBZAFCRKYEY-LAEOZQHASA-N Asp-Val-Gln Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O MFDPBZAFCRKYEY-LAEOZQHASA-N 0.000 description 11
- 241000282836 Camelus dromedarius Species 0.000 description 11
- 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 11
- 238000000338 in vitro Methods 0.000 description 11
- 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 10
- VHAQSYHSDKERBS-XPUUQOCRSA-N Ala-Val-Gly Chemical compound C[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)NCC(O)=O VHAQSYHSDKERBS-XPUUQOCRSA-N 0.000 description 10
- PMNHJLASAAWELO-FOHZUACHSA-N Gly-Asp-Thr Chemical compound [H]NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O PMNHJLASAAWELO-FOHZUACHSA-N 0.000 description 10
- 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 10
- XZKQVQKUZMAADP-IMJSIDKUSA-N Ser-Ser Chemical compound OC[C@H](N)C(=O)N[C@@H](CO)C(O)=O XZKQVQKUZMAADP-IMJSIDKUSA-N 0.000 description 10
- 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 10
- 238000002474 experimental method Methods 0.000 description 10
- 230000003647 oxidation Effects 0.000 description 10
- 238000007254 oxidation reaction Methods 0.000 description 10
- 102000004196 processed proteins & peptides Human genes 0.000 description 10
- 108010061238 threonyl-glycine Proteins 0.000 description 10
- 108010038745 tryptophylglycine Proteins 0.000 description 10
- VVJTWSRNMJNDPN-IUCAKERBSA-N Arg-Met-Gly Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCSC)C(=O)NCC(O)=O VVJTWSRNMJNDPN-IUCAKERBSA-N 0.000 description 9
- BCADFFUQHIMQAA-KKHAAJSZSA-N Asn-Thr-Val Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(O)=O BCADFFUQHIMQAA-KKHAAJSZSA-N 0.000 description 9
- 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 9
- 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 9
- 108010060035 arginylproline Proteins 0.000 description 9
- 230000035772 mutation Effects 0.000 description 9
- 229920001184 polypeptide Polymers 0.000 description 9
- 108010026333 seryl-proline Proteins 0.000 description 9
- FXKNPWNXPQZLES-ZLUOBGJFSA-N Ala-Asn-Ser Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(O)=O FXKNPWNXPQZLES-ZLUOBGJFSA-N 0.000 description 8
- PBAMJJXWDQXOJA-FXQIFTODSA-N Ala-Asp-Arg Chemical compound C[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(O)=O)CCCN=C(N)N PBAMJJXWDQXOJA-FXQIFTODSA-N 0.000 description 8
- PBSOQGZLPFVXPU-YUMQZZPRSA-N Arg-Glu-Gly Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(=O)NCC(O)=O PBSOQGZLPFVXPU-YUMQZZPRSA-N 0.000 description 8
- WLVLIYYBPPONRJ-GCJQMDKQSA-N Asn-Thr-Ala Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C)C(O)=O WLVLIYYBPPONRJ-GCJQMDKQSA-N 0.000 description 8
- RZSLYUUFFVHFRQ-FXQIFTODSA-N Gln-Ala-Glu Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(O)=O RZSLYUUFFVHFRQ-FXQIFTODSA-N 0.000 description 8
- 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 8
- DKDHTRVDOUZZTP-IFFSRLJSSA-N Thr-Gln-Val Chemical compound CC(C)[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)[C@@H](C)O)C(O)=O DKDHTRVDOUZZTP-IFFSRLJSSA-N 0.000 description 8
- 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 8
- 125000000539 amino acid group Chemical group 0.000 description 8
- 230000008859 change Effects 0.000 description 8
- 108010084264 glycyl-glycyl-cysteine Proteins 0.000 description 8
- 239000002609 medium Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 108010044292 tryptophyltyrosine Proteins 0.000 description 8
- OMDNCNKNEGFOMM-BQBZGAKWSA-N Ala-Met-Gly Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CCSC)C(=O)NCC(O)=O OMDNCNKNEGFOMM-BQBZGAKWSA-N 0.000 description 7
- WEZNQZHACPSMEF-QEJZJMRPSA-N Ala-Phe-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)C)CC1=CC=CC=C1 WEZNQZHACPSMEF-QEJZJMRPSA-N 0.000 description 7
- 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 7
- KGSJCPBERYUXCN-BPNCWPANSA-N Arg-Ala-Tyr Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O KGSJCPBERYUXCN-BPNCWPANSA-N 0.000 description 7
- ITVINTQUZMQWJR-QXEWZRGKSA-N Arg-Asn-Val Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](C(C)C)C(O)=O ITVINTQUZMQWJR-QXEWZRGKSA-N 0.000 description 7
- 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 7
- LTARLVHGOGBRHN-AAEUAGOBSA-N Asp-Trp-Gly Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)NCC(O)=O LTARLVHGOGBRHN-AAEUAGOBSA-N 0.000 description 7
- 101100505161 Caenorhabditis elegans mel-32 gene Proteins 0.000 description 7
- 241000282832 Camelidae Species 0.000 description 7
- VSRCAOIHMGCIJK-SRVKXCTJSA-N Glu-Leu-Arg Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O VSRCAOIHMGCIJK-SRVKXCTJSA-N 0.000 description 7
- 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 7
- IDOGEHIWMJMAHT-BYPYZUCNSA-N Gly-Gly-Cys Chemical compound NCC(=O)NCC(=O)N[C@@H](CS)C(O)=O IDOGEHIWMJMAHT-BYPYZUCNSA-N 0.000 description 7
- 101001023379 Homo sapiens Lysosome-associated membrane glycoprotein 1 Proteins 0.000 description 7
- 102100035133 Lysosome-associated membrane glycoprotein 1 Human genes 0.000 description 7
- VPFGPKIWSDVTOY-SRVKXCTJSA-N Pro-Glu-His Chemical compound C1C[C@H](NC1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC2=CN=CN2)C(=O)O VPFGPKIWSDVTOY-SRVKXCTJSA-N 0.000 description 7
- UGGWCAFQPKANMW-FXQIFTODSA-N Ser-Met-Ala Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](C)C(O)=O UGGWCAFQPKANMW-FXQIFTODSA-N 0.000 description 7
- 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 7
- PZVGOVRNGKEFCB-KKHAAJSZSA-N Thr-Asn-Val Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](C(C)C)C(=O)O)N)O PZVGOVRNGKEFCB-KKHAAJSZSA-N 0.000 description 7
- AOAMKFFPFOPMLX-BVSLBCMMSA-N Trp-Arg-Phe Chemical compound C([C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)N)C(O)=O)C1=CC=CC=C1 AOAMKFFPFOPMLX-BVSLBCMMSA-N 0.000 description 7
- 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 7
- 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 7
- 108010083476 phenylalanyltryptophan Proteins 0.000 description 7
- NJIFPLAJSVUQOZ-JBDRJPRFSA-N Ala-Cys-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CS)NC(=O)[C@H](C)N NJIFPLAJSVUQOZ-JBDRJPRFSA-N 0.000 description 6
- IFKQPMZRDQZSHI-GHCJXIJMSA-N Ala-Ile-Asn Chemical compound [H]N[C@@H](C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(N)=O)C(O)=O IFKQPMZRDQZSHI-GHCJXIJMSA-N 0.000 description 6
- ACKNRKFVYUVWAC-ZPFDUUQYSA-N Asn-Ile-Lys Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CC(=O)N)N ACKNRKFVYUVWAC-ZPFDUUQYSA-N 0.000 description 6
- UWMIZBCTVWVMFI-FXQIFTODSA-N Asp-Ala-Arg Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O UWMIZBCTVWVMFI-FXQIFTODSA-N 0.000 description 6
- 101100315624 Caenorhabditis elegans tyr-1 gene Proteins 0.000 description 6
- TZXOPHFCAATANZ-QEJZJMRPSA-N Glu-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](CCC(=O)O)N TZXOPHFCAATANZ-QEJZJMRPSA-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
- 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 6
- 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 6
- VLMIUSLQONKLDV-HEIBUPTGSA-N Ser-Thr-Thr Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O VLMIUSLQONKLDV-HEIBUPTGSA-N 0.000 description 6
- SLUWOCTZVGMURC-BFHQHQDPSA-N Thr-Gly-Ala Chemical compound C[C@@H](O)[C@H](N)C(=O)NCC(=O)N[C@@H](C)C(O)=O SLUWOCTZVGMURC-BFHQHQDPSA-N 0.000 description 6
- XPNSAQMEAVSQRD-FBCQKBJTSA-N Thr-Gly-Gly Chemical compound C[C@@H](O)[C@H](N)C(=O)NCC(=O)NCC(O)=O XPNSAQMEAVSQRD-FBCQKBJTSA-N 0.000 description 6
- KHTIUAKJRUIEMA-HOUAVDHOSA-N Thr-Trp-Asp Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@@H](N)[C@H](O)C)C(=O)N[C@@H](CC(O)=O)C(O)=O)=CNC2=C1 KHTIUAKJRUIEMA-HOUAVDHOSA-N 0.000 description 6
- 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 6
- 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 6
- 108010024078 alanyl-glycyl-serine Proteins 0.000 description 6
- 108010045023 alanyl-prolyl-tyrosine Proteins 0.000 description 6
- 108010047857 aspartylglycine Proteins 0.000 description 6
- 238000004113 cell culture Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000013604 expression vector Substances 0.000 description 6
- 238000000684 flow cytometry Methods 0.000 description 6
- 230000003053 immunization Effects 0.000 description 6
- 238000002649 immunization Methods 0.000 description 6
- 108010060857 isoleucyl-valyl-tyrosine Proteins 0.000 description 6
- 230000004048 modification Effects 0.000 description 6
- 238000012986 modification Methods 0.000 description 6
- 230000002829 reductive effect Effects 0.000 description 6
- 108010071207 serylmethionine Proteins 0.000 description 6
- 108010033670 threonyl-aspartyl-tyrosine Proteins 0.000 description 6
- 210000001519 tissue Anatomy 0.000 description 6
- HHGYNJRJIINWAK-FXQIFTODSA-N Ala-Ala-Arg Chemical compound C[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@H](C(O)=O)CCCN=C(N)N HHGYNJRJIINWAK-FXQIFTODSA-N 0.000 description 5
- IETUUAHKCHOQHP-KZVJFYERSA-N Ala-Thr-Val Chemical compound CC(C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](C)N)[C@@H](C)O)C(O)=O IETUUAHKCHOQHP-KZVJFYERSA-N 0.000 description 5
- AENHOIXXHKNIQL-AUTRQRHGSA-N Ala-Tyr-Ala Chemical compound [O-]C(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H]([NH3+])C)CC1=CC=C(O)C=C1 AENHOIXXHKNIQL-AUTRQRHGSA-N 0.000 description 5
- DEAGTWNKODHUIY-MRFFXTKBSA-N Ala-Tyr-Trp Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O DEAGTWNKODHUIY-MRFFXTKBSA-N 0.000 description 5
- REWSWYIDQIELBE-FXQIFTODSA-N Ala-Val-Ser Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CO)C(O)=O REWSWYIDQIELBE-FXQIFTODSA-N 0.000 description 5
- GOWZVQXTHUCNSQ-NHCYSSNCSA-N Arg-Glu-Val Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(O)=O GOWZVQXTHUCNSQ-NHCYSSNCSA-N 0.000 description 5
- 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 5
- 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 5
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 5
- QSVMIMFAAZPCAQ-PMVVWTBXSA-N Gly-His-Thr Chemical compound [H]NCC(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H]([C@@H](C)O)C(O)=O QSVMIMFAAZPCAQ-PMVVWTBXSA-N 0.000 description 5
- WNGHUXFWEWTKAO-YUMQZZPRSA-N Gly-Ser-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CO)NC(=O)CN WNGHUXFWEWTKAO-YUMQZZPRSA-N 0.000 description 5
- 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 5
- 108060003951 Immunoglobulin Proteins 0.000 description 5
- QTDBZORPVYTRJU-KKXDTOCCSA-N Phe-Tyr-Ala Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](C)C(O)=O QTDBZORPVYTRJU-KKXDTOCCSA-N 0.000 description 5
- 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 5
- HBBBLSVBQGZKOZ-GUBZILKMSA-N Pro-Met-Ala Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(=O)N[C@@H](C)C(O)=O HBBBLSVBQGZKOZ-GUBZILKMSA-N 0.000 description 5
- WIPAMEKBSHNFQE-IUCAKERBSA-N Pro-Met-Gly Chemical compound CSCC[C@@H](C(=O)NCC(=O)O)NC(=O)[C@@H]1CCCN1 WIPAMEKBSHNFQE-IUCAKERBSA-N 0.000 description 5
- UJGDFQRPYGJBEH-AAEUAGOBSA-N Trp-Ser-Gly Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CO)C(=O)NCC(=O)O)N UJGDFQRPYGJBEH-AAEUAGOBSA-N 0.000 description 5
- 230000004913 activation Effects 0.000 description 5
- 238000007385 chemical modification Methods 0.000 description 5
- 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 5
- 108010050848 glycylleucine Proteins 0.000 description 5
- 108010037850 glycylvaline Proteins 0.000 description 5
- 102000018358 immunoglobulin Human genes 0.000 description 5
- 230000002147 killing effect Effects 0.000 description 5
- 229930182817 methionine Natural products 0.000 description 5
- 239000013612 plasmid Substances 0.000 description 5
- 230000037452 priming Effects 0.000 description 5
- 238000001890 transfection Methods 0.000 description 5
- HDTRYLNUVZCQOY-UHFFFAOYSA-N α-D-glucopyranosyl-α-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(O)C(O)C(CO)O1 HDTRYLNUVZCQOY-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 4
- 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 4
- YJHKTAMKPGFJCT-NRPADANISA-N Ala-Val-Glu Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O YJHKTAMKPGFJCT-NRPADANISA-N 0.000 description 4
- FEZJJKXNPSEYEV-CIUDSAMLSA-N Arg-Gln-Ala Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(O)=O FEZJJKXNPSEYEV-CIUDSAMLSA-N 0.000 description 4
- 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 4
- 102100021277 Beta-secretase 2 Human genes 0.000 description 4
- 101710150190 Beta-secretase 2 Proteins 0.000 description 4
- 238000002965 ELISA Methods 0.000 description 4
- CGYDXNKRIMJMLV-GUBZILKMSA-N Glu-Arg-Glu Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(O)=O CGYDXNKRIMJMLV-GUBZILKMSA-N 0.000 description 4
- PXXGVUVQWQGGIG-YUMQZZPRSA-N Glu-Gly-Arg Chemical compound OC(=O)CC[C@H](N)C(=O)NCC(=O)N[C@H](C(O)=O)CCCN=C(N)N PXXGVUVQWQGGIG-YUMQZZPRSA-N 0.000 description 4
- 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 4
- 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 4
- 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 4
- 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 4
- 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 4
- KSOBNUBCYHGUKH-UWVGGRQHSA-N Gly-Val-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)CN KSOBNUBCYHGUKH-UWVGGRQHSA-N 0.000 description 4
- 108010065920 Insulin Lispro Proteins 0.000 description 4
- SITWEMZOJNKJCH-UHFFFAOYSA-N L-alanine-L-arginine Natural products CC(N)C(=O)NC(C(O)=O)CCCNC(N)=N SITWEMZOJNKJCH-UHFFFAOYSA-N 0.000 description 4
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 4
- CLVUXCBGKUECIT-HJGDQZAQSA-N Leu-Asp-Thr Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O CLVUXCBGKUECIT-HJGDQZAQSA-N 0.000 description 4
- 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 4
- KZNQNBZMBZJQJO-UHFFFAOYSA-N N-glycyl-L-proline Natural products NCC(=O)N1CCCC1C(O)=O KZNQNBZMBZJQJO-UHFFFAOYSA-N 0.000 description 4
- 102100021462 Natural killer cells antigen CD94 Human genes 0.000 description 4
- HTKNPQZCMLBOTQ-XVSYOHENSA-N Phe-Asn-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CC1=CC=CC=C1)N)O HTKNPQZCMLBOTQ-XVSYOHENSA-N 0.000 description 4
- 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 4
- 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 4
- 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 4
- 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 4
- 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 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
- NCXVJIQMWSGRHY-KXNHARMFSA-N Thr-Leu-Pro Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@@H]1C(=O)O)N)O NCXVJIQMWSGRHY-KXNHARMFSA-N 0.000 description 4
- 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 4
- LXXCHJKHJYRMIY-FQPOAREZSA-N Thr-Tyr-Ala 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(O)=O LXXCHJKHJYRMIY-FQPOAREZSA-N 0.000 description 4
- 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 4
- HDTRYLNUVZCQOY-WSWWMNSNSA-N Trehalose Natural products O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-WSWWMNSNSA-N 0.000 description 4
- OFCKFBGRYHOKFP-IHPCNDPISA-N Trp-Asp-Tyr Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC3=CC=C(C=C3)O)C(=O)O)N OFCKFBGRYHOKFP-IHPCNDPISA-N 0.000 description 4
- 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 4
- BURPTJBFWIOHEY-UWJYBYFXSA-N Tyr-Ala-Asp Chemical compound OC(=O)C[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 BURPTJBFWIOHEY-UWJYBYFXSA-N 0.000 description 4
- 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 4
- SMLCYZYQFRTLCO-UWJYBYFXSA-N Tyr-Cys-Ala 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(O)=O SMLCYZYQFRTLCO-UWJYBYFXSA-N 0.000 description 4
- AZSHAZJLOZQYAY-FXQIFTODSA-N Val-Ala-Ser Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(O)=O AZSHAZJLOZQYAY-FXQIFTODSA-N 0.000 description 4
- YTUABZMPYKCWCQ-XQQFMLRXSA-N Val-His-Pro Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N2CCC[C@@H]2C(=O)O)N YTUABZMPYKCWCQ-XQQFMLRXSA-N 0.000 description 4
- JXWGBRRVTRAZQA-ULQDDVLXSA-N Val-Tyr-Leu Chemical compound CC(C)C[C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)NC(=O)[C@H](C(C)C)N JXWGBRRVTRAZQA-ULQDDVLXSA-N 0.000 description 4
- 108010047495 alanylglycine Proteins 0.000 description 4
- HDTRYLNUVZCQOY-LIZSDCNHSA-N alpha,alpha-trehalose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-LIZSDCNHSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 238000003556 assay Methods 0.000 description 4
- 239000002299 complementary DNA Substances 0.000 description 4
- 238000010276 construction Methods 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 230000006240 deamidation Effects 0.000 description 4
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 108010078144 glutaminyl-glycine Proteins 0.000 description 4
- 108010027668 glycyl-alanyl-valine Proteins 0.000 description 4
- 108010079413 glycyl-prolyl-glutamic acid Proteins 0.000 description 4
- 108010087823 glycyltyrosine Proteins 0.000 description 4
- 230000028993 immune response Effects 0.000 description 4
- 230000008676 import Effects 0.000 description 4
- 108010003700 lysyl aspartic acid Proteins 0.000 description 4
- 108010009298 lysylglutamic acid Proteins 0.000 description 4
- 230000001404 mediated effect Effects 0.000 description 4
- 125000001360 methionine group Chemical group N[C@@H](CCSC)C(=O)* 0.000 description 4
- 239000013642 negative control Substances 0.000 description 4
- 210000000056 organ Anatomy 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000013641 positive control Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 108010065320 prolyl-lysyl-glutamyl-lysine Proteins 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 210000002966 serum Anatomy 0.000 description 4
- 230000009870 specific binding Effects 0.000 description 4
- 238000002054 transplantation Methods 0.000 description 4
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 4
- 235000002374 tyrosine Nutrition 0.000 description 4
- 108010017949 tyrosyl-glycyl-glycine Proteins 0.000 description 4
- 238000011144 upstream manufacturing Methods 0.000 description 4
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 4
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 3
- ZPXCNXMJEZKRLU-LSJOCFKGSA-N Ala-His-Arg Chemical compound NC(N)=NCCC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)C)CC1=CN=CN1 ZPXCNXMJEZKRLU-LSJOCFKGSA-N 0.000 description 3
- DHBKYZYFEXXUAK-ONGXEEELSA-N Ala-Phe-Gly Chemical compound OC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](N)C)CC1=CC=CC=C1 DHBKYZYFEXXUAK-ONGXEEELSA-N 0.000 description 3
- 235000002198 Annona diversifolia Nutrition 0.000 description 3
- CFGHCPUPFHWMCM-FDARSICLSA-N Arg-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](CCCN=C(N)N)N CFGHCPUPFHWMCM-FDARSICLSA-N 0.000 description 3
- PRLPSDIHSRITSF-UNQGMJICSA-N Arg-Phe-Thr Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)O)C(O)=O PRLPSDIHSRITSF-UNQGMJICSA-N 0.000 description 3
- CNBIWSCSSCAINS-UFYCRDLUSA-N Arg-Tyr-Tyr Chemical compound [H]N[C@@H](CCCNC(N)=N)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 CNBIWSCSSCAINS-UFYCRDLUSA-N 0.000 description 3
- DAPLJWATMAXPPZ-CIUDSAMLSA-N Asn-Asn-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](N)CC(N)=O DAPLJWATMAXPPZ-CIUDSAMLSA-N 0.000 description 3
- NCXTYSVDWLAQGZ-ZKWXMUAHSA-N Asn-Ser-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC(N)=O NCXTYSVDWLAQGZ-ZKWXMUAHSA-N 0.000 description 3
- YNCHFVRXEQFPBY-BQBZGAKWSA-N Asp-Gly-Arg Chemical compound OC(=O)C[C@H](N)C(=O)NCC(=O)N[C@H](C(O)=O)CCCN=C(N)N YNCHFVRXEQFPBY-BQBZGAKWSA-N 0.000 description 3
- VMVUDJUXJKDGNR-FXQIFTODSA-N Asp-Met-Asn Chemical compound CSCC[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)[C@H](CC(=O)O)N VMVUDJUXJKDGNR-FXQIFTODSA-N 0.000 description 3
- RVMXMLSYBTXCAV-VEVYYDQMSA-N Asp-Pro-Thr Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H]([C@@H](C)O)C(O)=O RVMXMLSYBTXCAV-VEVYYDQMSA-N 0.000 description 3
- PDIYGFYAMZZFCW-JIOCBJNQSA-N Asp-Thr-Pro Chemical compound C[C@H]([C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CC(=O)O)N)O PDIYGFYAMZZFCW-JIOCBJNQSA-N 0.000 description 3
- RSMZEHCMIOKNMW-GSSVUCPTSA-N Asp-Thr-Thr Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O RSMZEHCMIOKNMW-GSSVUCPTSA-N 0.000 description 3
- 102100038077 CD226 antigen Human genes 0.000 description 3
- KEBJBKIASQVRJS-WDSKDSINSA-N Cys-Gln-Gly Chemical compound C(CC(=O)N)[C@@H](C(=O)NCC(=O)O)NC(=O)[C@H](CS)N KEBJBKIASQVRJS-WDSKDSINSA-N 0.000 description 3
- KVGPYKUIHZJWGA-BQBZGAKWSA-N Cys-Met-Gly Chemical compound [H]N[C@@H](CS)C(=O)N[C@@H](CCSC)C(=O)NCC(O)=O KVGPYKUIHZJWGA-BQBZGAKWSA-N 0.000 description 3
- 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 3
- NSORZJXKUQFEKL-JGVFFNPUSA-N Gln-Gly-Pro Chemical compound C1C[C@@H](N(C1)C(=O)CNC(=O)[C@H](CCC(=O)N)N)C(=O)O NSORZJXKUQFEKL-JGVFFNPUSA-N 0.000 description 3
- MSHXWFKYXJTLEZ-CIUDSAMLSA-N Gln-Met-Asn Chemical compound CSCC[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)[C@H](CCC(=O)N)N MSHXWFKYXJTLEZ-CIUDSAMLSA-N 0.000 description 3
- QGWXAMDECCKGRU-XVKPBYJWSA-N Gln-Val-Gly Chemical compound CC(C)[C@H](NC(=O)[C@@H](N)CCC(N)=O)C(=O)NCC(O)=O QGWXAMDECCKGRU-XVKPBYJWSA-N 0.000 description 3
- VAZZOGXDUQSVQF-NUMRIWBASA-N Glu-Asn-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CCC(=O)O)N)O VAZZOGXDUQSVQF-NUMRIWBASA-N 0.000 description 3
- SBCYJMOOHUDWDA-NUMRIWBASA-N Glu-Asp-Thr Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O SBCYJMOOHUDWDA-NUMRIWBASA-N 0.000 description 3
- UJMNFCAHLYKWOZ-DCAQKATOSA-N Glu-Lys-Gln Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(O)=O UJMNFCAHLYKWOZ-DCAQKATOSA-N 0.000 description 3
- 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 3
- ZTVGZOIBLRPQNR-KKUMJFAQSA-N Glu-Met-Tyr Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O ZTVGZOIBLRPQNR-KKUMJFAQSA-N 0.000 description 3
- 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 3
- XBWMTPAIUQIWKA-BYULHYEWSA-N Gly-Asp-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)CN XBWMTPAIUQIWKA-BYULHYEWSA-N 0.000 description 3
- YYPFZVIXAVDHIK-IUCAKERBSA-N Gly-Glu-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)CN YYPFZVIXAVDHIK-IUCAKERBSA-N 0.000 description 3
- LRQXRHGQEVWGPV-NHCYSSNCSA-N Gly-Leu-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)CN LRQXRHGQEVWGPV-NHCYSSNCSA-N 0.000 description 3
- FOKISINOENBSDM-WLTAIBSBSA-N Gly-Thr-Tyr Chemical compound [H]NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O FOKISINOENBSDM-WLTAIBSBSA-N 0.000 description 3
- 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 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
- QCBYAHHNOHBXIH-UWVGGRQHSA-N His-Pro-Gly Chemical compound C([C@H](N)C(=O)N1[C@@H](CCC1)C(=O)NCC(O)=O)C1=CN=CN1 QCBYAHHNOHBXIH-UWVGGRQHSA-N 0.000 description 3
- KECFCPNPPYCGBL-PMVMPFDFSA-N His-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](CC4=CN=CN4)N KECFCPNPPYCGBL-PMVMPFDFSA-N 0.000 description 3
- 101000884298 Homo sapiens CD226 antigen Proteins 0.000 description 3
- 101001037140 Homo sapiens Immunoglobulin heavy variable 3-23 Proteins 0.000 description 3
- 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 3
- 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 3
- XDVKZSJODLMNLJ-GGQYPGDFSA-N Ile-Trp-Trp Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@H](CC=3C4=CC=CC=C4NC=3)NC(=O)[C@@H](N)[C@@H](C)CC)C(O)=O)=CNC2=C1 XDVKZSJODLMNLJ-GGQYPGDFSA-N 0.000 description 3
- PRTZQMBYUZFSFA-XEGUGMAKSA-N Ile-Tyr-Gly Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)NCC(=O)O)N PRTZQMBYUZFSFA-XEGUGMAKSA-N 0.000 description 3
- 108010021625 Immunoglobulin Fragments Proteins 0.000 description 3
- 102000008394 Immunoglobulin Fragments Human genes 0.000 description 3
- 102100040220 Immunoglobulin heavy variable 3-23 Human genes 0.000 description 3
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 description 3
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 3
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 3
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 3
- DLCOFDAHNMMQPP-SRVKXCTJSA-N Leu-Asp-Leu Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(O)=O DLCOFDAHNMMQPP-SRVKXCTJSA-N 0.000 description 3
- IFMPDNRWZZEZSL-SRVKXCTJSA-N Leu-Leu-Cys Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CS)C(O)=O IFMPDNRWZZEZSL-SRVKXCTJSA-N 0.000 description 3
- LXKNSJLSGPNHSK-KKUMJFAQSA-N Leu-Leu-Lys Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)O)N LXKNSJLSGPNHSK-KKUMJFAQSA-N 0.000 description 3
- RTIRBWJPYJYTLO-MELADBBJSA-N Leu-Lys-Pro Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@@H]1C(=O)O)N RTIRBWJPYJYTLO-MELADBBJSA-N 0.000 description 3
- 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 3
- CAODKDAPYGUMLK-FXQIFTODSA-N Met-Asn-Ser Chemical compound CSCC[C@H](N)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(O)=O CAODKDAPYGUMLK-FXQIFTODSA-N 0.000 description 3
- OIFHHODAXVWKJN-ULQDDVLXSA-N Met-Phe-Leu Chemical compound CSCC[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(O)=O)CC1=CC=CC=C1 OIFHHODAXVWKJN-ULQDDVLXSA-N 0.000 description 3
- PESQCPHRXOFIPX-UHFFFAOYSA-N N-L-methionyl-L-tyrosine Natural products CSCCC(N)C(=O)NC(C(O)=O)CC1=CC=C(O)C=C1 PESQCPHRXOFIPX-UHFFFAOYSA-N 0.000 description 3
- 108010002311 N-glycylglutamic acid Proteins 0.000 description 3
- 230000006051 NK cell activation Effects 0.000 description 3
- 108091028043 Nucleic acid sequence Proteins 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
- CDHURCQGUDNBMA-UBHSHLNASA-N Phe-Val-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)CC1=CC=CC=C1 CDHURCQGUDNBMA-UBHSHLNASA-N 0.000 description 3
- 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 3
- 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 3
- FNGOXVQBBCMFKV-CIUDSAMLSA-N Pro-Ser-Glu Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(O)=O FNGOXVQBBCMFKV-CIUDSAMLSA-N 0.000 description 3
- 206010039491 Sarcoma Diseases 0.000 description 3
- FUMGHWDRRFCKEP-CIUDSAMLSA-N Ser-Leu-Ala Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(O)=O FUMGHWDRRFCKEP-CIUDSAMLSA-N 0.000 description 3
- 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 3
- VZQRNAYURWAEFE-KKUMJFAQSA-N Ser-Leu-Phe Chemical compound OC[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 VZQRNAYURWAEFE-KKUMJFAQSA-N 0.000 description 3
- 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 3
- PIQRHJQWEPWFJG-UWJYBYFXSA-N Ser-Tyr-Ala Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](C)C(O)=O PIQRHJQWEPWFJG-UWJYBYFXSA-N 0.000 description 3
- PQEQXWRVHQAAKS-SRVKXCTJSA-N Ser-Tyr-Asn Chemical compound NC(=O)C[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CO)N)CC1=CC=C(O)C=C1 PQEQXWRVHQAAKS-SRVKXCTJSA-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
- 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 3
- 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 3
- VYVBSMCZNHOZGD-RCWTZXSCSA-N Thr-Val-Val Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(O)=O VYVBSMCZNHOZGD-RCWTZXSCSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- UIRPULWLRODAEQ-QEJZJMRPSA-N Trp-Ser-Glu Chemical compound C1=CC=C2C(C[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(O)=O)=CNC2=C1 UIRPULWLRODAEQ-QEJZJMRPSA-N 0.000 description 3
- GBEAUNVBIMLWIB-IHPCNDPISA-N Trp-Ser-Phe Chemical compound C([C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)N)C(O)=O)C1=CC=CC=C1 GBEAUNVBIMLWIB-IHPCNDPISA-N 0.000 description 3
- UIDJDMVRDUANDL-BVSLBCMMSA-N Trp-Tyr-Arg Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O UIDJDMVRDUANDL-BVSLBCMMSA-N 0.000 description 3
- TWAVEIJGFCBWCG-JYJNAYRXSA-N Tyr-Gln-Leu Chemical compound CC(C)C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CC1=CC=C(C=C1)O)N TWAVEIJGFCBWCG-JYJNAYRXSA-N 0.000 description 3
- 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 3
- SYFHQHYTNCQCCN-MELADBBJSA-N Tyr-Ser-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CO)NC(=O)[C@H](CC2=CC=C(C=C2)O)N)C(=O)O SYFHQHYTNCQCCN-MELADBBJSA-N 0.000 description 3
- XTAUQCGQFJQGEJ-NHCYSSNCSA-N Val-Gln-Arg Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)N XTAUQCGQFJQGEJ-NHCYSSNCSA-N 0.000 description 3
- HPANGHISDXDUQY-ULQDDVLXSA-N Val-Lys-Phe Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)N HPANGHISDXDUQY-ULQDDVLXSA-N 0.000 description 3
- 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 3
- 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 3
- 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 3
- 239000002671 adjuvant Substances 0.000 description 3
- 108010041407 alanylaspartic acid Proteins 0.000 description 3
- 108010087924 alanylproline Proteins 0.000 description 3
- 108010069926 arginyl-glycyl-serine Proteins 0.000 description 3
- 108010040443 aspartyl-aspartic acid Proteins 0.000 description 3
- 230000004071 biological effect Effects 0.000 description 3
- 210000000170 cell membrane Anatomy 0.000 description 3
- 230000001413 cellular effect Effects 0.000 description 3
- 230000001276 controlling effect Effects 0.000 description 3
- UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- 108010013768 glutamyl-aspartyl-proline Proteins 0.000 description 3
- 230000013595 glycosylation Effects 0.000 description 3
- 238000006206 glycosylation reaction Methods 0.000 description 3
- VPZXBVLAVMBEQI-UHFFFAOYSA-N glycyl-DL-alpha-alanine Natural products OC(=O)C(C)NC(=O)CN VPZXBVLAVMBEQI-UHFFFAOYSA-N 0.000 description 3
- 108010089804 glycyl-threonine Proteins 0.000 description 3
- 108010010147 glycylglutamine Proteins 0.000 description 3
- 108010081551 glycylphenylalanine Proteins 0.000 description 3
- 108010084389 glycyltryptophan Proteins 0.000 description 3
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 3
- 230000002998 immunogenetic effect Effects 0.000 description 3
- 239000003446 ligand Substances 0.000 description 3
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 3
- 108010017391 lysylvaline Proteins 0.000 description 3
- 210000003819 peripheral blood mononuclear cell Anatomy 0.000 description 3
- 108010031719 prolyl-serine Proteins 0.000 description 3
- 108010029020 prolylglycine Proteins 0.000 description 3
- 108010053725 prolylvaline Proteins 0.000 description 3
- 238000012216 screening Methods 0.000 description 3
- 108010048818 seryl-histidine Proteins 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 108010045269 tryptophyltryptophan Proteins 0.000 description 3
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 2
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide Chemical compound CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 2
- 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
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 208000031261 Acute myeloid leukaemia Diseases 0.000 description 2
- 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 2
- CSAHOYQKNHGDHX-ACZMJKKPSA-N Ala-Gln-Asn Chemical compound C[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O CSAHOYQKNHGDHX-ACZMJKKPSA-N 0.000 description 2
- FBHOPGDGELNWRH-DRZSPHRISA-N Ala-Glu-Phe Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O FBHOPGDGELNWRH-DRZSPHRISA-N 0.000 description 2
- VBRDBGCROKWTPV-XHNCKOQMSA-N Ala-Glu-Pro Chemical compound C[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N1CCC[C@@H]1C(=O)O)N VBRDBGCROKWTPV-XHNCKOQMSA-N 0.000 description 2
- PUBLUECXJRHTBK-ACZMJKKPSA-N Ala-Glu-Ser Chemical compound C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(O)=O PUBLUECXJRHTBK-ACZMJKKPSA-N 0.000 description 2
- UWIQWPWWZUHBAO-ZLIFDBKOSA-N Ala-Leu-Trp Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@@H](NC(=O)[C@H](C)N)CC(C)C)C(O)=O)=CNC2=C1 UWIQWPWWZUHBAO-ZLIFDBKOSA-N 0.000 description 2
- ARHJJAAWNWOACN-FXQIFTODSA-N Ala-Ser-Val Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(O)=O ARHJJAAWNWOACN-FXQIFTODSA-N 0.000 description 2
- JJHBEVZAZXZREW-LFSVMHDDSA-N Ala-Thr-Phe Chemical compound C[C@@H](O)[C@H](NC(=O)[C@H](C)N)C(=O)N[C@@H](Cc1ccccc1)C(O)=O JJHBEVZAZXZREW-LFSVMHDDSA-N 0.000 description 2
- PGNNQOJOEGFAOR-KWQFWETISA-N Ala-Tyr-Gly Chemical compound OC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](N)C)CC1=CC=C(O)C=C1 PGNNQOJOEGFAOR-KWQFWETISA-N 0.000 description 2
- ZDILXFDENZVOTL-BPNCWPANSA-N Ala-Val-Tyr Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O ZDILXFDENZVOTL-BPNCWPANSA-N 0.000 description 2
- OTOXOKCIIQLMFH-KZVJFYERSA-N Arg-Ala-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCCN=C(N)N OTOXOKCIIQLMFH-KZVJFYERSA-N 0.000 description 2
- DCGLNNVKIZXQOJ-FXQIFTODSA-N Arg-Asn-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CCCN=C(N)N)N DCGLNNVKIZXQOJ-FXQIFTODSA-N 0.000 description 2
- NONSEUUPKITYQT-BQBZGAKWSA-N Arg-Asn-Gly Chemical compound C(C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)NCC(=O)O)N)CN=C(N)N NONSEUUPKITYQT-BQBZGAKWSA-N 0.000 description 2
- KMSHNDWHPWXPEC-BQBZGAKWSA-N Arg-Asp-Gly Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)NCC(O)=O KMSHNDWHPWXPEC-BQBZGAKWSA-N 0.000 description 2
- YSUVMPICYVWRBX-VEVYYDQMSA-N Arg-Asp-Thr Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O YSUVMPICYVWRBX-VEVYYDQMSA-N 0.000 description 2
- BBYTXXRNSFUOOX-IHRRRGAJSA-N Arg-Cys-Phe Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CS)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O BBYTXXRNSFUOOX-IHRRRGAJSA-N 0.000 description 2
- 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 2
- UHFUZWSZQKMDSX-DCAQKATOSA-N Arg-Leu-Asn Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)[C@H](CCCN=C(N)N)N UHFUZWSZQKMDSX-DCAQKATOSA-N 0.000 description 2
- OTZMRMHZCMZOJZ-SRVKXCTJSA-N Arg-Leu-Glu Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O OTZMRMHZCMZOJZ-SRVKXCTJSA-N 0.000 description 2
- NMRHDSAOIURTNT-RWMBFGLXSA-N Arg-Leu-Pro Chemical compound CC(C)C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CCCN=C(N)N)N NMRHDSAOIURTNT-RWMBFGLXSA-N 0.000 description 2
- NGYHSXDNNOFHNE-AVGNSLFASA-N Arg-Pro-Leu Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(O)=O NGYHSXDNNOFHNE-AVGNSLFASA-N 0.000 description 2
- 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 2
- VLIJAPRTSXSGFY-STQMWFEESA-N Arg-Tyr-Gly Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@H](C(=O)NCC(O)=O)CC1=CC=C(O)C=C1 VLIJAPRTSXSGFY-STQMWFEESA-N 0.000 description 2
- QHUOOCKNNURZSL-IHRRRGAJSA-N Arg-Tyr-Ser Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CO)C(O)=O QHUOOCKNNURZSL-IHRRRGAJSA-N 0.000 description 2
- 239000004475 Arginine Substances 0.000 description 2
- GMRGSBAMMMVDGG-GUBZILKMSA-N Asn-Arg-Arg Chemical compound C(C[C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)NC(=O)[C@H](CC(=O)N)N)CN=C(N)N GMRGSBAMMMVDGG-GUBZILKMSA-N 0.000 description 2
- UDSVWSUXKYXSTR-QWRGUYRKSA-N Asn-Gly-Tyr Chemical compound [H]N[C@@H](CC(N)=O)C(=O)NCC(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O UDSVWSUXKYXSTR-QWRGUYRKSA-N 0.000 description 2
- RAKKBBHMTJSXOY-XVYDVKMFSA-N Asn-His-Ala Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](C)C(O)=O RAKKBBHMTJSXOY-XVYDVKMFSA-N 0.000 description 2
- JQBCANGGAVVERB-CFMVVWHZSA-N Asn-Ile-Tyr Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O)NC(=O)[C@H](CC(=O)N)N JQBCANGGAVVERB-CFMVVWHZSA-N 0.000 description 2
- YHXNKGKUDJCAHB-PBCZWWQYSA-N Asn-Thr-His Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)[C@H](CC(=O)N)N)O YHXNKGKUDJCAHB-PBCZWWQYSA-N 0.000 description 2
- YSYTWUMRHSFODC-QWRGUYRKSA-N Asn-Tyr-Gly Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)NCC(O)=O YSYTWUMRHSFODC-QWRGUYRKSA-N 0.000 description 2
- NYLBGYLHBDFRHL-VEVYYDQMSA-N Asp-Arg-Thr 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)O)C(O)=O NYLBGYLHBDFRHL-VEVYYDQMSA-N 0.000 description 2
- 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 2
- RKNIUWSZIAUEPK-PBCZWWQYSA-N Asp-His-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC1=CN=CN1)NC(=O)[C@H](CC(=O)O)N)O RKNIUWSZIAUEPK-PBCZWWQYSA-N 0.000 description 2
- PWAIZUBWHRHYKS-MELADBBJSA-N Asp-Phe-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CC(=O)O)N)C(=O)O PWAIZUBWHRHYKS-MELADBBJSA-N 0.000 description 2
- GPPIDDWYKJPRES-YDHLFZDLSA-N Asp-Phe-Val Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](C(C)C)C(O)=O GPPIDDWYKJPRES-YDHLFZDLSA-N 0.000 description 2
- DRCOAZZDQRCGGP-GHCJXIJMSA-N Asp-Ser-Ile Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O DRCOAZZDQRCGGP-GHCJXIJMSA-N 0.000 description 2
- JJQGZGOEDSSHTE-FOHZUACHSA-N Asp-Thr-Gly Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(O)=O JJQGZGOEDSSHTE-FOHZUACHSA-N 0.000 description 2
- PLNJUJGNLDSFOP-UWJYBYFXSA-N Asp-Tyr-Ala 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](C)C(O)=O PLNJUJGNLDSFOP-UWJYBYFXSA-N 0.000 description 2
- USENATHVGFXRNO-SRVKXCTJSA-N Asp-Tyr-Asp Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CC(O)=O)C(O)=O)CC1=CC=C(O)C=C1 USENATHVGFXRNO-SRVKXCTJSA-N 0.000 description 2
- RKXVTTIQNKPCHU-KKHAAJSZSA-N Asp-Val-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)CC(O)=O RKXVTTIQNKPCHU-KKHAAJSZSA-N 0.000 description 2
- DCXYFEDJOCDNAF-UHFFFAOYSA-N Asparagine Natural products OC(=O)C(N)CC(N)=O DCXYFEDJOCDNAF-UHFFFAOYSA-N 0.000 description 2
- 206010006187 Breast cancer Diseases 0.000 description 2
- 208000026310 Breast neoplasm Diseases 0.000 description 2
- 101100512078 Caenorhabditis elegans lys-1 gene Proteins 0.000 description 2
- 241000283707 Capra Species 0.000 description 2
- 201000009030 Carcinoma Diseases 0.000 description 2
- 206010009944 Colon cancer Diseases 0.000 description 2
- YFAFBAPQHGULQT-HJPIBITLSA-N Cys-Ile-Tyr Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O)NC(=O)[C@H](CS)N YFAFBAPQHGULQT-HJPIBITLSA-N 0.000 description 2
- SRIRHERUAMYIOQ-CIUDSAMLSA-N Cys-Leu-Ser Chemical compound [H]N[C@@H](CS)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(O)=O SRIRHERUAMYIOQ-CIUDSAMLSA-N 0.000 description 2
- 241000588724 Escherichia coli Species 0.000 description 2
- 208000000461 Esophageal Neoplasms Diseases 0.000 description 2
- 208000022072 Gallbladder Neoplasms Diseases 0.000 description 2
- MWLYSLMKFXWZPW-ZPFDUUQYSA-N Gln-Arg-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](N)CCC(N)=O MWLYSLMKFXWZPW-ZPFDUUQYSA-N 0.000 description 2
- ININBLZFFVOQIO-JHEQGTHGSA-N Gln-Thr-Gly Chemical compound C[C@H]([C@@H](C(=O)NCC(=O)O)NC(=O)[C@H](CCC(=O)N)N)O ININBLZFFVOQIO-JHEQGTHGSA-N 0.000 description 2
- 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 2
- 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 2
- YSWHPLCDIMUKFE-QWRGUYRKSA-N Glu-Tyr Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 YSWHPLCDIMUKFE-QWRGUYRKSA-N 0.000 description 2
- GWCRIHNSVMOBEQ-BQBZGAKWSA-N Gly-Arg-Ser Chemical compound [H]NCC(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(O)=O GWCRIHNSVMOBEQ-BQBZGAKWSA-N 0.000 description 2
- SCCPDJAQCXWPTF-VKHMYHEASA-N Gly-Asp Chemical compound NCC(=O)N[C@H](C(O)=O)CC(O)=O SCCPDJAQCXWPTF-VKHMYHEASA-N 0.000 description 2
- 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 2
- UPADCCSMVOQAGF-LBPRGKRZSA-N Gly-Gly-Trp Chemical compound C1=CC=C2C(C[C@H](NC(=O)CNC(=O)CN)C(O)=O)=CNC2=C1 UPADCCSMVOQAGF-LBPRGKRZSA-N 0.000 description 2
- SWQALSGKVLYKDT-UHFFFAOYSA-N Gly-Ile-Ala Natural products NCC(=O)NC(C(C)CC)C(=O)NC(C)C(O)=O SWQALSGKVLYKDT-UHFFFAOYSA-N 0.000 description 2
- ULZCYBYDTUMHNF-IUCAKERBSA-N Gly-Leu-Glu Chemical compound NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O ULZCYBYDTUMHNF-IUCAKERBSA-N 0.000 description 2
- 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 2
- 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 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
- 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 2
- GWNIGUKSRJBIHX-STQMWFEESA-N Gly-Tyr-Arg Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)NC(=O)CN)O GWNIGUKSRJBIHX-STQMWFEESA-N 0.000 description 2
- HQSKKSLNLSTONK-JTQLQIEISA-N Gly-Tyr-Gly Chemical compound OC(=O)CNC(=O)[C@@H](NC(=O)CN)CC1=CC=C(O)C=C1 HQSKKSLNLSTONK-JTQLQIEISA-N 0.000 description 2
- 239000004471 Glycine Substances 0.000 description 2
- 101710154606 Hemagglutinin Proteins 0.000 description 2
- SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 description 2
- FZKFYOXDVWDELO-KBPBESRZSA-N His-Gly-Tyr Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)NCC(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O FZKFYOXDVWDELO-KBPBESRZSA-N 0.000 description 2
- 108010093488 His-His-His-His-His-His Proteins 0.000 description 2
- YAEKRYQASVCDLK-JYJNAYRXSA-N His-Phe-Glu Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)O)NC(=O)[C@H](CC2=CN=CN2)N YAEKRYQASVCDLK-JYJNAYRXSA-N 0.000 description 2
- AJTBOTWDSRSUDV-ULQDDVLXSA-N His-Phe-Met Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCSC)C(O)=O AJTBOTWDSRSUDV-ULQDDVLXSA-N 0.000 description 2
- BRQKGRLDDDQWQJ-MBLNEYKQSA-N His-Thr-Ala Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C)C(O)=O BRQKGRLDDDQWQJ-MBLNEYKQSA-N 0.000 description 2
- DLTCGJZBNFOWFL-LKTVYLICSA-N His-Tyr-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)NC(=O)[C@H](CC2=CN=CN2)N DLTCGJZBNFOWFL-LKTVYLICSA-N 0.000 description 2
- 208000017604 Hodgkin disease Diseases 0.000 description 2
- 208000010747 Hodgkins lymphoma Diseases 0.000 description 2
- 101000935587 Homo sapiens Flavin reductase (NADPH) Proteins 0.000 description 2
- 101001109501 Homo sapiens NKG2-D type II integral membrane protein Proteins 0.000 description 2
- 101000971513 Homo sapiens Natural killer cells antigen CD94 Proteins 0.000 description 2
- 101000581981 Homo sapiens Neural cell adhesion molecule 1 Proteins 0.000 description 2
- DMHGKBGOUAJRHU-UHFFFAOYSA-N Ile-Arg-Pro Natural products CCC(C)C(N)C(=O)NC(CCCN=C(N)N)C(=O)N1CCCC1C(O)=O DMHGKBGOUAJRHU-UHFFFAOYSA-N 0.000 description 2
- FJWYJQRCVNGEAQ-ZPFDUUQYSA-N Ile-Asn-Lys Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CCCCN)C(=O)O)N FJWYJQRCVNGEAQ-ZPFDUUQYSA-N 0.000 description 2
- 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 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
- 102000006496 Immunoglobulin Heavy Chains Human genes 0.000 description 2
- 108010019476 Immunoglobulin Heavy Chains Proteins 0.000 description 2
- 108010002350 Interleukin-2 Proteins 0.000 description 2
- HGCNKOLVKRAVHD-UHFFFAOYSA-N L-Met-L-Phe Natural products CSCCC(N)C(=O)NC(C(O)=O)CC1=CC=CC=C1 HGCNKOLVKRAVHD-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
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 description 2
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 2
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 description 2
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 description 2
- 241000282842 Lama glama Species 0.000 description 2
- XIRYQRLFHWWWTC-QEJZJMRPSA-N Leu-Ala-Phe Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 XIRYQRLFHWWWTC-QEJZJMRPSA-N 0.000 description 2
- 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 2
- NEEOBPIXKWSBRF-IUCAKERBSA-N Leu-Glu-Gly Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)NCC(O)=O NEEOBPIXKWSBRF-IUCAKERBSA-N 0.000 description 2
- LAGPXKYZCCTSGQ-JYJNAYRXSA-N Leu-Glu-Phe Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O LAGPXKYZCCTSGQ-JYJNAYRXSA-N 0.000 description 2
- YFBBUHJJUXXZOF-UWVGGRQHSA-N Leu-Gly-Pro Chemical compound CC(C)C[C@H](N)C(=O)NCC(=O)N1CCC[C@H]1C(O)=O YFBBUHJJUXXZOF-UWVGGRQHSA-N 0.000 description 2
- USLNHQZCDQJBOV-ZPFDUUQYSA-N Leu-Ile-Asn Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(N)=O)C(O)=O USLNHQZCDQJBOV-ZPFDUUQYSA-N 0.000 description 2
- IEWBEPKLKUXQBU-VOAKCMCISA-N Leu-Leu-Thr Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O IEWBEPKLKUXQBU-VOAKCMCISA-N 0.000 description 2
- YRRCOJOXAJNSAX-IHRRRGAJSA-N Leu-Pro-Lys Chemical compound CC(C)C[C@@H](C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCCN)C(=O)O)N YRRCOJOXAJNSAX-IHRRRGAJSA-N 0.000 description 2
- 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 2
- ZJZNLRVCZWUONM-JXUBOQSCSA-N Leu-Thr-Ala Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C)C(O)=O ZJZNLRVCZWUONM-JXUBOQSCSA-N 0.000 description 2
- LSLUTXRANSUGFY-XIRDDKMYSA-N Leu-Trp-Asp Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CC(O)=O)C(O)=O LSLUTXRANSUGFY-XIRDDKMYSA-N 0.000 description 2
- HGZHSNBZDOLMLH-DCAQKATOSA-N Lys-Asn-Met Chemical compound CSCC[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CCCCN)N HGZHSNBZDOLMLH-DCAQKATOSA-N 0.000 description 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 2
- MIXPUVSPPOWTCR-FXQIFTODSA-N Met-Ser-Ser Chemical compound [H]N[C@@H](CCSC)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O MIXPUVSPPOWTCR-FXQIFTODSA-N 0.000 description 2
- 208000034578 Multiple myelomas Diseases 0.000 description 2
- 208000033776 Myeloid Acute Leukemia Diseases 0.000 description 2
- 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 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
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 2
- 108010079364 N-glycylalanine Proteins 0.000 description 2
- 108091008877 NK cell receptors Proteins 0.000 description 2
- 102100022680 NKG2-D type II integral membrane protein Human genes 0.000 description 2
- 102100027347 Neural cell adhesion molecule 1 Human genes 0.000 description 2
- 206010030155 Oesophageal carcinoma Diseases 0.000 description 2
- 101710093908 Outer capsid protein VP4 Proteins 0.000 description 2
- 101710135467 Outer capsid protein sigma-1 Proteins 0.000 description 2
- 206010033128 Ovarian cancer Diseases 0.000 description 2
- 206010061535 Ovarian neoplasm Diseases 0.000 description 2
- 102000004503 Perforin Human genes 0.000 description 2
- 108010056995 Perforin Proteins 0.000 description 2
- KHGNFPUMBJSZSM-UHFFFAOYSA-N Perforine Natural products COC1=C2CCC(O)C(CCC(C)(C)O)(OC)C2=NC2=C1C=CO2 KHGNFPUMBJSZSM-UHFFFAOYSA-N 0.000 description 2
- JXQVYPWVGUOIDV-MXAVVETBSA-N Phe-Ser-Ile Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O JXQVYPWVGUOIDV-MXAVVETBSA-N 0.000 description 2
- 206010035226 Plasma cell myeloma Diseases 0.000 description 2
- CGBYDGAJHSOGFQ-LPEHRKFASA-N Pro-Ala-Pro Chemical compound C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@@H]2CCCN2 CGBYDGAJHSOGFQ-LPEHRKFASA-N 0.000 description 2
- 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 2
- GZNYIXWOIUFLGO-ZJDVBMNYSA-N Pro-Thr-Thr Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O GZNYIXWOIUFLGO-ZJDVBMNYSA-N 0.000 description 2
- IIRBTQHFVNGPMQ-AVGNSLFASA-N Pro-Val-Lys Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@@H]1CCCN1 IIRBTQHFVNGPMQ-AVGNSLFASA-N 0.000 description 2
- 206010060862 Prostate cancer Diseases 0.000 description 2
- 208000000236 Prostatic Neoplasms Diseases 0.000 description 2
- 101710176177 Protein A56 Proteins 0.000 description 2
- 108010076504 Protein Sorting Signals Proteins 0.000 description 2
- 108010079005 RDV peptide Proteins 0.000 description 2
- 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 2
- BRKHVZNDAOMAHX-BIIVOSGPSA-N Ser-Ala-Pro Chemical compound C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CO)N BRKHVZNDAOMAHX-BIIVOSGPSA-N 0.000 description 2
- IDCKUIWEIZYVSO-WFBYXXMGSA-N Ser-Ala-Trp Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@@H](NC(=O)[C@@H](N)CO)C)C(O)=O)=CNC2=C1 IDCKUIWEIZYVSO-WFBYXXMGSA-N 0.000 description 2
- NLQUOHDCLSFABG-GUBZILKMSA-N Ser-Arg-Arg Chemical compound NC(N)=NCCC[C@H](NC(=O)[C@H](CO)N)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O NLQUOHDCLSFABG-GUBZILKMSA-N 0.000 description 2
- QFBNNYNWKYKVJO-DCAQKATOSA-N Ser-Arg-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)CO)CCCN=C(N)N QFBNNYNWKYKVJO-DCAQKATOSA-N 0.000 description 2
- RZUOXAKGNHXZTB-GUBZILKMSA-N Ser-Arg-Met Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCSC)C(O)=O RZUOXAKGNHXZTB-GUBZILKMSA-N 0.000 description 2
- NRCJWSGXMAPYQX-LPEHRKFASA-N Ser-Arg-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CO)N)C(=O)O NRCJWSGXMAPYQX-LPEHRKFASA-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
- 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 2
- FBLNYDYPCLFTSP-IXOXFDKPSA-N Ser-Phe-Thr Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)O)C(O)=O FBLNYDYPCLFTSP-IXOXFDKPSA-N 0.000 description 2
- 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 2
- 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 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
- ZWSZBWAFDZRBNM-UBHSHLNASA-N Ser-Trp-Ser Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CO)C(O)=O ZWSZBWAFDZRBNM-UBHSHLNASA-N 0.000 description 2
- FHXGMDRKJHKLKW-QWRGUYRKSA-N Ser-Tyr-Gly Chemical compound OC[C@H](N)C(=O)N[C@H](C(=O)NCC(O)=O)CC1=CC=C(O)C=C1 FHXGMDRKJHKLKW-QWRGUYRKSA-N 0.000 description 2
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 2
- 108010003723 Single-Domain Antibodies Proteins 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 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
- UKBSDLHIKIXJKH-HJGDQZAQSA-N Thr-Arg-Glu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(O)=O UKBSDLHIKIXJKH-HJGDQZAQSA-N 0.000 description 2
- CTONFVDJYCAMQM-IUKAMOBKSA-N Thr-Asn-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H]([C@@H](C)O)N CTONFVDJYCAMQM-IUKAMOBKSA-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
- NLJKZUGAIIRWJN-LKXGYXEUSA-N Thr-Asp-Cys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CS)C(=O)O)N)O NLJKZUGAIIRWJN-LKXGYXEUSA-N 0.000 description 2
- OHAJHDJOCKKJLV-LKXGYXEUSA-N Thr-Asp-Ser Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(O)=O OHAJHDJOCKKJLV-LKXGYXEUSA-N 0.000 description 2
- 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 2
- RCEHMXVEMNXRIW-IRIUXVKKSA-N Thr-Gln-Tyr Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O)N)O RCEHMXVEMNXRIW-IRIUXVKKSA-N 0.000 description 2
- JRAUIKJSEAKTGD-TUBUOCAGSA-N Thr-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]([C@@H](C)O)N JRAUIKJSEAKTGD-TUBUOCAGSA-N 0.000 description 2
- IHAPJUHCZXBPHR-WZLNRYEVSA-N Thr-Ile-Tyr Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O)NC(=O)[C@H]([C@@H](C)O)N IHAPJUHCZXBPHR-WZLNRYEVSA-N 0.000 description 2
- 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 2
- MEBDIIKMUUNBSB-RPTUDFQQSA-N Thr-Phe-Tyr Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O MEBDIIKMUUNBSB-RPTUDFQQSA-N 0.000 description 2
- QJIODPFLAASXJC-JHYOHUSXSA-N Thr-Thr-Phe Chemical compound C[C@H]([C@@H](C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)N)O QJIODPFLAASXJC-JHYOHUSXSA-N 0.000 description 2
- PWONLXBUSVIZPH-RHYQMDGZSA-N Thr-Val-Lys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)O)N)O PWONLXBUSVIZPH-RHYQMDGZSA-N 0.000 description 2
- 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 2
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 2
- 239000004473 Threonine Substances 0.000 description 2
- 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 2
- KIMOCKLJBXHFIN-YLVFBTJISA-N Trp-Ile-Gly Chemical compound C1=CC=C2C(C[C@H](N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(O)=O)=CNC2=C1 KIMOCKLJBXHFIN-YLVFBTJISA-N 0.000 description 2
- KULBQAVOXHQLIY-HSCHXYMDSA-N Trp-Ile-Leu Chemical compound C1=CC=C2C(C[C@H](N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(O)=O)=CNC2=C1 KULBQAVOXHQLIY-HSCHXYMDSA-N 0.000 description 2
- CRCHQCUINSOGFD-JBACZVJFSA-N Trp-Tyr-Glu Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CC3=CC=C(C=C3)O)C(=O)N[C@@H](CCC(=O)O)C(=O)O)N CRCHQCUINSOGFD-JBACZVJFSA-N 0.000 description 2
- 102000004142 Trypsin Human genes 0.000 description 2
- 108090000631 Trypsin Proteins 0.000 description 2
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 description 2
- SEFNTZYRPGBDCY-IHRRRGAJSA-N Tyr-Arg-Cys Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CS)C(=O)O)N)O SEFNTZYRPGBDCY-IHRRRGAJSA-N 0.000 description 2
- SGFIXFAHVWJKTD-KJEVXHAQSA-N Tyr-Arg-Thr 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@@H](C)O)C(O)=O SGFIXFAHVWJKTD-KJEVXHAQSA-N 0.000 description 2
- TZXFLDNBYYGLKA-BZSNNMDCSA-N Tyr-Asp-Tyr Chemical compound C([C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(O)=O)C1=CC=C(O)C=C1 TZXFLDNBYYGLKA-BZSNNMDCSA-N 0.000 description 2
- ZRPLVTZTKPPSBT-AVGNSLFASA-N Tyr-Glu-Ser Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(O)=O ZRPLVTZTKPPSBT-AVGNSLFASA-N 0.000 description 2
- HIINQLBHPIQYHN-JTQLQIEISA-N Tyr-Gly-Gly Chemical compound OC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1 HIINQLBHPIQYHN-JTQLQIEISA-N 0.000 description 2
- 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 2
- OHOVFPKXPZODHS-SJWGOKEGSA-N Tyr-Ile-Pro Chemical compound CC[C@H](C)[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CC2=CC=C(C=C2)O)N OHOVFPKXPZODHS-SJWGOKEGSA-N 0.000 description 2
- UBKKNELWDCBNCF-STQMWFEESA-N Tyr-Met-Gly Chemical compound OC(=O)CNC(=O)[C@H](CCSC)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 UBKKNELWDCBNCF-STQMWFEESA-N 0.000 description 2
- QPOUERMDWKKZEG-HJPIBITLSA-N Tyr-Ser-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 QPOUERMDWKKZEG-HJPIBITLSA-N 0.000 description 2
- UUBKSZNKJUJQEJ-JRQIVUDYSA-N Tyr-Thr-Asp Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)N)O UUBKSZNKJUJQEJ-JRQIVUDYSA-N 0.000 description 2
- ZZDYJFVIKVSUFA-WLTAIBSBSA-N Tyr-Thr-Gly Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(O)=O ZZDYJFVIKVSUFA-WLTAIBSBSA-N 0.000 description 2
- 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 2
- UUJHRSTVQCFDPA-UFYCRDLUSA-N Tyr-Tyr-Val Chemical compound C([C@@H](C(=O)N[C@@H](C(C)C)C(O)=O)NC(=O)[C@@H](N)CC=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 UUJHRSTVQCFDPA-UFYCRDLUSA-N 0.000 description 2
- XQVRMLRMTAGSFJ-QXEWZRGKSA-N Val-Asp-Arg Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)N XQVRMLRMTAGSFJ-QXEWZRGKSA-N 0.000 description 2
- OVBMCNDKCWAXMZ-NAKRPEOUSA-N Val-Ile-Ser Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](C(C)C)N OVBMCNDKCWAXMZ-NAKRPEOUSA-N 0.000 description 2
- KTEZUXISLQTDDQ-NHCYSSNCSA-N Val-Lys-Asp Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(=O)O)C(=O)O)N KTEZUXISLQTDDQ-NHCYSSNCSA-N 0.000 description 2
- SBJCTAZFSZXWSR-AVGNSLFASA-N Val-Met-His Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)N SBJCTAZFSZXWSR-AVGNSLFASA-N 0.000 description 2
- VTIAEOKFUJJBTC-YDHLFZDLSA-N Val-Tyr-Asp Chemical compound CC(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 VTIAEOKFUJJBTC-YDHLFZDLSA-N 0.000 description 2
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 description 2
- 108010081404 acein-2 Proteins 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 230000003213 activating effect Effects 0.000 description 2
- 238000001261 affinity purification Methods 0.000 description 2
- 235000004279 alanine Nutrition 0.000 description 2
- 108010044940 alanylglutamine Proteins 0.000 description 2
- 108010050025 alpha-glutamyltryptophan Proteins 0.000 description 2
- 230000003321 amplification Effects 0.000 description 2
- 230000000840 anti-viral effect Effects 0.000 description 2
- 230000000890 antigenic effect Effects 0.000 description 2
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 2
- 108010018691 arginyl-threonyl-arginine Proteins 0.000 description 2
- 235000009582 asparagine Nutrition 0.000 description 2
- 229960001230 asparagine Drugs 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004556 brain Anatomy 0.000 description 2
- 238000013368 capillary electrophoresis sodium dodecyl sulfate analysis Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 208000029742 colonic neoplasm Diseases 0.000 description 2
- 235000018417 cysteine Nutrition 0.000 description 2
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 2
- 108010060199 cysteinylproline Proteins 0.000 description 2
- 231100000433 cytotoxic Toxicity 0.000 description 2
- 210000001151 cytotoxic T lymphocyte Anatomy 0.000 description 2
- 230000001472 cytotoxic effect Effects 0.000 description 2
- 231100000135 cytotoxicity Toxicity 0.000 description 2
- 230000003013 cytotoxicity Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000005547 deoxyribonucleotide Substances 0.000 description 2
- 125000002637 deoxyribonucleotide group Chemical group 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 208000035475 disorder Diseases 0.000 description 2
- 201000004101 esophageal cancer Diseases 0.000 description 2
- 210000003527 eukaryotic cell Anatomy 0.000 description 2
- 238000001943 fluorescence-activated cell sorting Methods 0.000 description 2
- 229960000304 folic acid Drugs 0.000 description 2
- 235000019152 folic acid Nutrition 0.000 description 2
- 239000011724 folic acid Substances 0.000 description 2
- 201000010175 gallbladder cancer Diseases 0.000 description 2
- 238000010353 genetic engineering Methods 0.000 description 2
- 108010085059 glutamyl-arginyl-proline Proteins 0.000 description 2
- 108010001064 glycyl-glycyl-glycyl-glycine Proteins 0.000 description 2
- 108010045126 glycyl-tyrosyl-glycine Proteins 0.000 description 2
- 108010077515 glycylproline Proteins 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 239000000185 hemagglutinin Substances 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 230000001900 immune effect Effects 0.000 description 2
- 230000002163 immunogen Effects 0.000 description 2
- 230000005847 immunogenicity Effects 0.000 description 2
- 108091008042 inhibitory receptors Proteins 0.000 description 2
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 2
- 229960000367 inositol Drugs 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 230000003834 intracellular effect Effects 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 229960000310 isoleucine Drugs 0.000 description 2
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 description 2
- BPHPUYQFMNQIOC-NXRLNHOXSA-N isopropyl beta-D-thiogalactopyranoside Chemical compound CC(C)S[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O BPHPUYQFMNQIOC-NXRLNHOXSA-N 0.000 description 2
- 108010076756 leucyl-alanyl-phenylalanine Proteins 0.000 description 2
- 108010034529 leucyl-lysine Proteins 0.000 description 2
- 210000000265 leukocyte Anatomy 0.000 description 2
- 150000002632 lipids Chemical class 0.000 description 2
- 208000012804 lymphangiosarcoma Diseases 0.000 description 2
- 210000004698 lymphocyte Anatomy 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 210000000274 microglia Anatomy 0.000 description 2
- 230000000116 mitigating effect Effects 0.000 description 2
- 238000010369 molecular cloning Methods 0.000 description 2
- 238000003199 nucleic acid amplification method Methods 0.000 description 2
- 239000002773 nucleotide Substances 0.000 description 2
- 125000003729 nucleotide group Chemical group 0.000 description 2
- 230000002018 overexpression Effects 0.000 description 2
- 230000001717 pathogenic effect Effects 0.000 description 2
- 230000001575 pathological effect Effects 0.000 description 2
- 229930192851 perforin Natural products 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- 210000004976 peripheral blood cell Anatomy 0.000 description 2
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 2
- 235000008729 phenylalanine Nutrition 0.000 description 2
- 229960005190 phenylalanine Drugs 0.000 description 2
- 108010070409 phenylalanyl-glycyl-glycine Proteins 0.000 description 2
- 230000026731 phosphorylation Effects 0.000 description 2
- 238000006366 phosphorylation reaction Methods 0.000 description 2
- 230000004481 post-translational protein modification Effects 0.000 description 2
- 108010077112 prolyl-proline Proteins 0.000 description 2
- 108010079317 prolyl-tyrosine Proteins 0.000 description 2
- 108010070643 prolylglutamic acid Proteins 0.000 description 2
- 230000005180 public health Effects 0.000 description 2
- 230000002285 radioactive effect Effects 0.000 description 2
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 235000004400 serine Nutrition 0.000 description 2
- 239000012679 serum free medium Substances 0.000 description 2
- 108010069117 seryl-lysyl-aspartic acid Proteins 0.000 description 2
- 238000003998 size exclusion chromatography high performance liquid chromatography Methods 0.000 description 2
- 238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000012430 stability testing Methods 0.000 description 2
- 238000003153 stable transfection Methods 0.000 description 2
- 235000008521 threonine Nutrition 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 239000012588 trypsin Substances 0.000 description 2
- 108010005834 tyrosyl-alanyl-glycine Proteins 0.000 description 2
- 108010078580 tyrosylleucine Proteins 0.000 description 2
- 210000003708 urethra Anatomy 0.000 description 2
- 239000004474 valine Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- BRPMXFSTKXXNHF-IUCAKERBSA-N (2s)-1-[2-[[(2s)-pyrrolidine-2-carbonyl]amino]acetyl]pyrrolidine-2-carboxylic acid Chemical compound OC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H]1NCCC1 BRPMXFSTKXXNHF-IUCAKERBSA-N 0.000 description 1
- IGXNPQWXIRIGBF-KEOOTSPTSA-N (2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-amino-3-(1h-imidazol-5-yl)propanoyl]amino]-3-(1h-imidazol-5-yl)propanoyl]amino]-3-(1h-imidazol-5-yl)propanoyl]amino]-3-(1h-imidazol-5-yl)propanoyl]amino]-3-(1h-imidazol-5-yl)propanoic acid Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CC=1NC=NC=1)C(O)=O)C1=CN=CN1 IGXNPQWXIRIGBF-KEOOTSPTSA-N 0.000 description 1
- 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 1
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 1
- QMOQBVOBWVNSNO-UHFFFAOYSA-N 2-[[2-[[2-[(2-azaniumylacetyl)amino]acetyl]amino]acetyl]amino]acetate Chemical compound NCC(=O)NCC(=O)NCC(=O)NCC(O)=O QMOQBVOBWVNSNO-UHFFFAOYSA-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
- 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
- 102100033400 4F2 cell-surface antigen heavy chain Human genes 0.000 description 1
- 206010000830 Acute leukaemia Diseases 0.000 description 1
- 208000024893 Acute lymphoblastic leukemia Diseases 0.000 description 1
- 208000014697 Acute lymphocytic leukaemia Diseases 0.000 description 1
- 206010000871 Acute monocytic leukaemia Diseases 0.000 description 1
- 206010000890 Acute myelomonocytic leukaemia Diseases 0.000 description 1
- 208000036762 Acute promyelocytic leukaemia Diseases 0.000 description 1
- AAQGRPOPTAUUBM-ZLUOBGJFSA-N Ala-Ala-Asn Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(O)=O AAQGRPOPTAUUBM-ZLUOBGJFSA-N 0.000 description 1
- DKJPOZOEBONHFS-ZLUOBGJFSA-N Ala-Ala-Asp Chemical compound C[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@H](C(O)=O)CC(O)=O DKJPOZOEBONHFS-ZLUOBGJFSA-N 0.000 description 1
- BUANFPRKJKJSRR-ACZMJKKPSA-N Ala-Ala-Gln Chemical compound C[C@H]([NH3+])C(=O)N[C@@H](C)C(=O)N[C@H](C([O-])=O)CCC(N)=O BUANFPRKJKJSRR-ACZMJKKPSA-N 0.000 description 1
- CXRCVCURMBFFOL-FXQIFTODSA-N Ala-Ala-Pro Chemical compound C[C@H](N)C(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(O)=O CXRCVCURMBFFOL-FXQIFTODSA-N 0.000 description 1
- JBVSSSZFNTXJDX-YTLHQDLWSA-N Ala-Ala-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)N JBVSSSZFNTXJDX-YTLHQDLWSA-N 0.000 description 1
- SVBXIUDNTRTKHE-CIUDSAMLSA-N Ala-Arg-Glu Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(O)=O SVBXIUDNTRTKHE-CIUDSAMLSA-N 0.000 description 1
- JAMAWBXXKFGFGX-KZVJFYERSA-N Ala-Arg-Thr Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(O)=O JAMAWBXXKFGFGX-KZVJFYERSA-N 0.000 description 1
- GFBLJMHGHAXGNY-ZLUOBGJFSA-N Ala-Asn-Asp Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(O)=O)C(O)=O GFBLJMHGHAXGNY-ZLUOBGJFSA-N 0.000 description 1
- YSMPVONNIWLJML-FXQIFTODSA-N Ala-Asp-Pro Chemical compound C[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N1CCC[C@H]1C(O)=O YSMPVONNIWLJML-FXQIFTODSA-N 0.000 description 1
- 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 1
- KUDREHRZRIVKHS-UWJYBYFXSA-N Ala-Asp-Tyr Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O KUDREHRZRIVKHS-UWJYBYFXSA-N 0.000 description 1
- CXZFXHGJJPVUJE-CIUDSAMLSA-N Ala-Cys-Leu Chemical compound C[C@@H](C(=O)N[C@@H](CS)C(=O)N[C@@H](CC(C)C)C(=O)O)N CXZFXHGJJPVUJE-CIUDSAMLSA-N 0.000 description 1
- NKJBKNVQHBZUIX-ACZMJKKPSA-N Ala-Gln-Asp Chemical compound C[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(O)=O NKJBKNVQHBZUIX-ACZMJKKPSA-N 0.000 description 1
- IFTVANMRTIHKML-WDSKDSINSA-N Ala-Gln-Gly Chemical compound C[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(O)=O IFTVANMRTIHKML-WDSKDSINSA-N 0.000 description 1
- CZPAHAKGPDUIPJ-CIUDSAMLSA-N Ala-Gln-Pro Chemical compound C[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N1CCC[C@H]1C(O)=O CZPAHAKGPDUIPJ-CIUDSAMLSA-N 0.000 description 1
- WGDNWOMKBUXFHR-BQBZGAKWSA-N Ala-Gly-Arg Chemical compound C[C@H](N)C(=O)NCC(=O)N[C@H](C(O)=O)CCCN=C(N)N WGDNWOMKBUXFHR-BQBZGAKWSA-N 0.000 description 1
- WMYJZJRILUVVRG-WDSKDSINSA-N Ala-Gly-Gln Chemical compound C[C@H](N)C(=O)NCC(=O)N[C@H](C(O)=O)CCC(N)=O WMYJZJRILUVVRG-WDSKDSINSA-N 0.000 description 1
- VGPWRRFOPXVGOH-BYPYZUCNSA-N Ala-Gly-Gly Chemical compound C[C@H](N)C(=O)NCC(=O)NCC(O)=O VGPWRRFOPXVGOH-BYPYZUCNSA-N 0.000 description 1
- LMFXXZPPZDCPTA-ZKWXMUAHSA-N Ala-Gly-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)CNC(=O)[C@H](C)N LMFXXZPPZDCPTA-ZKWXMUAHSA-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
- QQACQIHVWCVBBR-GVARAGBVSA-N Ala-Ile-Tyr Chemical compound [H]N[C@@H](C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O QQACQIHVWCVBBR-GVARAGBVSA-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
- BLTRAARCJYVJKV-QEJZJMRPSA-N Ala-Lys-Phe Chemical compound C[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1ccccc1)C(O)=O BLTRAARCJYVJKV-QEJZJMRPSA-N 0.000 description 1
- 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 1
- KQESEZXHYOUIIM-CQDKDKBSSA-N Ala-Lys-Tyr Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O KQESEZXHYOUIIM-CQDKDKBSSA-N 0.000 description 1
- IPZQNYYAYVRKKK-FXQIFTODSA-N Ala-Pro-Ala Chemical compound C[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(O)=O IPZQNYYAYVRKKK-FXQIFTODSA-N 0.000 description 1
- MAZZQZWCCYJQGZ-GUBZILKMSA-N Ala-Pro-Arg Chemical compound [H]N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O MAZZQZWCCYJQGZ-GUBZILKMSA-N 0.000 description 1
- FFZJHQODAYHGPO-KZVJFYERSA-N Ala-Pro-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](C)N FFZJHQODAYHGPO-KZVJFYERSA-N 0.000 description 1
- 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 1
- 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 1
- HCBKAOZYACJUEF-XQXXSGGOSA-N Ala-Thr-Gln Chemical compound N[C@@H](C)C(=O)N[C@@H]([C@H](O)C)C(=O)N[C@@H](CCC(N)=O)C(=O)O HCBKAOZYACJUEF-XQXXSGGOSA-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
- QOIGKCBMXUCDQU-KDXUFGMBSA-N Ala-Thr-Pro Chemical compound C[C@H]([C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](C)N)O QOIGKCBMXUCDQU-KDXUFGMBSA-N 0.000 description 1
- 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 1
- VQBULXOHAZSTQY-GKCIPKSASA-N Ala-Trp-Phe Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O VQBULXOHAZSTQY-GKCIPKSASA-N 0.000 description 1
- TVUFMYKTYXTRPY-HERUPUMHSA-N Ala-Trp-Ser Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CO)C(O)=O TVUFMYKTYXTRPY-HERUPUMHSA-N 0.000 description 1
- ZXKNLCPUNZPFGY-LEWSCRJBSA-N Ala-Tyr-Pro Chemical compound C[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N2CCC[C@@H]2C(=O)O)N ZXKNLCPUNZPFGY-LEWSCRJBSA-N 0.000 description 1
- 201000003076 Angiosarcoma Diseases 0.000 description 1
- 108010032595 Antibody Binding Sites Proteins 0.000 description 1
- DBKNLHKEVPZVQC-LPEHRKFASA-N Arg-Ala-Pro Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H](C)C(=O)N1CCC[C@@H]1C(O)=O DBKNLHKEVPZVQC-LPEHRKFASA-N 0.000 description 1
- 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 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
- TTXYKSADPSNOIF-IHRRRGAJSA-N Arg-Asp-Phe Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O TTXYKSADPSNOIF-IHRRRGAJSA-N 0.000 description 1
- MFAMTAVAFBPXDC-LPEHRKFASA-N Arg-Asp-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCCN=C(N)N)N)C(=O)O MFAMTAVAFBPXDC-LPEHRKFASA-N 0.000 description 1
- VXXHDZKEQNGXNU-QXEWZRGKSA-N Arg-Asp-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H](N)CCCN=C(N)N VXXHDZKEQNGXNU-QXEWZRGKSA-N 0.000 description 1
- YHQGEARSFILVHL-HJGDQZAQSA-N Arg-Gln-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CCCN=C(N)N)N)O YHQGEARSFILVHL-HJGDQZAQSA-N 0.000 description 1
- HPKSHFSEXICTLI-CIUDSAMLSA-N Arg-Glu-Ala Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(O)=O HPKSHFSEXICTLI-CIUDSAMLSA-N 0.000 description 1
- QAODJPUKWNNNRP-DCAQKATOSA-N Arg-Glu-Arg Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O QAODJPUKWNNNRP-DCAQKATOSA-N 0.000 description 1
- OHYQKYUTLIPFOX-ZPFDUUQYSA-N Arg-Glu-Ile Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O OHYQKYUTLIPFOX-ZPFDUUQYSA-N 0.000 description 1
- NXDXECQFKHXHAM-HJGDQZAQSA-N Arg-Glu-Thr Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O NXDXECQFKHXHAM-HJGDQZAQSA-N 0.000 description 1
- JQFJNGVSGOUQDH-XIRDDKMYSA-N Arg-Glu-Trp Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCN=C(N)N)N)C(O)=O)=CNC2=C1 JQFJNGVSGOUQDH-XIRDDKMYSA-N 0.000 description 1
- CYXCAHZVPFREJD-LURJTMIESA-N Arg-Gly-Gly Chemical compound NC(=N)NCCC[C@H](N)C(=O)NCC(=O)NCC(O)=O CYXCAHZVPFREJD-LURJTMIESA-N 0.000 description 1
- NVUIWHJLPSZZQC-CYDGBPFRSA-N Arg-Ile-Arg Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O NVUIWHJLPSZZQC-CYDGBPFRSA-N 0.000 description 1
- FRMQITGHXMUNDF-GMOBBJLQSA-N Arg-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](CCCN=C(N)N)N FRMQITGHXMUNDF-GMOBBJLQSA-N 0.000 description 1
- FSNVAJOPUDVQAR-AVGNSLFASA-N Arg-Lys-Arg Chemical compound NC(=N)NCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O FSNVAJOPUDVQAR-AVGNSLFASA-N 0.000 description 1
- GSUFZRURORXYTM-STQMWFEESA-N Arg-Phe-Gly Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@H](C(=O)NCC(O)=O)CC1=CC=CC=C1 GSUFZRURORXYTM-STQMWFEESA-N 0.000 description 1
- BSYKSCBTTQKOJG-GUBZILKMSA-N Arg-Pro-Ala Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(O)=O BSYKSCBTTQKOJG-GUBZILKMSA-N 0.000 description 1
- OVQJAKFLFTZDNC-GUBZILKMSA-N Arg-Pro-Asp Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(O)=O)C(O)=O OVQJAKFLFTZDNC-GUBZILKMSA-N 0.000 description 1
- FVBZXNSRIDVYJS-AVGNSLFASA-N Arg-Pro-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCN=C(N)N FVBZXNSRIDVYJS-AVGNSLFASA-N 0.000 description 1
- ADPACBMPYWJJCE-FXQIFTODSA-N Arg-Ser-Asp Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(O)=O ADPACBMPYWJJCE-FXQIFTODSA-N 0.000 description 1
- URAUIUGLHBRPMF-NAKRPEOUSA-N Arg-Ser-Ile Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O URAUIUGLHBRPMF-NAKRPEOUSA-N 0.000 description 1
- BECXEHHOZNFFFX-IHRRRGAJSA-N Arg-Ser-Tyr Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O BECXEHHOZNFFFX-IHRRRGAJSA-N 0.000 description 1
- AIFHRTPABBBHKU-RCWTZXSCSA-N Arg-Thr-Arg Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H]([C@H](O)C)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O AIFHRTPABBBHKU-RCWTZXSCSA-N 0.000 description 1
- WCZXPVPHUMYLMS-VEVYYDQMSA-N Arg-Thr-Asp Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(O)=O WCZXPVPHUMYLMS-VEVYYDQMSA-N 0.000 description 1
- UZSQXCMNUPKLCC-FJXKBIBVSA-N Arg-Thr-Gly Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(O)=O UZSQXCMNUPKLCC-FJXKBIBVSA-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
- ZPWMEWYQBWSGAO-ZJDVBMNYSA-N Arg-Thr-Thr Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O ZPWMEWYQBWSGAO-ZJDVBMNYSA-N 0.000 description 1
- OGZBJJLRKQZRHL-KJEVXHAQSA-N Arg-Thr-Tyr Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H]([C@H](O)C)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 OGZBJJLRKQZRHL-KJEVXHAQSA-N 0.000 description 1
- XRNXPIGJPQHCPC-RCWTZXSCSA-N Arg-Thr-Val Chemical compound CC(C)[C@H](NC(=O)[C@@H](NC(=O)[C@@H](N)CCCNC(N)=N)[C@@H](C)O)C(O)=O XRNXPIGJPQHCPC-RCWTZXSCSA-N 0.000 description 1
- ZUVDFJXRAICIAJ-BPUTZDHNSA-N Arg-Trp-Asp Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@H](CCCN=C(N)N)N)C(=O)N[C@@H](CC(O)=O)C(O)=O)=CNC2=C1 ZUVDFJXRAICIAJ-BPUTZDHNSA-N 0.000 description 1
- NVPHRWNWTKYIST-BPNCWPANSA-N Arg-Tyr-Ala Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](C)C(O)=O)CC1=CC=C(O)C=C1 NVPHRWNWTKYIST-BPNCWPANSA-N 0.000 description 1
- BFDDUDQCPJWQRQ-IHRRRGAJSA-N Arg-Tyr-Cys Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CCCN=C(N)N)N)O BFDDUDQCPJWQRQ-IHRRRGAJSA-N 0.000 description 1
- PFOYSEIHFVKHNF-FXQIFTODSA-N Asn-Ala-Arg Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O PFOYSEIHFVKHNF-FXQIFTODSA-N 0.000 description 1
- GXMSVVBIAMWMKO-BQBZGAKWSA-N Asn-Arg-Gly Chemical compound NC(=O)C[C@H](N)C(=O)N[C@H](C(=O)NCC(O)=O)CCCN=C(N)N GXMSVVBIAMWMKO-BQBZGAKWSA-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
- IICZCLFBILYRCU-WHFBIAKZSA-N Asn-Gly-Asp Chemical compound [H]N[C@@H](CC(N)=O)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(O)=O IICZCLFBILYRCU-WHFBIAKZSA-N 0.000 description 1
- OOWSBIOUKIUWLO-RCOVLWMOSA-N Asn-Gly-Val Chemical compound [H]N[C@@H](CC(N)=O)C(=O)NCC(=O)N[C@@H](C(C)C)C(O)=O OOWSBIOUKIUWLO-RCOVLWMOSA-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
- 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 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
- AEZCCDMZZJOGII-DCAQKATOSA-N Asn-Met-Leu Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(C)C)C(O)=O AEZCCDMZZJOGII-DCAQKATOSA-N 0.000 description 1
- RLHANKIRBONJBK-IHRRRGAJSA-N Asn-Met-Phe Chemical compound CSCC[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)NC(=O)[C@H](CC(=O)N)N RLHANKIRBONJBK-IHRRRGAJSA-N 0.000 description 1
- GKKUBLFXKRDMFC-BQBZGAKWSA-N Asn-Pro-Gly Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N1CCC[C@H]1C(=O)NCC(O)=O GKKUBLFXKRDMFC-BQBZGAKWSA-N 0.000 description 1
- OOXUBGLNDRGOKT-FXQIFTODSA-N Asn-Ser-Arg Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O OOXUBGLNDRGOKT-FXQIFTODSA-N 0.000 description 1
- DOURAOODTFJRIC-CIUDSAMLSA-N Asn-Ser-His Chemical compound C1=C(NC=N1)C[C@@H](C(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(=O)N)N DOURAOODTFJRIC-CIUDSAMLSA-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
- QUMKPKWYDVMGNT-NUMRIWBASA-N Asn-Thr-Gln Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](CC(=O)N)N)O QUMKPKWYDVMGNT-NUMRIWBASA-N 0.000 description 1
- FYRVDDJMNISIKJ-UWVGGRQHSA-N Asn-Tyr Chemical compound NC(=O)C[C@H](N)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 FYRVDDJMNISIKJ-UWVGGRQHSA-N 0.000 description 1
- JPPLRQVZMZFOSX-UWJYBYFXSA-N Asn-Tyr-Ala Chemical compound NC(=O)C[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](C)C(O)=O)CC1=CC=C(O)C=C1 JPPLRQVZMZFOSX-UWJYBYFXSA-N 0.000 description 1
- RTFXPCYMDYBZNQ-SRVKXCTJSA-N Asn-Tyr-Asn Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC(N)=O)C(O)=O RTFXPCYMDYBZNQ-SRVKXCTJSA-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
- CBWCQCANJSGUOH-ZKWXMUAHSA-N Asn-Val-Ala Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C)C(O)=O CBWCQCANJSGUOH-ZKWXMUAHSA-N 0.000 description 1
- ZAESWDKAMDVHLL-RCOVLWMOSA-N Asn-Val-Gly Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](C(C)C)C(=O)NCC(O)=O ZAESWDKAMDVHLL-RCOVLWMOSA-N 0.000 description 1
- CBHVAFXKOYAHOY-NHCYSSNCSA-N Asn-Val-Leu Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(O)=O CBHVAFXKOYAHOY-NHCYSSNCSA-N 0.000 description 1
- ZLGKHJHFYSRUBH-FXQIFTODSA-N Asp-Arg-Asp Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(O)=O ZLGKHJHFYSRUBH-FXQIFTODSA-N 0.000 description 1
- MFMJRYHVLLEMQM-DCAQKATOSA-N Asp-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](CC(=O)O)N MFMJRYHVLLEMQM-DCAQKATOSA-N 0.000 description 1
- ILJQISGMGXRZQQ-IHRRRGAJSA-N Asp-Arg-Tyr Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O ILJQISGMGXRZQQ-IHRRRGAJSA-N 0.000 description 1
- XACXDSRQIXRMNS-OLHMAJIHSA-N Asp-Asn-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CC(=O)O)N)O XACXDSRQIXRMNS-OLHMAJIHSA-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
- JNNVNVRBYUJYGS-CIUDSAMLSA-N Asp-Leu-Ala Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(O)=O JNNVNVRBYUJYGS-CIUDSAMLSA-N 0.000 description 1
- XLILXFRAKOYEJX-GUBZILKMSA-N Asp-Leu-Gln Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O XLILXFRAKOYEJX-GUBZILKMSA-N 0.000 description 1
- DONWIPDSZZJHHK-HJGDQZAQSA-N Asp-Lys-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC(=O)O)N)O DONWIPDSZZJHHK-HJGDQZAQSA-N 0.000 description 1
- HJZLUGQGJWXJCJ-CIUDSAMLSA-N Asp-Pro-Gln Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(O)=O HJZLUGQGJWXJCJ-CIUDSAMLSA-N 0.000 description 1
- YFGUZQQCSDZRBN-DCAQKATOSA-N Asp-Pro-Leu Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(O)=O YFGUZQQCSDZRBN-DCAQKATOSA-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
- OZBXOELNJBSJOA-UBHSHLNASA-N Asp-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](CC(=O)O)N OZBXOELNJBSJOA-UBHSHLNASA-N 0.000 description 1
- IQCJOIHDVFJQFV-LKXGYXEUSA-N Asp-Thr-Cys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CC(=O)O)N)O IQCJOIHDVFJQFV-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
- KCOPOPKJRHVGPE-AQZXSJQPSA-N Asp-Thr-Trp Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O KCOPOPKJRHVGPE-AQZXSJQPSA-N 0.000 description 1
- YUELDQUPTAYEGM-XIRDDKMYSA-N Asp-Trp-Leu Chemical compound CC(C)C[C@@H](C(=O)O)NC(=O)[C@H](CC1=CNC2=CC=CC=C21)NC(=O)[C@H](CC(=O)O)N YUELDQUPTAYEGM-XIRDDKMYSA-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
- 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 1
- BYLPQJAWXJWUCJ-YDHLFZDLSA-N Asp-Tyr-Val 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](C(C)C)C(O)=O BYLPQJAWXJWUCJ-YDHLFZDLSA-N 0.000 description 1
- 206010003571 Astrocytoma Diseases 0.000 description 1
- 208000010839 B-cell chronic lymphocytic leukemia Diseases 0.000 description 1
- 208000032791 BCR-ABL1 positive chronic myelogenous leukemia Diseases 0.000 description 1
- 206010004146 Basal cell carcinoma Diseases 0.000 description 1
- 206010005003 Bladder cancer Diseases 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 206010006417 Bronchial carcinoma Diseases 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 208000010667 Carcinoma of liver and intrahepatic biliary tract Diseases 0.000 description 1
- 241000282693 Cercopithecidae Species 0.000 description 1
- 208000005243 Chondrosarcoma Diseases 0.000 description 1
- 201000009047 Chordoma Diseases 0.000 description 1
- 208000006332 Choriocarcinoma Diseases 0.000 description 1
- 208000010833 Chronic myeloid leukaemia Diseases 0.000 description 1
- 108091026890 Coding region Proteins 0.000 description 1
- 108010047041 Complementarity Determining Regions Proteins 0.000 description 1
- 208000009798 Craniopharyngioma Diseases 0.000 description 1
- ZLHPWFSAUJEEAN-KBIXCLLPSA-N Cys-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](CS)N ZLHPWFSAUJEEAN-KBIXCLLPSA-N 0.000 description 1
- BLGNLNRBABWDST-CIUDSAMLSA-N Cys-Leu-Asp Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)O)NC(=O)[C@H](CS)N BLGNLNRBABWDST-CIUDSAMLSA-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
- 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 1
- AFYGNOJUTMXQIG-FXQIFTODSA-N Cys-Met-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CS)N AFYGNOJUTMXQIG-FXQIFTODSA-N 0.000 description 1
- 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 1
- SWJYSDXMTPMBHO-FXQIFTODSA-N Cys-Pro-Ser Chemical compound [H]N[C@@H](CS)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(O)=O SWJYSDXMTPMBHO-FXQIFTODSA-N 0.000 description 1
- 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 1
- NRVQLLDIJJEIIZ-VZFHVOOUSA-N Cys-Thr-Ala Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](C)C(=O)O)NC(=O)[C@H](CS)N)O NRVQLLDIJJEIIZ-VZFHVOOUSA-N 0.000 description 1
- BUAUGQJXGNRTQE-AAEUAGOBSA-N Cys-Trp-Gly Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)NCC(=O)O)NC(=O)[C@H](CS)N BUAUGQJXGNRTQE-AAEUAGOBSA-N 0.000 description 1
- ZOMMHASZJQRLFS-IHRRRGAJSA-N Cys-Tyr-Val Chemical compound CC(C)[C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)NC(=O)[C@H](CS)N ZOMMHASZJQRLFS-IHRRRGAJSA-N 0.000 description 1
- 102000053602 DNA Human genes 0.000 description 1
- 229920002307 Dextran Polymers 0.000 description 1
- 201000009051 Embryonal Carcinoma Diseases 0.000 description 1
- 206010014967 Ependymoma Diseases 0.000 description 1
- 241000283086 Equidae Species 0.000 description 1
- 241000283074 Equus asinus Species 0.000 description 1
- 108010008177 Fd immunoglobulins Proteins 0.000 description 1
- 201000008808 Fibrosarcoma Diseases 0.000 description 1
- YJIUYQKQBBQYHZ-ACZMJKKPSA-N Gln-Ala-Ala Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(O)=O YJIUYQKQBBQYHZ-ACZMJKKPSA-N 0.000 description 1
- SHERTACNJPYHAR-ACZMJKKPSA-N Gln-Ala-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCC(N)=O SHERTACNJPYHAR-ACZMJKKPSA-N 0.000 description 1
- XXLBHPPXDUWYAG-XQXXSGGOSA-N Gln-Ala-Thr Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O XXLBHPPXDUWYAG-XQXXSGGOSA-N 0.000 description 1
- RGXXLQWXBFNXTG-CIUDSAMLSA-N Gln-Arg-Ala Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(O)=O RGXXLQWXBFNXTG-CIUDSAMLSA-N 0.000 description 1
- DTMLKCYOQKZXKZ-HJGDQZAQSA-N Gln-Arg-Thr Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(O)=O DTMLKCYOQKZXKZ-HJGDQZAQSA-N 0.000 description 1
- AAOBFSKXAVIORT-GUBZILKMSA-N Gln-Asn-Leu Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(O)=O AAOBFSKXAVIORT-GUBZILKMSA-N 0.000 description 1
- CKNUKHBRCSMKMO-XHNCKOQMSA-N Gln-Asn-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC(=O)N)NC(=O)[C@H](CCC(=O)N)N)C(=O)O CKNUKHBRCSMKMO-XHNCKOQMSA-N 0.000 description 1
- RMOCFPBLHAOTDU-ACZMJKKPSA-N Gln-Asn-Ser Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(O)=O RMOCFPBLHAOTDU-ACZMJKKPSA-N 0.000 description 1
- PKVWNYGXMNWJSI-CIUDSAMLSA-N Gln-Gln-Gln Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O PKVWNYGXMNWJSI-CIUDSAMLSA-N 0.000 description 1
- NVEASDQHBRZPSU-BQBZGAKWSA-N Gln-Gln-Gly Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(O)=O NVEASDQHBRZPSU-BQBZGAKWSA-N 0.000 description 1
- 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 1
- 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 1
- TWIAMTNJOMRDAK-GUBZILKMSA-N Gln-Lys-Asp Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(O)=O TWIAMTNJOMRDAK-GUBZILKMSA-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
- OZEQPCDLCDRCGY-SOUVJXGZSA-N Gln-Phe-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CCC(=O)N)N)C(=O)O OZEQPCDLCDRCGY-SOUVJXGZSA-N 0.000 description 1
- XUMFMAVDHQDATI-DCAQKATOSA-N Gln-Pro-Arg Chemical compound NC(=O)CC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(O)=O XUMFMAVDHQDATI-DCAQKATOSA-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
- 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
- SGVGIVDZLSHSEN-RYUDHWBXSA-N Gln-Tyr-Gly Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)NCC(O)=O SGVGIVDZLSHSEN-RYUDHWBXSA-N 0.000 description 1
- VYOILACOFPPNQH-UMNHJUIQSA-N Gln-Val-Pro Chemical compound CC(C)[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CCC(=O)N)N VYOILACOFPPNQH-UMNHJUIQSA-N 0.000 description 1
- CSMHMEATMDCQNY-DZKIICNBSA-N Gln-Val-Tyr Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O CSMHMEATMDCQNY-DZKIICNBSA-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
- UTKUTMJSWKKHEM-WDSKDSINSA-N Glu-Ala-Gly Chemical compound OC(=O)CNC(=O)[C@H](C)NC(=O)[C@@H](N)CCC(O)=O UTKUTMJSWKKHEM-WDSKDSINSA-N 0.000 description 1
- AVZHGSCDKIQZPQ-CIUDSAMLSA-N Glu-Arg-Ala Chemical compound C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](N)CCC(O)=O)C(O)=O AVZHGSCDKIQZPQ-CIUDSAMLSA-N 0.000 description 1
- VTTSANCGJWLPNC-ZPFDUUQYSA-N Glu-Arg-Ile Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O VTTSANCGJWLPNC-ZPFDUUQYSA-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
- ZOXBSICWUDAOHX-GUBZILKMSA-N Glu-Asn-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](N)CCC(O)=O ZOXBSICWUDAOHX-GUBZILKMSA-N 0.000 description 1
- HJIFPJUEOGZWRI-GUBZILKMSA-N Glu-Asp-Lys Chemical compound C(CCN)C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCC(=O)O)N HJIFPJUEOGZWRI-GUBZILKMSA-N 0.000 description 1
- HUFCEIHAFNVSNR-IHRRRGAJSA-N Glu-Gln-Tyr Chemical compound OC(=O)CC[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 HUFCEIHAFNVSNR-IHRRRGAJSA-N 0.000 description 1
- KOSRFJWDECSPRO-WDSKDSINSA-N Glu-Glu Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(O)=O KOSRFJWDECSPRO-WDSKDSINSA-N 0.000 description 1
- RAUDKMVXNOWDLS-WDSKDSINSA-N Glu-Gly-Ser Chemical compound OC(=O)CC[C@H](N)C(=O)NCC(=O)N[C@@H](CO)C(O)=O RAUDKMVXNOWDLS-WDSKDSINSA-N 0.000 description 1
- ZGKXAUIVGIBISK-SZMVWBNQSA-N Glu-His-Trp Chemical compound N[C@@H](CCC(O)=O)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(O)=O ZGKXAUIVGIBISK-SZMVWBNQSA-N 0.000 description 1
- XMBSYZWANAQXEV-QWRGUYRKSA-N Glu-Phe Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 XMBSYZWANAQXEV-QWRGUYRKSA-N 0.000 description 1
- CBWKURKPYSLMJV-SOUVJXGZSA-N Glu-Phe-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CCC(=O)O)N)C(=O)O CBWKURKPYSLMJV-SOUVJXGZSA-N 0.000 description 1
- NNQDRRUXFJYCCJ-NHCYSSNCSA-N Glu-Pro-Val Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(O)=O NNQDRRUXFJYCCJ-NHCYSSNCSA-N 0.000 description 1
- 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 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
- GPSHCSTUYOQPAI-JHEQGTHGSA-N Glu-Thr-Gly Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(O)=O GPSHCSTUYOQPAI-JHEQGTHGSA-N 0.000 description 1
- 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 1
- QGAJQIGFFIQJJK-IHRRRGAJSA-N Glu-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](CCC(=O)O)N)O QGAJQIGFFIQJJK-IHRRRGAJSA-N 0.000 description 1
- QEJKKJNDDDPSMU-KKUMJFAQSA-N Glu-Tyr-Met 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](CCSC)C(O)=O QEJKKJNDDDPSMU-KKUMJFAQSA-N 0.000 description 1
- 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 1
- 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 1
- JBRBACJPBZNFMF-YUMQZZPRSA-N Gly-Ala-Lys Chemical compound NCC(=O)N[C@@H](C)C(=O)N[C@H](C(O)=O)CCCCN JBRBACJPBZNFMF-YUMQZZPRSA-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
- UPOJUWHGMDJUQZ-IUCAKERBSA-N Gly-Arg-Arg Chemical compound NC(=N)NCCC[C@H](NC(=O)CN)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O UPOJUWHGMDJUQZ-IUCAKERBSA-N 0.000 description 1
- 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 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
- SUDUYJOBLHQAMI-WHFBIAKZSA-N Gly-Asp-Cys Chemical compound NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CS)C(O)=O SUDUYJOBLHQAMI-WHFBIAKZSA-N 0.000 description 1
- LCNXZQROPKFGQK-WHFBIAKZSA-N Gly-Asp-Ser Chemical compound NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(O)=O LCNXZQROPKFGQK-WHFBIAKZSA-N 0.000 description 1
- XXGQRGQPGFYECI-WDSKDSINSA-N Gly-Cys-Glu Chemical compound NCC(=O)N[C@@H](CS)C(=O)N[C@H](C(O)=O)CCC(O)=O XXGQRGQPGFYECI-WDSKDSINSA-N 0.000 description 1
- IANBSEOVTQNGBZ-BQBZGAKWSA-N Gly-Cys-Met Chemical compound [H]NCC(=O)N[C@@H](CS)C(=O)N[C@@H](CCSC)C(O)=O IANBSEOVTQNGBZ-BQBZGAKWSA-N 0.000 description 1
- GYAUWXXORNTCHU-QWRGUYRKSA-N Gly-Cys-Tyr Chemical compound NCC(=O)N[C@@H](CS)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 GYAUWXXORNTCHU-QWRGUYRKSA-N 0.000 description 1
- JLJLBWDKDRYOPA-RYUDHWBXSA-N Gly-Gln-Tyr Chemical compound NCC(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 JLJLBWDKDRYOPA-RYUDHWBXSA-N 0.000 description 1
- QPDUVFSVVAOUHE-XVKPBYJWSA-N Gly-Gln-Val Chemical compound CC(C)[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)CN)C(O)=O QPDUVFSVVAOUHE-XVKPBYJWSA-N 0.000 description 1
- XTQFHTHIAKKCTM-YFKPBYRVSA-N Gly-Glu-Gly Chemical compound NCC(=O)N[C@@H](CCC(O)=O)C(=O)NCC(O)=O XTQFHTHIAKKCTM-YFKPBYRVSA-N 0.000 description 1
- ZQIMMEYPEXIYBB-IUCAKERBSA-N Gly-Glu-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)CN ZQIMMEYPEXIYBB-IUCAKERBSA-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
- INLIXXRWNUKVCF-JTQLQIEISA-N Gly-Gly-Tyr Chemical compound NCC(=O)NCC(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 INLIXXRWNUKVCF-JTQLQIEISA-N 0.000 description 1
- SWQALSGKVLYKDT-ZKWXMUAHSA-N Gly-Ile-Ala Chemical compound NCC(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(O)=O SWQALSGKVLYKDT-ZKWXMUAHSA-N 0.000 description 1
- 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 1
- HAXARWKYFIIHKD-ZKWXMUAHSA-N Gly-Ile-Ser Chemical compound NCC(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(O)=O HAXARWKYFIIHKD-ZKWXMUAHSA-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
- LHYJCVCQPWRMKZ-WEDXCCLWSA-N Gly-Leu-Thr Chemical compound [H]NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O LHYJCVCQPWRMKZ-WEDXCCLWSA-N 0.000 description 1
- FHQRLHFYVZAQHU-IUCAKERBSA-N Gly-Lys-Gln Chemical compound [H]NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(O)=O FHQRLHFYVZAQHU-IUCAKERBSA-N 0.000 description 1
- OQQKUTVULYLCDG-ONGXEEELSA-N Gly-Lys-Val Chemical compound CC(C)[C@H](NC(=O)[C@H](CCCCN)NC(=O)CN)C(O)=O OQQKUTVULYLCDG-ONGXEEELSA-N 0.000 description 1
- OJNZVYSGVYLQIN-BQBZGAKWSA-N Gly-Met-Asp Chemical compound [H]NCC(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(O)=O OJNZVYSGVYLQIN-BQBZGAKWSA-N 0.000 description 1
- FJWSJWACLMTDMI-WPRPVWTQSA-N Gly-Met-Val Chemical compound [H]NCC(=O)N[C@@H](CCSC)C(=O)N[C@@H](C(C)C)C(O)=O FJWSJWACLMTDMI-WPRPVWTQSA-N 0.000 description 1
- WMGHDYWNHNLGBV-ONGXEEELSA-N Gly-Phe-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)CN)CC1=CC=CC=C1 WMGHDYWNHNLGBV-ONGXEEELSA-N 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
- GLACUWHUYFBSPJ-FJXKBIBVSA-N Gly-Pro-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)CN GLACUWHUYFBSPJ-FJXKBIBVSA-N 0.000 description 1
- BMWFDYIYBAFROD-WPRPVWTQSA-N Gly-Pro-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)CN BMWFDYIYBAFROD-WPRPVWTQSA-N 0.000 description 1
- 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 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
- 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
- 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
- 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 1
- JKSMZVCGQWVTBW-STQMWFEESA-N Gly-Trp-Asn Chemical compound [H]NCC(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CC(N)=O)C(O)=O JKSMZVCGQWVTBW-STQMWFEESA-N 0.000 description 1
- UMRIXLHPZZIOML-OALUTQOASA-N Gly-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)CN UMRIXLHPZZIOML-OALUTQOASA-N 0.000 description 1
- MREVELMMFOLESM-HOCLYGCPSA-N Gly-Trp-Val Chemical compound [H]NCC(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](C(C)C)C(O)=O MREVELMMFOLESM-HOCLYGCPSA-N 0.000 description 1
- YJDALMUYJIENAG-QWRGUYRKSA-N Gly-Tyr-Asn Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)CN)O YJDALMUYJIENAG-QWRGUYRKSA-N 0.000 description 1
- WRFOZIJRODPLIA-QWRGUYRKSA-N Gly-Tyr-Cys Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)CN)O WRFOZIJRODPLIA-QWRGUYRKSA-N 0.000 description 1
- UVTSZKIATYSKIR-RYUDHWBXSA-N Gly-Tyr-Glu Chemical compound [H]NCC(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CCC(O)=O)C(O)=O UVTSZKIATYSKIR-RYUDHWBXSA-N 0.000 description 1
- 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 1
- DKJWUIYLMLUBDX-XPUUQOCRSA-N Gly-Val-Cys Chemical compound NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CS)C(=O)O DKJWUIYLMLUBDX-XPUUQOCRSA-N 0.000 description 1
- 108090000288 Glycoproteins Proteins 0.000 description 1
- 102000003886 Glycoproteins Human genes 0.000 description 1
- 239000007995 HEPES buffer Substances 0.000 description 1
- 208000001258 Hemangiosarcoma Diseases 0.000 description 1
- 206010073069 Hepatic cancer Diseases 0.000 description 1
- 229920000209 Hexadimethrine bromide Polymers 0.000 description 1
- FYVHHKMHFPMBBG-GUBZILKMSA-N His-Gln-Asp Chemical compound C1=C(NC=N1)C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC(=O)O)C(=O)O)N FYVHHKMHFPMBBG-GUBZILKMSA-N 0.000 description 1
- BDFCIKANUNMFGB-PMVVWTBXSA-N His-Gly-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)CC1=CN=CN1 BDFCIKANUNMFGB-PMVVWTBXSA-N 0.000 description 1
- DYKZGTLPSNOFHU-DEQVHRJGSA-N His-Ile-Pro Chemical compound CC[C@H](C)[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CC2=CN=CN2)N DYKZGTLPSNOFHU-DEQVHRJGSA-N 0.000 description 1
- HZWWOGWOBQBETJ-CUJWVEQBSA-N His-Thr-Cys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CC1=CN=CN1)N)O HZWWOGWOBQBETJ-CUJWVEQBSA-N 0.000 description 1
- HTOOKGDPMXSJSY-STQMWFEESA-N His-Tyr Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(O)=O)C1=CN=CN1 HTOOKGDPMXSJSY-STQMWFEESA-N 0.000 description 1
- LPBWRHRHEIYAIP-KKUMJFAQSA-N His-Tyr-Asp 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(O)=O)C(O)=O LPBWRHRHEIYAIP-KKUMJFAQSA-N 0.000 description 1
- YKUAGFAXQRYUQW-KKUMJFAQSA-N His-Tyr-Cys Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CC2=CN=CN2)N)O YKUAGFAXQRYUQW-KKUMJFAQSA-N 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 101000800023 Homo sapiens 4F2 cell-surface antigen heavy chain Proteins 0.000 description 1
- 101000690301 Homo sapiens Aldo-keto reductase family 1 member C4 Proteins 0.000 description 1
- 101001037139 Homo sapiens Immunoglobulin heavy variable 3-30 Proteins 0.000 description 1
- 101000878605 Homo sapiens Low affinity immunoglobulin epsilon Fc receptor Proteins 0.000 description 1
- 101001109503 Homo sapiens NKG2-C type II integral membrane protein Proteins 0.000 description 1
- 101000589305 Homo sapiens Natural cytotoxicity triggering receptor 2 Proteins 0.000 description 1
- 101001116548 Homo sapiens Protein CBFA2T1 Proteins 0.000 description 1
- 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 1
- 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 1
- TZCGZYWNIDZZMR-NAKRPEOUSA-N Ile-Arg-Ala Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](C)C(=O)O)N TZCGZYWNIDZZMR-NAKRPEOUSA-N 0.000 description 1
- TZCGZYWNIDZZMR-UHFFFAOYSA-N Ile-Arg-Ala Natural products CCC(C)C(N)C(=O)NC(C(=O)NC(C)C(O)=O)CCCN=C(N)N TZCGZYWNIDZZMR-UHFFFAOYSA-N 0.000 description 1
- VZIFYHYNQDIPLI-HJWJTTGWSA-N Ile-Arg-Phe Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)N VZIFYHYNQDIPLI-HJWJTTGWSA-N 0.000 description 1
- YPQDTQJBOFOTJQ-SXTJYALSSA-N Ile-Asn-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)O)N YPQDTQJBOFOTJQ-SXTJYALSSA-N 0.000 description 1
- JDAWAWXGAUZPNJ-ZPFDUUQYSA-N Ile-Glu-Arg Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)N JDAWAWXGAUZPNJ-ZPFDUUQYSA-N 0.000 description 1
- BEWFWZRGBDVXRP-PEFMBERDSA-N Ile-Glu-Asn Chemical compound [H]N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O BEWFWZRGBDVXRP-PEFMBERDSA-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
- JXMSHKFPDIUYGS-SIUGBPQLSA-N Ile-Glu-Tyr Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O)N JXMSHKFPDIUYGS-SIUGBPQLSA-N 0.000 description 1
- NYEYYMLUABXDMC-NHCYSSNCSA-N Ile-Gly-Leu Chemical compound CC[C@H](C)[C@@H](C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)O)N NYEYYMLUABXDMC-NHCYSSNCSA-N 0.000 description 1
- SVBAHOMTJRFSIC-SXTJYALSSA-N Ile-Ile-Asn Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(=O)N)C(=O)O)N SVBAHOMTJRFSIC-SXTJYALSSA-N 0.000 description 1
- YNMQUIVKEFRCPH-QSFUFRPTSA-N Ile-Ile-Gly Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)O)N YNMQUIVKEFRCPH-QSFUFRPTSA-N 0.000 description 1
- OWSWUWDMSNXTNE-GMOBBJLQSA-N Ile-Pro-Asp Chemical compound CC[C@H](C)[C@@H](C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(=O)O)C(=O)O)N OWSWUWDMSNXTNE-GMOBBJLQSA-N 0.000 description 1
- MITYXXNZSZLHGG-OBAATPRFSA-N Ile-Trp-Tyr Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)N[C@@H](CC3=CC=C(C=C3)O)C(=O)O)N MITYXXNZSZLHGG-OBAATPRFSA-N 0.000 description 1
- NGKPIPCGMLWHBX-WZLNRYEVSA-N Ile-Tyr-Thr 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)O)C(=O)O)N NGKPIPCGMLWHBX-WZLNRYEVSA-N 0.000 description 1
- JZBVBOKASHNXAD-NAKRPEOUSA-N Ile-Val-Ser Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CO)C(=O)O)N JZBVBOKASHNXAD-NAKRPEOUSA-N 0.000 description 1
- 108010054477 Immunoglobulin Fab Fragments Proteins 0.000 description 1
- 102000001706 Immunoglobulin Fab Fragments Human genes 0.000 description 1
- 108010067060 Immunoglobulin Variable Region Proteins 0.000 description 1
- 102000017727 Immunoglobulin Variable Region Human genes 0.000 description 1
- 102100040219 Immunoglobulin heavy variable 3-30 Human genes 0.000 description 1
- 102000002698 KIR Receptors Human genes 0.000 description 1
- 108010043610 KIR Receptors Proteins 0.000 description 1
- 101150069255 KLRC1 gene Proteins 0.000 description 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 1
- 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 1
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 1
- UGTHTQWIQKEDEH-BQBZGAKWSA-N L-alanyl-L-prolylglycine zwitterion Chemical compound C[C@H](N)C(=O)N1CCC[C@H]1C(=O)NCC(O)=O UGTHTQWIQKEDEH-BQBZGAKWSA-N 0.000 description 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 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
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- 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 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-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
- 241000282838 Lama Species 0.000 description 1
- 208000018142 Leiomyosarcoma Diseases 0.000 description 1
- KVRKAGGMEWNURO-CIUDSAMLSA-N Leu-Ala-Cys Chemical compound C[C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CC(C)C)N KVRKAGGMEWNURO-CIUDSAMLSA-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
- XVSJMWYYLHPDKY-DCAQKATOSA-N Leu-Asp-Met Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCSC)C(O)=O XVSJMWYYLHPDKY-DCAQKATOSA-N 0.000 description 1
- GZAUZBUKDXYPEH-CIUDSAMLSA-N Leu-Cys-Cys Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CS)C(=O)N[C@@H](CS)C(=O)O)N GZAUZBUKDXYPEH-CIUDSAMLSA-N 0.000 description 1
- FOEHRHOBWFQSNW-KATARQTJSA-N Leu-Cys-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CS)NC(=O)[C@H](CC(C)C)N)O FOEHRHOBWFQSNW-KATARQTJSA-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
- QDSKNVXKLPQNOJ-GVXVVHGQSA-N Leu-Gln-Val Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C(C)C)C(O)=O QDSKNVXKLPQNOJ-GVXVVHGQSA-N 0.000 description 1
- HVJVUYQWFYMGJS-GVXVVHGQSA-N Leu-Glu-Val Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(O)=O HVJVUYQWFYMGJS-GVXVVHGQSA-N 0.000 description 1
- HYIFFZAQXPUEAU-QWRGUYRKSA-N Leu-Gly-Leu Chemical compound CC(C)C[C@H](N)C(=O)NCC(=O)N[C@H](C(O)=O)CC(C)C HYIFFZAQXPUEAU-QWRGUYRKSA-N 0.000 description 1
- 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 1
- MPSBSKHOWJQHBS-IHRRRGAJSA-N Leu-His-Met Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N[C@@H](CCSC)C(=O)O)N MPSBSKHOWJQHBS-IHRRRGAJSA-N 0.000 description 1
- XBCWOTOCBXXJDG-BZSNNMDCSA-N Leu-His-Phe Chemical compound C([C@H](NC(=O)[C@@H](N)CC(C)C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CN=CN1 XBCWOTOCBXXJDG-BZSNNMDCSA-N 0.000 description 1
- PDQDCFBVYXEFSD-SRVKXCTJSA-N Leu-Leu-Asp Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(O)=O)C(O)=O PDQDCFBVYXEFSD-SRVKXCTJSA-N 0.000 description 1
- 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 1
- ZDBMWELMUCLUPL-QEJZJMRPSA-N Leu-Phe-Ala Chemical compound CC(C)C[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](C)C(O)=O)CC1=CC=CC=C1 ZDBMWELMUCLUPL-QEJZJMRPSA-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
- KZZCOWMDDXDKSS-CIUDSAMLSA-N Leu-Ser-Asn Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(O)=O KZZCOWMDDXDKSS-CIUDSAMLSA-N 0.000 description 1
- 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 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
- SIGZKCWZEBFNAK-QAETUUGQSA-N Leu-Ser-Ser-Tyr Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 SIGZKCWZEBFNAK-QAETUUGQSA-N 0.000 description 1
- 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 1
- SVBJIZVVYJYGLA-DCAQKATOSA-N Leu-Ser-Val Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(O)=O SVBJIZVVYJYGLA-DCAQKATOSA-N 0.000 description 1
- LJBVRCDPWOJOEK-PPCPHDFISA-N Leu-Thr-Ile 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)CC)C(O)=O LJBVRCDPWOJOEK-PPCPHDFISA-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
- DAYQSYGBCUKVKT-VOAKCMCISA-N Leu-Thr-Lys Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(O)=O DAYQSYGBCUKVKT-VOAKCMCISA-N 0.000 description 1
- 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 1
- WBRJVRXEGQIDRK-XIRDDKMYSA-N Leu-Trp-Ser Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@@H](N)CC(C)C)C(=O)N[C@@H](CO)C(O)=O)=CNC2=C1 WBRJVRXEGQIDRK-XIRDDKMYSA-N 0.000 description 1
- RIHIGSWBLHSGLV-CQDKDKBSSA-N Leu-Tyr-Ala 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](C)C(O)=O RIHIGSWBLHSGLV-CQDKDKBSSA-N 0.000 description 1
- 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 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
- NTXYXFDMIHXTHE-WDSOQIARSA-N Leu-Val-Trp Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)CC(C)C)C(O)=O)=CNC2=C1 NTXYXFDMIHXTHE-WDSOQIARSA-N 0.000 description 1
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 1
- 102100038007 Low affinity immunoglobulin epsilon Fc receptor Human genes 0.000 description 1
- 208000031422 Lymphocytic Chronic B-Cell Leukemia Diseases 0.000 description 1
- XFIHDSBIPWEYJJ-YUMQZZPRSA-N Lys-Ala-Gly Chemical compound OC(=O)CNC(=O)[C@H](C)NC(=O)[C@@H](N)CCCCN XFIHDSBIPWEYJJ-YUMQZZPRSA-N 0.000 description 1
- 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 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
- QUYCUALODHJQLK-CIUDSAMLSA-N Lys-Asp-Asp Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(O)=O)C(O)=O QUYCUALODHJQLK-CIUDSAMLSA-N 0.000 description 1
- IBQMEXQYZMVIFU-SRVKXCTJSA-N Lys-Asp-His Chemical compound C1=C(NC=N1)C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCCCN)N IBQMEXQYZMVIFU-SRVKXCTJSA-N 0.000 description 1
- HEWWNLVEWBJBKA-WDCWCFNPSA-N Lys-Gln-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)CCCCN HEWWNLVEWBJBKA-WDCWCFNPSA-N 0.000 description 1
- DRCILAJNUJKAHC-SRVKXCTJSA-N Lys-Glu-Arg Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O DRCILAJNUJKAHC-SRVKXCTJSA-N 0.000 description 1
- FGMHXLULNHTPID-KKUMJFAQSA-N Lys-His-Lys Chemical compound NCCCC[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(O)=O)CC1=CN=CN1 FGMHXLULNHTPID-KKUMJFAQSA-N 0.000 description 1
- 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 1
- OIQSIMFSVLLWBX-VOAKCMCISA-N Lys-Leu-Thr Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O OIQSIMFSVLLWBX-VOAKCMCISA-N 0.000 description 1
- XFOAWKDQMRMCDN-ULQDDVLXSA-N Lys-Phe-Arg Chemical compound NC(N)=NCCC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)CCCCN)CC1=CC=CC=C1 XFOAWKDQMRMCDN-ULQDDVLXSA-N 0.000 description 1
- BPDXWKVZNCKUGG-BZSNNMDCSA-N Lys-Phe-His Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CC2=CN=CN2)C(=O)O)NC(=O)[C@H](CCCCN)N BPDXWKVZNCKUGG-BZSNNMDCSA-N 0.000 description 1
- 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 1
- QBHGXFQJFPWJIH-XUXIUFHCSA-N Lys-Pro-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCCN QBHGXFQJFPWJIH-XUXIUFHCSA-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
- UQJOKDAYFULYIX-AVGNSLFASA-N Lys-Pro-Pro Chemical compound NCCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1[C@H](C(O)=O)CCC1 UQJOKDAYFULYIX-AVGNSLFASA-N 0.000 description 1
- 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 1
- QVTDVTONTRSQMF-WDCWCFNPSA-N Lys-Thr-Glu Chemical compound OC(=O)CC[C@@H](C(O)=O)NC(=O)[C@H]([C@H](O)C)NC(=O)[C@@H](N)CCCCN QVTDVTONTRSQMF-WDCWCFNPSA-N 0.000 description 1
- MIMXMVDLMDMOJD-BZSNNMDCSA-N Lys-Tyr-Leu Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC(C)C)C(O)=O MIMXMVDLMDMOJD-BZSNNMDCSA-N 0.000 description 1
- OZVXDDFYCQOPFD-XQQFMLRXSA-N Lys-Val-Pro Chemical compound CC(C)[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CCCCN)N OZVXDDFYCQOPFD-XQQFMLRXSA-N 0.000 description 1
- 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 1
- 239000004472 Lysine Substances 0.000 description 1
- 102000043129 MHC class I family Human genes 0.000 description 1
- 108091054437 MHC class I family Proteins 0.000 description 1
- 241000282553 Macaca Species 0.000 description 1
- 241000282560 Macaca mulatta Species 0.000 description 1
- 101100404845 Macaca mulatta NKG2A gene Proteins 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 208000007054 Medullary Carcinoma Diseases 0.000 description 1
- 208000000172 Medulloblastoma Diseases 0.000 description 1
- 102000018697 Membrane Proteins Human genes 0.000 description 1
- 108010052285 Membrane Proteins Proteins 0.000 description 1
- 206010027406 Mesothelioma Diseases 0.000 description 1
- WXHHTBVYQOSYSL-FXQIFTODSA-N Met-Ala-Ser Chemical compound CSCC[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(O)=O WXHHTBVYQOSYSL-FXQIFTODSA-N 0.000 description 1
- MVBZBRKNZVJEKK-DTWKUNHWSA-N Met-Gly-Pro Chemical compound CSCC[C@@H](C(=O)NCC(=O)N1CCC[C@@H]1C(=O)O)N MVBZBRKNZVJEKK-DTWKUNHWSA-N 0.000 description 1
- MHQXIBRPDKXDGZ-ZFWWWQNUSA-N Met-Gly-Trp Chemical compound C1=CC=C2C(C[C@H](NC(=O)CNC(=O)[C@@H](N)CCSC)C(O)=O)=CNC2=C1 MHQXIBRPDKXDGZ-ZFWWWQNUSA-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
- 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
- RMLWDZINJUDMEB-IHRRRGAJSA-N Met-Tyr-Asn Chemical compound CSCC[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](CC(=O)N)C(=O)O)N RMLWDZINJUDMEB-IHRRRGAJSA-N 0.000 description 1
- VYDLZDRMOFYOGV-TUAOUCFPSA-N Met-Val-Pro Chemical compound CC(C)[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CCSC)N VYDLZDRMOFYOGV-TUAOUCFPSA-N 0.000 description 1
- 206010027476 Metastases Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 208000035489 Monocytic Acute Leukemia Diseases 0.000 description 1
- 241000699666 Mus <mouse, genus> Species 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 101710135898 Myc proto-oncogene protein Proteins 0.000 description 1
- 102100038895 Myc proto-oncogene protein Human genes 0.000 description 1
- 208000033761 Myelogenous Chronic BCR-ABL Positive Leukemia Diseases 0.000 description 1
- 208000033835 Myelomonocytic Acute Leukemia Diseases 0.000 description 1
- NQTADLQHYWFPDB-UHFFFAOYSA-N N-Hydroxysuccinimide Chemical compound ON1C(=O)CCC1=O NQTADLQHYWFPDB-UHFFFAOYSA-N 0.000 description 1
- 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 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
- 102100022682 NKG2-A/NKG2-B type II integral membrane protein Human genes 0.000 description 1
- 102100022683 NKG2-C type II integral membrane protein Human genes 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 108010004222 Natural Cytotoxicity Triggering Receptor 3 Proteins 0.000 description 1
- 102100032851 Natural cytotoxicity triggering receptor 2 Human genes 0.000 description 1
- 102100032852 Natural cytotoxicity triggering receptor 3 Human genes 0.000 description 1
- 206010029260 Neuroblastoma Diseases 0.000 description 1
- 201000010133 Oligodendroglioma Diseases 0.000 description 1
- 208000002606 Paramyxoviridae Infections Diseases 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 102000000447 Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase Human genes 0.000 description 1
- 108010055817 Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase Proteins 0.000 description 1
- VHWOBXIWBDWZHK-IHRRRGAJSA-N Phe-Arg-Asp Chemical compound NC(N)=NCCC[C@@H](C(=O)N[C@@H](CC(O)=O)C(O)=O)NC(=O)[C@@H](N)CC1=CC=CC=C1 VHWOBXIWBDWZHK-IHRRRGAJSA-N 0.000 description 1
- XWBJLKDCHJVKAK-KKUMJFAQSA-N Phe-Arg-Gln Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(=O)N)C(=O)O)N XWBJLKDCHJVKAK-KKUMJFAQSA-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
- MFQXSDWKUXTOPZ-DZKIICNBSA-N Phe-Gln-Val Chemical compound CC(C)[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CC1=CC=CC=C1)N MFQXSDWKUXTOPZ-DZKIICNBSA-N 0.000 description 1
- FIRWJEJVFFGXSH-RYUDHWBXSA-N Phe-Glu-Gly Chemical compound OC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](N)CC1=CC=CC=C1 FIRWJEJVFFGXSH-RYUDHWBXSA-N 0.000 description 1
- BFYHIHGIHGROAT-HTUGSXCWSA-N Phe-Glu-Thr Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O BFYHIHGIHGROAT-HTUGSXCWSA-N 0.000 description 1
- ZZVUXQCQPXSUFH-JBACZVJFSA-N Phe-Glu-Trp Chemical compound C([C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(O)=O)C1=CC=CC=C1 ZZVUXQCQPXSUFH-JBACZVJFSA-N 0.000 description 1
- HGNGAMWHGGANAU-WHOFXGATSA-N Phe-Gly-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)CC1=CC=CC=C1 HGNGAMWHGGANAU-WHOFXGATSA-N 0.000 description 1
- 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 1
- DZVXMMSUWWUIQE-ACRUOGEOSA-N Phe-His-Tyr Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CC2=CN=CN2)C(=O)N[C@@H](CC3=CC=C(C=C3)O)C(=O)O)N DZVXMMSUWWUIQE-ACRUOGEOSA-N 0.000 description 1
- GXDPQJUBLBZKDY-IAVJCBSLSA-N Phe-Ile-Ile Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O GXDPQJUBLBZKDY-IAVJCBSLSA-N 0.000 description 1
- NRKNYPRRWXVELC-NQCBNZPSSA-N Phe-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=CC=CC=C3)N NRKNYPRRWXVELC-NQCBNZPSSA-N 0.000 description 1
- YTILBRIUASDGBL-BZSNNMDCSA-N Phe-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=CC=CC=C1 YTILBRIUASDGBL-BZSNNMDCSA-N 0.000 description 1
- DMEYUTSDVRCWRS-ULQDDVLXSA-N Phe-Lys-Arg Chemical compound NC(=N)NCCC[C@@H](C(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CC1=CC=CC=C1 DMEYUTSDVRCWRS-ULQDDVLXSA-N 0.000 description 1
- IWZRODDWOSIXPZ-IRXDYDNUSA-N Phe-Phe-Gly Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC(O)=O)C1=CC=CC=C1 IWZRODDWOSIXPZ-IRXDYDNUSA-N 0.000 description 1
- FENSZYFJQOFSQR-FIRPJDEBSA-N Phe-Phe-Ile Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(O)=O)NC(=O)[C@@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FENSZYFJQOFSQR-FIRPJDEBSA-N 0.000 description 1
- AAERWTUHZKLDLC-IHRRRGAJSA-N Phe-Pro-Asp Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(O)=O)C(O)=O AAERWTUHZKLDLC-IHRRRGAJSA-N 0.000 description 1
- FKFCKDROTNIVSO-JYJNAYRXSA-N Phe-Pro-Met Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(O)=O FKFCKDROTNIVSO-JYJNAYRXSA-N 0.000 description 1
- NJJBATPLUQHRBM-IHRRRGAJSA-N Phe-Pro-Ser Chemical compound C1C[C@H](N(C1)C(=O)[C@H](CC2=CC=CC=C2)N)C(=O)N[C@@H](CO)C(=O)O NJJBATPLUQHRBM-IHRRRGAJSA-N 0.000 description 1
- YMIZSYUAZJSOFL-SRVKXCTJSA-N Phe-Ser-Asn Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(O)=O YMIZSYUAZJSOFL-SRVKXCTJSA-N 0.000 description 1
- RAGOJJCBGXARPO-XVSYOHENSA-N Phe-Thr-Asp Chemical compound OC(=O)C[C@@H](C(O)=O)NC(=O)[C@H]([C@H](O)C)NC(=O)[C@@H](N)CC1=CC=CC=C1 RAGOJJCBGXARPO-XVSYOHENSA-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
- VFDRDMOMHBJGKD-UFYCRDLUSA-N Phe-Tyr-Arg 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](CCCN=C(N)N)C(=O)O)N VFDRDMOMHBJGKD-UFYCRDLUSA-N 0.000 description 1
- CVAUVSOFHJKCHN-BZSNNMDCSA-N Phe-Tyr-Cys Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CS)C(O)=O)C1=CC=CC=C1 CVAUVSOFHJKCHN-BZSNNMDCSA-N 0.000 description 1
- 208000007641 Pinealoma Diseases 0.000 description 1
- 208000007452 Plasmacytoma Diseases 0.000 description 1
- 208000006664 Precursor Cell Lymphoblastic Leukemia-Lymphoma Diseases 0.000 description 1
- 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 1
- ZSKJPKFTPQCPIH-RCWTZXSCSA-N Pro-Arg-Thr Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(O)=O ZSKJPKFTPQCPIH-RCWTZXSCSA-N 0.000 description 1
- SGCZFWSQERRKBD-BQBZGAKWSA-N Pro-Asp-Gly Chemical compound OC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@@H]1CCCN1 SGCZFWSQERRKBD-BQBZGAKWSA-N 0.000 description 1
- QVIZLAUEAMQKGS-GUBZILKMSA-N Pro-Asp-Met Chemical compound CSCC[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H]1CCCN1 QVIZLAUEAMQKGS-GUBZILKMSA-N 0.000 description 1
- 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 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
- ULIWFCCJIOEHMU-BQBZGAKWSA-N Pro-Gly-Asp Chemical compound OC(=O)C[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H]1CCCN1 ULIWFCCJIOEHMU-BQBZGAKWSA-N 0.000 description 1
- FEPSEIDIPBMIOS-QXEWZRGKSA-N Pro-Gly-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H]1CCCN1 FEPSEIDIPBMIOS-QXEWZRGKSA-N 0.000 description 1
- AFXCXDQNRXTSBD-FJXKBIBVSA-N Pro-Gly-Thr Chemical compound [H]N1CCC[C@H]1C(=O)NCC(=O)N[C@@H]([C@@H](C)O)C(O)=O AFXCXDQNRXTSBD-FJXKBIBVSA-N 0.000 description 1
- LNOWDSPAYBWJOR-PEDHHIEDSA-N Pro-Ile-Ile Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O LNOWDSPAYBWJOR-PEDHHIEDSA-N 0.000 description 1
- INDVYIOKMXFQFM-SRVKXCTJSA-N Pro-Lys-Gln Chemical compound C1C[C@H](NC1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)N)C(=O)O INDVYIOKMXFQFM-SRVKXCTJSA-N 0.000 description 1
- MHBSUKYVBZVQRW-HJWJTTGWSA-N Pro-Phe-Ile Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O MHBSUKYVBZVQRW-HJWJTTGWSA-N 0.000 description 1
- HWLKHNDRXWTFTN-GUBZILKMSA-N Pro-Pro-Cys Chemical compound C1C[C@H](NC1)C(=O)N2CCC[C@H]2C(=O)N[C@@H](CS)C(=O)O HWLKHNDRXWTFTN-GUBZILKMSA-N 0.000 description 1
- RFWXYTJSVDUBBZ-DCAQKATOSA-N Pro-Pro-Glu Chemical compound OC(=O)CC[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H]1NCCC1 RFWXYTJSVDUBBZ-DCAQKATOSA-N 0.000 description 1
- 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 1
- POQFNPILEQEODH-FXQIFTODSA-N Pro-Ser-Ala Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(O)=O POQFNPILEQEODH-FXQIFTODSA-N 0.000 description 1
- GOMUXSCOIWIJFP-GUBZILKMSA-N Pro-Ser-Arg Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O GOMUXSCOIWIJFP-GUBZILKMSA-N 0.000 description 1
- 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 1
- 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 1
- 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 1
- 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 1
- QUBVFEANYYWBTM-VEVYYDQMSA-N Pro-Thr-Asp Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(O)=O QUBVFEANYYWBTM-VEVYYDQMSA-N 0.000 description 1
- FDMCIBSQRKFSTJ-RHYQMDGZSA-N Pro-Thr-Leu Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(O)=O FDMCIBSQRKFSTJ-RHYQMDGZSA-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
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 1
- 102220621241 Proline-rich membrane anchor 1_S32A_mutation Human genes 0.000 description 1
- 208000033826 Promyelocytic Acute Leukemia Diseases 0.000 description 1
- 238000010802 RNA extraction kit Methods 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 208000006265 Renal cell carcinoma Diseases 0.000 description 1
- 201000000582 Retinoblastoma Diseases 0.000 description 1
- 206010038997 Retroviral infections Diseases 0.000 description 1
- 201000010208 Seminoma Diseases 0.000 description 1
- MMGJPDWSIOAGTH-ACZMJKKPSA-N Ser-Ala-Gln Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(O)=O MMGJPDWSIOAGTH-ACZMJKKPSA-N 0.000 description 1
- WTUJZHKANPDPIN-CIUDSAMLSA-N Ser-Ala-Lys Chemical compound C[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CO)N WTUJZHKANPDPIN-CIUDSAMLSA-N 0.000 description 1
- GXXTUIUYTWGPMV-FXQIFTODSA-N Ser-Arg-Ala Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(O)=O GXXTUIUYTWGPMV-FXQIFTODSA-N 0.000 description 1
- VQBLHWSPVYYZTB-DCAQKATOSA-N Ser-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](CO)N VQBLHWSPVYYZTB-DCAQKATOSA-N 0.000 description 1
- KYKKKSWGEPFUMR-NAKRPEOUSA-N Ser-Arg-Ile Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O KYKKKSWGEPFUMR-NAKRPEOUSA-N 0.000 description 1
- OYEDZGNMSBZCIM-XGEHTFHBSA-N Ser-Arg-Thr Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(O)=O OYEDZGNMSBZCIM-XGEHTFHBSA-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
- 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 1
- 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 1
- FIDMVVBUOCMMJG-CIUDSAMLSA-N Ser-Asn-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](N)CO FIDMVVBUOCMMJG-CIUDSAMLSA-N 0.000 description 1
- MMAPOBOTRUVNKJ-ZLUOBGJFSA-N Ser-Asp-Ser Chemical compound C([C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](CO)N)C(=O)O MMAPOBOTRUVNKJ-ZLUOBGJFSA-N 0.000 description 1
- RNFKSBPHLTZHLU-WHFBIAKZSA-N Ser-Cys-Gly Chemical compound C([C@@H](C(=O)N[C@@H](CS)C(=O)NCC(=O)O)N)O RNFKSBPHLTZHLU-WHFBIAKZSA-N 0.000 description 1
- RFBKULCUBJAQFT-BIIVOSGPSA-N Ser-Cys-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CS)NC(=O)[C@H](CO)N)C(=O)O RFBKULCUBJAQFT-BIIVOSGPSA-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
- PPNPDKGQRFSCAC-CIUDSAMLSA-N Ser-Lys-Asp Chemical compound NCCCC[C@H](NC(=O)[C@@H](N)CO)C(=O)N[C@@H](CC(O)=O)C(O)=O PPNPDKGQRFSCAC-CIUDSAMLSA-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
- VXYQOFXBIXKPCX-BQBZGAKWSA-N Ser-Met-Gly Chemical compound CSCC[C@@H](C(=O)NCC(=O)O)NC(=O)[C@H](CO)N VXYQOFXBIXKPCX-BQBZGAKWSA-N 0.000 description 1
- VIIJCAQMJBHSJH-FXQIFTODSA-N Ser-Met-Ser Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(O)=O VIIJCAQMJBHSJH-FXQIFTODSA-N 0.000 description 1
- 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 1
- MHVXPTAMDHLTHB-IHPCNDPISA-N Ser-Phe-Trp Chemical compound C([C@H](NC(=O)[C@H](CO)N)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(O)=O)C1=CC=CC=C1 MHVXPTAMDHLTHB-IHPCNDPISA-N 0.000 description 1
- RHAPJNVNWDBFQI-BQBZGAKWSA-N Ser-Pro-Gly Chemical compound OC[C@H](N)C(=O)N1CCC[C@H]1C(=O)NCC(O)=O RHAPJNVNWDBFQI-BQBZGAKWSA-N 0.000 description 1
- PPCZVWHJWJFTFN-ZLUOBGJFSA-N Ser-Ser-Asp Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(O)=O PPCZVWHJWJFTFN-ZLUOBGJFSA-N 0.000 description 1
- ILZAUMFXKSIUEF-SRVKXCTJSA-N Ser-Ser-Phe Chemical compound OC[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 ILZAUMFXKSIUEF-SRVKXCTJSA-N 0.000 description 1
- 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 1
- 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 1
- ATEQEHCGZKBEMU-GQGQLFGLSA-N Ser-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](CO)N ATEQEHCGZKBEMU-GQGQLFGLSA-N 0.000 description 1
- SYCFMSYTIFXWAJ-DCAQKATOSA-N Ser-Val-His Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)[C@H](CO)N SYCFMSYTIFXWAJ-DCAQKATOSA-N 0.000 description 1
- MFQMZDPAZRZAPV-NAKRPEOUSA-N Ser-Val-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CO)N MFQMZDPAZRZAPV-NAKRPEOUSA-N 0.000 description 1
- 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 1
- 206010041067 Small cell lung cancer Diseases 0.000 description 1
- 208000000102 Squamous Cell Carcinoma of Head and Neck Diseases 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- NHUHCSRWZMLRLA-UHFFFAOYSA-N Sulfisoxazole Chemical compound CC1=NOC(NS(=O)(=O)C=2C=CC(N)=CC=2)=C1C NHUHCSRWZMLRLA-UHFFFAOYSA-N 0.000 description 1
- 210000001744 T-lymphocyte Anatomy 0.000 description 1
- 208000024313 Testicular Neoplasms Diseases 0.000 description 1
- 206010057644 Testis cancer Diseases 0.000 description 1
- STGXWWBXWXZOER-MBLNEYKQSA-N Thr-Ala-His Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@H](C(O)=O)CC1=CN=CN1 STGXWWBXWXZOER-MBLNEYKQSA-N 0.000 description 1
- 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 1
- BSNZTJXVDOINSR-JXUBOQSCSA-N Thr-Ala-Leu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(O)=O BSNZTJXVDOINSR-JXUBOQSCSA-N 0.000 description 1
- GFDUZZACIWNMPE-KZVJFYERSA-N Thr-Ala-Met Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCSC)C(O)=O GFDUZZACIWNMPE-KZVJFYERSA-N 0.000 description 1
- LVHHEVGYAZGXDE-KDXUFGMBSA-N Thr-Ala-Pro Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](C)C(=O)N1CCC[C@@H]1C(=O)O)N)O LVHHEVGYAZGXDE-KDXUFGMBSA-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
- TWLMXDWFVNEFFK-FJXKBIBVSA-N Thr-Arg-Gly Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(O)=O TWLMXDWFVNEFFK-FJXKBIBVSA-N 0.000 description 1
- VOGXLRKCWFLJBY-HSHDSVGOSA-N Thr-Arg-Trp Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)O)N)O VOGXLRKCWFLJBY-HSHDSVGOSA-N 0.000 description 1
- UNURFMVMXLENAZ-KJEVXHAQSA-N Thr-Arg-Tyr Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O UNURFMVMXLENAZ-KJEVXHAQSA-N 0.000 description 1
- JHBHMCMKSPXRHV-NUMRIWBASA-N Thr-Asn-Gln Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CCC(=O)N)C(=O)O)N)O JHBHMCMKSPXRHV-NUMRIWBASA-N 0.000 description 1
- GCXFWAZRHBRYEM-NUMRIWBASA-N Thr-Gln-Asn Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC(=O)N)C(=O)O)N)O GCXFWAZRHBRYEM-NUMRIWBASA-N 0.000 description 1
- WLDUCKSCDRIVLJ-NUMRIWBASA-N Thr-Gln-Asp Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC(=O)O)C(=O)O)N)O WLDUCKSCDRIVLJ-NUMRIWBASA-N 0.000 description 1
- KGKWKSSSQGGYAU-SUSMZKCASA-N Thr-Gln-Thr Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H]([C@@H](C)O)C(=O)O)N)O KGKWKSSSQGGYAU-SUSMZKCASA-N 0.000 description 1
- BIENEHRYNODTLP-HJGDQZAQSA-N Thr-Glu-Met Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCSC)C(=O)O)N)O BIENEHRYNODTLP-HJGDQZAQSA-N 0.000 description 1
- NIEWSKWFURSECR-FOHZUACHSA-N Thr-Gly-Asp Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(O)=O NIEWSKWFURSECR-FOHZUACHSA-N 0.000 description 1
- WYKJENSCCRJLRC-ZDLURKLDSA-N Thr-Gly-Cys Chemical compound C[C@H]([C@@H](C(=O)NCC(=O)N[C@@H](CS)C(=O)O)N)O WYKJENSCCRJLRC-ZDLURKLDSA-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
- MSIYNSBKKVMGFO-BHNWBGBOSA-N Thr-Gly-Pro Chemical compound C[C@H]([C@@H](C(=O)NCC(=O)N1CCC[C@@H]1C(=O)O)N)O MSIYNSBKKVMGFO-BHNWBGBOSA-N 0.000 description 1
- 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 1
- CYVQBKQYQGEELV-NKIYYHGXSA-N Thr-His-Gln Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N[C@@H](CCC(=O)N)C(=O)O)N)O CYVQBKQYQGEELV-NKIYYHGXSA-N 0.000 description 1
- DDDLIMCZFKOERC-SVSWQMSJSA-N Thr-Ile-Cys Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H]([C@@H](C)O)N DDDLIMCZFKOERC-SVSWQMSJSA-N 0.000 description 1
- GMXIJHCBTZDAPD-QPHKQPEJSA-N Thr-Ile-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)O)NC(=O)[C@H]([C@@H](C)O)N GMXIJHCBTZDAPD-QPHKQPEJSA-N 0.000 description 1
- XYFISNXATOERFZ-OSUNSFLBSA-N Thr-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]([C@@H](C)O)N XYFISNXATOERFZ-OSUNSFLBSA-N 0.000 description 1
- 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 1
- XIULAFZYEKSGAJ-IXOXFDKPSA-N Thr-Leu-His Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(O)=O)CC1=CNC=N1 XIULAFZYEKSGAJ-IXOXFDKPSA-N 0.000 description 1
- IJVNLNRVDUTWDD-MEYUZBJRSA-N Thr-Leu-Tyr 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=C(O)C=C1)C(O)=O IJVNLNRVDUTWDD-MEYUZBJRSA-N 0.000 description 1
- QHUWWSQZTFLXPQ-FJXKBIBVSA-N Thr-Met-Gly Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCSC)C(=O)NCC(O)=O QHUWWSQZTFLXPQ-FJXKBIBVSA-N 0.000 description 1
- IVDFVBVIVLJJHR-LKXGYXEUSA-N Thr-Ser-Asp Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(O)=O IVDFVBVIVLJJHR-LKXGYXEUSA-N 0.000 description 1
- 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 1
- AHERARIZBPOMNU-KATARQTJSA-N Thr-Ser-Leu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(O)=O AHERARIZBPOMNU-KATARQTJSA-N 0.000 description 1
- XZUBGOYOGDRYFC-XGEHTFHBSA-N Thr-Ser-Met Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCSC)C(O)=O XZUBGOYOGDRYFC-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
- 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 1
- QYDKSNXSBXZPFK-ZJDVBMNYSA-N Thr-Thr-Arg Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O QYDKSNXSBXZPFK-ZJDVBMNYSA-N 0.000 description 1
- MFMGPEKYBXFIRF-SUSMZKCASA-N Thr-Thr-Gln Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCC(N)=O)C(O)=O MFMGPEKYBXFIRF-SUSMZKCASA-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
- XGUAUKUYQHBUNY-SWRJLBSHSA-N Thr-Trp-Glu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CCC(O)=O)C(O)=O XGUAUKUYQHBUNY-SWRJLBSHSA-N 0.000 description 1
- XEVHXNLPUBVQEX-DVJZZOLTSA-N Thr-Trp-Gly Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)NCC(=O)O)N)O XEVHXNLPUBVQEX-DVJZZOLTSA-N 0.000 description 1
- VMSSYINFMOFLJM-KJEVXHAQSA-N Thr-Tyr-Met Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](CCSC)C(=O)O)N)O VMSSYINFMOFLJM-KJEVXHAQSA-N 0.000 description 1
- CYCGARJWIQWPQM-YJRXYDGGSA-N Thr-Tyr-Ser Chemical compound C[C@@H](O)[C@H]([NH3+])C(=O)N[C@H](C(=O)N[C@@H](CO)C([O-])=O)CC1=CC=C(O)C=C1 CYCGARJWIQWPQM-YJRXYDGGSA-N 0.000 description 1
- BPGDJSUFQKWUBK-KJEVXHAQSA-N Thr-Val-Tyr Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 BPGDJSUFQKWUBK-KJEVXHAQSA-N 0.000 description 1
- 101710150448 Transcriptional regulator Myc Proteins 0.000 description 1
- 108020004566 Transfer RNA Proteins 0.000 description 1
- 102100023935 Transmembrane glycoprotein NMB Human genes 0.000 description 1
- 206010052779 Transplant rejections Diseases 0.000 description 1
- KZTLJLFVOIMRAQ-IHPCNDPISA-N Trp-Asn-Tyr Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O KZTLJLFVOIMRAQ-IHPCNDPISA-N 0.000 description 1
- NKUIXQOJUAEIET-AQZXSJQPSA-N Trp-Asp-Thr Chemical compound C1=CC=C2C(C[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@H](O)C)C(O)=O)=CNC2=C1 NKUIXQOJUAEIET-AQZXSJQPSA-N 0.000 description 1
- VMBBTANKMSRJSS-JSGCOSHPSA-N Trp-Glu-Gly Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CCC(O)=O)C(=O)NCC(O)=O VMBBTANKMSRJSS-JSGCOSHPSA-N 0.000 description 1
- HQJOVVWAPQPYDS-ZFWWWQNUSA-N Trp-Gly-Arg Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(O)=O HQJOVVWAPQPYDS-ZFWWWQNUSA-N 0.000 description 1
- RPVDDQYNBOVWLR-HOCLYGCPSA-N Trp-Gly-Leu Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)NCC(=O)N[C@@H](CC(C)C)C(O)=O RPVDDQYNBOVWLR-HOCLYGCPSA-N 0.000 description 1
- OGXQLUCMJZSJPW-LYSGOOTNSA-N Trp-Gly-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)CNC(=O)[C@H](CC1=CNC2=CC=CC=C21)N)O OGXQLUCMJZSJPW-LYSGOOTNSA-N 0.000 description 1
- YRXXUYPYPHRJPB-RXVVDRJESA-N Trp-Gly-Trp Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)NCC(=O)N[C@@H](CC3=CNC4=CC=CC=C43)C(=O)O)N YRXXUYPYPHRJPB-RXVVDRJESA-N 0.000 description 1
- AZBIIKDSDLVJAK-VHWLVUOQSA-N Trp-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](CC1=CNC2=CC=CC=C21)N AZBIIKDSDLVJAK-VHWLVUOQSA-N 0.000 description 1
- YTCNLMSUXPCFBW-SXNHZJKMSA-N Trp-Ile-Glu Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCC(O)=O)C(O)=O YTCNLMSUXPCFBW-SXNHZJKMSA-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
- RWAYYYOZMHMEGD-XIRDDKMYSA-N Trp-Leu-Ser Chemical compound C1=CC=C2C(C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(O)=O)=CNC2=C1 RWAYYYOZMHMEGD-XIRDDKMYSA-N 0.000 description 1
- KWTRGSQOQHZKIA-PMVMPFDFSA-N Trp-Lys-Tyr Chemical compound C([C@H](NC(=O)[C@@H](NC(=O)[C@@H](N)CC=1C2=CC=CC=C2NC=1)CCCCN)C(O)=O)C1=CC=C(O)C=C1 KWTRGSQOQHZKIA-PMVMPFDFSA-N 0.000 description 1
- YCQKQFKXBPJXRY-PMVMPFDFSA-N Trp-Tyr-Lys Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CC3=CC=C(C=C3)O)C(=O)N[C@@H](CCCCN)C(=O)O)N YCQKQFKXBPJXRY-PMVMPFDFSA-N 0.000 description 1
- VCXWRWYFJLXITF-AUTRQRHGSA-N Tyr-Ala-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 VCXWRWYFJLXITF-AUTRQRHGSA-N 0.000 description 1
- WTXQBCCKXIKKHB-JYJNAYRXSA-N Tyr-Arg-Arg 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](CCCNC(N)=N)C(O)=O WTXQBCCKXIKKHB-JYJNAYRXSA-N 0.000 description 1
- PZXUIGWOEWWFQM-SRVKXCTJSA-N Tyr-Asn-Asn 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](CC(N)=O)C(O)=O PZXUIGWOEWWFQM-SRVKXCTJSA-N 0.000 description 1
- NSTPFWRAIDTNGH-BZSNNMDCSA-N Tyr-Asn-Tyr 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](CC1=CC=C(O)C=C1)C(O)=O NSTPFWRAIDTNGH-BZSNNMDCSA-N 0.000 description 1
- NLMXVDDEQFKQQU-CFMVVWHZSA-N Tyr-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)CC1=CC=C(O)C=C1 NLMXVDDEQFKQQU-CFMVVWHZSA-N 0.000 description 1
- MNMYOSZWCKYEDI-JRQIVUDYSA-N Tyr-Asp-Thr 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@@H](C)O)C(O)=O MNMYOSZWCKYEDI-JRQIVUDYSA-N 0.000 description 1
- KLGFILUOTCBNLJ-IHRRRGAJSA-N Tyr-Cys-Arg Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CS)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)N)O KLGFILUOTCBNLJ-IHRRRGAJSA-N 0.000 description 1
- UMXSDHPSMROQRB-YJRXYDGGSA-N Tyr-Cys-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CS)NC(=O)[C@H](CC1=CC=C(C=C1)O)N)O UMXSDHPSMROQRB-YJRXYDGGSA-N 0.000 description 1
- KCPFDGNYAMKZQP-KBPBESRZSA-N Tyr-Gly-Leu Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)NCC(=O)N[C@@H](CC(C)C)C(O)=O KCPFDGNYAMKZQP-KBPBESRZSA-N 0.000 description 1
- KHCSOLAHNLOXJR-BZSNNMDCSA-N Tyr-Leu-Leu Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(O)=O KHCSOLAHNLOXJR-BZSNNMDCSA-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
- BIWVVOHTKDLRMP-ULQDDVLXSA-N Tyr-Pro-Leu Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(O)=O BIWVVOHTKDLRMP-ULQDDVLXSA-N 0.000 description 1
- KWKJGBHDYJOVCR-SRVKXCTJSA-N Tyr-Ser-Cys Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CS)C(=O)O)N)O KWKJGBHDYJOVCR-SRVKXCTJSA-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
- UMSZZGTXGKHTFJ-SRVKXCTJSA-N Tyr-Ser-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 UMSZZGTXGKHTFJ-SRVKXCTJSA-N 0.000 description 1
- XUIOBCQESNDTDE-FQPOAREZSA-N Tyr-Thr-Ala Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](C)C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)N)O XUIOBCQESNDTDE-FQPOAREZSA-N 0.000 description 1
- BIVIUZRBCAUNPW-JRQIVUDYSA-N Tyr-Thr-Asn 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(N)=O)C(O)=O BIVIUZRBCAUNPW-JRQIVUDYSA-N 0.000 description 1
- VSYROIRKNBCULO-BWAGICSOSA-N Tyr-Thr-His Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)[C@H](CC2=CC=C(C=C2)O)N)O VSYROIRKNBCULO-BWAGICSOSA-N 0.000 description 1
- OJCISMMNNUNNJA-BZSNNMDCSA-N Tyr-Tyr-Asp Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CC(O)=O)C(O)=O)C1=CC=C(O)C=C1 OJCISMMNNUNNJA-BZSNNMDCSA-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
- PQPWEALFTLKSEB-DZKIICNBSA-N Tyr-Val-Glu 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](CCC(O)=O)C(O)=O PQPWEALFTLKSEB-DZKIICNBSA-N 0.000 description 1
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 description 1
- 208000002495 Uterine Neoplasms Diseases 0.000 description 1
- LTFLDDDGWOVIHY-NAKRPEOUSA-N Val-Ala-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](C(C)C)N LTFLDDDGWOVIHY-NAKRPEOUSA-N 0.000 description 1
- LABUITCFCAABSV-UHFFFAOYSA-N Val-Ala-Tyr Natural products CC(C)C(N)C(=O)NC(C)C(=O)NC(C(O)=O)CC1=CC=C(O)C=C1 LABUITCFCAABSV-UHFFFAOYSA-N 0.000 description 1
- LNYOXPDEIZJDEI-NHCYSSNCSA-N Val-Asn-Leu Chemical compound CC(C)C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](C(C)C)N LNYOXPDEIZJDEI-NHCYSSNCSA-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
- DLYOEFGPYTZVSP-AEJSXWLSSA-N Val-Cys-Pro Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CS)C(=O)N1CCC[C@@H]1C(=O)O)N DLYOEFGPYTZVSP-AEJSXWLSSA-N 0.000 description 1
- GBESYURLQOYWLU-LAEOZQHASA-N Val-Glu-Asp Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)O)N GBESYURLQOYWLU-LAEOZQHASA-N 0.000 description 1
- JTWIMNMUYLQNPI-WPRPVWTQSA-N Val-Gly-Arg Chemical compound CC(C)[C@H](N)C(=O)NCC(=O)N[C@H](C(O)=O)CCCNC(N)=N JTWIMNMUYLQNPI-WPRPVWTQSA-N 0.000 description 1
- DJEVQCWNMQOABE-RCOVLWMOSA-N Val-Gly-Asp Chemical compound CC(C)[C@@H](C(=O)NCC(=O)N[C@@H](CC(=O)O)C(=O)O)N DJEVQCWNMQOABE-RCOVLWMOSA-N 0.000 description 1
- WFENBJPLZMPVAX-XVKPBYJWSA-N Val-Gly-Glu Chemical compound CC(C)[C@H](N)C(=O)NCC(=O)N[C@H](C(O)=O)CCC(O)=O WFENBJPLZMPVAX-XVKPBYJWSA-N 0.000 description 1
- PIFJAFRUVWZRKR-QMMMGPOBSA-N Val-Gly-Gly Chemical compound CC(C)[C@H]([NH3+])C(=O)NCC(=O)NCC([O-])=O PIFJAFRUVWZRKR-QMMMGPOBSA-N 0.000 description 1
- URIRWLJVWHYLET-ONGXEEELSA-N Val-Gly-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)C(C)C URIRWLJVWHYLET-ONGXEEELSA-N 0.000 description 1
- XXROXFHCMVXETG-UWVGGRQHSA-N Val-Gly-Val Chemical compound CC(C)[C@H](N)C(=O)NCC(=O)N[C@@H](C(C)C)C(O)=O XXROXFHCMVXETG-UWVGGRQHSA-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
- BZMIYHIJVVJPCK-QSFUFRPTSA-N Val-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(C)C)N BZMIYHIJVVJPCK-QSFUFRPTSA-N 0.000 description 1
- DIOSYUIWOQCXNR-ONGXEEELSA-N Val-Lys-Gly Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)NCC(O)=O DIOSYUIWOQCXNR-ONGXEEELSA-N 0.000 description 1
- ZRSZTKTVPNSUNA-IHRRRGAJSA-N Val-Lys-Leu Chemical compound CC(C)C[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)C(C)C)C(O)=O ZRSZTKTVPNSUNA-IHRRRGAJSA-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
- XBJKAZATRJBDCU-GUBZILKMSA-N Val-Pro-Ala Chemical compound CC(C)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(O)=O XBJKAZATRJBDCU-GUBZILKMSA-N 0.000 description 1
- RYQUMYBMOJYYDK-NHCYSSNCSA-N Val-Pro-Glu Chemical compound CC(C)[C@@H](C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(=O)O)C(=O)O)N RYQUMYBMOJYYDK-NHCYSSNCSA-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
- 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
- YQYFYUSYEDNLSD-YEPSODPASA-N Val-Thr-Gly Chemical compound CC(C)[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(O)=O YQYFYUSYEDNLSD-YEPSODPASA-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
- PDDJTOSAVNRJRH-UNQGMJICSA-N Val-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](C(C)C)N)O PDDJTOSAVNRJRH-UNQGMJICSA-N 0.000 description 1
- OFTXTCGQJXTNQS-XGEHTFHBSA-N Val-Thr-Ser Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](C(C)C)N)O OFTXTCGQJXTNQS-XGEHTFHBSA-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
- 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 1
- 241000251539 Vertebrata <Metazoa> Species 0.000 description 1
- 208000014070 Vestibular schwannoma Diseases 0.000 description 1
- 208000036142 Viral infection Diseases 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 208000033559 Waldenström macroglobulinemia Diseases 0.000 description 1
- 208000008383 Wilms tumor Diseases 0.000 description 1
- 230000021736 acetylation Effects 0.000 description 1
- 238000006640 acetylation reaction Methods 0.000 description 1
- 208000004064 acoustic neuroma Diseases 0.000 description 1
- 208000017733 acquired polycythemia vera Diseases 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 208000011912 acute myelomonocytic leukemia M4 Diseases 0.000 description 1
- 210000005006 adaptive immune system Anatomy 0.000 description 1
- 208000009956 adenocarcinoma Diseases 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
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 description 1
- 229960000723 ampicillin Drugs 0.000 description 1
- 230000003698 anagen phase Effects 0.000 description 1
- 230000000259 anti-tumor effect Effects 0.000 description 1
- 230000009830 antibody antigen interaction Effects 0.000 description 1
- 230000006907 apoptotic process Effects 0.000 description 1
- 108010013835 arginine glutamate Proteins 0.000 description 1
- 108010001271 arginyl-glutamyl-arginine Proteins 0.000 description 1
- 230000010516 arginylation Effects 0.000 description 1
- 108010062796 arginyllysine Proteins 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001507 asparagine derivatives Chemical class 0.000 description 1
- 108010077245 asparaginyl-proline Proteins 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-L aspartate group Chemical group N[C@@H](CC(=O)[O-])C(=O)[O-] CKLJMWTZIZZHCS-REOHCLBHSA-L 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 108010093581 aspartyl-proline Proteins 0.000 description 1
- 108010038633 aspartylglutamate Proteins 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
- 238000012575 bio-layer interferometry Methods 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 210000000481 breast Anatomy 0.000 description 1
- 201000010983 breast ductal carcinoma Diseases 0.000 description 1
- 208000003362 bronchogenic carcinoma Diseases 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 210000004899 c-terminal region Anatomy 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 210000000845 cartilage Anatomy 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000012412 chemical coupling Methods 0.000 description 1
- 210000004978 chinese hamster ovary cell Anatomy 0.000 description 1
- 210000000349 chromosome Anatomy 0.000 description 1
- 208000024207 chronic leukemia Diseases 0.000 description 1
- 208000032852 chronic lymphocytic leukemia Diseases 0.000 description 1
- 238000010367 cloning Methods 0.000 description 1
- 238000000975 co-precipitation Methods 0.000 description 1
- 230000006957 competitive inhibition Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011970 concomitant therapy Methods 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 239000012531 culture fluid Substances 0.000 description 1
- 239000012228 culture supernatant Substances 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 description 1
- 230000021953 cytokinesis Effects 0.000 description 1
- 230000009089 cytolysis Effects 0.000 description 1
- 210000005220 cytoplasmic tail Anatomy 0.000 description 1
- 230000034994 death Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000007123 defense Effects 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 238000000612 dual polarization interferometry Methods 0.000 description 1
- 238000002296 dynamic light scattering Methods 0.000 description 1
- 230000004064 dysfunction Effects 0.000 description 1
- 239000012636 effector Substances 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 238000004520 electroporation Methods 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 230000003511 endothelial effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000007071 enzymatic hydrolysis Effects 0.000 description 1
- 238000006047 enzymatic hydrolysis reaction Methods 0.000 description 1
- 208000037828 epithelial carcinoma Diseases 0.000 description 1
- 210000003238 esophagus Anatomy 0.000 description 1
- 230000017188 evasion or tolerance of host immune response Effects 0.000 description 1
- 239000013613 expression plasmid Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 230000005714 functional activity Effects 0.000 description 1
- 108020001507 fusion proteins Proteins 0.000 description 1
- 102000037865 fusion proteins Human genes 0.000 description 1
- 210000000232 gallbladder Anatomy 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 108010055341 glutamyl-glutamic acid Proteins 0.000 description 1
- 108010049041 glutamylalanine Proteins 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 108010074027 glycyl-seryl-phenylalanine Proteins 0.000 description 1
- 108010015792 glycyllysine Proteins 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 229960000789 guanidine hydrochloride Drugs 0.000 description 1
- PJJJBBJSCAKJQF-UHFFFAOYSA-N guanidinium chloride Chemical compound [Cl-].NC(N)=[NH2+] PJJJBBJSCAKJQF-UHFFFAOYSA-N 0.000 description 1
- 201000000459 head and neck squamous cell carcinoma Diseases 0.000 description 1
- 210000002216 heart Anatomy 0.000 description 1
- 201000002222 hemangioblastoma Diseases 0.000 description 1
- 206010073071 hepatocellular carcinoma Diseases 0.000 description 1
- 238000000703 high-speed centrifugation Methods 0.000 description 1
- 108010040030 histidinoalanine Proteins 0.000 description 1
- 108010036413 histidylglycine Proteins 0.000 description 1
- 108010028295 histidylhistidine Proteins 0.000 description 1
- 108010092114 histidylphenylalanine Proteins 0.000 description 1
- 108010085325 histidylproline Proteins 0.000 description 1
- 102000054751 human RUNX1T1 Human genes 0.000 description 1
- 210000004408 hybridoma Anatomy 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 210000002865 immune cell Anatomy 0.000 description 1
- 230000006058 immune tolerance Effects 0.000 description 1
- 238000003119 immunoblot Methods 0.000 description 1
- 230000009851 immunogenic response Effects 0.000 description 1
- 230000016784 immunoglobulin production Effects 0.000 description 1
- 229940072221 immunoglobulins Drugs 0.000 description 1
- 238000001114 immunoprecipitation Methods 0.000 description 1
- 230000001024 immunotherapeutic effect Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 210000005007 innate immune system Anatomy 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 230000009545 invasion Effects 0.000 description 1
- 230000026045 iodination Effects 0.000 description 1
- 238000006192 iodination reaction Methods 0.000 description 1
- PGLTVOMIXTUURA-UHFFFAOYSA-N iodoacetamide Chemical compound NC(=O)CI PGLTVOMIXTUURA-UHFFFAOYSA-N 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 108010027338 isoleucylcysteine Proteins 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 238000000111 isothermal titration calorimetry Methods 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 238000011005 laboratory method Methods 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 108010073472 leucyl-prolyl-proline Proteins 0.000 description 1
- 108010091871 leucylmethionine Proteins 0.000 description 1
- 108010057821 leucylproline Proteins 0.000 description 1
- 108010012058 leucyltyrosine Proteins 0.000 description 1
- 230000029226 lipidation Effects 0.000 description 1
- 238000001638 lipofection Methods 0.000 description 1
- 206010024627 liposarcoma Diseases 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 201000002250 liver carcinoma Diseases 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 210000001165 lymph node Anatomy 0.000 description 1
- 108010064235 lysylglycine Proteins 0.000 description 1
- 201000000564 macroglobulinemia Diseases 0.000 description 1
- 230000036210 malignancy Effects 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 208000023356 medullary thyroid gland carcinoma Diseases 0.000 description 1
- 201000001441 melanoma Diseases 0.000 description 1
- 230000009401 metastasis Effects 0.000 description 1
- 150000002741 methionine derivatives Chemical class 0.000 description 1
- 108010016686 methionyl-alanyl-serine Proteins 0.000 description 1
- 108010068488 methionylphenylalanine Proteins 0.000 description 1
- 230000011987 methylation Effects 0.000 description 1
- 238000007069 methylation reaction Methods 0.000 description 1
- 238000000520 microinjection Methods 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229940126619 mouse monoclonal antibody Drugs 0.000 description 1
- 208000001611 myxosarcoma Diseases 0.000 description 1
- 230000001613 neoplastic effect Effects 0.000 description 1
- 201000008026 nephroblastoma Diseases 0.000 description 1
- 238000007857 nested PCR Methods 0.000 description 1
- 208000007538 neurilemmoma Diseases 0.000 description 1
- 210000004498 neuroglial cell Anatomy 0.000 description 1
- 230000009701 normal cell proliferation Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 201000008968 osteosarcoma Diseases 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 210000003101 oviduct Anatomy 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 208000004019 papillary adenocarcinoma Diseases 0.000 description 1
- 201000010198 papillary carcinoma Diseases 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- 239000000816 peptidomimetic Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 108010084525 phenylalanyl-phenylalanyl-glycine Proteins 0.000 description 1
- 108010024654 phenylalanyl-prolyl-alanine Proteins 0.000 description 1
- 108010073101 phenylalanylleucine Proteins 0.000 description 1
- 108010073025 phenylalanylphenylalanine Proteins 0.000 description 1
- 208000024724 pineal body neoplasm Diseases 0.000 description 1
- 210000004180 plasmocyte Anatomy 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 208000037244 polycythemia vera Diseases 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000013823 prenylation Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000004393 prognosis Methods 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 108700042769 prolyl-leucyl-glycine Proteins 0.000 description 1
- 210000002307 prostate Anatomy 0.000 description 1
- 230000002797 proteolythic effect Effects 0.000 description 1
- 210000001938 protoplast Anatomy 0.000 description 1
- 230000006340 racemization Effects 0.000 description 1
- 238000003259 recombinant expression Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 238000010839 reverse transcription Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 201000009410 rhabdomyosarcoma Diseases 0.000 description 1
- 239000012723 sample buffer Substances 0.000 description 1
- 206010039667 schwannoma Diseases 0.000 description 1
- 201000008407 sebaceous adenocarcinoma Diseases 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 238000002864 sequence alignment Methods 0.000 description 1
- 238000013207 serial dilution Methods 0.000 description 1
- 125000003607 serino group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(O[H])([H])[H] 0.000 description 1
- 108010048397 seryl-lysyl-leucine Proteins 0.000 description 1
- 230000011664 signaling Effects 0.000 description 1
- 210000002027 skeletal muscle Anatomy 0.000 description 1
- 235000020183 skimmed milk Nutrition 0.000 description 1
- 210000003491 skin Anatomy 0.000 description 1
- 208000000587 small cell lung carcinoma Diseases 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 210000000278 spinal cord Anatomy 0.000 description 1
- 210000000952 spleen Anatomy 0.000 description 1
- 206010041823 squamous cell carcinoma Diseases 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000001370 static light scattering Methods 0.000 description 1
- 210000000130 stem cell Anatomy 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000019635 sulfation Effects 0.000 description 1
- 238000005670 sulfation reaction Methods 0.000 description 1
- 238000002198 surface plasmon resonance spectroscopy Methods 0.000 description 1
- 201000010965 sweat gland carcinoma Diseases 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000000946 synaptic effect Effects 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 201000003120 testicular cancer Diseases 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 210000001550 testis Anatomy 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 108010071097 threonyl-lysyl-proline Proteins 0.000 description 1
- 210000001541 thymus gland Anatomy 0.000 description 1
- 210000001685 thyroid gland Anatomy 0.000 description 1
- 210000003437 trachea Anatomy 0.000 description 1
- 239000012096 transfection reagent Substances 0.000 description 1
- 238000003146 transient transfection Methods 0.000 description 1
- 108091007466 transmembrane glycoproteins Proteins 0.000 description 1
- 108700004896 tripeptide FEG Proteins 0.000 description 1
- 210000004881 tumor cell Anatomy 0.000 description 1
- 230000004614 tumor growth Effects 0.000 description 1
- 208000013706 tumor of meninges Diseases 0.000 description 1
- 108010003137 tyrosyltyrosine Proteins 0.000 description 1
- 230000034512 ubiquitination Effects 0.000 description 1
- 238000010798 ubiquitination Methods 0.000 description 1
- 241000712461 unidentified influenza virus Species 0.000 description 1
- 210000000626 ureter Anatomy 0.000 description 1
- 210000003932 urinary bladder Anatomy 0.000 description 1
- 201000005112 urinary bladder cancer Diseases 0.000 description 1
- 206010046766 uterine cancer Diseases 0.000 description 1
- 210000004291 uterus Anatomy 0.000 description 1
- 238000010200 validation analysis Methods 0.000 description 1
- 108010052774 valyl-lysyl-glycyl-phenylalanyl-tyrosine Proteins 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 230000009385 viral infection Effects 0.000 description 1
- 239000013603 viral vector Substances 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 238000002424 x-ray crystallography Methods 0.000 description 1
Images
Classifications
-
- 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
- C07K16/2803—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6801—Drug-antibody or immunoglobulin conjugates defined by the pharmacologically or therapeutically active agent
- A61K47/6803—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6835—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
- A61K47/6849—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a receptor, a cell surface antigen or a cell surface determinant
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/001—Preparation for luminescence or biological staining
- A61K49/0013—Luminescence
- A61K49/0017—Fluorescence in vivo
- A61K49/005—Fluorescence in vivo characterised by the carrier molecule carrying the fluorescent agent
- A61K49/0058—Antibodies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
- A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
- A61K51/04—Organic compounds
- A61K51/08—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins
- A61K51/10—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody
- A61K51/1027—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody against receptors, cell-surface antigens or cell-surface determinants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/569—Immunoassay; Biospecific binding assay; Materials therefor for microorganisms, e.g. protozoa, bacteria, viruses
- G01N33/56966—Animal cells
- G01N33/56972—White blood cells
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/22—Immunoglobulins specific features characterized by taxonomic origin from camelids, e.g. camel, llama or dromedary
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/33—Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity
-
- 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
- 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
- C07K2317/569—Single domain, e.g. dAb, sdAb, VHH, VNAR or nanobody®
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/75—Agonist effect on antigen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
- C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
- C07K2317/94—Stability, e.g. half-life, pH, temperature or enzyme-resistance
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/705—Assays involving receptors, cell surface antigens or cell surface determinants
- G01N2333/70596—Molecules with a "CD"-designation not provided for elsewhere in G01N2333/705
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Immunology (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Cell Biology (AREA)
- Hematology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- Biomedical Technology (AREA)
- Urology & Nephrology (AREA)
- Microbiology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Analytical Chemistry (AREA)
- Virology (AREA)
- Biotechnology (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Zoology (AREA)
- Food Science & Technology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Mycology (AREA)
- Optics & Photonics (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
提供NKp46受體的抗體或其抗原結合片段、包含所述抗體或其抗原結合片段的衍生物、藥物組成物及其在治療癌症方面的相關應用。
Description
本揭露屬於免疫學領域,更具體地,本揭露有關針對NKp46受體的抗體或其抗原結合片段、包含所述抗體或其抗原結合片段的衍生物、藥物組成物及其在治療癌症方面的相關應用。
NK細胞屬於先天性免疫系統中的效應淋巴細胞,是機體抵抗病毒感染和防止腫瘤發生的第一道防線。它與獲得性免疫系統中的細胞毒性T細胞,扮演著相近的角色,但它們之間不同的是:通常情況下,細胞毒性T細胞需要檢測到病毒細胞表面的MHC,才會引起細胞因數的釋放,進而導致靶細胞裂解或凋亡;而NK細胞可以在沒有抗體或MHC的情況下,識別這些細胞並進行快速的免疫回應。對於那些失去自身標記的MHC-I型的細胞,NK細胞不經過啟動就可以進行殺傷,而這些細胞通常是有害但不能被其他免疫細胞發現並消滅的。
NK細胞通過表面活化性受體和抑制性受體的平衡調控NK細胞的活性。NK細胞表面的活化性受體分為人類白細胞抗原I(human leukocyte antigen-I,HLA-I)類分子相關受體和非相關受體,前者包括殺傷細胞免疫球蛋白樣受體二區域(killer cell immunogloblin-like receptor,2 domains short,KIR2DS),殺傷細胞免疫球蛋白樣受體三區域(killer cell immunogloblin-like receptor,3 domains short,KIR3DS)及NK細胞受體2C(natural killer cell group 2C,CD94/NKG2C);後者主要有NK細胞受體2區域(natural killer cell group 2D,NKG2D)和自然細胞毒性受體(natural cytotoxicity receptors, NCR;包括NKp46,NKp30,NKp44)及DNAX輔助分子1(DNAX accessory molecule-1,DNAM-1);相應的抑制性受體為KIR2DL,KIR3DL及CD94/NKG2A等。
Sivori等於1997年發現了NKp46受體,是最早發現的自然細胞毒性受體,也是最主要的自然細胞毒受體,表達於所有NK細胞(包括成熟、未成熟、靜止和活化NK細胞)表面,在自然殺傷作用中起關鍵作用。因其特異表達於NK細胞表面,分子量大小為46kD,故命名為NKp46。NKp46基因位於19號染色體,為I型跨膜糖蛋白,NKp46胞外區含有2個Ig樣結構域,即D1和D2,D2(靠近細胞膜區域)是腫瘤及病毒感染細胞配體結合的區域。跨膜區有一個帶正電荷的精氨酸和一個缺乏基於免疫受體酪氨酸活化序列的細胞質尾部,可以與CD3ζ和FcγR穿膜區天冬氨酸殘基建立鹽橋,後者通過受體結合使得酪氨酸磷酸化故而介導NKp46的信號轉導。目前為止鑒定的NKp46的配體只有流感病毒血凝素和副流感病毒血凝素,而細胞性配體還不知曉。
NK細胞殺傷靶細胞時,毒性顆粒將達到漿膜面並與細胞膜融合,引起顆粒內容物釋放,最終導致靶細胞的死亡。隨著脫顆粒的發生,CD107a分子被轉運到細胞膜表面,並且CD107a分子的表達上調與穿孔素的分泌一致。故,CD107a分子陽性表達的NK細胞可代表具有殺傷活性的NK細胞。
NKp46在抗腫瘤中的作用:活化的NK細胞具有較強的殺傷腫瘤細胞作用,而NKp46受體是傳遞活化刺激所必需的。已經知道NKp46的表達減少有關宮頸癌及其前驅病損的免疫逃逸,NKp46/NCR1表達缺失,增加淋巴瘤的生長。Yasser等證實NKp46對所有MM細胞株的殺傷都是必須的。此外,NKp46在中樞神經系統中小膠質細胞的清除也有著重要的作用,Lunemann等證實,大腦內浸潤的NK細胞通過NKp46,NKG2D的介導識別,使活化的NK細胞與小膠質細胞形成突觸連接,後者的穿孔素極化至細胞介面而發揮殺傷作用。
本揭露提供了一種抗NKp46的抗體或其抗原結合片段,所述抗體或其抗原結合片段特異性地結合人類和食蟹猴NKp46。
在一些實施方案中,提供一種抗NKp46的抗體或其抗原結合片段,所述抗體或其抗原結合片段能夠特異性結合NKp46,其包含3個選自SEQ ID NO:44-133序列所示的CDR。
在一些實施方案中,提供一種抗NKp46的抗體或其抗原結合片段,所述抗體或其抗原結合片段能夠特異性結合NKp46,其包含選自SEQ ID NO:44,47,50,53,56,59,62,65,68,71,74,77,80,83,86,89,92,95,98,101,104,107,110,113,116,119,122,125,128,131所示的HCDR1;以及,選自SEQ ID NO: 45,48,51,54,57,60,63,66,69,72,75,78,81,84,87,90,93,96,99,102,105,108,111,114,117,120,123,126,129,132所示的HCDR2;以及,選自SEQ ID NO: 46,49,52,55,58,61,64,67,70,73,76,79,82,85,88,91,94,97,100,103,106,109,112,115,118,121,124,127,130,133所示的HCDR3。
在一些實施方案中,提供一種抗NKp46的抗體或其抗原結合片段,所述抗體或其抗原結合片段能夠特異性結合NKp46,包含重鏈可變區,所述重鏈可變區包含選自下組的HCDR1、HCDR2和HCDR3:SEQ ID NO:44、SEQ ID NO:45和SEQ ID NO:46;或SEQ ID NO:47、SEQ ID NO:48和SEQ ID NO:49;或SEQ ID NO:50、SEQ ID NO:51和SEQ ID NO:52;或SEQ ID NO:53、SEQ ID NO:54和SEQ ID NO:55;或SEQ ID NO:56、SEQ ID NO:57和SEQ ID NO:58;或SEQ ID NO:59、SEQ ID NO:60和SEQ ID NO:61;或SEQ ID NO:62、SEQ ID NO:63和SEQ ID NO:64;或SEQ ID NO:65、SEQ ID NO:66和SEQ ID NO:67;或SEQ ID NO:68、SEQ ID NO:69和SEQ ID NO:70;或SEQ ID NO:71、SEQ ID NO:72和SEQ ID NO:73;或SEQ ID NO:74、SEQ ID NO:75和SEQ ID NO:76;或SEQ ID NO:77、SEQ ID NO:78和SEQ ID NO:79;或SEQ ID NO:80、SEQ ID NO:81和SEQ ID NO:82;或SEQ ID NO:83、SEQ ID NO:84和SEQ ID NO:85;或SEQ ID NO:86、SEQ ID NO:87和SEQ ID NO:88;或SEQ ID NO:89、SEQ ID NO:90和SEQ ID NO:91;或SEQ ID NO:92、SEQ ID NO:93和SEQ ID NO:94;或SEQ ID NO:95、SEQ ID NO:96和SEQ ID NO:97;或SEQ ID NO:98、SEQ ID NO:99和SEQ ID NO:100;或SEQ ID NO:101、SEQ ID NO:102和SEQ ID NO:103;或SEQ ID NO:104、SEQ ID NO:105和SEQ ID NO:106;或SEQ ID NO:107、SEQ ID NO:108和SEQ ID NO:109;或SEQ ID NO:110、SEQ ID NO:111和SEQ ID NO:112;或SEQ ID NO:113、SEQ ID NO:114和SEQ ID NO:115;或SEQ ID NO:116、SEQ ID NO:117和SEQ ID NO:118;或SEQ ID NO:119、SEQ ID NO:120和SEQ ID NO:121;或SEQ ID NO:122、SEQ ID NO:123和SEQ ID NO:124;或SEQ ID NO:125、SEQ ID NO:126和SEQ ID NO:127;或SEQ ID NO:128、SEQ ID NO:129和SEQ ID NO:130;或SEQ ID NO:131、SEQ ID NO:132和SEQ ID NO:133。
在一些實施方案中,提供一種抗NKp46的抗體或其抗原結合片段,所述抗體或其抗原結合片段能夠特異性結合NKp46,其包含HCDR1、HCDR2和HCDR3,所述HCDR1、HCDR2和HCDR3來自於SEQ ID NO: 14-43,136-152所示的重鏈可變區。
在一些實施方案中,提供一種抗NKp46的抗體或其抗原結合片段,所述抗體或其抗原結合片段能夠特異性結合NKp46,包含重鏈可變區,所述重鏈可變區具有與SEQ ID NO: 14-43,136-152所示序列至少80%、81%、82%、83%、84%、85%、86%、87%、88%、89%、90%、91%、92%、93%、94%、95%、96%、97%、98%、99%或100%同一性。
在一些實施方案中,提供所述的抗NKp46的抗體或其抗原結合片段,其中所述單克隆抗體是重組抗體,優選的,為羊駝源抗體、嵌合抗體或人源化抗體。
在一些實施方案中,提供根據本揭露所述的抗NKp46的抗體或其抗原結合片段,其中所述單克隆抗體是奈米抗體,優選的,為人源化的駱駝科VHH。
在一些實施方案中,提供本揭露所述的抗NKp46的抗體或其抗原結合片段,其更包括重鏈恒定區及/或輕鏈恒定區,優選的,所述重鏈恒定區包括Fc或變體Fc,Fc來源於鼠或人。
在一些實施方案中,提供本揭露所述的抗NKp46的抗體或其抗原結合片段,其為IgG1、IgG2、IgG3或IgG4形式。
在一些實施方案中,提供本揭露所述的一種偶聯物,將前述任一抗NKp46的抗體或其抗原結合片段與捕獲標記物或檢測標記物偶聯形成,所述的檢測標記物包括放射性核素、發光物質、有色物質或酶。
在一些實施方案中,提供一種雙特異性抗體,其中的一個抗原結合結構域包含前述任一抗NKp46的抗體或其抗原結合片段。
在一些實施方案中,提供一種多特異性抗體,其中的一個抗原結合結構域包含前述任一抗NKp46的抗體或其抗原結合片段。
在一些實施方案中,提供一種抗體藥物綴合物,含有前述任一抗NKp46的抗體或其抗原結合片段,所述的抗體藥物綴合物由抗體-接頭-毒素相互連接形成。
在一些實施方案中,提供一種嵌合抗原受體,其胞外識別單元包含前述任一抗NKp46的抗體或其抗原結合片段。
在一些實施方案中,提供編碼前述任一抗NKp46的抗體或其抗原結合片段的核酸。
在一些實施方案中,提供本揭露所述的核酸的重組載體。
在一些實施方案中,提供一種宿主細胞,其包含本揭露所述的重組載體或基因組中整合本揭露所述的核酸。
在一些實施方案中,提供本揭露所述抗NKp46的抗體或其抗原結合片段的方法,包括:在適合的條件下培養本揭露所述的宿主細胞,並從所述細胞中純化獲得表達產物。
在一些實施方案中,提供本揭露所述的抗NKp46的抗體或其抗原結合片段在製備特異性靶向表達NKp46的細胞的藥物中的用途,優選的,所述細胞是NK細胞。
在一些實施方案中,提供本揭露所述的抗NKp46的抗體或其抗原結合片段在製備癌症、感染性疾病或者炎性或自身免疫性疾病藥物中的用途,優選的,所述腫瘤包括:白血病,侵襲性淋巴瘤,非霍奇金淋巴瘤,腦膠質瘤,宮頸癌,頭頸癌,直腸癌,腎癌,肝癌,肺癌,胰腺癌,胃癌等。
在一些實施方案中,提供本揭露所述的抗NKp46的抗體或其抗原結合片段在製備表達NKp46的NK的診斷試劑中的用途。
在一些實施方案中,提供一種含有NKp46的抗體的溶液製劑,其包含抗NKp46的抗體或其抗原結合片段和緩衝液。
在一些實施方案中,提供本揭露所述的一種用於鑒定個體中NKp46表達細胞的存在的方法,所述方法包括從包含細胞的個體獲得生物樣品,使所述細胞與本揭露所述的抗NKp46的抗體或其抗原結合片段接觸,以及評估所述抗體是否與所述細胞結合。
在一些實施方案中,提供一種藥物組成物,其包含有效量的前述任一抗NKp46的抗體或其抗原結合片段、或包含有效量的雙特異性抗體、或包含有效量的多特異性抗體、或包含有效量的抗體藥物綴合物、或包含有效量的嵌合抗原受體、或包含有效量的核酸、或包含有效量的重組載體、或包含有效量的宿主細胞。
在一些實施方案中,提供本揭露所述的藥物組成物,更包括藥學上可接受的載體。
在一些實施方案中,提供本揭露所述的藥物組成物,更包括一種或多種額外的其他治療劑,優選的所述一種或多種額外的其他治療劑包括:化學治療劑、細胞毒性劑、放射性治療劑、癌症疫苗、減瘤劑、靶向性抗癌劑、抗血管生成劑、生物反應修飾劑、細胞因數、激素、抗轉移劑和免疫治療劑。
在一些實施方案中,提供一種藥盒或試劑盒,其包括容器,以及位於容器中的本揭露所述的藥物組成物。
術語
本說明書中提及的所有公佈、專利和專利申請都以引用的方式併入本文,所述引用的程度就如同已特定地和個別地指示將各個別公佈、專利或專利申請以引用的方式併入一般。
在下文詳細描述本揭露前,應理解本揭露不限於本文中描述的特定方法學、方案和試劑,因為這些可以變化。還應理解本文中使用的術語僅為了描述具體實施方案,而並不意圖限制本揭露的範圍。除非另外定義,本文中使用的所有技術和科學術語與本揭露所屬領域中普通技術人員通常的理解具有相同的含義。
本文所公開的某些實施方案包含了數值範圍,並且本揭露的某些方面可採用範圍的方式描述。除非另有說明,應當理解數值範圍或者以範圍描述的方式僅是出於簡潔、便利的目的,並不應當認為是對本揭露的範圍的嚴格限定。因此,採用範圍方式的描述應當被認為具體地公開了所有可能的子範圍以及在該範圍內的所有可能的具體數值點,正如這些子範圍和數值點在本文中已經明確寫出。例如,從1至6的範圍的描述應當被認為具體公開了從1至3、1至4、1至5、2至4、2至6、3至6等的子範圍,以及在這些範圍內的具體的數值點,例如1、2、3、4、5、6。不論所述數值的寬窄,上述原則均同等適用。當採用範圍描述時,該範圍包括範圍的端點。
當有關可測量值比如量、暫時持續時間等時,術語“約”是指包括指定值的±20%、或在某些情況下±10%、或在某些情況下±5%、或在某些情況下±1%、或在某些情況下±0.1%的變化。
本文所用氨基酸三字母代碼和單字母代碼如J. Biol. Chem,243,p3558(1968)中所述。
常規的免疫球蛋白是四聚體,由兩條重鏈和兩條輕鏈組成,組合分子量約150kDa。在駱駝科(Camelidae)成員中,相當比例的血清抗體是同源二聚體IgG,分子量約80kD(Hamers-Casterman等人. 1993 Nature, 363, 446-448)。這些重鏈免疫球蛋白(Ig)包含三個結構域,其可變區被稱為VHH(variable domain of heavy chain of heavy-chain antibody)。重組VHH(約12至14kD)構成完整的抗原結合結構域並顯示出廣闊的抗原結合譜。擴大它們的高變區,並表現出獨特的特性,如三至四個(與常規抗體VL相互作用的)疏水框架殘基被更多親水性氨基酸取代。為了穩定擴大的CDR,除了常規的二硫鍵以外,在單峰駱駝CDR1和CDR3之間,在美洲駝的CDR2和CDR3之間,VHH可具有額外的二硫鍵(Harmsen和De Haard 2007 Appl Microbiol Biotechnol., 77, 13-22; Muyldermans 2001 J Biotechnol., 74, 277-302)。擴大的CDR3環可以採取凸面構象,而常規的互補位被限制在凹的或者平面結構(Muyldermans 2001 J Biotechnol., 74, 277-302)。這些特徵允許VHH識別對於常規抗體而言免疫原性較差的獨特表位(Lafaye等人. 2009 Mol Immuno., 46, 695-704;Wernery 2001 J Vet Med B Infect Dis Vet Public Health., 48, 561-568)。儘管VHH被定義為單價抗體,默認排除任何親合力效果,被測量表示為體外IC
50的生物活性可類似於常規的二價抗體分子(Thys等人. 2010 Antiviral Res., 87: 257-264)。
術語“單克隆抗體”是指由一群基本同源的抗體獲得的抗體,即包含在該群體中的各個抗體是相同的(除了可能以少量存在的可能的天然突變以外)。單克隆抗體針對單個抗原位點具有高度特異性。此外,與常規的多克隆抗體製劑(其通常包括針對抗原上不同決定簇(表位)的不同抗體)不同的是,每個單克隆抗體只針對抗原上的單個決定簇或表位。
在某些實施方式中,本揭露可有關嵌合的駱駝科動物/人抗體,特別是其中VH及/或VL結構域完全是駱駝科動物序列(例如大羊駝或阿爾帕卡羊駝),而抗體的其餘部分完全是人序列的嵌合抗體。在本揭露的一些優選實施方式中,更包括“人源化”或“種系化”的駱駝科抗體以及駱駝科/人嵌合抗體,其中VH及/或VL結構域相對於通過主動免疫獲得的駱駝科VH及/或VL結構域來說在框架區包含一個或多個氨基酸替換。用人種系VH或VL結構域中的對應殘基來取代起始駱駝科VH或VL結構域中的不匹配氨基酸殘基,這樣的“人源化”過程提高了與人種系VH或VL結構域的序列一致性百分比。
本揭露包括天然、重組的VHH或VH。
“重組”有關採用遺傳工程的方法(克隆、擴增)來生產所述VHH或VH。
根據本揭露的VHH能夠是單體的形式或者同源多聚體的形式,如同源二聚體或同源三聚體。
本揭露的抗體包括羊駝源抗體、嵌合抗體、人源化抗體,優選人源化抗體。
“嵌合抗體(chimeric antibody)”,是將羊駝源性抗體的可變區與人抗體的恒定區(或Fc區)融合而成的抗體,可以減輕羊駝源性抗體誘發的免疫應答反應。建立嵌合抗體,要先建立分泌羊駝源性特異性單抗的雜交瘤或抗體文庫,然後將羊駝抗體可變區基因與人恒定區基因(或Fc區基因)連接成嵌合基因後插入表達載體中,最後在真核系統或原核系統中表達嵌合抗體分子。
“人源化抗體(humanized antibody)”,是指將羊駝的CDR序列移植到人的抗體可變區框架,即不同類型的人種系抗體框架序列中產生的抗體。可以克服嵌合抗體由於攜帶大量羊駝蛋白成分,從而誘導的異源性反應。此類框架序列可以從包括種系抗體基因序列的公共DNA資料庫或公開的參考文獻獲得。如人重鏈和輕鏈可變區基因的種系DNA序列可以在“VBase”人種系序列資料庫(https://www2.mrc-lmb.cam.ac.uk/vbase/)中獲得,以及在Kabat,E.A.等人,1991 Sequences of Proteins of Immunological Interest第5版中找到。為避免免疫原性下降的同時,引起的活性下降,可對所述的人抗體可變區框架序列進行最少反向突變或回復突變,以保持活性。
“VHH”有關來自駱駝科(駱駝、單峰駱駝、美洲駝、羊駝等)重鏈抗體的可變抗原結合結構域(參見Nguyen等人.2000 EMBO J.,19,921-930;Muyldermans 2001 J Biotechnol.,74, 277-302以及綜述Vanlandschoot等人. 2011 Antiviral Res.92,389-407)。
通常奈米抗體可以定義為具有下述(通用)結構的氨基酸序列:FR1-CDR1-FR2-CDR2-FR3-CDR3-FR4。其中,FR1-FR4分別是指框架區(Frame)1-4,並且其中CDR1-CDR3分別是指互補決定區1-3。
本領域已知五個主要類別的抗體:IgA,IgD,IgE,IgG和IgM,對應的重鏈恒定結構域分別被稱為α,δ,ε,γ和μ,IgG和IgA可以進一步分為不同的亞類,例如IgG可分為IgG1,IgG2,IgG3,IgG4,IgA可分為IgA1和IgA2。來自任何脊椎動物物種的抗體的輕鏈基於其恒定結構域的氨基酸序列可以被分配到兩種明顯相異的類型之一,稱為κ和λ。
在IgG、IgA和IgD抗體的情形中,該恒定區包含稱為CH1、CH2和CH3的三個結構域(IgM和IgE具有第四結構域CH4)。在IgG、IgA和IgD類別中,CH1和CH2結構域被柔性鉸鏈區分離,該鉸鏈區是可變長度的富含脯氨酸和半胱氨酸的區段。每類抗體進一步包含由配對半胱氨酸殘基形成的鏈間和鏈內二硫鍵。
術語“Fc”在本文中用於定義免疫球蛋白重鏈的C端區域,所述區域包含至少一部分的恒定區。該術語包括天然序列Fc區和變體Fc區。除非另外說明,Fc區或恒定區中的氨基酸殘基的編號是根據EU編號系統,其也被稱為EU索引,如在Kabat等,Sequences of Proteins of Immunological Interest,5thEd.Public Health Service,National Institutes of Health,Bethesda,MD,1991中所述。
需說明的是,本揭露的單克隆抗體可變區的CDR和FR的劃分是根據Kabat定義確定的。而其他命名和編號系統,例如Chothia、IMGT或AHo等,也是本領域技術人員已知的。因此,以本揭露的單抗序列為基礎,包含任何命名系統衍生的一種或多種CDR的人源化抗體均明確地保持在本揭露的範圍內。
術語“序列同一性”或“序列相似性”或“序列同源性”,是指在將所述序列進行比對(並在必要時導入空位)以獲取最大百分比序列同一性,且不將任何保守置換視為序列同一性的部分之後,候選序列中的氨基酸殘基與參比多肽序列中的相同氨基酸殘基的百分比。可使用本領域各種方法進行序列比對以便測定百分比氨基酸序列同一性,例如,使用公眾可得到的電腦軟體如BLAST、BLAST-2、ALIGN或MEGALIGN(DNASTAR)軟體。本領域技術人員可以決定測量比對的適宜參數,包括對所比較的序列全長獲得最大比對所需的任何演算法。
術語“抗體片段”包含完整抗體的至少一部分。如在此所使用,抗體分子的“片段”包括抗體的“抗原結合片段”,並且術語“抗原結合片段”是指免疫球蛋白或抗體中與所選抗原或其抗原表位特異性結合或反應的多肽片段,或由此片段進一步衍生的融合蛋白產物,例如單鏈抗體,嵌合抗原受體中的胞外結合區等。示例性的抗體片段或其抗原結合片段包括但不限於:可變輕鏈片段(VL)、可變重鏈片段(VH)、Fab片段、F(ab’)
2片段、Fd片段、Fv片段、單結構域抗體、線性抗體、單鏈抗體(scFv)及由抗體片段形成的雙特異性抗體或多特異性抗體等。
術語“多特異性抗體”是指,將抗體通過功能連接(例如化學偶聯、基因融合、非共價結合或其他方法)至一個或多個其他結合分子上,從而形成與兩個以上不同位點及/或靶點結合的新的抗體構建體。其中,使用較多的是“雙特異性抗體”,其特指針對兩種不同抗原具有特異性的抗體構建體。通常,雙特異性抗體或多特異性抗體至少包括2個抗原結合結構域。
術語“抗原”是指被抗體或抗體結合片段識別並特異性結合的物質,廣義上,抗原可以包括所選靶標的任何免疫原性片段或決定簇,包括單表位、多表位元、單結構域、多結構域、或完整的胞外結構域(ECD)或蛋白質。肽、蛋白質、糖蛋白、多糖和脂質,其部分及其組合均可構成抗原。非限制性示例性抗原包括腫瘤抗原或病原體抗原等。“抗原”也可以指引發免疫反應的分子。任何形式的抗原或含有該抗原的細胞或製劑都可以用於生成對抗原決定簇具有特異性的抗體。抗原可以是分離的全長蛋白質、細胞表面蛋白(例如,用在其表面上表達至少一部分抗原的細胞進行免疫的)、或可溶性蛋白質(例如,僅用該蛋白質的ECD部分進行免疫的)或蛋白質構建體(例如,Fc抗原)。該抗原可以在基因修飾的細胞中產生。前述任何抗原可以單獨或與本領域已知的一種或多種免疫原性增強佐劑組合使用。編碼該抗原的DNA可以是基因組的或非基因組的(例如,cDNA),並且可以編碼足以引起免疫原性應答的至少一部分ECD。可以使用任何載體來轉化其中表達抗原的細胞,所述載體包括但不限於腺病毒載體、慢病毒載體、質粒以及非病毒載體如陽離子脂質。
術語“表位”是指抗原上與免疫球蛋白或抗體特異性結合的位點。表位可以由相鄰的氨基酸、或通過蛋白質的三級折疊而並列的不相鄰的氨基酸形成。由相鄰的氨基酸形成的表位通常在暴露於變性溶劑後保持,而通過三級折疊形成的表位通常在變性溶劑處理後喪失。表位通常以獨特的空間構象包括至少3-15個氨基酸。由給定的抗體確定其結合的表位的方法是本領域熟知的,包括免疫印跡和免疫沉澱檢測分析等。確定表位的空間構象的方法包括本領域中的技術和本文所述的技術,例如X射線晶體分析法和二維核磁共振等。
術語“多肽”、“肽”和“蛋白質”在本文中可互換使用以指任何長度的氨基酸的聚合物。聚合物可以是直鏈、環狀或支鏈的,它可以包含修飾的氨基酸,特別是保守修飾的氨基酸,並且它可以被非氨基酸中斷。該術語更包括改性的氨基酸聚合物例如已經通過硫酸化、糖基化、脂化、乙醯化、磷酸化、碘化、甲基化、氧化、蛋白水解加工、異戊二烯化、外消旋化、硒醯化、轉移-RNA介導的氨基加成如精氨酸化、泛在化、或任何其他操作如與標記組分綴合等改性的氨基酸聚合物。如本文所用,術語“氨基酸”是指天然及/或非天然或合成氨基酸,包括甘氨酸以及D或L光學異構體,以及氨基酸類似物和肽模擬物。“衍生自”指定的蛋白質的多肽或氨基酸序列是指多肽的來源。該術語更包括由指定的核酸序列表達的多肽。
術語“氨基酸修飾”(或“修飾的氨基酸”)包括在多肽序列中的氨基酸取代、插入及/或缺失。本文中的“氨基酸取代”或“取代”意指用另一種氨基酸替換親本多肽序列中特定位置上的氨基酸。例如,取代S32A指第32位的絲氨酸被丙氨酸替換。
人源化抗體可變區與人類受體可變區的序列同一性或同源性可以如在此所論述的進行測定,並且當這樣測量時,將優選地共用至少60%或65%的序列同一性,更優選至少70%、75%、80%、85%或90%的序列同一性,甚至更優選至少93%、95%、98%或99%的序列同一性。優選地,不相同的殘基位置因保守性氨基酸置換而不同。“保守取代”是一個氨基酸殘基被具有類似化學特性(例如,電荷或疏水性)的側鏈(R基團)的另一個氨基酸殘基替換的氨基酸取代。一般而言,保守氨基酸取代不會實質上改變蛋白質的功能特性。本領域已經定義了具有相似側鏈的氨基酸殘基家族。這些家族包括含鹼性側鏈的氨基酸(例如,賴氨酸、精氨酸、組氨酸)、酸性側鏈(例如,天冬氨酸、谷氨酸)、不帶電的極性側鏈(例如,甘氨酸、天冬醯胺、絲氨酸、蘇氨酸、酪氨酸、半胱氨酸、色氨酸)、非極性側鏈(例如,丙氨酸、纈氨酸、亮氨酸、異亮氨酸、脯氨酸、苯丙氨酸、甲硫氨酸)、β分支側鏈(例如,蘇氨酸、纈氨酸、異亮氨酸)和芳香族側鏈(例如,酪氨酸、苯丙氨酸、色氨酸、組氨酸)。因而,可以用其他相似側鏈的氨基酸殘基替換本揭露抗體的CDR區中或框架區中的一個或多個氨基酸殘基。在兩個或更多個氨基酸序列因保守取代而彼此不同的情形中,序列同一性百分比或相似性程度可以向上調整以校正該取代的保守性質。
術語“親和力”或“結合親和力”指分子(例如抗體)的單一結合位點與其結合配偶體(例如抗原)之間全部非共價相互作用總和的強度。術語“K
D”是指特定的抗體-抗原相互作用的解離常數。可以使用本領域已知的各種技術來確定結合親和力,例如表面電漿共振、生物層干涉法、雙極化干涉法、靜態光散射、動態光散射、等溫滴定量熱法、ELISA、分析超速離心和流式細胞術等。
術語“競爭結合”或“競爭性抗體”通常是指,與本揭露的抗體結合相同表位的抗體,其結合導致本揭露的抗體與抗原表位的結合被抑制或阻斷,在競爭測定中可以得到競爭性抑制的程度。
術語“藥物組成物”指這樣的製劑,其以允許包含在其中的活性成分的生物學活性有效的形式存在,並且不包含對施用所述製劑的受試者具有不可接受的毒性的另外的成分。
術語“藥用載體”或“藥學上可接受的載體”指與治療劑一起施用的稀釋劑、佐劑(例如弗氏佐劑(完全和不完全的))、賦形劑或媒介物。
術語“有效量”指本揭露的抗體或片段的藥物製劑的劑量,其以單一或多次劑量施用患者後,在治療的患者中產生預期效果。有效量可以由作為本領域技術人員的主治醫師通過考慮以下多種因素來容易地確定:諸如人種差異;體重、年齡和健康狀況;有關的具體疾病;疾病的嚴重程度;個體患者的應答;施用的具體抗體;施用模式;施用製劑的生物利用率特徵;選擇的給藥方案;和任何伴隨療法的使用。
術語“宿主細胞”、“宿主細胞系”和“宿主細胞培養物”可交換地使用且是指其中引入外源核酸的細胞,包括這種細胞的後代。宿主細胞包括“轉化體”和“轉化的細胞”,其包括初級轉化的細胞和來源於其的後代,而不考慮傳代的數目。後代在核酸含量上可能與親本細胞不完全相同,而是可以包含突變。本文中包括與在最初轉化的細胞中篩選或選擇的具有相同功能或生物學活性的突變體後代。
本文所用的術語“轉染”是指將外源核酸引入真核細胞。轉染可以通過本領域已知的各種手段來實現,包括磷酸鈣-DNA共沉澱、DEAE-葡聚糖介導的轉染、聚凝胺介導的轉染、電穿孔、顯微注射、脂質體融合、脂質轉染、原生質體融合、逆轉錄病毒感染和生物彈道技術(biolistics)。
術語“穩定轉染”或“穩轉”是指將外源核酸、DNA或RNA引入和整合到轉染細胞的基因組中。術語“穩定轉染體”(stable transfectant)是指將外來DNA穩定地整合到基因組DNA中的細胞。
術語“核酸分子編碼”、“編碼DNA序列”和“編碼DNA”是指沿著去氧核糖核酸鏈的去氧核糖核苷酸的順序。這些去氧核糖核苷酸的順序決定了沿著多肽(蛋白質)鏈的氨基酸的順序。因此,核酸序列編碼氨基酸序列。
生產和純化抗體和抗原結合片段的方法在現有技術中熟知和能找到,如冷泉港的抗體實驗技術指南,5-8章和15章。本揭露所述的抗體或其抗原結合片段用基因工程方法在非人源的CDR區加上一個或多個人FR區。人FR種系序列可以從ImMunoGeneTics(IMGT)的網站(http://imgt.cines.fr)得到,或者從免疫球蛋白雜誌(The Immunoglobulin FactsBook,(2001) ISBN:012441351)上獲得。
本揭露工程化的抗體或其抗原結合片段可用常規方法製備和純化。比如,編碼重鏈和輕鏈的cDNA序列,可以克隆並重組至表達載體。重組的免疫球蛋白表達載體可以穩定地轉染CHO細胞。作為一種更推薦的現有技術,哺乳動物類表達系統會導致抗體的糖基化,特別是在Fc區的高度保守N端。通過表達與人源抗原特異性結合的抗體得到穩定的克隆。陽性的克隆在生物反應器的無血清培養基中擴大培養以生產抗體。分泌了抗體的培養液可以用常規技術純化、收集。抗體可用常規方法進行過濾濃縮。可溶的混合物和多聚體,也可以用常規方法去除,比如分子篩、離子交換。
本文所用的術語“個體”或“受試者”是指任何動物,例如哺乳動物或有袋動物。本揭露的個體包括但不限於人類、非人類靈長類動物(例如食蟹猴或恒河猴或其他類型的獼猴)、小鼠、豬、馬、驢、牛、綿羊、大鼠和任何種類的家禽。
本文所用的術語“腫瘤”指的是一種以細胞或組織的病理性增生為特徵的疾病,及其隨後的遷移或侵襲其他組織或器官。腫瘤生長通常是不受控制的和進行性的,不誘導或抑制正常細胞增殖。腫瘤可影響多種細胞、組織或器官,包括但不限於選自膀胱、骨、腦、乳腺、軟骨、神經膠質細胞、食管、輸卵管、膽囊、心臟、腸、腎、肝、肺、淋巴結、神經組織、卵巢、胰腺、前列腺、骨骼肌、皮膚、脊髓、脾、胃、睾丸、胸腺、甲狀腺、氣管、尿道、輸尿管、尿道、子宮、陰道器官,或組織或相應的細胞。腫瘤包括癌症,如肉瘤,癌,或漿細胞瘤(漿細胞的惡性腫瘤)。本揭露所述的腫瘤,可包括,但不限於白血病(如急性白血病、急性淋巴細胞白血病、急性髓細胞性白血病,急性粒細胞白血病,急性早幼粒細胞白血病、急性粒-單核細胞白血病、急性單核細胞白血病、慢性白血病、慢性粒細胞白血病、慢性淋巴細胞白血病、真性紅細胞增多症),淋巴瘤(霍奇金病、非霍奇金病)、原發性巨球蛋白血症,重鏈病,實體瘤如肉瘤和癌症(如纖維肉瘤、粘液肉瘤、脂肪肉瘤、軟骨肉瘤、骨肉瘤、脊索瘤、內皮肉瘤、淋巴管肉瘤、血管肉瘤、淋巴管內皮肉瘤,間皮瘤,尤文氏瘤、平滑肌肉瘤、橫紋肌肉瘤、結腸癌、胰腺癌、乳腺癌、卵巢癌、前列腺癌、鱗狀細胞癌、基底細胞癌、腺癌、汗腺癌、皮脂腺癌、乳頭狀癌、乳頭狀腺癌、支氣管癌、髓樣癌、腎細胞癌、肝癌,尼羅河管癌,絨癌、精原細胞瘤、胚胎癌、腎母細胞瘤、宮頸癌、子宮癌、睾丸癌、肺癌、小細胞肺癌、膀胱癌、上皮癌、膠質瘤、星形細胞瘤、髓母細胞瘤,顱咽管瘤、室管膜瘤、松果體瘤、血管母細胞瘤,聽神經瘤,少突膠質瘤、神經鞘瘤、腦膜瘤、黑色素瘤、神經母細胞瘤、視網膜母細胞瘤)、食管癌、膽囊癌、腎癌、多發性骨髓瘤。較佳地,所述的“腫瘤”包括但不限於:胰腺癌、肝癌、肺癌、胃癌、食管癌、頭頸部鱗狀細胞癌、前列腺癌、結腸癌、乳腺癌、淋巴瘤、膽囊癌、腎癌、白血病、多發性骨髓瘤、卵巢癌、宮頸癌和膠質瘤。
本文所用的術語“疾病”或“病症”或“紊亂”等是指任何損害或干擾細胞、組織或器官的正常功能的改變或失調。例如,所述的“疾病”包括但不限於:腫瘤、病原體感染、自身免疫性疾病、T細胞功能障礙性疾病、或免疫耐受能力缺陷(如移植排斥)。
本文所用的術語“治療”是指在試圖改變個人或處理細胞引起的疾病過程中的臨床干預,既可以進行預防也可以在臨床病理過程干預。治療效果包括但不限於,防止疾病的發生或復發、減輕症狀、減少任何疾病直接或間接的病理後果、防止轉移、減慢疾病的進展速度、改善或緩解病情、緩解或改善預後等。
術語“藥盒”或“試劑盒”包括有效量的一種或多種單位劑型的本揭露的藥物組成物。在一些實施方案中,藥盒或“試劑盒”可含有無菌容器;這樣的容器可以是盒、安瓿、瓶、小瓶、管、袋、泡罩包裝或本領域已知的其它合適的容器形式。這種容器可以由塑膠、玻璃、層壓紙、金屬箔或其他適合於保持藥物的材料製成。此外,藥盒更包括將本揭露的藥物組成物給予個體的說明書。說明書中通常包含使用本揭露的藥物組成物來治療疾病的方法。
實施例
下面結合具體實施例,進一步闡述本揭露。應理解,這些實施例僅用於說明本揭露而不用於限制本揭露的範圍。下列實施例中未注明具體條件的實驗方法,通常按照常規條件如分子克隆實驗指南(J.薩姆布魯克等編著,分子克隆實驗指南,第三版,科學出版社,2002)中所述的條件,或按照製造廠商所建議的條件。
實施例
1
人
NKp46
及食蟹猴
NKp46
抗原信息
表1 序列資訊
名稱 | 序號 | 備註 |
人NKp46全長氨基酸序列 | SEQ ID NO:1 | 第1-21位元為信號肽,第22-258位為NKp46胞外區,第259-279位為跨膜區,第280-304位為胞內區 |
食蟹猴NKp46全長氨基酸序列 | SEQ ID NO:2 | 第1-21位元為信號肽,第22-257位為NKp46胞外區,第258-278位為跨膜區,第279-306位為胞內區 |
免疫,篩選及檢測用人NKp46抗原(愷佧生物,NKP-HM146) | SEQ ID NO:3 | - |
免疫,篩選及檢測用食蟹猴NKp46抗原(愷佧生物,NKP-CM146) | SEQ ID NO:4 | - |
實施例
2
人
NKp46
及食蟹猴
NKp46
細胞系的製備
將編碼SEQ ID NO:1所示的人NKp46氨基酸的核苷酸序列,克隆至pCMV3(SinoBiological,貨號CV011)載體中,獲得用於人NKp46細胞系構建的載體。將所獲得的載體轉染至CHOK1細胞(ATCC,貨號CCL-61)中,獲得表達人NKp46的CHOK1細胞系(簡稱:人NKp46-CHOK1細胞系)。
將編碼SEQ ID NO:2所示的食蟹猴NKp46氨基酸的核苷酸序列,克隆至pCMV3載體中,獲得用於食蟹猴NKp46細胞系構建的載體。將所獲得的載體轉染至CHOK1細胞中,獲得表達食蟹猴NKp46的CHOK1細胞系(簡稱:食蟹猴NKp46-CHOK1細胞系)。
使用陽性對照抗體(Santa Cruz Biotechnology,貨號sc-59343),使用FACS測定方法,檢測上述獲得的人NKp46-CHOK1細胞系中人NKp46的表達情況,並在實驗中設立陰性對照anti-HEL human IgG1 LALA(百英生物,貨號B109802)。
使用陽性對照抗體(Santa Cruz Biotechnology,貨號sc-59343),使用FACS測定方法,檢測上述獲得的食蟹猴NKp46-CHOK1細胞系中食蟹猴NKp46的表達情況,並在實驗中設立陰性對照anti-HEL human IgG1 LALA(百英生物,貨號 B109802)。
結果顯示:
人NKp46-CHOK1細胞系中人NKp46的表達情況如圖1所示,結果表明人NKp46在CHOK1細胞中有很好的過表達現象,可以用於後續實驗驗證NKp46單抗與人NKp46在細胞水平的結合情況。
食蟹猴NKp46-CHOK1細胞系中食蟹猴NKp46的表達情況如圖2所示,結果表明食蟹猴NKp46在CHOK1細胞中有很好的過表達現象,可以用於後續實驗驗證NKp46單抗與食蟹猴NKp46在細胞水平的結合情況。
實施例
3
羊駝
/
駱駝
VHH
重鏈抗體免疫文庫的構建
分別用SEQ ID NO:3所示的人NKp46抗原和SEQ ID NO:4所示的食蟹猴NKp46抗原間隔對羊駝/駱駝進行免疫。免疫的日期分別為第0天,第14天,第28天,第42天,共免疫4次。分別在第28天,第42天,第56天抽取血樣分離出血清,利用流式細胞術檢測血清中免疫應答反應情況。檢測血清效價大於1:10000時,結束免疫。對免疫的羊駝/駱駝重新抽取血樣各100mL,進行如下操作:
1. 使用淋巴細胞分離液(Solarbio公司),按照操作分別分離駱駝/羊駝PBMC;
2. 使用細胞總RNA提取試劑盒(OMEGA公司),按照操作分別提取駱駝/羊駝總RNA;
3. 使用PrimeScript™ II反轉錄試劑盒(Takara公司),按照操作分別合成駱駝/羊駝cDNA;
4. 以上述獲得的cDNA做範本,使用下述SEQ ID NO:5- SEQ ID NO:13所示的特異性引物進行巢式PCR擴增;
第一輪PCR
SEQ ID NO:5(上游引物):GTCCTGGCTGCTCTTCTACAAGG;
SEQ ID NO:6(下游引物):GGTACGTGCTGTTGAACTGTTCC。
第二輪PCR
SEQ ID NO:7(上游引物):
ACTCGCGGCCCAGCCGGCCATGGCCGAGGTGCAGCTGGTGGAGTCTGGGGGAG;
SEQ ID NO:8(上游引物):
ACTCGCGGCCCAGCCGGCCATGGCCCAGGTRCAGCTGGTGGAGTCTGGGGGAG;
SEQ ID NO:9(上游引物):
ACTCGCGGCCCAGCCGGCCATGGCCGATGTGCAGCTGGTGGAGTCTGGGGGAG;
SEQ ID NO:10(下游引物):
GGTGTTGGCCTCCCGGGCCACTAGTGCTKGAGACRGTGACCTGGGT;
SEQ ID NO:11(下游引物):
GGTGTTGGCCTCCCGGGCCACTAGTGCTKGAGACRGTGACCAGGGT;
SEQ ID NO:12(下游引物):
GGTGTTGGCCTCCCGGGCCACTAGTTGAKGAGACRGTGACCTGGGT;
SEQ ID NO:13(下游引物):
GGTGTTGGCCTCCCGGGCCACTAGTTGAKGAGACRGTGACCAGGGT。
5. 擴增獲得駱駝/羊駝VHH基因片段。
回收上述擴增獲得的駱駝/羊駝VHH片段,通過Sfi I酶切,連接到pADL-23c(Biovector)噬菌粒載體上,電轉化TG1大腸桿菌感受態細胞建成羊駝/駱駝VHH重鏈抗體免疫文庫。其中,NKp46駱駝免疫文庫庫容為5.2E7,羊駝免疫文庫庫容為7.8E7。
實施例
4
特異性結合
NKp46
的陽性克隆的篩選
為了獲得可與人NKp46和食蟹猴NKp46交叉結合的陽性抗體,將上述文庫擴增加入M13K07 helper phage組裝成噬菌體後,分別投入1x10
12pfu駱駝和羊駝免疫文庫,噬菌體與結合在磁珠上生物素化的人NKp46蛋白(8µg/mL)室溫孵育1h,0.05%PBST洗去未結合噬菌體後,用100mM三乙基胺將與NKp46特異性結合的噬菌體洗脫下來,梯度稀釋後侵染對數期生長的大腸桿菌SS320,在氨苄平板上37℃過夜培養;挑取單克隆進行IPTG誘導表達,上清用於ELISA檢測。ELISA板上分別包被2µg/mL人NKp46或食蟹猴NKp46抗原4℃過夜,0.05%PBST清洗3次後用5%脫脂牛奶室溫封閉1h,0.05%PBST清洗3次後每孔加入誘導的上清30μL,陰性對照孔加入培養基,室溫孵育1h,最後用anti-Myc HRP檢測(IPTG誘導表達出的VHH帶有his和c-Myc標籤);將ELISA測試得到的結合人和食蟹猴NKp46的OD450值大於1.0,且與結合培養基陰性對照的ELISA OD450比值均大於3的克隆進行測序,獲得本揭露的30個重鏈抗體可變區的氨基酸序列,結果如表2所示:
表2 30個重鏈抗體可變區的氨基酸序列
克隆號 | 重鏈可變區(VHH) |
NKp46-PC1 | SEQ ID NO:14 |
NKp46-PC2 | SEQ ID NO:15 |
NKp46-PC3 | SEQ ID NO:16 |
NKp46-PC4 | SEQ ID NO:17 |
NKp46-PC6 | SEQ ID NO:18 |
NKp46-PC7 | SEQ ID NO:19 |
NKp46-PC8 | SEQ ID NO:20 |
NKp46-PC9 | SEQ ID NO:21 |
NKp46-PC11 | SEQ ID NO:22 |
NKp46-PC12 | SEQ ID NO:23 |
NKp46-PC13 | SEQ ID NO:24 |
NKp46-PC16 | SEQ ID NO:25 |
NKp46-PA2 | SEQ ID NO:26 |
NKp46-PA3 | SEQ ID NO:27 |
NKp46-PA11 | SEQ ID NO:28 |
NKp46-PA15 | SEQ ID NO:29 |
NKp46-PA19 | SEQ ID NO:30 |
NKp46-PA22 | SEQ ID NO:31 |
NKp46-PA24 | SEQ ID NO:32 |
NKp46-PA26 | SEQ ID NO:33 |
NKp46-PA27 | SEQ ID NO:34 |
NKp46-PA28 | SEQ ID NO:35 |
NKp46-PA29 | SEQ ID NO:36 |
NKp46-PA31 | SEQ ID NO:37 |
NKp46-PA34 | SEQ ID NO:38 |
NKp46-PA36 | SEQ ID NO:39 |
NKp46-PA40 | SEQ ID NO:40 |
NKp46-PA45 | SEQ ID NO:41 |
NKp46-PA63 | SEQ ID NO:42 |
NKp46-PA69 | SEQ ID NO:43 |
在上述氨基酸序列的基礎上,利用Kabat編號規則劃分抗體可變區的CDR和FR,每個抗體的3個CDR序列組成如下表3所示。表3中括弧內數字表示序號,例如(44)即代表SEQ ID NO:44。
表3 30個重鏈抗體的CDR序列
克隆號 | HCDR1 | HCDR2 | HCDR3 |
NKp46-PC1 | TDCMG (44) | TIYTSDGRTDYANSVKG (45) | DPQYGGVCPSGGWNY (46) |
NKp46-PC2 | NYNMF (47) | VINRGGDTADYAASVKG (48) | DPLGTT (49) |
NKp46-PC3 | TMG (50) | CIYTGPTTTFTDYADSVKG (51) | NLAYPLTIIPDTR (52) |
NKp46-PC4 | IEYMGWG (53) | YINTGGGTSVYDDSVKG (54) | GSFFGIWYKVPATQYFHY (55) |
NKp46-PC6 | HYCMG (56) | LINTGGPTTFYADFVEG (57) | GPPSSDSGSGCYVPEYMYNY (58) |
NKp46-PC7 | TDCMG (59) | TIYTSDGRTAYADSVKG (60) | DLQYGGSCPSGGWKY (61) |
NKp46-PC8 | TGCMA (62) | IINISGTTRYTDSVKG (63) | TQNPRTVGRGYCTGDYFQVGGGGYSF (64) |
NKp46-PC9 | RYCMA (65) | CLDRDGSTTYADSVKG (66) | AQPGDCWGRRYGFNT (67) |
NKp46-PC11 | SFSMA (68) | CIQAESGSTNVAPSVKG (69) | FKRNVGGCELRPEHWRF (70) |
NKp46-PC12 | SCGMD (71) | RIRPDGRTDYVESVKG (72) | WGLCTAKFR (73) |
NKp46-PC13 | IYYMG (74) | VMHTGGGSTYYTDSVKG (75) | SKYLLAFGGVEWILRPAGGWDY (76) |
NKp46-PC16 | IVSMS (77) | WINGDSSNTSYADSVKG (78) | QNSHYDIRFGY (79) |
NKp46-PA2 | SYAMG (80) | AISRISGDTYSPDSVKG (81) | SATPSATNIYTNQYAYGD (82) |
NKp46-PA3 | TIH (83) | RIWWIERTTFYAASVKG (84) | DARYTGSRRWESDY (85) |
NKp46-PA11 | WYRMG (86) | RISGSPGILYYAGSVKG (87) | DRTGATWDY (88) |
NKp46-PA15 | TYAMG (89) | ASSRDGTTTYYADSVKG (90) | SRPLSTTQVGIASAWYEY (91) |
NKp46-PA19 | TYAMG (92) | AISRNGGTTYYADSVKG (93) | SRPLSNTQVGVASAWYEF (94) |
NKp46-PA22 | TLH (95) | RIWWIGGATFYADSVKG (96) | DARYTSNRRWESDY (97) |
NKp46-PA24 | IYGMG (98) | AINWSSGHTYYADSVKG (99) | DSIYGLSFTVKDYDY (100) |
NKp46-PA26 | TIH (101) | RIWWIGGATFYADSVKG (102) | DARYTSHGYYESDY (103) |
NKp46-PA27 | WYRMG (104) | RISGDTNIKYYAGSVKG (105) | DRTGATWDY (106) |
NKp46-PA28 | TYAMG (107) | AISRNADTTYYADSVKG (108) | DRYSSNTQVGVARTYYDY (109) |
NKp46-PA29 | IYGMG (110) | AINWNSGHTYYADSVKG (111) | DSIIGLSFTVKDYDY (112) |
NKp46-PA31 | RLPMG (113) | AISWSSSTTYYADSVKG (114) | VGGSLDYSATVVYTAARAYAD (115) |
NKp46-PA34 | FYRMG (116) | RISSSAGLIYYVDSVKG (117) | DRHGTRWDY (118) |
NKp46-PA36 | RYAMG (119) | AISSSGDPTYYADSVKG (120) | GLTARDTTVVVHPNGYSY (121) |
NKp46-PA40 | RYSMG (122) | AISSSGDVTHYADSAKG (123) | SLTARATTVTVHPNGYNY (124) |
NKp46-PA45 | RLPMA (125) | AISWSGGSTYYADSMKG (126) | VGDSAPYSATIVYTDARAYAY (127) |
NKp46-PA63 | SYAMG (128) | AINRSGDFPYYADSVKG (129) | APRAPATQVVISAFGYEY (130) |
NKp46-PA69 | LYAMG (131) | GISRTGDTTYSPDSVKG (132) | SATYSATNIYTHQRAYGD (133) |
實施例
5
抗
NKp46
嵌合抗體的構建及其在真核細胞中的暫態轉染表達
將測序完成的本揭露的單抗可變區與氨基酸序列如SEQ ID NO:134所示的人IgG1恒定區拼接後生成的目的基因片段克隆到pTT5表達載體(Nova lifetech)中,製備轉染級別的表達質粒。
在無血清培養基中培養Expi293F
TM細胞(Thermo Fisher Scientific),將細胞接種在搖瓶(Corning公司)中,並在37°C,8% CO
2的環境中置於搖床上培養。調整細胞密度,將含有目的基因片段的pTT5重組表達載體和PEI轉染試劑按照合適的比例混合,並添加進細胞培養搖瓶中,細胞培養6天後收集表達上清,高速離心去除細胞碎片,用Protein A柱進行親和純化。用PBS沖洗柱子,至A280讀數降至基線。用pH3.0-pH3.5的酸性洗脫液洗脫目的蛋白,用1M Tris-HCl,pH8.0-9.0中和。洗脫樣品適當濃縮後,換液到PBS分裝備用。對最終純化的嵌合抗體進行SDS-PAGE及HPLC純度分析和A280濃度測定。
實施例
6
抗
NKp46
嵌合抗體與表達
NKp46
細胞的結合
培養實施例2中所製備得到的人NKp46-CHOK1和食蟹猴NKp46-CHOK1穩定細胞株,用0.25%胰酶(含EDTA)消化細胞約5分鐘,加入完全培養基終止反應。1500 rpm離心5分鐘棄上清,使用含有1%BSA的PBS重懸後計數。將細胞密度調整到1E6/mL,以100μL/孔,接種到corning-3799號96孔培養板中培養,在37℃,8% CO
2的環境中培養過夜,之後將96孔培養板以1500 rpm離心5分鐘棄上清,4℃放置備用。
選取上述實施例中獲得的24個抗NKp46嵌合抗體,用含有1%BSA的PBS分別配置抗NKp46嵌合抗體溶液,起始濃度為100nM,10倍稀釋,獲得7個梯度,分別為:10
-4nM、10
-3nM、10
-2nM、10
-1nM、10
0nM、10
1nM和10
2nM。
用配置好的抗體重懸細胞培養板,100μL/孔。將重懸好的細胞培養板在4℃冰箱孵育1小時。1500 rpm離心5分鐘,棄上清,160μL含1%BSA的PBS洗滌一遍,棄上清備用。用含1%BSA的PBS配置二抗(goat anti human IgG Fc PE),1:200稀釋。用配置好的二抗重懸細胞,100μL/孔,4℃冰箱孵育0.5小時。1500 rpm離心5分鐘,棄上清,160μL含1%BSA的PBS洗滌一遍,棄上清,100μL含1%BSA的PBS重懸細胞,300目紗布過濾細胞,然後在流式細胞儀上分析抗體與細胞結合的平均螢光強度。從流式細胞儀匯出FCS檔,用Flowjo軟體分析PE通道平均螢光強度(以下簡稱MFI),將分析得出的平均螢光強度導入Graphpad分析抗體與細胞的半數結合濃度(以下簡稱EC
50)和最高平均螢光強度(Top MFI),結果如表4及附圖3-10所示。抗NKp46嵌合抗體均與過表達人及食蟹猴NKp46細胞有較好的結合。
表4A 抗NKp46嵌合抗體與表達NKp46細胞的結合
克隆號 | 人NKp46-CHOK1 | 食蟹猴NKp46-CHOK1 | ||
EC 50(nM) | 最高平均螢光強度 (Top MFI) | EC 50(nM) | 最高平均螢光強度 (Top MFI) | |
Anti-HEL human IgG1 LALA | / | 223 | / | 118 |
NKp46-PA3 | 0.149 | 9307 | 0.076 | 5445 |
NKp46-PA11 | 0.162 | 7602 | 0.104 | 4178 |
NKp46-PA19 | 0.09 | 7480 | 1.443 | 1788 |
NKp46-PA22 | 0.365 | 7846 | 0.241 | 4413 |
NKp46-PA24 | 0.495 | 7856 | 0.49 | 4190 |
NKp46-PA26 | 0.396 | 8088 | 0.289 | 4747 |
NKp46-PA27 | 0.155 | 7230 | 0.099 | 3935 |
NKp46-PA29 | 0.2 | 7430 | 0.164 | 4018 |
NKp46-PA31 | 0.535 | 10700 | 4.429 | 5140 |
表4B 抗NKp46嵌合抗體與表達NKp46細胞的結合
克隆號 | 人NKp46-CHOK1 | 食蟹猴NKp46-CHOK1 | ||
EC 50(nM) | 最高平均螢光強度 (Top MFI) | EC 50(nM) | 最高平均螢光強度 (Top MFI) | |
Anti-HEL human IgG1 LALA | / | 98 | / | 86 |
NKp46-PC1 | 7.052 | 310 | 9.813 | 180 |
NKp46-PC2 | 18.82 | 3727 | 77.27 | 371 |
NKp46-PC6 | 0.196 | 3828 | 1.06 | 2682 |
NKp46-PC7 | 6.539 | 262 | 8.421 | 155 |
NKp46-PC11 | 0.416 | 4196 | 0.549 | 3646 |
NKp46-PC12 | 0.138 | 3896 | 0.132 | 3669 |
NKp46-PC13 | 0.911 | 4123 | 1.541 | 2808 |
NKp46-PA2 | 0.075 | 3927 | 0.241 | 3414 |
NKp46-PA15 | 0.102 | 3912 | 0.476 | 2549 |
NKp46-PA28 | 0.093 | 3894 | 3.977 | 225 |
NKp46-PA34 | 0.198 | 4122 | 0.169 | 3631 |
NKp46-PA36 | 0.1 | 3757 | 0.483 | 2574 |
NKp46-PA40 | 0.084 | 3516 | 26.83 | 453 |
NKp46-PA45 | 0.237 | 3464 | 3.014 | 3105 |
NKp46-PA69 | 0.096 | 3513 | 5.774 | 1502 |
實施例
7
抗
NKp46
嵌合抗體的體外
NK
細胞啟動實驗
取人新鮮外周血細胞(PBMC),使用EasySep™ Human NK Cell Isolation Kit(StemCell)分離NK細胞並計數。使用α-MEM培養基培養細胞,添加15%熱滅活FBS,0.2mM肌醇,0.1mM β-巰基乙醇,0.02mM葉酸,200U/mL IL-2。將NK細胞密度調整到1E6/mL,在37℃ 5% CO
2培養箱中培養6-8天。用PBS稀釋抗體,最高濃度為20nM,3倍稀釋,獲得7個梯度濃度,分別為20nM、6.67nM、2.23nM、0.74nM、0.247nM、0.083nM和0.027nM。將稀釋好的抗體包被在corning-3599號96孔培養板中,100μL/孔,4℃包被過夜。使用150μL/孔PBS將96孔板洗滌兩次。使用完全培養基將啟動後的NK細胞密度調整到1E6/mL,然後鋪到洗滌過的96孔板中,100μL/孔,37℃ 5%CO
2培養箱中培養4小時。將細胞從corning-3599號培養板轉移到corning-3799號培養板,1500rpm離心5分鐘,棄上清,備用。
按照說明書要求分別稀釋CD3-APC(BD®555335),CD56-BV421(BD®562751),CD107a-PE(BD®560948)。將上述獲得的備用細胞重懸,以50μL/孔的濃度添加上述稀釋後的CD3-APC,CD56-BV421,CD107a-PE抗體,4℃孵育0.5小時。1500 rpm離心5分鐘,棄上清,160μL含1%BSA的PBS洗滌一遍,棄上清,100μL含1%BSA的PBS洗滌一遍,300目紗布過濾細胞。然後在流式細胞儀上分析CD107a陽性的細胞在NK中的比例。從流式細胞儀匯出FCS檔,用Flowjo軟體分析CD107a陽性細胞在NK(CD3
-CD56
+)細胞中的比例,並導入Graphpad求出NK活化的半數有效濃度(以下簡稱EC
50)和最高平均螢光強度(Top MFI),結果如表5及附圖11-12所示。抗NKp46嵌合抗體表現出不同的體外NK細胞啟動能力。
表5A 抗NKp46嵌合抗體的體外NK細胞啟動
克隆號 | EC 50(nM) | 最高平均螢光強度 (Top MFI) |
Anti-HEL human IgG1 LALA | / | / |
NKp46-PA11 | 2.20 | 16 |
NKp46-PA24 | 0.31 | 15 |
NKp46-PA27 | 1.93 | 20 |
NKp46-PA31 | 0.08 | 23 |
表5B 抗NKp46嵌合抗體的體外NK細胞啟動
克隆號 | EC 50(nM) | 最高平均螢光強度 (Top MFI) |
Anti-HEL human IgG1 LALA | / | / |
NKp46-PC6 | 0.51 | 30 |
NKp46-PC11 | 0.54 | 26 |
NKp46-PC12 | 0.65 | 30 |
NKp46-PA2 | 0.33 | 26 |
NKp46-PA15 | 0.08 | 22 |
NKp46-PA34 | 1.50 | 20 |
NKp46-PA36 | 0.11 | 20 |
NKp46-PA45 | 0.14 | 27 |
NKp46-PA69 | 0.40 | 31 |
實施例
8
抗
NKp46
抗體的人源化設計
選擇上述編號為NKp46-PC11,NKp46-PA27,NKp46-PA31和NKp46-PA45的抗NKp46嵌合抗體進行人源化設計。
實施例
8.1 NKp46-PC11
的人源化
NKp46-PC11人源化框架選擇
通過序列比對選擇與克隆號NKp46-PC11同源性較高的胚系基因序列作為VHH移植框架範本:IGHV3-23*04(序列一致性64.3%)和IGHJ4_01(序列一致性73.3%)。將NKp46-PC11 CDR區嫁接至選定的人抗體可變區框架後,得到人源化抗體hPC11,人源化可變區hPC11 VHH-CDR graft序列如SEQ ID NO:135所示:
EVQLVESGGGLVQPGGSLRLSCAAS PYSANSFSMA WVRQAPGKGLEWVS CIQAESGSTNVAPSVKG RFTISRDNSKNTLYLQMNSLRAEDTAVYYC AAFKRNVGGCELRPEHWRF WGQGTLVTVSS(SEQ ID NO:135),順序為FR1-CDR1-FR2-CDR2-FR3-CDR3-FR4,序列中斜體為FR序列,底線為CDR序列,graft代表嵌合抗體的CDR植入人種系FR區後獲得的人源化可變區VHH序列。
對hPC11進行回復突變,獲得H1-PC11(序列如SEQ ID NO:136所示)、H2-PC11(序列如SEQ ID NO:137所示)、H3-PC11(序列如SEQ ID NO:138所示)、H4-PC11(序列如SEQ ID NO:139所示)和H5-PC11(序列如SEQ ID NO:140所示),5條人源化抗體。
實施例
8.2 NKp46-PA27
的人源化
NKp46-PA27人源化框架選擇
通過序列比對選擇與克隆號NKp46-PA27同源性較高的胚系基因序列作為VHH移植框架範本:IGHV3-30*15(序列一致性74.5%)和IGHJ4_01(序列一致性80%)。將NKp46-PA27 CDR區嫁接至選定的人抗體可變區框架後,得到人源化抗體hPA27,人源化可變區hPA27 VHH-CDR graft序列SEQ ID NO:141所示:
QVQLVESGGGVVQPGRSLRLSCAAS GRTESWYRMG WVRQAPGKGLEWVA RISGDTNIKYYAGSVKG RFTISRDNSKNTLYLQMSSLRAEDTAVYYC AADRTGATWDY WGQGTLVTVSS(SEQ ID NO:141),順序為FR1-CDR1-FR2-CDR2-FR3-CDR3-FR4,序列中斜體為FR序列,底線為CDR序列,graft代表嵌合抗體的CDR 植入人種系FR 區後獲得的人源化可變區VHH序列。
對hPA27進行回復突變,獲得H1-PA27(序列如SEQ ID NO:141所示,原grafted序列)、H2-PA27(序列如SEQ ID NO:142所示)、H3-PA27(序列如SEQ ID NO:143所示)、H4-PA27(序列如SEQ ID NO:144所示),4條人源化抗體。
實施例
8.3 NKp46-PA31
的人源化
NKp46-PA31人源化框架選擇
通過序列比對選擇與克隆號NKp46-PA31同源性較高的胚系基因序列作為VHH移植框架範本:IGHV3-23*04(序列一致性74.5%)和IGHJ4_01(序列一致性73.3%)。將NKp46-PA31 CDR區嫁接至選定的人抗體可變區框架後,得到人源化抗體hPA31,人源化可變區hPA31 VHH-CDR graft序列如SEQ ID NO:145所示:
EVQLVESGGGLVQPGGSLRLSCAAS GRTFSRLPMG WVRQAPGKGLEWVS AISWSSSTTYYADSVKG RFTISRDNSKNTLYLQMNSLRAEDTAVYYC AAVGGSLDYSATVVYTAARAYAD WGQGTLVTVSS(SEQ ID NO:145),順序為FR1-CDR1-FR2-CDR2-FR3-CDR3-FR4,序列中斜體為FR序列,底線為CDR序列,graft代表嵌合抗體的CDR 植入人種系FR 區後獲得的人源化可變區VHH序列。
對hPA27進行回復突變,獲得H1-PA31(序列如SEQ ID NO:145所示,原graft序列)、H2-PA31(序列如SEQ ID NO:146所示)、H3-PA31(序列如SEQ ID NO:147所示)、H4-PA31(序列如SEQ ID NO:148所示),4條人源化抗體。
實施例
8.4 NKp46-PA45
的人源化
NKp46-PA45人源化框架選擇
通過序列比對選擇與克隆號NKp46-PA45同源性較高的胚系基因序列作為VHH移植框架範本:IGHV3-23*04(序列一致性79.6%)和IGHJ4_01(序列一致性73.3%)。將NKp46-PA45 CDR區嫁接至選定的人抗體可變區框架後,得到人源化抗體hPA45,人源化可變區hPA45 VHH-CDR graft序列SEQ ID NO:149所示:
EVQLVESGGGLVQPGGSLRLSCAAS GRTFSRLPMA WVRQAPGKGLEWVS AISWSGGSTYYADSMKG RFTISRDNSKNTLYLQMNSLRAEDTAVYYC AAVGDSAPYSATIVYTDARAYAY WGQGTLVTVSS(SEQ ID NO:149),順序為FR1-CDR1-FR2-CDR2-FR3-CDR3-FR4,序列中斜體為FR序列,底線為CDR序列,graft代表嵌合抗體的CDR植入人種系FR區後獲得的人源化可變區VHH序列。
對hPA45進行回復突變,獲得H1-PA45(序列如SEQ ID NO:149所示,原graft序列)、H2-PA45(序列如SEQ ID NO:150所示)、H3-PA45(序列如SEQ ID NO:151所示)、H4- PA45(序列如SEQ ID NO:152所示),4條人源化抗體。
實施例
9
特異性結合
NKp46
的人源化抗體的製備
通過本領域技術人員已知的標準方法,將人源化抗體的可變區與人IgG1恒定區拼接後生成的目的基因片段亞克隆到pTT5表達載體(Nova lifetech)中,採用ExpiFectamine
TM293轉染試劑暫態轉染對數生長期的Expi293F
TM細胞,收集培養上清,並進行親和純化,對最終純化的人源化抗體進行SDS-PAGE及HPLC純度分析和A280濃度測定。
實施例
10
特異性結合
NKp46
人源化抗體的體外細胞結合驗證
培養實施例2得到的人NKp46-CHOK1和食蟹猴NKp46-CHOK1穩定細胞株,用0.25%胰酶EDTA消化細胞約5分鐘,完全培養基終止。1500 rpm離心5分鐘棄上清,用含有1%BSA的PBS重懸後計數。將細胞密度調整到1E6/mL,鋪到corning-3799號96孔培養板中,100μL/孔。1500 rpm離心5分鐘棄上清,4℃放置備用。用含有1%BSA的PBS配置抗體,起始濃度為100nM,10倍稀釋,獲得7個梯度,分別為:10
-4nM、10
-3nM、10
-2nM、10
-1nM、10
0nM、10
1nM和10
2nM。配置好的抗體重懸細胞,100μL/孔。將重懸好的細胞培養板在4℃冰箱孵育1小時。1500 rpm離心5分鐘,棄上清,160μL含有1%BSA的PBS洗滌一遍,棄上清備用。
用含有1%BSA的PBS配置二抗(goat anti human IgG Fc PE),1:200稀釋。用配置好的二抗重懸細胞,100μL/孔,4℃冰箱孵育0.5小時。1500 rpm離心5分鐘,棄上清,160μL含有1%BSA的PBS洗滌一遍,棄上清,100μL含有1%BSA的PBS重懸細胞,300目紗布過濾細胞。然後在流式細胞儀上分析抗體與細胞結合的平均螢光強度。從流式細胞儀匯出FCS檔,用Flowjo軟體分析PE通道平均螢光強度(以下簡稱MFI),將分析得出的平均螢光強度導入Graphpad分析抗體與細胞的半數結合濃度(以下簡稱EC
50)和最高平均螢光強度(Top MFI),結果如表6及附圖13-20所示。抗NKp46人源化抗體和對應嵌合抗體相比,在過表達人及食蟹猴NKp46細胞上的結合能力相當。
表6 抗NKp46人源化抗體與表達NKp46細胞的結合
克隆號 | 人NKp46-CHOK1 | 食蟹猴NKp46-CHOK1 | ||
EC 50(nM) | 最高平均螢光強度 (Top MFI) | EC 50(nM) | 最高平均螢光強度 (Top MFI) | |
NKp46-PC11 | 0.318 | 7887 | 0.261 | 3587 |
H1-PC11 | 0.389 | 6710 | 0.345 | 3255 |
H2-PC11 | 0.363 | 6936 | 0.301 | 3535 |
H3-PC11 | 0.328 | 6833 | 0.297 | 3285 |
H4-PC11 | 0.305 | 7240 | 0.274 | 3617 |
H5-PC11 | 0.302 | 7370 | 0.270 | 3656 |
NKp46-PA27 | 0.170 | 7094 | 0.077 | 3761 |
H1-PA27 | 0.253 | 5995 | 0.338 | 2538 |
H2-PA27 | 0.153 | 6938 | 0.069 | 3797 |
H3-PA27 | 0.153 | 6818 | 0.072 | 4055 |
H4-PA27 | 0.145 | 6646 | 0.074 | 3879 |
NKp46-PA31 | 0.932 | 9082 | 3.708 | 4732 |
H2-PA31 | 0.203 | 5938 | 2.107 | 3269 |
H3-PA31 | 0.148 | 5979 | 1.157 | 3214 |
H4-PA31 | 0.162 | 5954 | 1.301 | 3337 |
NKp46-PA45 | 0.226 | 5517 | 2.064 | 3287 |
H1-PA45 | 0.543 | 5093 | 11.11 | 3117 |
H2-PA45 | 0.274 | 5613 | 2.762 | 3591 |
H3-PA45 | 0.188 | 5720 | 1.516 | 3328 |
H4-PA45 | 0.205 | 5762 | 1.533 | 3395 |
實施例
11
抗
NKp46
人源化抗體的體外
NK
細胞啟動實驗
取人新鮮外周血細胞(PBMC),使用EasySep
TMHuman NK Cell Isolation Kit分離NK細胞並計數。使用α-MEM培養基培養細胞,添加15%熱滅活FBS,0.2mM肌醇,0.1mM β-巰基乙醇,0.02mM葉酸,200U/mL IL-2。將NK細胞密度調整到1E6/mL,在37℃ 5%CO
2培養箱中培養6-8天。用PBS稀釋抗體,最高濃度為20nM,獲得7個梯度濃度,分別為20nM、6.67nM、2.23nM、0.74nM、0.247nM、0.083nM和0.027nM。將稀釋好的抗體包被在corning-3599號96孔培養板中,100μL/孔,4℃包被過夜。使用150μL/孔PBS將96孔板洗滌兩次。使用完全培養基將啟動後的NK細胞密度調整到1E6/mL,然後鋪到洗滌過的96孔板中,100μL/孔,37℃ 5%CO
2培養箱中培養4小時。將細胞從corning-3599培養板轉移到corning-3799培養板,1500rpm離心5分鐘,棄上清,備用。
按照說明書稀釋抗體(CD3-APC,CD56-BV421,CD107a-PE),重懸細胞,50μL/孔,4℃孵育0.5小時。1500rpm離心5分鐘,棄上清,160μL含有1%BSA的PBS洗滌一遍,棄上清,100μL的含有1%BSA的PBS懸細胞,300目紗布過濾細胞。然後在流式細胞儀上分析CD107a陽性的細胞在NK中的比例。從流式細胞儀匯出FCS檔,用Flowjo軟體分析CD107a陽性細胞在NK(CD3
-CD56
+)細胞中的比例,並導入Graphpad求出NK活化的半數有效濃度(以下簡稱EC
50)和最高平均螢光強度(Top MFI),結果如表7及附圖21-24所示。抗NKp46人源化抗體和對應嵌合抗體相比,體外NK細胞的啟動能力保持或略微減弱。
表7 抗NKp46人源化抗體的體外NK細胞啟動
克隆號 | EC 50(nM) | 最高平均螢光強度 (Top MFI) |
NKp46-PC11 | 0.97 | 24.4 |
H1-PC11 | 0.85 | 21.0 |
H2-PC11 | 0.87 | 18.8 |
H3-PC11 | 1.21 | 19.6 |
H4-PC11 | 1.84 | 19.3 |
H5-PC11 | 0.95 | 23.6 |
NKp46-PA27 | 15.92 | 30.9 |
H1-PA27 | >20 | 6.3 |
H2-PA27 | >20 | 14.1 |
H3-PA27 | 7.39 | 14.4 |
H4-PA27 | 10.73 | 18.1 |
NKp46-PA31 | 0.62 | 34.4 |
H2-PA31 | 0.63 | 35.3 |
H3-PA31 | 0.75 | 31.6 |
H4-PA31 | 0.38 | 34.1 |
NKp46-PA45 | 0.63 | 38.1 |
H1-PA45 | 7.39 | 30.8 |
H2-PA45 | 0.75 | 39.1 |
H3-PA45 | 0.58 | 34.0 |
H4-PA45 | 0.40 | 37.6 |
實施例
12
特異性結合
NKp46
人源化抗體的
Biacore
親和力實驗
使用Biacore 8K儀器分析特異性結合NKp46人源化抗體與人NKp46(愷佧生物,NKP-HM146)和食蟹猴NKp46(愷佧生物,NKP-CM146)的親和力和動力學性質。將Biacore儀器CM5晶片先用乙基-二甲氨基丙基-碳二亞胺EDC和羥基丁二醯亞胺NHS活化,然後固定抗人Fc的鼠單抗,再用乙醇胺封閉。
為測定與人NKp46的親和力與動力學性質,NKp46人源化抗體用HBS-EP+緩衝液(10 mM HEPES,pH 7.4,150 mM NaCl,3 mM EDTA,0.05% P20)稀釋至0.8μg/mL,以10μL/min的流速捕獲60s。人NKp46兩倍逐級稀釋至系列濃度(400nM-3.125nM),以50μL/min的流速結合90s,解離500s。
為測定與食蟹猴NKp46的親和力與動力學性質,NKp46人源化抗體用HBS-EP+緩衝液(10 mM HEPES,pH 7.4,150 mM NaCl,3 mM EDTA,0.05% P20)稀釋至0.8μg/mL,以10μL/min的流速捕獲60s。食蟹猴NKp46兩倍逐級稀釋至系列濃度(400nM-3.125nM),以50μL/min的流速結合90s,解離500s。
每一輪實驗結束後,使用3M MgCl
2溶液以30μL/min的流速沖洗30s,將捕獲的抗體連同抗原一起去除,完成晶片的再生。原始資料使用Biacore Insight Evaluation Software(版本3.0.12.15655)軟體進行分析,以(1:1)Langmuir模型進行擬合,結果如表8所示。抗NKp46人源化抗體和對應嵌合抗體相比,與人NKp46抗原蛋白的親和力基本保持。
表8A抗NKp46人源化抗體與人NKp46抗原蛋白的親和力測定結果
克隆號 | ka (1/Ms) | kd(1/s) | KD(M) | Rmax (RU) |
NKp46-PC11 | 7.02E+04 | 3.40E-04 | 4.84E-09 | 72.4 |
H1-PC11 | 5.08E+04 | 3.07E-04 | 6.05E-09 | 93.9 |
H2-PC11 | 6.13E+04 | 1.26E-04 | 2.05E-09 | 55.1 |
H3-PC11 | 6.78E+04 | 7.75E-05 | 1.14E-09 | 50 |
NKp46-PA27 | 1.12E+05 | 3.62E-03 | 3.25E-08 | 94.7 |
H2-PA27 | 9.77E+04 | 2.16E-03 | 2.21E-08 | 119.3 |
H4-PA27 | 1.12E+05 | 2.66E-03 | 2.37E-08 | 117.1 |
NKp46-PA31 | 1.68E+05 | 1.00E-03 | 5.97E-09 | 77.3 |
H2-PA31 | 8.78E+04 | 9.59E-04 | 1.09E-08 | 45.4 |
H4-PA31 | 1.75E+05 | 1.03E-03 | 5.89E-09 | 46.6 |
NKp46-PA45 | 8.59E+04 | 1.87E-03 | 2.18E-08 | 48.2 |
H2-PA45 | 6.38E+04 | 1.54E-03 | 2.41E-08 | 59.7 |
H4-PA45 | 9.30E+04 | 2.04E-03 | 2.19E-08 | 68.2 |
表8B抗NKp46人源化抗體與猴NKp46抗原蛋白的親和力測定結果
克隆號 | ka (1/Ms) | kd(1/s) | KD(M) | Rmax (RU) |
H1-PC11 | 5.13E+04 | 5.89E-03 | 1.15E-07 | 102.1 |
H2-PA27 | 2.52E+05 | 5.90E-03 | 2.34E-08 | 171.7 |
H2-PA31 | 7.75E+04 | 5.96E-04 | 7.69E-09 | 44.8 |
H2-PA45 | 7.67E+04 | 5.63E-04 | 7.34E-09 | 39.5 |
實施例
13
抗
NKp46
人源化抗體的物理穩定性測試
利用NanoDSF(差示螢光掃描技術)檢測不同抗體在pH7.4 PBS緩衝液中的熱穩定性。樣品濃度在1mg/mL左右,利用Prometheus NT.Plex儀器進行檢測。檢測前,將各個樣品10000g離心10分鐘。樣品板每個孔加入40μL樣品(儀器上樣量為10μL,每個樣品均有一個複孔)。掃描溫度從30℃開始到95℃結束,掃描速率0.5℃/min。實驗結果如表9所示。
表9 抗NKp46人源化抗體的NanoDSF檢測結果
克隆號 | Tm Onset | Tm1 | Tm2 | Tm3 | Tagg |
NKp46-PC11 | 62.6°C | 68.5°C | 76.9°C | / | 76.5°C |
H1-PC11 | 61.2°C | 69.0°C | 79.4°C | / | 77.3°C |
H2-PC11 | 61.1°C | 68.4°C | 77.2°C | / | 76.4°C |
H3-PC11 | 62.5°C | 67.6°C | 75.6°C | / | 76.8°C |
H4-PC11 | 62.0°C | 65.8°C | 74.8°C | / | 76.0°C |
H5-PC11 | 62.0°C | 67.3°C | 75.8°C | / | 77.0°C |
NKp46-PA27 | 62.4°C | 67.3°C | 73.6°C | 80.3°C | 70.1°C |
H2-PA27 | 58.9°C | 62.5°C | / | / | 62.1°C |
H3-PA27 | 57.6°C | 60.9°C | 79.9°C | / | 60.1°C |
H4-PA27 | 58.9°C | 61.4°C | 80.7°C | / | 61.2°C |
NKp46-PA31 | 62.7°C | 64.2°C | 80.0°C | / | 64.9°C |
H2-PA31 | 60.7°C | 67.9°C | 80.3°C | / | 69.0°C |
H3-PA31 | / | 64.9°C | 80.4°C | / | 65.8°C |
H4-PA31 | 73.9°C | 80.1°C | / | / | 66.3°C |
NKp46-PA45 | 65.3°C | 67.4°C | 80.4°C | / | 67.9°C |
H2-PA45 | 62.1°C | 69.5°C | 76.8°C | 81.3°C | 75.6°C |
H3-PA45 | 63.6°C | 66.3°C | 73.1°C | 81.0°C | 72.1°C |
H4-PA45 | 63.1°C | 67.0°C | 73.9°C | 81.3°C | 72.9°C |
通過SEC-HPLC監測樣品純度考察一定濃度條件下週期性穩定性。示例性的條件比如將樣品濃度控制在10mg/mL,10mM醋酸鹽,9%海藻糖(pH 5.5)緩衝液中和將濃度控制在1mg/mL PBS(PH 7.4)緩衝液中,比較在40℃保存0、7、14天的穩定性情況。利用Waters Xbridge Protein BEH SEC 3.5μm 7.8*300mm柱子檢測,流動相為PBS緩衝液,使用H
3PO
4調整至pH 6.8;流速為0.5 mL/min。實驗結果如表10所示。
表10 抗NKp46人源化抗體的週期穩定性結果(SEC-HPLC)
H1-PC11 | H2-PA27 | H2-PA31 | H2-PA45 | |||||
pH5.5 | pH7.4 | pH5.5 | pH7.4 | pH5.5 | pH7.4 | pH5.5 | pH7.4 | |
0天 | 98.81% | 98.93% | 99.43% | 99.52% | 97.81% | 97.66% | 98.65% | 98.72% |
7天 | 98.69% | 98.90% | 99.35% | 99.47% | 97.78% | 97.63% | 98.23% | 98.62% |
14天 | 98.50% | 98.32% | 99.51% | 98.77% | 97.64% | 97.32% | 98.36% | 98.38% |
變化值 | -0.31% | -0.61% | +0.08% | -0.75% | -0.17% | -0.34% | -0.29% | -0.34% |
通過CE-SDS監測樣品分子完整性,考察一定濃度條件下週期性穩定性。將樣品濃度控制在10mg/mL,10mM醋酸鹽,9%海藻糖(pH 5.5)緩衝液中,在還原和非還原條件下比較在40℃保存0、7、14天的分子完整性情況。取200μg樣本(100μg還原,100μg非還原)加入樣本緩衝液至97μL,還原樣本加入5μL 2-巰基乙醇,非還原樣本加入5μL250mM碘乙醯胺,樣本均在70℃加熱10分鐘。利用PA 800 Plus(Beckman Sciex)檢測,電泳時間40分鐘。實驗結果如表11所示。
表11 抗NKp46人源化抗體的週期穩定性結果(CE-SDS)
H1-PC11 | H2-PA27 | H2-PA31 | H2-PA45 | |||||
非還原 | 還原 | 非還原 | 還原 | 非還原 | 還原 | 非還原 | 還原 | |
0天 | 100% | 99.78% | 99.51% | 99.59% | 100% | 99.42% | 98.80% | 99.64% |
7天 | 98.68% | 99.48% | 99.31% | 99.83% | 98.88% | 99.49% | 98.74% | 99.62% |
14天 | 98.62% | 99.53% | 97.64% | 99.66% | 97.66% | 99.43% | 97.65% | 99.50% |
變化值 | -1.38% | -0.25% | -1.87% | +0.07% | -2.34% | +0.01% | -1.15% | -0.14% |
實施例
14
抗
NKp46
人源化抗體的化學穩定性測試
通過cIEF監測樣品分子的電荷異質性。抗體具有很多翻譯後修飾,包括脫醯氨作用、異構化、末端的改變、糖基化、氧化、斷裂、聚合等。這些修飾可能會引起抗體表面電荷的改變,導致電荷異質性。cIEF是基於抗體所帶電荷,對其進行分離,進而對抗體電荷異質性進行分析。將樣品濃度控制在10mg/mL,10mM醋酸鹽,9%海藻糖(pH 5.5)緩衝液中,比較在40℃保存0、7、14天的電荷異質性情況。取20ug樣本,加入到Separation Mix緩衝液中,利用Maurice.C(ProteinSimple)聚焦7分鐘檢測抗體樣本的電荷分佈。實驗結果如表12所示。
表12 抗NKp46人源化抗體的週期穩定性結果(cIEF)
H1-PC11 | H2-PA27 | H2-PA31 | H2-PA45 | |
酸性峰變化 | + 11.5% | + 11.4% | + 7.7% | + 9.7% |
主峰變化 | - 16.3% | -12.5% | - 20.5% | - 15.3% |
鹼性峰變化 | + 4.7% | + 1% | + 12.8% | + 5.6% |
通過LC-MS技術檢測抗體樣本的翻譯後修飾。脫醯胺修飾是抗體中可能影響後期穩定性的一種常見的化學修飾,尤其是CDR區域的部分氨基酸高度脫醯胺修飾一般選擇儘量避免或者突變降低。示例性的條件比如將待測抗體濃度控制在10mg/mL,10mM醋酸鹽,9%海藻糖(pH 5.5)緩衝液中和將濃度控制在1mg/mL PBS(pH 7.4)緩衝液中,40℃恒溫箱存放;分別於0、7、14天取樣,用於酶解實驗。取30μg的抗體樣品,加入6 μL 8M鹽酸胍和3 μL 200 mM DTT,60 ℃水浴20 min,再加入46 μL 20 mM Histidine緩衝液(pH6.0)和2 μL PNGase F酶(Promega,V5111),37℃水浴16h。在Q-Exactive Plus儀器上,進行LC-MS檢測脫醯胺修飾情況。實驗結果如表13所示。
表13 抗NKp46人源化抗體的週期穩定性結果(化學修飾)
H1-PC11 | 化學修飾種類 | pH5.5 | pH7.4 | ||
0天起始值 | 14天變化值 | 0天起始值 | 14天變化值 | ||
M34 Oxidation 第34位甲硫氨酸氧化 | 10.06% | -2.25% | 4.95% | -0.05% | |
N59 Loss N 第59位天冬醯胺脫氮 | 7.91% | 0.59% | 22.34% | -0.94% | |
M83 Oxidation 第83位甲硫氨酸氧化 | 10.94% | -2.64% | 9.91% | -1.01% | |
H2-PA27 | M34 Oxidation 第34位甲硫氨酸氧化 | 8.02% | 1.22% | 10.09% | -0.45% |
H2-PA31 | M34 Oxidation 第34位甲硫氨酸氧化 | 9.72% | -0.02% | 9.29% | 0.77% |
H2-PA45 | 未檢測到明顯化學修飾變化 | / | / | / | / |
備註:N代表檢測到修飾的天冬醯胺,M代表檢測到修飾的甲硫氨酸,數字代表所處輕鏈或者重鏈N端開始計數所處的位置。百分含量代表LC-MS檢測到的脫醯胺修飾占該位元點所處全部肽段信號的比例。
從上述實驗資料可以看出,H1-PC11,H2-PA27,H2-PA31和H2-PA45等4個人源化抗體表現出較高的熱變形溫度,且在40℃高溫條件下儲存14天後,聚體及碎片比例變化較小,發生化學修飾的變化比例較低,這4個人源化抗體的物理穩定性及化學穩定性均較好。
上文所述的本揭露的實施方案僅為示例性的,任何本領域技術人員都可以認識到或者可以確定無數的特定化合物、材料和操作的等價物,而不需要進行超出常規的試驗。所有這些等價物都是在本揭露範圍之內的,並且被申請專利範圍所包含。
無
附圖更進一步說明了本說明書所公開的新特性。參照這些附圖將能更好地理解本說明書中所公開的特性和優點,但應當理解,這些附圖僅用於說明本文所公開原理的具體的實施方案,而非意欲對申請專利範圍加以限制。
圖1顯示了流式細胞術檢測的抗NKp46陽性對照抗體驗證CHOK1細胞上人NKp46的表達情況;圖中實線所示為未轉任何質粒的CHOK1母本細胞上人NKp46的表達情況,圖中虛線所示為CHOK1母本細胞轉染人NKp46質粒後,人NKp46蛋白過表達情況。
圖2顯示了流式細胞術檢測的抗NKp46陽性對照抗體驗證CHOK1細胞上食蟹猴NKp46的表達情況;圖中實線所示為未轉任何質粒的CHOK1母本細胞上食蟹猴NKp46的表達情況,圖中虛線所示為CHOK1母本細胞轉染食蟹猴NKp46質粒後,食蟹猴NKp46蛋白過表達情況。
圖3-6顯示了本揭露的抗NKp46嵌合抗體與表達NKp46細胞(人NKp46-CHOK1)的結合情況。
圖7-10顯示了本揭露的抗NKp46嵌合抗體與表達NKp46細胞(食蟹猴NKp46-CHOK1)的結合情況。
圖11-12顯示了本揭露的抗NKp46嵌合抗體的體外NK細胞啟動結果。
圖13-16顯示了本揭露的抗NKp46人源化抗體與表達NKp46細胞(人NKp46-CHOK1)的結合情況。
圖17-20顯示了本揭露的抗NKp46人源化抗體與表達NKp46細胞(食蟹猴NKp46-CHOK1)的結合情況。
圖21-24顯示了本揭露的抗NKp46人源化抗體的體外NK細胞啟動結果。
序列表 <![CDATA[<110> 上海齊魯製藥研究中心有限公司]]> <![CDATA[<120> 針對NKp46的抗體及其應用]]> <![CDATA[<130> MTTW21497]]> <![CDATA[<150> CN2021102436015]]> <![CDATA[<151> 2021-03-05]]> <![CDATA[<160> 152]]> <![CDATA[<170> SIPOSequenceListing 1.0]]> <![CDATA[<210> 1]]> <![CDATA[<211> 304]]> <![CDATA[<212> PRT]]> <![CDATA[<213> human]]> <![CDATA[<220>]]> <![CDATA[<223> human NKp46 protein]]> <![CDATA[<400> 1]]> Met Ser Ser Thr Leu Pro Ala Leu Leu Cys Val Gly Leu Cys Leu Ser 1 5 10 15 Gln Arg Ile Ser Ala Gln Gln Gln Thr Leu Pro Lys Pro Phe Ile Trp 20 25 30 Ala Glu Pro His Phe Met Val Pro Lys Glu Lys Gln Val Thr Ile Cys 35 40 45 Cys Gln Gly Asn Tyr Gly Ala Val Glu Tyr Gln Leu His Phe Glu Gly 50 55 60 Ser Leu Phe Ala Val Asp Arg Pro Lys Pro Pro Glu Arg Ile Asn Lys 65 70 75 80 Val Lys Phe Tyr Ile Pro Asp Met Asn Ser Arg Met Ala Gly Gln Tyr 85 90 95 Ser Cys Ile Tyr Arg Val Gly Glu Leu Trp Ser Glu Pro Ser Asn Leu 100 105 110 Leu Asp Leu Val Val Thr Glu Met Tyr Asp Thr Pro Thr Leu Ser Val 115 120 125 His Pro Gly Pro Glu Val Ile Ser Gly Glu Lys Val Thr Phe Tyr Cys 130 135 140 Arg Leu Asp Thr Ala Thr Ser Met Phe Leu Leu Leu Lys Glu Gly Arg 145 150 155 160 Ser Ser His Val Gln Arg Gly Tyr Gly Lys Val Gln Ala Glu Phe Pro 165 170 175 Leu Gly Pro Val Thr Thr Ala His Arg Gly Thr Tyr Arg Cys Phe Gly 180 185 190 Ser Tyr Asn Asn His Ala Trp Ser Phe Pro Ser Glu Pro Val Lys Leu 195 200 205 Leu Val Thr Gly Asp Ile Glu Asn Thr Ser Leu Ala Pro Glu Asp Pro 210 215 220 Thr Phe Pro Ala Asp Thr Trp Gly Thr Tyr Leu Leu Thr Thr Glu Thr 225 230 235 240 Gly Leu Gln Lys Asp His Ala Leu Trp Asp His Thr Ala Gln Asn Leu 245 250 255 Leu Arg Met Gly Leu Ala Phe Leu Val Leu Val Ala Leu Val Trp Phe 260 265 270 Leu Val Glu Asp Trp Leu Ser Arg Lys Arg Thr Arg Glu Arg Ala Ser 275 280 285 Arg Ala Ser Thr Trp Glu Gly Arg Arg Arg Leu Asn Thr Gln Thr Leu 290 295 300 <![CDATA[<210> 2]]> <![CDATA[<211> 306]]> <![CDATA[<212> PRT]]> <![CDATA[<213> Macaca fascicularis]]> <![CDATA[<220>]]> <![CDATA[<223> Macaca fascicularis NKp46 protein]]> <![CDATA[<400> 2]]> Met Ser Ser Thr Leu Arg Ala Leu Leu Cys Leu Gly Leu Cys Leu Ser 1 5 10 15 Gln Arg Ile Ser Ala Pro Lys Gln Thr Leu Pro Lys Pro Ile Ile Arg 20 25 30 Ala Glu Ser Thr Tyr Met Val Pro Lys Glu Lys Gln Ala Thr Leu Cys 35 40 45 Cys Gln Gly Ser Tyr Gly Ala Val Glu Tyr Gln Leu His Phe Glu Gly 50 55 60 Ser Leu Phe Ala Val Glu Arg Pro Lys Pro Pro Glu Arg Ile Asn Gly 65 70 75 80 Val Lys Phe His Ile Pro Asp Met Asn Ser Arg Lys Ala Gly Arg Tyr 85 90 95 Ser Cys Ile Tyr Arg Val Gly Glu Leu Trp Ser Glu Arg Ser Asp Leu 100 105 110 Leu Asp Leu Val Val Thr Glu Met Tyr Asp Thr Pro Thr Leu Ser Val 115 120 125 His Pro Gly Pro Glu Val Thr Ser Gly Glu Lys Val Thr Phe Tyr Cys 130 135 140 Arg Leu Asp Thr Ala Thr Ser Met Phe Leu Leu Leu Lys Glu Gly Arg 145 150 155 160 Ser Arg Asp Val Gln Arg Ser Tyr Gly Lys Val Gln Ala Glu Phe Pro 165 170 175 Met Gly Pro Val Thr Thr Ala His Arg Gly Ser Tyr Arg Cys Phe Gly 180 185 190 Ser Tyr Asn Asn Tyr Ala Trp Ser Phe Pro Ser Glu Pro Val Lys Leu 195 200 205 Leu Val Thr Gly Asp Ile Glu Asn Thr Ser Leu Ala Pro Thr Asp Pro 210 215 220 Thr Phe Pro Asp Ser Trp Asp Thr Cys Leu Leu Thr Arg Glu Thr Gly 225 230 235 240 Leu Gln Lys Asp Leu Ala Leu Trp Asp His Thr Ala Gln Asn Leu Leu 245 250 255 Arg Met Gly Leu Ala Phe Leu Val Leu Val Ala Leu Val Cys Leu Leu 260 265 270 Val Glu Asp Trp Leu Ser Arg Lys Arg Thr Arg Glu Gln Ala Ser Arg 275 280 285 Ala Ser Thr Trp Glu Gly Arg Arg Arg Leu Asn Lys His Lys Asp Ser 290 295 300 Glu Glu 305 <![CDATA[<210> 3]]> <![CDATA[<211> 241]]> <![CDATA[<212> PRT]]> <![CDATA[<213> human]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 3]]> His His His His His His His His Gln Gln Gln Thr Leu Pro Lys Pro 1 5 10 15 Phe Ile Trp Ala Glu Pro His Phe Met Val Pro Lys Glu Lys Gln Val 20 25 30 Thr Ile Cys Cys Gln Gly Asn Tyr Gly Ala Val Glu Tyr Gln Leu His 35 40 45 Phe Glu Gly Ser Leu Phe Ala Val Asp Arg Pro Lys Pro Pro Glu Arg 50 55 60 Ile Asn Lys Val Lys Phe Tyr Ile Pro Asp Met Asn Ser Arg Met Ala 65 70 75 80 Gly Gln Tyr Ser Cys Ile Tyr Arg Val Gly Glu Leu Trp Ser Glu Pro 85 90 95 Ser Asn Leu Leu Asp Leu Val Val Thr Glu Met Tyr Asp Thr Pro Thr 100 105 110 Leu Ser Val His Pro Gly Pro Glu Val Ile Ser Gly Glu Lys Val Thr 115 120 125 Phe Tyr Cys Arg Leu Asp Thr Ala Thr Ser Met Phe Leu Leu Leu Lys 130 135 140 Glu Gly Arg Ser Ser His Val Gln Arg Gly Tyr Gly Lys Val Gln Ala 145 150 155 160 Glu Phe Pro Leu Gly Pro Val Thr Thr Ala His Arg Gly Thr Tyr Arg 165 170 175 Cys Phe Gly Ser Tyr Asn Asn His Ala Trp Ser Phe Pro Ser Glu Pro 180 185 190 Val Lys Leu Leu Val Thr Gly Asp Ile Glu Asn Thr Ser Leu Ala Pro 195 200 205 Glu Asp Pro Thr Phe Pro Asp Thr Trp Gly Thr Tyr Leu Leu Thr Thr 210 215 220 Glu Thr Gly Leu Gln Lys Asp His Ala Leu Trp Asp His Thr Ala Gln 225 230 235 240 Asn <![CDATA[<210> 4]]> <![CDATA[<211> 241]]> <![CDATA[<212> PRT]]> <![CDATA[<213> Macaca fascicularis]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 4]]> Pro Lys Gln Thr Leu Pro Lys Pro Ile Ile Arg Ala Glu Ser Thr Tyr 1 5 10 15 Met Val Pro Lys Glu Lys Gln Ala Thr Leu Cys Cys Gln Gly Ser Tyr 20 25 30 Gly Ala Val Glu Tyr Gln Leu His Phe Glu Gly Ser Leu Phe Ala Val 35 40 45 Glu Arg Pro Lys Pro Pro Glu Arg Ile Asn Gly Val Lys Phe His Ile 50 55 60 Pro Asp Met Asn Ser Arg Lys Ala Gly Arg Tyr Ser Cys Ile Tyr Arg 65 70 75 80 Val Gly Glu Leu Trp Ser Glu Arg Ser Asp Leu Leu Asp Leu Val Val 85 90 95 Thr Glu Met Tyr Asp Thr Pro Thr Leu Ser Val His Pro Gly Pro Glu 100 105 110 Val Thr Ser Gly Glu Lys Val Thr Phe Tyr Cys Arg Leu Asp Thr Ala 115 120 125 Thr Ser Met Phe Leu Leu Leu Lys Glu Gly Arg Ser Arg Asp Val Gln 130 135 140 Arg Ser Tyr Gly Lys Val Gln Ala Glu Phe Pro Met Gly Pro Val Thr 145 150 155 160 Thr Ala His Arg Gly Ser Tyr Arg Cys Phe Gly Ser Tyr Asn Asn Tyr 165 170 175 Ala Trp Ser Phe Pro Ser Glu Pro Val Lys Leu Leu Val Thr Gly Asp 180 185 190 Ile Glu Asn Thr Ser Leu Ala Pro Thr Asp Pro Thr Phe Pro Asp Ser 195 200 205 Trp Asp Thr Cys Leu Leu Thr Arg Glu Thr Gly Leu Gln Lys Asp Leu 210 215 220 Ala Leu Trp Asp His Thr Ala Gln Asn His His His His His His His 225 230 235 240 His <![CDATA[<210> 5]]> <![CDATA[<211> 23]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> primer]]> <![CDATA[<400> 5]]> gtcctggctg ctcttctaca agg 23 <![CDATA[<210> 6]]> <![CDATA[<211> 23]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> primer]]> <![CDATA[<400> 6]]> ggtacgtgct gttgaactgt tcc 23 <![CDATA[<210> 7]]> <![CDATA[<211> 53]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> primer]]> <![CDATA[<400> 7]]> actcgcggcc cagccggcca tggccgaggt gcagctggtg gagtctgggg gag 53 <![CDATA[<210> 8]]> <![CDATA[<211> 53]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> primer]]> <![CDATA[<400> 8]]> actcgcggcc cagccggcca tggcccaggt rcagctggtg gagtctgggg gag 53 <![CDATA[<210> 9]]> <![CDATA[<211> 53]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> primer]]> <![CDATA[<400> 9]]> actcgcggcc cagccggcca tggccgatgt gcagctggtg gagtctgggg gag 53 <![CDATA[<210> 10]]> <![CDATA[<211> 46]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> primer]]> <![CDATA[<400> 10]]> ggtgttggcc tcccgggcca ctagtgctkg agacrgtgac ctgggt 46 <![CDATA[<210> 11]]> <![CDATA[<211> 46]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> primer]]> <![CDATA[<400> 11]]> ggtgttggcc tcccgggcca ctagtgctkg agacrgtgac cagggt 46 <![CDATA[<210> 12]]> <![CDATA[<211> 46]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> primer]]> <![CDATA[<400> 12]]> ggtgttggcc tcccgggcca ctagttgakg agacrgtgac ctgggt 46 <![CDATA[<210> 13]]> <![CDATA[<211> 46]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> primer]]> <![CDATA[<400> 13]]> ggtgttggcc tcccgggcca ctagttgakg agacrgtgac cagggt 46 <![CDATA[<210> 14]]> <![CDATA[<211> 124]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 14]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Ser Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Thr Leu Ser Cys Ala Thr Ser Gly Tyr Thr Tyr Arg Thr Asp 20 25 30 Cys Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Gly Leu 35 40 45 Ala Thr Ile Tyr Thr Ser Asp Gly Arg Thr Asp Tyr Ala Asn Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Gln Asp Asn Ala Lys Asn Thr Leu Tyr 65 70 75 80 Leu His Met Asn Asn Leu Lys Pro Glu Asp Thr Ala Ile Tyr Tyr Cys 85 90 95 Ala Ala Asp Pro Gln Tyr Gly Gly Val Cys Pro Ser Gly Gly Trp Asn 100 105 110 Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser 115 120 <![CDATA[<210> 15]]> <![CDATA[<211> 115]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 15]]> Gln Val Gln Leu Val 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 Ala Phe Ser Asn Tyr 20 25 30 Asn Met Phe Trp Val Arg Gln Ala Pro Gly Glu Gly Phe Glu Trp Ile 35 40 45 Ser Val Ile Asn Arg Gly Gly Asp Thr Ala Asp Tyr Ala Ala 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 Asn Ser Leu Lys Thr Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Arg Asp Pro Leu Gly Thr Thr Arg Gly Gln Gly Thr Leu Val Thr 100 105 110 Val Ser Ser 115 <![CDATA[<210> 16]]> <![CDATA[<211> 122]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 16]]> Asp Val Gln Leu Val Glu Ser Gly Gly Gly Ser Val Glu Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Tyr Arg Gln Arg Thr Met 20 25 30 Gly Trp Phe Arg Gln Ala Pro Gly Lys Ala Arg Glu Gly Val Ala Cys 35 40 45 Ile Tyr Thr Gly Pro Thr Thr Thr Phe Thr Asp Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Thr Gln Asp Asn Ala Lys Asn Thr Val Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Met Tyr Tyr Cys 85 90 95 Ala Ala Asn Leu Ala Tyr Pro Leu Thr Ile Ile Pro Asp Thr Arg Trp 100 105 110 Gly Gln Gly Thr Gln Val Thr Val Ser Ser 115 120 <![CDATA[<210> 17]]> <![CDATA[<211> 129]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 17]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Ser Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Thr Val Ser Gly Tyr Thr Gly Thr Ile Glu 20 25 30 Tyr Met Gly Trp Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu 35 40 45 Gly Val Ala Tyr Ile Asn Thr Gly Gly Gly Thr Ser Val Tyr Asp Asp 50 55 60 Ser Val Lys Gly Arg Phe Thr Ile Ser Lys Asp Asp Val Asn Leu Thr 65 70 75 80 Val Tyr Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Ile Tyr 85 90 95 Tyr Cys Ala Thr Gly Ser Phe Phe Gly Ile Trp Tyr Lys Val Pro Ala 100 105 110 Thr Gln Tyr Phe His Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser 115 120 125 Ser <![CDATA[<210> 18]]> <![CDATA[<211> 129]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 18]]> Asp Val Gln Leu Val Glu Ser Gly Gly Gly Ser Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Tyr Arg Ser Arg His Tyr 20 25 30 Cys Met Gly Trp Phe Arg Gln Phe Pro Gly Lys Glu Arg Glu Arg Val 35 40 45 Ala Leu Ile Asn Thr Gly Gly Pro Thr Thr Phe Tyr Ala Asp Phe Val 50 55 60 Glu Gly Arg Phe Thr Ile Ser Leu Asp Asn Ala Lys Asn Thr Leu Ser 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Met Tyr Tyr Cys 85 90 95 Ala Ala Gly Pro Pro Ser Ser Asp Ser Gly Ser Gly Cys Tyr Val Pro 100 105 110 Glu Tyr Met Tyr Asn Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser 115 120 125 Ser <![CDATA[<210> 19]]> <![CDATA[<211> 124]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 19]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Ser Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Tyr Thr Tyr Arg Thr Asp 20 25 30 Cys Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Gly Leu 35 40 45 Ala Thr Ile Tyr Thr Ser Asp Gly Arg Thr Ala Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Gln Asp Asn Ala Lys Asn Thr Leu Tyr 65 70 75 80 Leu Asp Met Asn Thr Leu Lys Pro Glu Asp Thr Ala Met Tyr Tyr Cys 85 90 95 Ala Ala Asp Leu Gln Tyr Gly Gly Ser Cys Pro Ser Gly Gly Trp Lys 100 105 110 Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 20]]> <![CDATA[<211> 135]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 20]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Ser Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Val Ser Arg Gly Ser Met Ala Ser Thr 20 25 30 Gly Cys Met Ala Trp Phe Arg Gln Thr Pro Gly Lys Glu Arg Glu Ala 35 40 45 Val Ala Ile Ile Asn Ile Ser Gly Thr Thr Arg Tyr Thr Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ala Gln Asp Ser Ala Lys Asn Thr Leu Thr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Gly Met Tyr Tyr Cys 85 90 95 Ala Ala Thr Gln Asn Pro Arg Thr Val Gly Arg Gly Tyr Cys Thr Gly 100 105 110 Asp Tyr Phe Gln Val Gly Gly Gly Gly Tyr Ser Phe Trp Gly Gln Gly 115 120 125 Thr Gln Val Thr Val Ser Ser 130 135 <![CDATA[<210> 21]]> <![CDATA[<211> 123]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 21]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Ser Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Tyr Thr Tyr Arg Arg Tyr 20 25 30 Cys Met Ala Trp Phe Arg Gln Gly Pro Gly Lys Glu Arg Glu Gly Val 35 40 45 Ala Cys Leu Asp Arg Asp Gly Ser Thr Thr Tyr Ala Asp Ser Val Lys 50 55 60 Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Asn Asp Thr Leu Tyr Leu 65 70 75 80 Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Leu Tyr Arg Cys Ala 85 90 95 Ala Ala Gln Pro Gly Asp Cys Trp Gly Arg Arg Tyr Gly Phe Asn Thr 100 105 110 Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 22]]> <![CDATA[<211> 126]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 22]]> Asp Val Gln Leu Val Glu Ser Gly Gly Gly Ser Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Pro Ser Pro Tyr Ser Ala Asn Ser Phe 20 25 30 Ser Met Ala Trp Phe Arg Gln Val Pro Gly Lys Glu Arg Glu Gly Ile 35 40 45 Ala Cys Ile Gln Ala Glu Ser Gly Ser Thr Asn Val Ala Pro Ser Val 50 55 60 Lys Gly Arg Phe Ser Ile Ser Gln Asp Asn Ala Lys Asn Thr Leu Tyr 65 70 75 80 Leu Gln Met Asn Asn Leu Lys Pro Glu Asp Thr Ala Met Tyr Tyr Cys 85 90 95 Ala Ala Phe Lys Arg Asn Val Gly Gly Cys Glu Leu Arg Pro Glu His 100 105 110 Trp Arg Phe Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 23]]> <![CDATA[<211> 117]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 23]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Ser Val Gln Thr Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Thr Ala Pro Gly Phe Thr Thr Asp Ser Cys 20 25 30 Gly Met Asp Trp Tyr Arg Gln Ala Ala Gly Lys Gln Arg Glu Trp Val 35 40 45 Ser Arg Ile Arg Pro Asp Gly Arg Thr Asp Tyr Val Glu Ser Val Lys 50 55 60 Gly Arg Phe Thr Ile Ser Glu Asp Lys Ala Lys Tyr Thr Val Tyr Leu 65 70 75 80 Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Met Tyr Ser Cys Thr 85 90 95 Thr Trp Gly Leu Cys Thr Ala Lys Phe Arg Trp Gly Gln Gly Thr Gln 100 105 110 Val Thr Val Ser Ser 115 <![CDATA[<210> 24]]> <![CDATA[<211> 131]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 24]]> Asp Val Gln Leu Val Glu Ser Gly Gly Gly Ser Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Tyr Thr Arg Ser Ile Tyr 20 25 30 Tyr Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Gly Val 35 40 45 Ala Val Met His Thr Gly Gly Gly Ser Thr Tyr Tyr Thr Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Gln Asp Asn Ala Lys Asn Thr Val Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Met Tyr Tyr Cys 85 90 95 Ala Ala Ser Lys Tyr Leu Leu Ala Phe Gly Gly Val Glu Trp Ile Leu 100 105 110 Arg Pro Ala Gly Gly Trp Asp Tyr Trp Ala Gln Gly Thr Gln Val Thr 115 120 125 Val Ser Ser 130 <![CDATA[<210> 25]]> <![CDATA[<211> 120]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 25]]> Asp Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ile Ser Gly Phe Thr Phe Ser Ile Val 20 25 30 Ser Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Pro Glu Arg Val 35 40 45 Ser Trp Ile Asn Gly Asp Ser Ser Asn Thr Ser Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Arg Asn Met Leu Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Ser Glu Asp Thr Ala Arg Tyr Tyr Cys 85 90 95 Thr Thr Gln Asn Ser His Tyr Asp Ile Arg Phe Gly Tyr Trp Gly Gln 100 105 110 Gly Thr Gln Val Thr Val Ser Ser 115 120 <![CDATA[<210> 26]]> <![CDATA[<211> 127]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 26]]> Asp Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Leu Ser Ser Tyr 20 25 30 Ala Met Gly Trp Phe Arg Gln Ala Pro Gly Leu Glu Arg Glu Phe Val 35 40 45 Ala Ala Ile Ser Arg Ile Ser Gly Asp Thr Tyr Ser Pro 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 Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Ser Ala Thr Pro Ser Ala Thr Asn Ile Tyr Thr Asn Gln Tyr 100 105 110 Ala Tyr Gly Asp Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 27]]> <![CDATA[<211> 121]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 27]]> Asp Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Phe Asn Thr Ile 20 25 30 His Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Val Ala Arg 35 40 45 Ile Trp Trp Ile Glu Arg Thr Thr Phe Tyr Ala Ala Ser Val Lys Gly 50 55 60 Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Met Val Tyr Leu Gln 65 70 75 80 Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys Ala Ala 85 90 95 Asp Ala Arg Tyr Thr Gly Ser Arg Arg Trp Glu Ser Asp Tyr Trp Gly 100 105 110 Gln Gly Thr Gln Val Thr Val Ser Ser 115 120 <![CDATA[<210> 28]]> <![CDATA[<211> 118]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 28]]> Asp Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly His Thr Glu Ser Trp Tyr 20 25 30 Arg Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Gly Arg Glu Val Val 35 40 45 Gly Arg Ile Ser Gly Ser Pro Gly Ile Leu Tyr Tyr Ala Gly 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 Thr Asn Leu Lys Pro Glu Asp Thr Ala Arg Tyr Tyr Cys 85 90 95 Ala Ala Asp Arg Thr Gly Ala Thr Trp Asp Tyr Trp Gly Gln Gly Thr 100 105 110 Gln Val Thr Val Ser Ser 115 <![CDATA[<210> 29]]> <![CDATA[<211> 127]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 29]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Asp 1 5 10 15 Ser Leu Arg Val Ser Cys Ala Ala Ser Gly Arg Thr Phe Ser Thr Tyr 20 25 30 Ala Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Val 35 40 45 Ala Ala Ser Ser Arg Asp Gly Thr Thr Thr Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Val Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Ser Arg Pro Leu Ser Thr Thr Gln Val Gly Ile Ala Ser Ala 100 105 110 Trp Tyr Glu Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 30]]> <![CDATA[<211> 127]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 30]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ala Cys Ala Ala Ser Gly Arg Thr Phe Ser Thr Tyr 20 25 30 Ala Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Val 35 40 45 Ala Ala Ile Ser Arg Asn Gly Gly Thr Thr Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Val Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Ser Arg Pro Leu Ser Asn Thr Gln Val Gly Val Ala Ser Ala 100 105 110 Trp Tyr Glu Phe Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 31]]> <![CDATA[<211> 121]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 31]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Thr Ala Ser Gly Arg Thr Phe Glu Thr Leu 20 25 30 His Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Val Ala Arg 35 40 45 Ile Trp Trp Ile Gly Gly Ala Thr Phe Tyr Ala Asp Ser Val Lys Gly 50 55 60 Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Met Val Tyr Leu Gln 65 70 75 80 Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Ile Tyr Tyr Cys Ala Ala 85 90 95 Asp Ala Arg Tyr Thr Ser Asn Arg Arg Trp Glu Ser Asp Tyr Trp Gly 100 105 110 Gln Gly Thr Gln Val Thr Val Ser Ser 115 120 <![CDATA[<210> 32]]> <![CDATA[<211> 124]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 32]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Gln Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Val Ala Ser Gly Arg Thr Tyr Ser Ile Tyr 20 25 30 Gly Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Val Val 35 40 45 Ala Ala Ile Asn Trp Ser Ser Gly His Thr Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Lys Asp Asn Ala Lys Asn Thr His Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Asp Ser Ile Tyr Gly Leu Ser Phe Thr Val Lys Asp Tyr Asp 100 105 110 Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 33]]> <![CDATA[<211> 121]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 33]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Met Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Phe Asn Thr Ile 20 25 30 His Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Val Ala Arg 35 40 45 Ile Trp Trp Ile Gly Gly Ala Thr Phe Tyr Ala Asp Ser Val Lys Gly 50 55 60 Arg Phe Thr Ile Ser Arg Asp Asn Thr Glu Asn Leu Val Tyr Leu Gln 65 70 75 80 Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys Ala Ala 85 90 95 Asp Ala Arg Tyr Thr Ser His Gly Tyr Tyr Glu Ser Asp Tyr Trp Gly 100 105 110 Pro Gly Thr Gln Val Thr Val Ser Ser 115 120 <![CDATA[<210> 34]]> <![CDATA[<211> 118]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 34]]> Asp Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Ala 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Glu Ser Trp Tyr 20 25 30 Arg Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Gly Arg Glu Val Val 35 40 45 Ala Arg Ile Ser Gly Asp Thr Asn Ile Lys Tyr Tyr Ala Gly 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 Thr Asn Leu Lys Pro Glu Asp Thr Ala Arg Tyr Tyr Cys 85 90 95 Ala Ala Asp Arg Thr Gly Ala Thr Trp Asp Tyr Trp Gly Gln Gly Thr 100 105 110 Gln Val Thr Val Ser Ser 115 <![CDATA[<210> 35]]> <![CDATA[<211> 127]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 35]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Asp 1 5 10 15 Ser Leu Arg Leu Ser Cys Val Ala Ser Gly Arg Thr Phe Ser Thr Tyr 20 25 30 Ala Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Val 35 40 45 Ala Ala Ile Ser Arg Asn Ala Asp Thr Thr Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Val Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Asp Arg Tyr Ser Ser Asn Thr Gln Val Gly Val Ala Arg Thr 100 105 110 Tyr Tyr Asp Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 36]]> <![CDATA[<211> 124]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 36]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Trp Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Tyr Ser Ile Tyr 20 25 30 Gly Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Ile Val 35 40 45 Ala Ala Ile Asn Trp Asn Ser Gly His Thr Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr His Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Asp Ser Ile Ile Gly Leu Ser Phe Thr Val Lys Asp Tyr Asp 100 105 110 Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser 115 120 <![CDATA[<210> 37]]> <![CDATA[<211> 130]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 37]]> Asp Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Asp 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Val Ser Gly Arg Thr Phe Ser Arg Leu 20 25 30 Pro Met Gly Trp Phe Arg Gln Gly Pro Gly Lys Asp Arg Glu Phe Val 35 40 45 Ala Ala Ile Ser Trp Ser Ser Ser Thr Thr Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Phe Ile Ser Arg Asp Asn Ala Lys Asn Thr Ala Tyr 65 70 75 80 Leu Gln Met Asn Asn Leu Arg Leu Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Val Gly Gly Ser Leu Asp Tyr Ser Ala Thr Val Val Tyr Thr 100 105 110 Ala Ala Arg Ala Tyr Ala Asp Trp Gly Gln Gly Thr Leu Val Thr Val 115 120 125 Ser Ser 130 <![CDATA[<210> 38]]> <![CDATA[<211> 118]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 38]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Thr Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Ser Thr Ser Ser Phe Tyr 20 25 30 Arg Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Ala Val 35 40 45 Ala Arg Ile Ser Ser Ser Ala Gly Leu Ile Tyr Tyr Val Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Ala Gly Ala Lys Asn Thr Val Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Asp Arg His Gly Thr Arg Trp Asp Tyr Trp Gly Gln Gly Thr 100 105 110 Gln Val Thr Val Ser Ser 115 <![CDATA[<210> 39]]> <![CDATA[<211> 127]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 39]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Ser Phe Ser Arg Tyr 20 25 30 Ala Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Asp Phe Val 35 40 45 Ala Ala Ile Ser Ser Ser Gly Asp Pro Thr Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Val Asn Ala Lys Asn Thr Val Tyr 65 70 75 80 Leu Gln Met Asn Ser Val Asn Pro Gly Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Gly Leu Thr Ala Arg Asp Thr Thr Val Val Val His Pro Asn 100 105 110 Gly Tyr Ser Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 40]]> <![CDATA[<211> 127]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 40]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Phe Ser Arg Tyr 20 25 30 Ser Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Val 35 40 45 Ala Ala Ile Ser Ser Ser Gly Asp Val Thr His Tyr Ala Asp Ser Ala 50 55 60 Lys Gly Arg Phe Ile Ile Ser Arg Asp Asn Ala Lys Asn Thr Val Ser 65 70 75 80 Leu Gln Val Asn Ser Val Asn Leu Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Ser Leu Thr Ala Arg Ala Thr Thr Val Thr Val His Pro Asn 100 105 110 Gly Tyr Asn Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 41]]> <![CDATA[<211> 130]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 41]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Leu Cys Ala Ala Ser Gly Arg Thr Phe Ser Arg Leu 20 25 30 Pro Met Ala Trp Phe Arg Gln Gly Pro Gly Lys Asp Arg Glu Phe Val 35 40 45 Ala Ala Ile Ser Trp Ser Gly Gly Ser Thr Tyr Tyr Ala Asp Ser Met 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Ala Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Arg Leu Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Val Gly Asp Ser Ala Pro Tyr Ser Ala Thr Ile Val Tyr Thr 100 105 110 Asp Ala Arg Ala Tyr Ala Tyr Trp Gly Gln Gly Thr Gln Val Thr Val 115 120 125 Ser Ser 130 <![CDATA[<210> 42]]> <![CDATA[<211> 127]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 42]]> Glu Val Gln Leu Val 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 Arg Thr Ser Thr Ser Tyr 20 25 30 Ala Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Val 35 40 45 Ala Ala Ile Asn Arg Ser Gly Asp Phe Pro Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Phe Arg Asp Asn Ala Lys Asn Thr Val Tyr 65 70 75 80 Leu Gln Met Ser Ser Val Lys Pro Glu Asp Thr Gly Val Tyr Phe Cys 85 90 95 Ala Ala Ala Pro Arg Ala Pro Ala Thr Gln Val Val Ile Ser Ala Phe 100 105 110 Gly Tyr Glu Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 43]]> <![CDATA[<211> 127]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 43]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Leu Ile Gln Ala Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Val Ala Ser Glu Arg Ser Leu Thr Leu Tyr 20 25 30 Ala Met Gly Trp Phe Arg Gln Ala Pro Gly Leu Glu Arg Glu Phe Val 35 40 45 Ala Gly Ile Ser Arg Thr Gly Asp Thr Thr Tyr Ser Pro Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Val Leu Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Pro Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Ser Ala Thr Tyr Ser Ala Thr Asn Ile Tyr Thr His Gln Arg 100 105 110 Ala Tyr Gly Asp Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 44]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 44]]> Thr Asp Cys Met Gly 1 5 <![CDATA[<210> 45]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 45]]> Thr Ile Tyr Thr Ser Asp Gly Arg Thr Asp Tyr Ala Asn Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 46]]> <![CDATA[<211> 15]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 46]]> Asp Pro Gln Tyr Gly Gly Val Cys Pro Ser Gly Gly Trp Asn Tyr 1 5 10 15 <![CDATA[<210> 47]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 47]]> Asn Tyr Asn Met Phe 1 5 <![CDATA[<210> 48]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 48]]> Val Ile Asn Arg Gly Gly Asp Thr Ala Asp Tyr Ala Ala Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 49]]> <![CDATA[<211> 6]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 49]]> Asp Pro Leu Gly Thr Thr 1 5 <![CDATA[<210> 50]]> <![CDATA[<211> 3]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 50]]> Thr Met Gly 1 <![CDATA[<210> 51]]> <![CDATA[<211> 19]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 51]]> Cys Ile Tyr Thr Gly Pro Thr Thr Thr Phe Thr Asp Tyr Ala Asp Ser 1 5 10 15 Val Lys Gly <![CDATA[<210> 52]]> <![CDATA[<211> 13]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 52]]> Asn Leu Ala Tyr Pro Leu Thr Ile Ile Pro Asp Thr Arg 1 5 10 <![CDATA[<210> 53]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 53]]> Ile Glu Tyr Met Gly Trp Gly 1 5 <![CDATA[<210> 54]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 54]]> Tyr Ile Asn Thr Gly Gly Gly Thr Ser Val Tyr Asp Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 55]]> <![CDATA[<211> 18]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 55]]> Gly Ser Phe Phe Gly Ile Trp Tyr Lys Val Pro Ala Thr Gln Tyr Phe 1 5 10 15 His Tyr <![CDATA[<210> 56]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 56]]> His Tyr Cys Met Gly 1 5 <![CDATA[<210> 57]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 57]]> Leu Ile Asn Thr Gly Gly Pro Thr Thr Phe Tyr Ala Asp Phe Val Glu 1 5 10 15 Gly <![CDATA[<210> 58]]> <![CDATA[<211> 20]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 58]]> Gly Pro Pro Ser Ser Asp Ser Gly Ser Gly Cys Tyr Val Pro Glu Tyr 1 5 10 15 Met Tyr Asn Tyr 20 <![CDATA[<210> 59]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 59]]> Thr Asp Cys Met Gly 1 5 <![CDATA[<210> 60]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 60]]> Thr Ile Tyr Thr Ser Asp Gly Arg Thr Ala Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 61]]> <![CDATA[<211> 15]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 61]]> Asp Leu Gln Tyr Gly Gly Ser Cys Pro Ser Gly Gly Trp Lys Tyr 1 5 10 15 <![CDATA[<210> 62]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 62]]> Thr Gly Cys Met Ala 1 5 <![CDATA[<210> 63]]> <![CDATA[<211> 16]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 63]]> Ile Ile Asn Ile Ser Gly Thr Thr Arg Tyr Thr Asp Ser Val Lys Gly 1 5 10 15 <![CDATA[<210> 64]]> <![CDATA[<211> 26]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 64]]> Thr Gln Asn Pro Arg Thr Val Gly Arg Gly Tyr Cys Thr Gly Asp Tyr 1 5 10 15 Phe Gln Val Gly Gly Gly Gly Tyr Ser Phe 20 25 <![CDATA[<210> 65]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 65]]> Arg Tyr Cys Met Ala 1 5 <![CDATA[<210> 66]]> <![CDATA[<211> 16]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 66]]> Cys Leu Asp Arg Asp Gly Ser Thr Thr Tyr Ala Asp Ser Val Lys Gly 1 5 10 15 <![CDATA[<210> 67]]> <![CDATA[<211> 15]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 67]]> Ala Gln Pro Gly Asp Cys Trp Gly Arg Arg Tyr Gly Phe Asn Thr 1 5 10 15 <![CDATA[<210> 68]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 68]]> Ser Phe Ser Met Ala 1 5 <![CDATA[<210> 69]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 69]]> Cys Ile Gln Ala Glu Ser Gly Ser Thr Asn Val Ala Pro Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 70]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 70]]> Phe Lys Arg Asn Val Gly Gly Cys Glu Leu Arg Pro Glu His Trp Arg 1 5 10 15 Phe <![CDATA[<210> 71]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 71]]> Ser Cys Gly Met Asp 1 5 <![CDATA[<210> 72]]> <![CDATA[<211> 16]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 72]]> Arg Ile Arg Pro Asp Gly Arg Thr Asp Tyr Val Glu Ser Val Lys Gly 1 5 10 15 <![CDATA[<210> 73]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 73]]> Trp Gly Leu Cys Thr Ala Lys Phe Arg 1 5 <![CDATA[<210> 74]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 74]]> Ile Tyr Tyr Met Gly 1 5 <![CDATA[<210> 75]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 75]]> Val Met His Thr Gly Gly Gly Ser Thr Tyr Tyr Thr Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 76]]> <![CDATA[<211> 22]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 76]]> Ser Lys Tyr Leu Leu Ala Phe Gly Gly Val Glu Trp Ile Leu Arg Pro 1 5 10 15 Ala Gly Gly Trp Asp Tyr 20 <![CDATA[<210> 77]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 77]]> Ile Val Ser Met Ser 1 5 <![CDATA[<210> 78]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 78]]> Trp Ile Asn Gly Asp Ser Ser Asn Thr Ser Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 79]]> <![CDATA[<211> 11]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 79]]> Gln Asn Ser His Tyr Asp Ile Arg Phe Gly Tyr 1 5 10 <![CDATA[<210> 80]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 80]]> Ser Tyr Ala Met Gly 1 5 <![CDATA[<210> 81]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 81]]> Ala Ile Ser Arg Ile Ser Gly Asp Thr Tyr Ser Pro Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 82]]> <![CDATA[<211> 18]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 82]]> Ser Ala Thr Pro Ser Ala Thr Asn Ile Tyr Thr Asn Gln Tyr Ala Tyr 1 5 10 15 Gly Asp <![CDATA[<210> 83]]> <![CDATA[<211> 3]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 83]]> Thr Ile His 1 <![CDATA[<210> 84]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 84]]> Arg Ile Trp Trp Ile Glu Arg Thr Thr Phe Tyr Ala Ala Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 85]]> <![CDATA[<211> 14]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 85]]> Asp Ala Arg Tyr Thr Gly Ser Arg Arg Trp Glu Ser Asp Tyr 1 5 10 <![CDATA[<210> 86]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 86]]> Trp Tyr Arg Met Gly 1 5 <![CDATA[<210> 87]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 87]]> Arg Ile Ser Gly Ser Pro Gly Ile Leu Tyr Tyr Ala Gly Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 88]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 88]]> Asp Arg Thr Gly Ala Thr Trp Asp Tyr 1 5 <![CDATA[<210> 89]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 89]]> Thr Tyr Ala Met Gly 1 5 <![CDATA[<210> 90]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 90]]> Ala Ser Ser Arg Asp Gly Thr Thr Thr Tyr Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 91]]> <![CDATA[<211> 18]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 91]]> Ser Arg Pro Leu Ser Thr Thr Gln Val Gly Ile Ala Ser Ala Trp Tyr 1 5 10 15 Glu Tyr <![CDATA[<210> 92]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 92]]> Thr Tyr Ala Met Gly 1 5 <![CDATA[<210> 93]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 93]]> Ala Ile Ser Arg Asn Gly Gly Thr Thr Tyr Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 94]]> <![CDATA[<211> 18]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 94]]> Ser Arg Pro Leu Ser Asn Thr Gln Val Gly Val Ala Ser Ala Trp Tyr 1 5 10 15 Glu Phe <![CDATA[<210> 95]]> <![CDATA[<211> 3]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 95]]> Thr Leu His 1 <![CDATA[<210> 96]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 96]]> Arg Ile Trp Trp Ile Gly Gly Ala Thr Phe Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 97]]> <![CDATA[<211> 14]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 97]]> Asp Ala Arg Tyr Thr Ser Asn Arg Arg Trp Glu Ser Asp Tyr 1 5 10 <![CDATA[<210> 98]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 98]]> Ile Tyr Gly Met Gly 1 5 <![CDATA[<210> 99]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 99]]> Ala Ile Asn Trp Ser Ser Gly His Thr Tyr Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 100]]> <![CDATA[<211> 15]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 100]]> Asp Ser Ile Tyr Gly Leu Ser Phe Thr Val Lys Asp Tyr Asp Tyr 1 5 10 15 <![CDATA[<210> 101]]> <![CDATA[<211> 3]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 101]]> Thr Ile His 1 <![CDATA[<210> 102]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 102]]> Arg Ile Trp Trp Ile Gly Gly Ala Thr Phe Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 103]]> <![CDATA[<211> 14]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 103]]> Asp Ala Arg Tyr Thr Ser His Gly Tyr Tyr Glu Ser Asp Tyr 1 5 10 <![CDATA[<210> 104]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 104]]> Trp Tyr Arg Met Gly 1 5 <![CDATA[<210> 105]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 105]]> Arg Ile Ser Gly Asp Thr Asn Ile Lys Tyr Tyr Ala Gly Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 106]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 106]]> Asp Arg Thr Gly Ala Thr Trp Asp Tyr 1 5 <![CDATA[<210> 107]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 107]]> Thr Tyr Ala Met Gly 1 5 <![CDATA[<210> 108]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 108]]> Ala Ile Ser Arg Asn Ala Asp Thr Thr Tyr Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 109]]> <![CDATA[<211> 18]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 109]]> Asp Arg Tyr Ser Ser Asn Thr Gln Val Gly Val Ala Arg Thr Tyr Tyr 1 5 10 15 Asp Tyr <![CDATA[<210> 110]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 110]]> Ile Tyr Gly Met Gly 1 5 <![CDATA[<210> 111]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 111]]> Ala Ile Asn Trp Asn Ser Gly His Thr Tyr Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 112]]> <![CDATA[<211> 15]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 112]]> Asp Ser Ile Ile Gly Leu Ser Phe Thr Val Lys Asp Tyr Asp Tyr 1 5 10 15 <![CDATA[<210> 113]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 113]]> Arg Leu Pro Met Gly 1 5 <![CDATA[<210> 114]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 114]]> Ala Ile Ser Trp Ser Ser Ser Thr Thr Tyr Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 115]]> <![CDATA[<211> 21]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 115]]> Val Gly Gly Ser Leu Asp Tyr Ser Ala Thr Val Val Tyr Thr Ala Ala 1 5 10 15 Arg Ala Tyr Ala Asp 20 <![CDATA[<210> 116]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 116]]> Phe Tyr Arg Met Gly 1 5 <![CDATA[<210> 117]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 117]]> Arg Ile Ser Ser Ser Ala Gly Leu Ile Tyr Tyr Val Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 118]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 118]]> Asp Arg His Gly Thr Arg Trp Asp Tyr 1 5 <![CDATA[<210> 119]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 119]]> Arg Tyr Ala Met Gly 1 5 <![CDATA[<210> 120]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 120]]> Ala Ile Ser Ser Ser Gly Asp Pro Thr Tyr Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 121]]> <![CDATA[<211> 18]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 121]]> Gly Leu Thr Ala Arg Asp Thr Thr Val Val Val His Pro Asn Gly Tyr 1 5 10 15 Ser Tyr <![CDATA[<210> 122]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 122]]> Arg Tyr Ser Met Gly 1 5 <![CDATA[<210> 123]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 123]]> Ala Ile Ser Ser Ser Gly Asp Val Thr His Tyr Ala Asp Ser Ala Lys 1 5 10 15 Gly <![CDATA[<210> 124]]> <![CDATA[<211> 18]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 124]]> Ser Leu Thr Ala Arg Ala Thr Thr Val Thr Val His Pro Asn Gly Tyr 1 5 10 15 Asn Tyr <![CDATA[<210> 125]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 125]]> Arg Leu Pro Met Ala 1 5 <![CDATA[<210> 126]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 126]]> Ala Ile Ser Trp Ser Gly Gly Ser Thr Tyr Tyr Ala Asp Ser Met Lys 1 5 10 15 Gly <![CDATA[<210> 127]]> <![CDATA[<211> 21]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 127]]> Val Gly Asp Ser Ala Pro Tyr Ser Ala Thr Ile Val Tyr Thr Asp Ala 1 5 10 15 Arg Ala Tyr Ala Tyr 20 <![CDATA[<210> 128]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 128]]> Ser Tyr Ala Met Gly 1 5 <![CDATA[<210> 129]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 129]]> Ala Ile Asn Arg Ser Gly Asp Phe Pro Tyr Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 130]]> <![CDATA[<211> 18]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 130]]> Ala Pro Arg Ala Pro Ala Thr Gln Val Val Ile Ser Ala Phe Gly Tyr 1 5 10 15 Glu Tyr <![CDATA[<210> 131]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 131]]> Leu Tyr Ala Met Gly 1 5 <![CDATA[<210> 132]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 132]]> Gly Ile Ser Arg Thr Gly Asp Thr Thr Tyr Ser Pro Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 133]]> <![CDATA[<211> 18]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 133]]> Ser Ala Thr Tyr Ser Ala Thr Asn Ile Tyr Thr His Gln Arg Ala Tyr 1 5 10 15 Gly Asp <![CDATA[<210> 134]]> <![CDATA[<211> 233]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<220>]]> <![CDATA[<221> UNSURE]]> <![CDATA[<222> (1)..(1)]]> <![CDATA[<223> The 'Xaa' at location 1 stands for Gln, Arg, Pro, or Leu.]]> <![CDATA[<220>]]> <![CDATA[<221> UNSURE]]> <![CDATA[<222> (2)..(2)]]> <![CDATA[<223> The 'Xaa' at location 2 stands for Gln, Arg, Pro, or Leu.]]> <![CDATA[<400> 134]]> Xaa Xaa Gly Gly Gly Gly Ser Asp Lys Thr His Thr Cys Pro Pro Cys 1 5 10 15 Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val Phe Leu Phe Pro Pro 20 25 30 Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr Pro Glu Val Thr Cys 35 40 45 Val Val Val Asp Val Ser His Glu Asp Pro Glu Val Lys Phe Asn Trp 50 55 60 Tyr Val Asp Gly Val Glu Val His Asn Ala Lys Thr Lys Pro Arg Glu 65 70 75 80 Glu Gln Tyr Asn Ser Thr Tyr Arg Val Val Ser Val Leu Thr Val Leu 85 90 95 His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys Cys Lys Val Ser Asn 100 105 110 Lys Ala Leu Pro Ala Pro Ile Glu Lys Thr Ile Ser Lys Ala Lys Gly 115 120 125 Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro Pro Ser Arg Asp Glu 130 135 140 Leu Thr Lys Asn Gln Val Ser Leu Thr Cys Leu Val Lys Gly Phe Tyr 145 150 155 160 Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn Gly Gln Pro Glu Asn 165 170 175 Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser Asp Gly Ser Phe Phe 180 185 190 Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg Trp Gln Gln Gly Asn 195 200 205 Val Phe Ser Cys Ser Val Met His Glu Ala Leu His Asn His Tyr Thr 210 215 220 Gln Lys Ser Leu Ser Leu Ser Pro Gly 225 230 <![CDATA[<210> 135]]> <![CDATA[<211> 126]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 135]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Pro Tyr Ser Ala Asn Ser Phe 20 25 30 Ser Met Ala Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45 Ser Cys Ile Gln Ala Glu Ser Gly Ser Thr Asn Val Ala Pro 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 Ala Phe Lys Arg Asn Val Gly Gly Cys Glu Leu Arg Pro Glu His 100 105 110 Trp Arg Phe Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 136]]> <![CDATA[<211> 126]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 136]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Pro Tyr Ser Ala Asn Ser Phe 20 25 30 Ser Met Ala Trp Phe Arg Gln Ala Pro Gly Lys Gly Leu Glu Gly Val 35 40 45 Ala Cys Ile Gln Ala Glu Ser Gly Ser Thr Asn Val Ala Pro Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Gln 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 Ala Phe Lys Arg Asn Val Gly Gly Cys Glu Leu Arg Pro Glu His 100 105 110 Trp Arg Phe Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 137]]> <![CDATA[<211> 126]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 137]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Pro Ser Pro Tyr Ser Ala Asn Ser Phe 20 25 30 Ser Met Ala Trp Phe Arg Gln Ala Pro Gly Lys Gly Leu Glu Gly Ile 35 40 45 Ala Cys Ile Gln Ala Glu Ser Gly Ser Thr Asn Val Ala Pro Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Gln 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 Ala Phe Lys Arg Asn Val Gly Gly Cys Glu Leu Arg Pro Glu His 100 105 110 Trp Arg Phe Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 138]]> <![CDATA[<211> 126]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 138]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Pro Tyr Ser Ala Asn Ser Phe 20 25 30 Ser Met Ala Trp Phe Arg Gln Ala Pro Gly Lys Gly Arg Glu Gly Val 35 40 45 Ala Cys Ile Gln Ala Glu Ser Gly Ser Thr Asn Val Ala Pro Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Gln 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 Ala Phe Lys Arg Asn Val Gly Gly Cys Glu Leu Arg Pro Glu His 100 105 110 Trp Arg Phe Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 139]]> <![CDATA[<211> 126]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 139]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Pro Ser Pro Tyr Ser Ala Asn Ser Phe 20 25 30 Ser Met Ala Trp Phe Arg Gln Ala Pro Gly Lys Gly Arg Glu Gly Ile 35 40 45 Ala Cys Ile Gln Ala Glu Ser Gly Ser Thr Asn Val Ala Pro Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Gln 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 Ala Phe Lys Arg Asn Val Gly Gly Cys Glu Leu Arg Pro Glu His 100 105 110 Trp Arg Phe Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 140]]> <![CDATA[<211> 126]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 140]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Pro Ser Pro Tyr Ser Ala Asn Ser Phe 20 25 30 Ser Met Ala Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Gly Ile 35 40 45 Ala Cys Ile Gln Ala Glu Ser Gly Ser Thr Asn Val Ala Pro Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Gln 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 Ala Phe Lys Arg Asn Val Gly Gly Cys Glu Leu Arg Pro Glu His 100 105 110 Trp Arg Phe Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 125 <![CDATA[<210> 141]]> <![CDATA[<211> 118]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 141]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Val Val Gln Pro Gly Arg 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Glu Ser Trp Tyr 20 25 30 Arg Met Gly Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45 Ala Arg Ile Ser Gly Asp Thr Asn Ile Lys Tyr Tyr Ala Gly 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 Ser Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Asp Arg Thr Gly Ala Thr Trp Asp Tyr Trp Gly Gln Gly Thr 100 105 110 Leu Val Thr Val Ser Ser 115 <![CDATA[<210> 142]]> <![CDATA[<211> 118]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 142]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Val Val Gln Pro Gly Arg 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Glu Ser Trp Tyr 20 25 30 Arg Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Gly Leu Glu Val Val 35 40 45 Ala Arg Ile Ser Gly Asp Thr Asn Ile Lys Tyr Tyr Ala Gly 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 Ser Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Asp Arg Thr Gly Ala Thr Trp Asp Tyr Trp Gly Gln Gly Thr 100 105 110 Leu Val Thr Val Ser Ser 115 <![CDATA[<210> 143]]> <![CDATA[<211> 118]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 143]]> Gln Val Gln Leu Val Glu Ser Gly Gly Gly Val Val Gln Pro Gly Arg 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Glu Ser Trp Tyr 20 25 30 Arg Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Gly Arg Glu Val Val 35 40 45 Ala Arg Ile Ser Gly Asp Thr Asn Ile Lys Tyr Tyr Ala Gly 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 Ser Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Asp Arg Thr Gly Ala Thr Trp Asp Tyr Trp Gly Gln Gly Thr 100 105 110 Leu Val Thr Val Ser Ser 115 <![CDATA[<210> 144]]> <![CDATA[<211> 118]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 144]]> Asp Val Gln Leu Val Glu Ser Gly Gly Gly Val Val Gln Pro Gly Arg 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Glu Ser Trp Tyr 20 25 30 Arg Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Gly Arg Glu Val Val 35 40 45 Ala Arg Ile Ser Gly Asp Thr Asn Ile Lys Tyr Tyr Ala Gly 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 Ser Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ala Asp Arg Thr Gly Ala Thr Trp Asp Tyr Trp Gly Gln Gly Thr 100 105 110 Leu Val Thr Val Ser Ser 115 <![CDATA[<210> 145]]> <![CDATA[<211> 130]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 145]]> Glu Val Gln Leu Val 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 Arg Thr Phe Ser Arg Leu 20 25 30 Pro Met Gly Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45 Ser Ala Ile Ser Trp Ser Ser Ser Thr Thr 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 Ala Val Gly Gly Ser Leu Asp Tyr Ser Ala Thr Val Val Tyr Thr 100 105 110 Ala Ala Arg Ala Tyr Ala Asp Trp Gly Gln Gly Thr Leu Val Thr Val 115 120 125 Ser Ser 130 <![CDATA[<210> 146]]> <![CDATA[<211> 130]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 146]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Val Ser Gly Arg Thr Phe Ser Arg Leu 20 25 30 Pro Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Gly Leu Glu Phe Val 35 40 45 Ala Ala Ile Ser Trp Ser Ser Ser Thr Thr Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Ala 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 Ala Val Gly Gly Ser Leu Asp Tyr Ser Ala Thr Val Val Tyr Thr 100 105 110 Ala Ala Arg Ala Tyr Ala Asp Trp Gly Gln Gly Thr Leu Val Thr Val 115 120 125 Ser Ser 130 <![CDATA[<210> 147]]> <![CDATA[<211> 130]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 147]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Val Ser Gly Arg Thr Phe Ser Arg Leu 20 25 30 Pro Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Gly Arg Glu Phe Val 35 40 45 Ala Ala Ile Ser Trp Ser Ser Ser Thr Thr Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Ala 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 Ala Val Gly Gly Ser Leu Asp Tyr Ser Ala Thr Val Val Tyr Thr 100 105 110 Ala Ala Arg Ala Tyr Ala Asp Trp Gly Gln Gly Thr Leu Val Thr Val 115 120 125 Ser Ser 130 <![CDATA[<210> 148]]> <![CDATA[<211> 130]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 148]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Val Ser Gly Arg Thr Phe Ser Arg Leu 20 25 30 Pro Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Asp Arg Glu Phe Val 35 40 45 Ala Ala Ile Ser Trp Ser Ser Ser Thr Thr Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Ala 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 Ala Val Gly Gly Ser Leu Asp Tyr Ser Ala Thr Val Val Tyr Thr 100 105 110 Ala Ala Arg Ala Tyr Ala Asp Trp Gly Gln Gly Thr Leu Val Thr Val 115 120 125 Ser Ser 130 <![CDATA[<210> 149]]> <![CDATA[<211> 130]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 149]]> Glu Val Gln Leu Val 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 Arg Thr Phe Ser Arg Leu 20 25 30 Pro Met Ala Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45 Ser Ala Ile Ser Trp Ser Gly Gly Ser Thr Tyr Tyr Ala Asp Ser Met 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 Ala Val Gly Asp Ser Ala Pro Tyr Ser Ala Thr Ile Val Tyr Thr 100 105 110 Asp Ala Arg Ala Tyr Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val 115 120 125 Ser Ser 130 <![CDATA[<210> 150]]> <![CDATA[<211> 130]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 150]]> Glu Val Gln Leu Val 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 Arg Thr Phe Ser Arg Leu 20 25 30 Pro Met Ala Trp Phe Arg Gln Ala Pro Gly Lys Gly Leu Glu Phe Val 35 40 45 Ala Ala Ile Ser Trp Ser Gly Gly Ser Thr Tyr Tyr Ala Asp Ser Met 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Ala 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 Ala Val Gly Asp Ser Ala Pro Tyr Ser Ala Thr Ile Val Tyr Thr 100 105 110 Asp Ala Arg Ala Tyr Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val 115 120 125 Ser Ser 130 <![CDATA[<210> 151]]> <![CDATA[<211> 130]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 151]]> Glu Val Gln Leu Val 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 Arg Thr Phe Ser Arg Leu 20 25 30 Pro Met Ala Trp Phe Arg Gln Ala Pro Gly Lys Gly Arg Glu Phe Val 35 40 45 Ala Ala Ile Ser Trp Ser Gly Gly Ser Thr Tyr Tyr Ala Asp Ser Met 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Ala 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 Ala Val Gly Asp Ser Ala Pro Tyr Ser Ala Thr Ile Val Tyr Thr 100 105 110 Asp Ala Arg Ala Tyr Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val 115 120 125 Ser Ser 130 <![CDATA[<210> 152]]> <![CDATA[<211> 130]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列(Artificial Sequence)]]> <![CDATA[<220>]]> <![CDATA[<223> synthetically generated protein]]> <![CDATA[<400> 152]]> Glu Val Gln Leu Val 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 Arg Thr Phe Ser Arg Leu 20 25 30 Pro Met Ala Trp Phe Arg Gln Ala Pro Gly Lys Asp Arg Glu Phe Val 35 40 45 Ala Ala Ile Ser Trp Ser Gly Gly Ser Thr Tyr Tyr Ala Asp Ser Met 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Ala 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 Ala Val Gly Asp Ser Ala Pro Tyr Ser Ala Thr Ile Val Tyr Thr 100 105 110 Asp Ala Arg Ala Tyr Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val 115 120 125 Ser Ser 130
Claims (17)
- 一種抗NKp46的抗體或其抗原結合片段,所述抗體或其抗原結合片段能夠特異性結合NKp46,其包含3個選自SEQ ID NO:44-133序列所示的CDR。
- 一種抗NKp46的抗體或其抗原結合片段,所述抗體或其抗原結合片段能夠特異性結合NKp46,其包含重鏈可變區,所述重鏈可變區包含選自SEQ ID NO:44,47,50,53,56,59,62,65,68,71,74,77,80,83,86,89,92,95,98,101,104,107,110,113,116,119,122,125,128,131所示的HCDR1;以及,選自SEQ ID NO: 45,48,51,54,57,60,63,66,69,72,75,78,81,84,87,90,93,96,99,102,105,108,111,114,117,120,123,126,129,132所示的HCDR2;以及,選自SEQ ID NO: 46,49,52,55,58,61,64,67,70,73,76,79,82,85,88,91,94,97,100,103,106,109,112,115,118,121,124,127,130,133所示的HCDR3; 優選的,所述重鏈可變區包含選自下組的HCDR1、HCDR2和HCDR3:SEQ ID NO:44、SEQ ID NO:45和SEQ ID NO:46;或SEQ ID NO:47、SEQ ID NO:48和SEQ ID NO:49;或SEQ ID NO:50、SEQ ID NO:51和SEQ ID NO:52;或SEQ ID NO:53、SEQ ID NO:54和SEQ ID NO:55;或SEQ ID NO:56、SEQ ID NO:57和SEQ ID NO:58;或SEQ ID NO:59、SEQ ID NO:60和SEQ ID NO:61;或SEQ ID NO:62、SEQ ID NO:63和SEQ ID NO:64;或SEQ ID NO:65、SEQ ID NO:66和SEQ ID NO:67;或SEQ ID NO:68、SEQ ID NO:69和SEQ ID NO:70;或SEQ ID NO:71、SEQ ID NO:72和SEQ ID NO:73;或SEQ ID NO:74、SEQ ID NO:75和SEQ ID NO:76;或SEQ ID NO:77、SEQ ID NO:78和SEQ ID NO:79;或SEQ ID NO:80、SEQ ID NO:81和SEQ ID NO:82;或SEQ ID NO:83、SEQ ID NO:84和SEQ ID NO:85;或SEQ ID NO:86、SEQ ID NO:87和SEQ ID NO:88;或SEQ ID NO:89、SEQ ID NO:90和SEQ ID NO:91;或SEQ ID NO:92、SEQ ID NO:93和SEQ ID NO:94;或SEQ ID NO:95、SEQ ID NO:96和SEQ ID NO:97;或SEQ ID NO:98、SEQ ID NO:99和SEQ ID NO:100;或SEQ ID NO:101、SEQ ID NO:102和SEQ ID NO:103;或SEQ ID NO:104、SEQ ID NO:105和SEQ ID NO:106;或SEQ ID NO:107、SEQ ID NO:108和SEQ ID NO:109;或SEQ ID NO:110、SEQ ID NO:111和SEQ ID NO:112;或SEQ ID NO:113、SEQ ID NO:114和SEQ ID NO:115;或SEQ ID NO:116、SEQ ID NO:117和SEQ ID NO:118;或SEQ ID NO:119、SEQ ID NO:120和SEQ ID NO:121;或SEQ ID NO:122、SEQ ID NO:123和SEQ ID NO:124;或SEQ ID NO:125、SEQ ID NO:126和SEQ ID NO:127;或SEQ ID NO:128、SEQ ID NO:129和SEQ ID NO:130;或SEQ ID NO:131、SEQ ID NO:132和SEQ ID NO:133。
- 一種抗NKp46的抗體或其抗原結合片段,所述抗體或其抗原結合片段能夠特異性結合NKp46,其包含HCDR1、HCDR2和HCDR3,所述HCDR1、HCDR2和HCDR3來自於SEQ ID NO: 14-43,136-152所示的重鏈可變區;優選的,所述重鏈可變區具有與SEQ ID NO: 14-43,136-152所示序列至少80%至100%的序列同一性。
- 如請求項1-3任一項所述的抗NKp46的抗體或其抗原結合片段,其中所述抗體是重組抗體,優選的,為羊駝源抗體、嵌合抗體或人源化抗體;更優選的,所述抗體為奈米抗體;進一步優選的,所述抗體為人源化的駱駝科VHH。
- 如前述請求項任一項所述的抗NKp46的抗體或其抗原結合片段,其更包括重鏈恒定區及/或輕鏈恒定區,優選的,所述重鏈恒定區包括Fc或變體Fc,Fc來源於鼠或人;及/或, 所述的抗NKp46的抗體或其抗原結合片段為IgG1、IgG2、IgG3或IgG4形式。
- 一種偶聯物,將前述請求項任一項所述的抗NKp46的抗體或其抗原結合片段與捕獲標記物或檢測標記物偶聯形成,所述的檢測標記物包括放射性核素、發光物質、有色物質或酶。
- 一種雙特異性抗體或多特異性抗體,其中的一個抗原結合結構域包含前述任一請求項所述的抗NKp46的抗體或其抗原結合片段。
- 一種抗體藥物綴合物,含有前述任一請求項所述的抗NKp46的抗體或其抗原結合片段,所述的抗體藥物綴合物由抗體-接頭-毒素相互連接形成。
- 一種嵌合抗原受體,其胞外識別單元包含前述任一請求項所述的抗NKp46的抗體或其抗原結合片段。
- 編碼前述任一請求項所述的抗NKp46的抗體或其抗原結合片段的核酸;或包含所述核酸的重組載體;或包含所述重組載體或基因組中整合有所述核酸的宿主細胞。
- 製備前述任一請求項所述的抗NKp46的抗體或其抗原結合片段的方法,包括:在適合的條件下培養請求項10的宿主細胞,並從所述細胞中純化獲得表達產物。
- 前述任一請求項所述的抗NKp46的抗體或其抗原結合片段在製備特異性靶向表達NKp46的細胞的藥物中的用途;前述任一請求項所述的抗NKp46的抗體或其抗原結合片段在治療、預防或檢測特異性表達NKp46疾病中的用途;優選的,所述細胞是NK細胞。
- 前述任一請求項所述的抗NKp46的抗體或其抗原結合片段在製備癌症、感染性疾病或者炎性或自身免疫性疾病藥物中的用途;前述任一請求項所述的抗NKp46的抗體或其抗原結合片段在治療癌症、感染性疾病或者炎性或自身免疫性疾病中的用途;優選的,所述癌症包括:白血病,侵襲性淋巴瘤,非霍奇金淋巴瘤,腦膠質瘤,宮頸癌,頭頸癌,直腸癌,腎癌,肝癌,肺癌,胰腺癌,胃癌等。
- 前述任一請求項所述的抗NKp46的抗體或其抗原結合片段在製備表達NKp46的診斷試劑中的用途。
- 一種含有抗NKp46的抗體的溶液製劑,其包含前述任一請求項所述的抗NKp46的抗體或其抗原結合片段和緩衝液。
- 一種用於鑒定個體中NKp46表達細胞的存在的方法,所述方法包括從包含細胞的個體獲得生物樣品,使所述細胞與如請求項1-5所述的抗NKp46的抗體或其抗原結合片段接觸,以及評估所述抗體是否與所述細胞結合。
- 一種藥物組成物,其包含有效量的前述請求項1-5任一項所述的抗NKp46的抗體或其抗原結合片段、或有效量的包含請求項6所述的偶聯物,或包含有效量的請求項7所述的雙特異性抗體或多特異性抗體、或包含有效量的請求項8所述的抗體藥物綴合物、或包含有效量的請求項9所述的嵌合抗原受體、或包含有效量的請求項10所述的核酸、重組載體、或宿主細胞;優選的,更包括藥學上可接受的載體;更優選的,更包括一種或多種額外的其他治療劑,優選的,所述一種或多種額外的其他治療劑包括:化學治療劑、細胞毒性劑、放射性治療劑、癌症疫苗、減瘤劑、靶向性抗癌劑、抗血管生成劑、生物反應修飾劑、細胞因數、激素、抗轉移劑和免疫治療劑。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110243601 | 2021-03-05 | ||
CN202110243601.5 | 2021-03-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
TW202246341A true TW202246341A (zh) | 2022-12-01 |
Family
ID=83154752
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW111107983A TW202246341A (zh) | 2021-03-05 | 2022-03-04 | 針對NKp46的抗體及其應用 |
Country Status (10)
Country | Link |
---|---|
US (1) | US20240141038A1 (zh) |
EP (1) | EP4303234A1 (zh) |
JP (1) | JP2024509557A (zh) |
KR (1) | KR20230154235A (zh) |
CN (1) | CN116964099A (zh) |
AU (1) | AU2022230011A1 (zh) |
BR (1) | BR112023017556A2 (zh) |
CA (1) | CA3210582A1 (zh) |
TW (1) | TW202246341A (zh) |
WO (1) | WO2022184162A1 (zh) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116284396A (zh) * | 2022-12-20 | 2023-06-23 | 合肥天港免疫药物有限公司 | NKp46抗体及其用途 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL137419A0 (en) * | 2000-07-20 | 2001-07-24 | Yissum Res Dev Co | Nk cells activating receptors and their therapeutic and diagnostic uses |
EP2408468B1 (en) * | 2009-03-19 | 2014-04-30 | Yissum Research Development Company of the Hebrew University of Jerusalem, Ltd. | USE OF NKp46 FOR PREVENTING TYPE 1 DIABETES |
WO2012175613A1 (en) * | 2011-06-21 | 2012-12-27 | Innate Pharma | NKp46-MEDIATED NK CELL TUNING |
WO2013113641A1 (en) * | 2012-01-31 | 2013-08-08 | Roche Glycart Ag | Use of nkp46 as a predictive biomarker for cancer treatment with adcc- enhanced antibodies |
EP2828291A1 (en) * | 2012-03-21 | 2015-01-28 | Yissum Research Development Company of The Hebrew University of Jerusalem Ltd. | Peptides derived from the d1-domain of nkp46 |
EP3161002A1 (en) * | 2014-06-27 | 2017-05-03 | Innate Pharma | MULTISPECIFIC NKp46 BINDING PROTEINS |
WO2018047154A1 (en) * | 2016-09-07 | 2018-03-15 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. | Anti-nkp46 antibodies and therapeutic use of same |
-
2022
- 2022-03-04 WO PCT/CN2022/079236 patent/WO2022184162A1/zh active Application Filing
- 2022-03-04 TW TW111107983A patent/TW202246341A/zh unknown
- 2022-03-04 AU AU2022230011A patent/AU2022230011A1/en active Pending
- 2022-03-04 US US18/280,248 patent/US20240141038A1/en active Pending
- 2022-03-04 CA CA3210582A patent/CA3210582A1/en active Pending
- 2022-03-04 JP JP2023553738A patent/JP2024509557A/ja active Pending
- 2022-03-04 BR BR112023017556A patent/BR112023017556A2/pt unknown
- 2022-03-04 KR KR1020237033784A patent/KR20230154235A/ko active Search and Examination
- 2022-03-04 CN CN202280019014.0A patent/CN116964099A/zh active Pending
- 2022-03-04 EP EP22762624.9A patent/EP4303234A1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
BR112023017556A2 (pt) | 2023-10-10 |
EP4303234A1 (en) | 2024-01-10 |
KR20230154235A (ko) | 2023-11-07 |
AU2022230011A1 (en) | 2023-10-19 |
WO2022184162A1 (zh) | 2022-09-09 |
US20240141038A1 (en) | 2024-05-02 |
CA3210582A1 (en) | 2022-09-09 |
CN116964099A (zh) | 2023-10-27 |
JP2024509557A (ja) | 2024-03-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US11472882B2 (en) | Anti-B7-H4 antibody, antigen-binding fragment thereof and pharmaceutical use thereof | |
WO2018161872A1 (zh) | 抗b7-h3抗体、其抗原结合片段及其医药用途 | |
JP2021519610A (ja) | 多価抗体 | |
TW201922784A (zh) | 4﹘1bb抗體及其製備方法和應用 | |
CN112243443B (zh) | 抗trop-2抗体、其抗原结合片段及其医药用途 | |
WO2021155635A1 (zh) | 抗cd3和cd123双特异性抗体及其用途 | |
US20230090014A1 (en) | Anti-cd47/anti-pd-l1 antibody and applications thereof | |
WO2021143914A1 (zh) | 一种激活型抗ox40抗体、生产方法及应用 | |
US20230192861A1 (en) | Anti-pd-l1/anti-b7-h3 multispecific antibodies and uses thereof | |
WO2022184162A1 (zh) | 针对NKp46的抗体及其应用 | |
WO2019192493A1 (zh) | 抗人lag-3单克隆抗体及其应用 | |
WO2022166876A1 (zh) | 特异性识别磷脂酰肌醇蛋白聚糖3的单克隆抗体及其应用 | |
WO2021244371A1 (zh) | 一种抗pd-l1/vegf融合蛋白 | |
AU2022273136A1 (en) | Binding molecule against dll3 and use thereof | |
KR20220035367A (ko) | 항-dll3 키메라 항원 수용체 및 이의 용도 | |
WO2019174637A1 (zh) | 一种针对tim-3的全人源化抗体分子、抗原结合片段及其医药用途 | |
WO2022174808A1 (zh) | 针对IL-13Rα2的抗体及其应用 | |
WO2024094017A1 (zh) | 一种针对磷脂酰肌醇蛋白聚糖3的双特异性抗体及其应用 | |
WO2022268168A1 (zh) | 靶向lag-3和pd-l1的新型双特异抗体及其应用 | |
WO2022171100A1 (zh) | Gpc3人源化抗体及其应用 | |
WO2023036215A1 (zh) | 双特异性抗原结合分子及其应用 | |
WO2024094159A1 (zh) | 靶向人源ror1的单域抗体 | |
WO2024078558A1 (zh) | 抗cd100抗体及其用途 | |
US20220064323A1 (en) | Therapeutic Anti-CD9 Antibody | |
CA3229250A1 (en) | Anti-vegf a and vegf c bispecific antibodies and use thereof |