CN101265503A - 检测间充质干细胞的标记和采用该标记识别间充质干细胞的方法 - Google Patents
检测间充质干细胞的标记和采用该标记识别间充质干细胞的方法 Download PDFInfo
- Publication number
- CN101265503A CN101265503A CNA200810081304XA CN200810081304A CN101265503A CN 101265503 A CN101265503 A CN 101265503A CN A200810081304X A CNA200810081304X A CN A200810081304XA CN 200810081304 A CN200810081304 A CN 200810081304A CN 101265503 A CN101265503 A CN 101265503A
- Authority
- CN
- China
- Prior art keywords
- gene
- stem cell
- mescenchymal stem
- sequence number
- people
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims abstract description 63
- 210000002901 mesenchymal stem cell Anatomy 0.000 title claims abstract description 26
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 371
- 210000004027 cell Anatomy 0.000 claims abstract description 39
- 229920001184 polypeptide Polymers 0.000 claims abstract description 36
- 102000004196 processed proteins & peptides Human genes 0.000 claims abstract description 34
- 108090000765 processed proteins & peptides Proteins 0.000 claims abstract description 34
- 239000000523 sample Substances 0.000 claims abstract description 32
- 210000000130 stem cell Anatomy 0.000 claims description 213
- 108020004999 messenger RNA Proteins 0.000 claims description 179
- 108020004414 DNA Proteins 0.000 claims description 117
- 230000014509 gene expression Effects 0.000 claims description 93
- 239000003550 marker Substances 0.000 claims description 55
- 102000004169 proteins and genes Human genes 0.000 claims description 51
- 238000003757 reverse transcription PCR Methods 0.000 claims description 45
- 239000002771 cell marker Substances 0.000 claims description 31
- 230000002068 genetic effect Effects 0.000 claims description 24
- 238000001514 detection method Methods 0.000 claims description 14
- 238000000018 DNA microarray Methods 0.000 claims description 12
- 238000002372 labelling Methods 0.000 claims description 7
- 108010049955 Bone Morphogenetic Protein 4 Proteins 0.000 claims description 6
- 108091028043 Nucleic acid sequence Proteins 0.000 claims description 6
- 238000002493 microarray Methods 0.000 claims description 6
- 102100028530 Cytoplasmic dynein 1 intermediate chain 1 Human genes 0.000 claims description 5
- 101000915295 Homo sapiens Cytoplasmic dynein 1 intermediate chain 1 Proteins 0.000 claims description 5
- 238000009396 hybridization Methods 0.000 claims description 5
- 102000004219 Brain-derived neurotrophic factor Human genes 0.000 claims description 4
- 108090000715 Brain-derived neurotrophic factor Proteins 0.000 claims description 4
- 102000016611 Proteoglycans Human genes 0.000 claims description 3
- 108010067787 Proteoglycans Proteins 0.000 claims description 3
- 229940077737 brain-derived neurotrophic factor Drugs 0.000 claims description 3
- 102000043253 matrix Gla protein Human genes 0.000 claims description 3
- 108010057546 matrix Gla protein Proteins 0.000 claims description 3
- 210000004739 secretory vesicle Anatomy 0.000 claims description 3
- 102000008137 Bone Morphogenetic Protein 4 Human genes 0.000 claims 2
- 101000999079 Homo sapiens Radiation-inducible immediate-early gene IEX-1 Proteins 0.000 claims 1
- 101000879840 Homo sapiens Serglycin Proteins 0.000 claims 1
- 101000766349 Homo sapiens Tribbles homolog 2 Proteins 0.000 claims 1
- 102000004257 Potassium Channel Human genes 0.000 claims 1
- 102100037344 Serglycin Human genes 0.000 claims 1
- 102100026394 Tribbles homolog 2 Human genes 0.000 claims 1
- 108020001213 potassium channel Proteins 0.000 claims 1
- 238000005215 recombination Methods 0.000 claims 1
- 230000006798 recombination Effects 0.000 claims 1
- 230000000692 anti-sense effect Effects 0.000 description 114
- 235000018102 proteins Nutrition 0.000 description 50
- 102000004190 Enzymes Human genes 0.000 description 20
- 108090000790 Enzymes Proteins 0.000 description 20
- 229940088598 enzyme Drugs 0.000 description 20
- 108700018351 Major Histocompatibility Complex Proteins 0.000 description 13
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 13
- 230000020382 suppression by virus of host antigen processing and presentation of peptide antigen via MHC class I Effects 0.000 description 13
- 230000002950 deficient Effects 0.000 description 12
- 210000001519 tissue Anatomy 0.000 description 12
- 230000004069 differentiation Effects 0.000 description 11
- 239000003814 drug Substances 0.000 description 11
- 210000002950 fibroblast Anatomy 0.000 description 11
- 239000000370 acceptor Substances 0.000 description 10
- 230000001172 regenerating effect Effects 0.000 description 10
- 102100024458 Cyclin-dependent kinase inhibitor 2A Human genes 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 101000575639 Homo sapiens Ribonucleoside-diphosphate reductase subunit M2 Proteins 0.000 description 8
- 102100023408 KH domain-containing, RNA-binding, signal transduction-associated protein 1 Human genes 0.000 description 8
- 101710094958 KH domain-containing, RNA-binding, signal transduction-associated protein 1 Proteins 0.000 description 8
- 108091000080 Phosphotransferase Proteins 0.000 description 8
- 102100026006 Ribonucleoside-diphosphate reductase subunit M2 Human genes 0.000 description 8
- 108091006207 SLC-Transporter Proteins 0.000 description 8
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 8
- 102100034838 Thymidine kinase, cytosolic Human genes 0.000 description 8
- 235000013399 edible fruits Nutrition 0.000 description 8
- 230000006698 induction Effects 0.000 description 8
- 102000020233 phosphotransferase Human genes 0.000 description 8
- 238000000926 separation method Methods 0.000 description 8
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 7
- 102000009333 Apolipoprotein D Human genes 0.000 description 7
- 108010025614 Apolipoproteins D Proteins 0.000 description 7
- 102100032306 Aurora kinase B Human genes 0.000 description 7
- 102000005483 Cell Cycle Proteins Human genes 0.000 description 7
- 108010031896 Cell Cycle Proteins Proteins 0.000 description 7
- 108010060273 Cyclin A2 Proteins 0.000 description 7
- 102100025191 Cyclin-A2 Human genes 0.000 description 7
- 101000798306 Homo sapiens Aurora kinase B Proteins 0.000 description 7
- 102100039813 Inactive tyrosine-protein kinase 7 Human genes 0.000 description 7
- 101710099452 Inactive tyrosine-protein kinase 7 Proteins 0.000 description 7
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 7
- 108010000684 Matrix Metalloproteinases Proteins 0.000 description 7
- 102000002274 Matrix Metalloproteinases Human genes 0.000 description 7
- 102000037054 SLC-Transporter Human genes 0.000 description 7
- 210000000988 bone and bone Anatomy 0.000 description 7
- 230000001419 dependent effect Effects 0.000 description 7
- 102000004379 Adrenomedullin Human genes 0.000 description 6
- 101800004616 Adrenomedullin Proteins 0.000 description 6
- 102100038099 Cell division cycle protein 20 homolog Human genes 0.000 description 6
- 101000583797 Homo sapiens Protein MCM10 homolog Proteins 0.000 description 6
- 101000620559 Homo sapiens Ras-related protein Rab-3B Proteins 0.000 description 6
- 102100030962 Protein MCM10 homolog Human genes 0.000 description 6
- 102100022306 Ras-related protein Rab-3B Human genes 0.000 description 6
- ULCUCJFASIJEOE-NPECTJMMSA-N adrenomedullin Chemical compound C([C@@H](C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC(=O)N[C@@H]1C(N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CSSC1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(N)=O)[C@@H](C)O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](N)CC=1C=CC(O)=CC=1)C1=CC=CC=C1 ULCUCJFASIJEOE-NPECTJMMSA-N 0.000 description 6
- 230000003321 amplification Effects 0.000 description 6
- 108010050848 glycylleucine Proteins 0.000 description 6
- 239000003112 inhibitor Substances 0.000 description 6
- 230000000394 mitotic effect Effects 0.000 description 6
- 238000003199 nucleic acid amplification method Methods 0.000 description 6
- 108010035532 Collagen Proteins 0.000 description 5
- 102000008186 Collagen Human genes 0.000 description 5
- 108010009392 Cyclin-Dependent Kinase Inhibitor p16 Proteins 0.000 description 5
- 102000004245 Proteasome Endopeptidase Complex Human genes 0.000 description 5
- 108090000708 Proteasome Endopeptidase Complex Proteins 0.000 description 5
- 101710133283 RNA-binding protein 2 Proteins 0.000 description 5
- 108050002982 RuvB-like helicase 1 Proteins 0.000 description 5
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000002596 correlated effect Effects 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 230000001939 inductive effect Effects 0.000 description 5
- 108010034529 leucyl-lysine Proteins 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000000137 peptide hydrolase inhibitor Substances 0.000 description 5
- DCWXELXMIBXGTH-UHFFFAOYSA-N phosphotyrosine Chemical compound OC(=O)C(N)CC1=CC=C(OP(O)(O)=O)C=C1 DCWXELXMIBXGTH-UHFFFAOYSA-N 0.000 description 5
- 102000055046 tissue-factor-pathway inhibitor 2 Human genes 0.000 description 5
- 108010016054 tissue-factor-pathway inhibitor 2 Proteins 0.000 description 5
- 108010013043 Acetylesterase Proteins 0.000 description 4
- 101710159080 Aconitate hydratase A Proteins 0.000 description 4
- 101710159078 Aconitate hydratase B Proteins 0.000 description 4
- 102100033393 Anillin Human genes 0.000 description 4
- 102100032311 Aurora kinase A Human genes 0.000 description 4
- 102100024505 Bone morphogenetic protein 4 Human genes 0.000 description 4
- 108090000342 C-Type Lectins Proteins 0.000 description 4
- 102000003930 C-Type Lectins Human genes 0.000 description 4
- 102100026194 C-type lectin domain family 2 member B Human genes 0.000 description 4
- 101150047144 CDC28 gene Proteins 0.000 description 4
- 108010078791 Carrier Proteins Proteins 0.000 description 4
- 102100025832 Centromere-associated protein E Human genes 0.000 description 4
- 102100031219 Centrosomal protein of 55 kDa Human genes 0.000 description 4
- 102000002734 Collagen Type VI Human genes 0.000 description 4
- 108010043741 Collagen Type VI Proteins 0.000 description 4
- 102100032952 Condensin complex subunit 3 Human genes 0.000 description 4
- 102100024829 DNA polymerase delta catalytic subunit Human genes 0.000 description 4
- 102100036740 DNA replication complex GINS protein PSF3 Human genes 0.000 description 4
- 102100036109 Dual specificity protein kinase TTK Human genes 0.000 description 4
- 102100024501 Histone H3-like centromeric protein A Human genes 0.000 description 4
- 102100038147 Histone chaperone ASF1B Human genes 0.000 description 4
- 102100022107 Holliday junction recognition protein Human genes 0.000 description 4
- 102100022373 Homeobox protein DLX-5 Human genes 0.000 description 4
- 101000798300 Homo sapiens Aurora kinase A Proteins 0.000 description 4
- 101000912618 Homo sapiens C-type lectin domain family 2 member B Proteins 0.000 description 4
- 101000884317 Homo sapiens Cell division cycle protein 20 homolog Proteins 0.000 description 4
- 101000914247 Homo sapiens Centromere-associated protein E Proteins 0.000 description 4
- 101000776447 Homo sapiens Centrosomal protein of 55 kDa Proteins 0.000 description 4
- 101000942622 Homo sapiens Condensin complex subunit 3 Proteins 0.000 description 4
- 101000868333 Homo sapiens Cyclin-dependent kinase 1 Proteins 0.000 description 4
- 101000909198 Homo sapiens DNA polymerase delta catalytic subunit Proteins 0.000 description 4
- 101001136564 Homo sapiens DNA replication complex GINS protein PSF3 Proteins 0.000 description 4
- 101000659223 Homo sapiens Dual specificity protein kinase TTK Proteins 0.000 description 4
- 101000981071 Homo sapiens Histone H3-like centromeric protein A Proteins 0.000 description 4
- 101000884473 Homo sapiens Histone chaperone ASF1B Proteins 0.000 description 4
- 101001045907 Homo sapiens Holliday junction recognition protein Proteins 0.000 description 4
- 101000901627 Homo sapiens Homeobox protein DLX-5 Proteins 0.000 description 4
- 101000994365 Homo sapiens Integrin alpha-6 Proteins 0.000 description 4
- 101001039762 Homo sapiens Multiple C2 and transmembrane domain-containing protein 2 Proteins 0.000 description 4
- 101001111320 Homo sapiens Nestin Proteins 0.000 description 4
- 101000991410 Homo sapiens Nucleolar and spindle-associated protein 1 Proteins 0.000 description 4
- 101001062751 Homo sapiens Pseudokinase FAM20A Proteins 0.000 description 4
- 101000873502 Homo sapiens S-adenosylmethionine decarboxylase proenzyme Proteins 0.000 description 4
- 101000831940 Homo sapiens Stathmin Proteins 0.000 description 4
- 101000596086 Homo sapiens TATA box-binding protein-associated factor RNA polymerase I subunit D Proteins 0.000 description 4
- 102100032816 Integrin alpha-6 Human genes 0.000 description 4
- 102000003815 Interleukin-11 Human genes 0.000 description 4
- 108090000177 Interleukin-11 Proteins 0.000 description 4
- 108010063296 Kinesin Proteins 0.000 description 4
- 102000010638 Kinesin Human genes 0.000 description 4
- 102100040886 Multiple C2 and transmembrane domain-containing protein 2 Human genes 0.000 description 4
- 102100024014 Nestin Human genes 0.000 description 4
- 102100030991 Nucleolar and spindle-associated protein 1 Human genes 0.000 description 4
- 108700020796 Oncogene Proteins 0.000 description 4
- 108010000598 Polycomb Repressive Complex 1 Proteins 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- RJKFOVLPORLFTN-LEKSSAKUSA-N Progesterone Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](C(=O)C)[C@@]1(C)CC2 RJKFOVLPORLFTN-LEKSSAKUSA-N 0.000 description 4
- 102100033947 Protein regulator of cytokinesis 1 Human genes 0.000 description 4
- 102100030553 Pseudokinase FAM20A Human genes 0.000 description 4
- 102000044126 RNA-Binding Proteins Human genes 0.000 description 4
- 101710105008 RNA-binding protein Proteins 0.000 description 4
- 102100027160 RuvB-like 1 Human genes 0.000 description 4
- 102100035914 S-adenosylmethionine decarboxylase proenzyme Human genes 0.000 description 4
- 102100024237 Stathmin Human genes 0.000 description 4
- 102100035207 TATA box-binding protein-associated factor RNA polymerase I subunit D Human genes 0.000 description 4
- 102100030951 Tissue factor pathway inhibitor Human genes 0.000 description 4
- 108090000848 Ubiquitin Proteins 0.000 description 4
- 102000044159 Ubiquitin Human genes 0.000 description 4
- 102100028718 Ubiquitin-conjugating enzyme E2 S Human genes 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
- 230000027455 binding Effects 0.000 description 4
- 210000000845 cartilage Anatomy 0.000 description 4
- 108010060199 cysteinylproline Proteins 0.000 description 4
- 210000000805 cytoplasm Anatomy 0.000 description 4
- 102000028416 insulin-like growth factor binding Human genes 0.000 description 4
- 108091022911 insulin-like growth factor binding Proteins 0.000 description 4
- 229940074383 interleukin-11 Drugs 0.000 description 4
- 108010044374 isoleucyl-tyrosine Proteins 0.000 description 4
- 229940043355 kinase inhibitor Drugs 0.000 description 4
- 108010013555 lipoprotein-associated coagulation inhibitor Proteins 0.000 description 4
- 230000008774 maternal effect Effects 0.000 description 4
- 201000001441 melanoma Diseases 0.000 description 4
- 229940067626 phosphatidylinositols Drugs 0.000 description 4
- 150000003905 phosphatidylinositols Chemical class 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 239000003757 phosphotransferase inhibitor Substances 0.000 description 4
- 108010026333 seryl-proline Proteins 0.000 description 4
- -1 solubility (TK1) Proteins 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 108010061238 threonyl-glycine Proteins 0.000 description 4
- 108010036901 thymidine kinase 1 Proteins 0.000 description 4
- 102000004217 thyroid hormone receptors Human genes 0.000 description 4
- 108090000721 thyroid hormone receptors Proteins 0.000 description 4
- 102000029816 Collagenase Human genes 0.000 description 3
- 108060005980 Collagenase Proteins 0.000 description 3
- 102000034534 Cotransporters Human genes 0.000 description 3
- 108020003264 Cotransporters Proteins 0.000 description 3
- 102000016736 Cyclin Human genes 0.000 description 3
- 108050006400 Cyclin Proteins 0.000 description 3
- 108010025464 Cyclin-Dependent Kinase 4 Proteins 0.000 description 3
- 102100036252 Cyclin-dependent kinase 4 Human genes 0.000 description 3
- 101001008945 Dictyostelium discoideum Kinesin-related protein 12 Proteins 0.000 description 3
- 101001031598 Dictyostelium discoideum Probable serine/threonine-protein kinase fhkC Proteins 0.000 description 3
- SJPMNHCEWPTRBR-BQBZGAKWSA-N Glu-Glu-Gly Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)NCC(O)=O SJPMNHCEWPTRBR-BQBZGAKWSA-N 0.000 description 3
- 102000042092 Glucose transporter family Human genes 0.000 description 3
- 108091052347 Glucose transporter family Proteins 0.000 description 3
- NNCSJUBVFBDDLC-YUMQZZPRSA-N Gly-Leu-Ser Chemical compound NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(O)=O NNCSJUBVFBDDLC-YUMQZZPRSA-N 0.000 description 3
- 101001050607 Homo sapiens KH domain-containing, RNA-binding, signal transduction-associated protein 3 Proteins 0.000 description 3
- 102100035692 Importin subunit alpha-1 Human genes 0.000 description 3
- 108010041100 Integrin alpha6 Proteins 0.000 description 3
- 102000000426 Integrin alpha6 Human genes 0.000 description 3
- 102100023428 KH domain-containing, RNA-binding, signal transduction-associated protein 3 Human genes 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
- KAFOIVJDVSZUMD-UHFFFAOYSA-N Leu-Gln-Gln Natural products CC(C)CC(N)C(=O)NC(CCC(N)=O)C(=O)NC(CCC(N)=O)C(O)=O KAFOIVJDVSZUMD-UHFFFAOYSA-N 0.000 description 3
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 3
- 102000005741 Metalloproteases Human genes 0.000 description 3
- 108010006035 Metalloproteases Proteins 0.000 description 3
- 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 3
- 238000000636 Northern blotting Methods 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 102000035195 Peptidases Human genes 0.000 description 3
- 108091005804 Peptidases Proteins 0.000 description 3
- 102000005831 Pituitary Hormone Release Inhibiting Hormones Human genes 0.000 description 3
- 108010005172 Pituitary Hormone Release Inhibiting Hormones Proteins 0.000 description 3
- 102000001253 Protein Kinase Human genes 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
- 239000004141 Sodium laurylsulphate Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 210000000577 adipose tissue Anatomy 0.000 description 3
- 108010070944 alanylhistidine Proteins 0.000 description 3
- 239000000427 antigen Substances 0.000 description 3
- 108091007433 antigens Proteins 0.000 description 3
- 102000036639 antigens Human genes 0.000 description 3
- 108010068380 arginylarginine Proteins 0.000 description 3
- 238000003556 assay Methods 0.000 description 3
- 230000004087 circulation Effects 0.000 description 3
- 229920001436 collagen Polymers 0.000 description 3
- 229960002424 collagenase Drugs 0.000 description 3
- 230000009274 differential gene expression Effects 0.000 description 3
- 230000003328 fibroblastic effect Effects 0.000 description 3
- 108010049041 glutamylalanine Proteins 0.000 description 3
- 108010000434 glycyl-alanyl-leucine Proteins 0.000 description 3
- 230000001900 immune effect Effects 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 108010073025 phenylalanylphenylalanine Proteins 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- DCWXELXMIBXGTH-QMMMGPOBSA-N phosphonotyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(OP(O)(O)=O)C=C1 DCWXELXMIBXGTH-QMMMGPOBSA-N 0.000 description 3
- 239000003072 pituitary hormone release inhibiting hormone Substances 0.000 description 3
- 108060006633 protein kinase Proteins 0.000 description 3
- 210000002966 serum Anatomy 0.000 description 3
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 3
- 230000002103 transcriptional effect Effects 0.000 description 3
- 108010073969 valyllysine Proteins 0.000 description 3
- 101150084750 1 gene Proteins 0.000 description 2
- TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 description 2
- 102100035988 60S ribosomal protein L39 Human genes 0.000 description 2
- 102100036605 AN1-type zinc finger protein 6 Human genes 0.000 description 2
- 102100037651 AP-2 complex subunit sigma Human genes 0.000 description 2
- 102100022117 Abnormal spindle-like microcephaly-associated protein Human genes 0.000 description 2
- 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 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
- MQIGTEQXYCRLGK-BQBZGAKWSA-N Ala-Gly-Pro Chemical compound C[C@H](N)C(=O)NCC(=O)N1CCC[C@H]1C(O)=O MQIGTEQXYCRLGK-BQBZGAKWSA-N 0.000 description 2
- 102000000412 Annexin Human genes 0.000 description 2
- 108050008874 Annexin Proteins 0.000 description 2
- NVGWESORMHFISY-SRVKXCTJSA-N Asn-Asn-Phe Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O NVGWESORMHFISY-SRVKXCTJSA-N 0.000 description 2
- 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 2
- GGBQDSHTXKQSLP-NHCYSSNCSA-N Asp-Val-Lys Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CC(=O)O)N GGBQDSHTXKQSLP-NHCYSSNCSA-N 0.000 description 2
- 241000271566 Aves Species 0.000 description 2
- 101100079025 Avian myeloblastosis virus V-MYB gene Proteins 0.000 description 2
- 108700020472 CDC20 Proteins 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 101150023302 Cdc20 gene Proteins 0.000 description 2
- 108010060385 Cyclin B1 Proteins 0.000 description 2
- 102100034770 Cyclin-dependent kinase inhibitor 3 Human genes 0.000 description 2
- YNJBLTDKTMKEET-ZLUOBGJFSA-N Cys-Ser-Ser Chemical compound SC[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O YNJBLTDKTMKEET-ZLUOBGJFSA-N 0.000 description 2
- 102100035474 DNA polymerase kappa Human genes 0.000 description 2
- 102100036238 Dihydropyrimidinase Human genes 0.000 description 2
- 102100039577 ETS translocation variant 5 Human genes 0.000 description 2
- 108010089760 Electron Transport Complex I Proteins 0.000 description 2
- 102000008013 Electron Transport Complex I Human genes 0.000 description 2
- 102000010180 Endothelin receptor Human genes 0.000 description 2
- 108050001739 Endothelin receptor Proteins 0.000 description 2
- 206010053177 Epidermolysis Diseases 0.000 description 2
- 102000012858 Eukaryotic Initiation Factor-4G Human genes 0.000 description 2
- 108010057192 Eukaryotic Initiation Factor-4G Proteins 0.000 description 2
- 102100039737 Eukaryotic translation initiation factor 4 gamma 2 Human genes 0.000 description 2
- 102000010834 Extracellular Matrix Proteins Human genes 0.000 description 2
- 108010037362 Extracellular Matrix Proteins Proteins 0.000 description 2
- 102000018233 Fibroblast Growth Factor Human genes 0.000 description 2
- 108050007372 Fibroblast Growth Factor Proteins 0.000 description 2
- 102100020921 Follistatin Human genes 0.000 description 2
- 101150082239 G gene Proteins 0.000 description 2
- 102100024165 G1/S-specific cyclin-D1 Human genes 0.000 description 2
- 102100032340 G2/mitotic-specific cyclin-B1 Human genes 0.000 description 2
- 102100034004 Gamma-adducin Human genes 0.000 description 2
- 102100041007 Glia maturation factor gamma Human genes 0.000 description 2
- FALJZCPMTGJOHX-SRVKXCTJSA-N Gln-Met-Leu Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(C)C)C(O)=O FALJZCPMTGJOHX-SRVKXCTJSA-N 0.000 description 2
- FVGOGEGGQLNZGH-DZKIICNBSA-N Glu-Val-Phe Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 FVGOGEGGQLNZGH-DZKIICNBSA-N 0.000 description 2
- 102100031132 Glucose-6-phosphate isomerase Human genes 0.000 description 2
- 108010070600 Glucose-6-phosphate isomerase Proteins 0.000 description 2
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 2
- LYZYGGWCBLBDMC-QWHCGFSZSA-N Gly-Tyr-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CC=C(C=C2)O)NC(=O)CN)C(=O)O LYZYGGWCBLBDMC-QWHCGFSZSA-N 0.000 description 2
- ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 description 2
- 102000003886 Glycoproteins Human genes 0.000 description 2
- 108090000288 Glycoproteins Proteins 0.000 description 2
- 102100034523 Histone H4 Human genes 0.000 description 2
- 102000009331 Homeodomain Proteins Human genes 0.000 description 2
- 108010048671 Homeodomain Proteins Proteins 0.000 description 2
- 101000782083 Homo sapiens AN1-type zinc finger protein 6 Proteins 0.000 description 2
- 101000900939 Homo sapiens Abnormal spindle-like microcephaly-associated protein Proteins 0.000 description 2
- 101000623903 Homo sapiens Cell surface glycoprotein MUC18 Proteins 0.000 description 2
- 101001094659 Homo sapiens DNA polymerase kappa Proteins 0.000 description 2
- 101000865085 Homo sapiens DNA polymerase theta Proteins 0.000 description 2
- 101000813745 Homo sapiens ETS translocation variant 5 Proteins 0.000 description 2
- 101001034811 Homo sapiens Eukaryotic translation initiation factor 4 gamma 2 Proteins 0.000 description 2
- 101000980756 Homo sapiens G1/S-specific cyclin-D1 Proteins 0.000 description 2
- 101000868643 Homo sapiens G2/mitotic-specific cyclin-B1 Proteins 0.000 description 2
- 101000799011 Homo sapiens Gamma-adducin Proteins 0.000 description 2
- 101001039458 Homo sapiens Glia maturation factor gamma Proteins 0.000 description 2
- 101000887490 Homo sapiens Guanine nucleotide-binding protein G(z) subunit alpha Proteins 0.000 description 2
- 101001067880 Homo sapiens Histone H4 Proteins 0.000 description 2
- 101001000302 Homo sapiens Max-interacting protein 1 Proteins 0.000 description 2
- 101000957259 Homo sapiens Mitotic spindle assembly checkpoint protein MAD2A Proteins 0.000 description 2
- 101000611427 Homo sapiens Polyglutamine-binding protein 1 Proteins 0.000 description 2
- 101000974747 Homo sapiens Potassium channel subfamily K member 12 Proteins 0.000 description 2
- 101000741967 Homo sapiens Presequence protease, mitochondrial Proteins 0.000 description 2
- 101000610537 Homo sapiens Prokineticin-1 Proteins 0.000 description 2
- 101000856696 Homo sapiens Rho GDP-dissociation inhibitor 2 Proteins 0.000 description 2
- 101001103771 Homo sapiens Ribonuclease H2 subunit A Proteins 0.000 description 2
- 101001129076 Homo sapiens Serine/threonine-protein kinase N1 Proteins 0.000 description 2
- 101000837565 Homo sapiens Ubiquitin-conjugating enzyme E2 S Proteins 0.000 description 2
- 101000837581 Homo sapiens Ubiquitin-conjugating enzyme E2 T Proteins 0.000 description 2
- 108090000144 Human Proteins Proteins 0.000 description 2
- 102000003839 Human Proteins Human genes 0.000 description 2
- 102000014150 Interferons Human genes 0.000 description 2
- 108010050904 Interferons 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
- JNDYEOUZBLOVOF-AVGNSLFASA-N Leu-Leu-Gln Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O JNDYEOUZBLOVOF-AVGNSLFASA-N 0.000 description 2
- ILDSIMPXNFWKLH-KATARQTJSA-N Leu-Thr-Ser Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(O)=O ILDSIMPXNFWKLH-KATARQTJSA-N 0.000 description 2
- NQCJGQHHYZNUDK-DCAQKATOSA-N Lys-Arg-Ser Chemical compound NCCCC[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CO)C(O)=O)CCCN=C(N)N NQCJGQHHYZNUDK-DCAQKATOSA-N 0.000 description 2
- BYPMOIFBQPEWOH-CIUDSAMLSA-N Lys-Asn-Asp Chemical compound C(CCN)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC(=O)O)C(=O)O)N BYPMOIFBQPEWOH-CIUDSAMLSA-N 0.000 description 2
- FLCMXEFCTLXBTL-DCAQKATOSA-N Lys-Asp-Arg Chemical compound C(CCN)C[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)N FLCMXEFCTLXBTL-DCAQKATOSA-N 0.000 description 2
- 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 2
- SVSQSPICRKBMSZ-SRVKXCTJSA-N Lys-Pro-Gln Chemical compound [H]N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(O)=O SVSQSPICRKBMSZ-SRVKXCTJSA-N 0.000 description 2
- 102000000380 Matrix Metalloproteinase 1 Human genes 0.000 description 2
- 108010016113 Matrix Metalloproteinase 1 Proteins 0.000 description 2
- 108010040897 Microfilament Proteins Proteins 0.000 description 2
- 102100038792 Mitotic spindle assembly checkpoint protein MAD2A Human genes 0.000 description 2
- 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 2
- 206010028980 Neoplasm Diseases 0.000 description 2
- 108010027206 Nucleopolyhedrovirus inhibitor of apoptosis Proteins 0.000 description 2
- 102000011931 Nucleoproteins Human genes 0.000 description 2
- 108010061100 Nucleoproteins Proteins 0.000 description 2
- XMQSOOJRRVEHRO-ULQDDVLXSA-N Phe-Leu-Arg Chemical compound NC(N)=NCCC[C@@H](C(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CC1=CC=CC=C1 XMQSOOJRRVEHRO-ULQDDVLXSA-N 0.000 description 2
- 102100030477 Plectin Human genes 0.000 description 2
- 108010054050 Plectin Proteins 0.000 description 2
- 102100040748 Polyglutamine-binding protein 1 Human genes 0.000 description 2
- 102100022801 Potassium channel subfamily K member 12 Human genes 0.000 description 2
- 102100038632 Presequence protease, mitochondrial Human genes 0.000 description 2
- 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 2
- 229940124158 Protease/peptidase inhibitor Drugs 0.000 description 2
- 102000004022 Protein-Tyrosine Kinases Human genes 0.000 description 2
- 108090000412 Protein-Tyrosine Kinases Proteins 0.000 description 2
- 102100025622 Rho GDP-dissociation inhibitor 2 Human genes 0.000 description 2
- 102100039493 Ribonuclease H2 subunit A Human genes 0.000 description 2
- 101100010298 Schizosaccharomyces pombe (strain 972 / ATCC 24843) pol2 gene Proteins 0.000 description 2
- HRNQLKCLPVKZNE-CIUDSAMLSA-N Ser-Ala-Leu Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(O)=O HRNQLKCLPVKZNE-CIUDSAMLSA-N 0.000 description 2
- CDVFZMOFNJPUDD-ACZMJKKPSA-N Ser-Gln-Asn Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O CDVFZMOFNJPUDD-ACZMJKKPSA-N 0.000 description 2
- PTWIYDNFWPXQSD-GARJFASQSA-N Ser-Lys-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CCCCN)NC(=O)[C@H](CO)N)C(=O)O PTWIYDNFWPXQSD-GARJFASQSA-N 0.000 description 2
- XQJCEKXQUJQNNK-ZLUOBGJFSA-N Ser-Ser-Ser Chemical compound OC[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O XQJCEKXQUJQNNK-ZLUOBGJFSA-N 0.000 description 2
- 102100031206 Serine/threonine-protein kinase N1 Human genes 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 208000022758 Sorsby fundus dystrophy Diseases 0.000 description 2
- 108010002687 Survivin Proteins 0.000 description 2
- 102000000763 Survivin Human genes 0.000 description 2
- ABWNZPOIUJMNKT-IXOXFDKPSA-N Thr-Phe-Ser Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(O)=O ABWNZPOIUJMNKT-IXOXFDKPSA-N 0.000 description 2
- 108010000499 Thromboplastin Proteins 0.000 description 2
- 102000002262 Thromboplastin Human genes 0.000 description 2
- 108060008682 Tumor Necrosis Factor Proteins 0.000 description 2
- 102100028705 Ubiquitin-conjugating enzyme E2 T Human genes 0.000 description 2
- DOBHJKVVACOQTN-DZKIICNBSA-N Val-Tyr-Gln Chemical compound NC(=O)CC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)C(C)C)CC1=CC=C(O)C=C1 DOBHJKVVACOQTN-DZKIICNBSA-N 0.000 description 2
- 241000700605 Viruses Species 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 210000001789 adipocyte Anatomy 0.000 description 2
- 108010044940 alanylglutamine Proteins 0.000 description 2
- 108010047495 alanylglycine Proteins 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 108010061189 anillin Proteins 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 108010062796 arginyllysine Proteins 0.000 description 2
- 108010077245 asparaginyl-proline Proteins 0.000 description 2
- 108010047857 aspartylglycine Proteins 0.000 description 2
- 210000000721 basilar membrane Anatomy 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000005340 bisphosphate group Chemical group 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 230000022131 cell cycle Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- AGVAZMGAQJOSFJ-WZHZPDAFSA-M cobalt(2+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+2].N#[C-].[N-]([C@@H]1[C@H](CC(N)=O)[C@@]2(C)CCC(=O)NC[C@@H](C)OP(O)(=O)O[C@H]3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)\C2=C(C)/C([C@H](C\2(C)C)CCC(N)=O)=N/C/2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O AGVAZMGAQJOSFJ-WZHZPDAFSA-M 0.000 description 2
- 239000002299 complementary DNA Substances 0.000 description 2
- 238000013016 damping Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 108091022884 dihydropyrimidinase Proteins 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 230000009762 endothelial cell differentiation Effects 0.000 description 2
- 210000002744 extracellular matrix Anatomy 0.000 description 2
- 229940126864 fibroblast growth factor Drugs 0.000 description 2
- 102000006482 fibulin Human genes 0.000 description 2
- 108010044392 fibulin Proteins 0.000 description 2
- 230000004992 fission Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 230000006377 glucose transport Effects 0.000 description 2
- VPZXBVLAVMBEQI-UHFFFAOYSA-N glycyl-DL-alpha-alanine Natural products OC(=O)C(C)NC(=O)CN VPZXBVLAVMBEQI-UHFFFAOYSA-N 0.000 description 2
- 108010037850 glycylvaline Proteins 0.000 description 2
- 208000006454 hepatitis Diseases 0.000 description 2
- 231100000283 hepatitis Toxicity 0.000 description 2
- 102000047813 human CCNB1 Human genes 0.000 description 2
- 102000052301 human GNAZ Human genes 0.000 description 2
- 230000001965 increasing effect Effects 0.000 description 2
- 229940079322 interferon Drugs 0.000 description 2
- 210000003963 intermediate filament Anatomy 0.000 description 2
- 108010028930 invariant chain Proteins 0.000 description 2
- 108010011989 karyopherin alpha 2 Proteins 0.000 description 2
- 108010009298 lysylglutamic acid Proteins 0.000 description 2
- 108010054155 lysyllysine Proteins 0.000 description 2
- 210000004379 membrane Anatomy 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 230000004060 metabolic process Effects 0.000 description 2
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 2
- 210000003205 muscle Anatomy 0.000 description 2
- 210000004498 neuroglial cell Anatomy 0.000 description 2
- 150000002891 organic anions Chemical class 0.000 description 2
- 230000002018 overexpression Effects 0.000 description 2
- 229920002643 polyglutamic acid Polymers 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000186 progesterone Substances 0.000 description 2
- 229960003387 progesterone Drugs 0.000 description 2
- 230000035755 proliferation Effects 0.000 description 2
- 230000022983 regulation of cell cycle Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000000837 restrainer Substances 0.000 description 2
- 108091008146 restriction endonucleases Proteins 0.000 description 2
- 150000004492 retinoid derivatives Chemical class 0.000 description 2
- 108010025387 ribosomal protein L39 Proteins 0.000 description 2
- 229920002477 rna polymer Polymers 0.000 description 2
- 108010069117 seryl-lysyl-aspartic acid Proteins 0.000 description 2
- 108010048397 seryl-lysyl-leucine Proteins 0.000 description 2
- 230000017423 tissue regeneration Effects 0.000 description 2
- 230000001131 transforming effect Effects 0.000 description 2
- 108010084736 ubiquitin carrier proteins Proteins 0.000 description 2
- 230000002792 vascular Effects 0.000 description 2
- 210000004885 white matter Anatomy 0.000 description 2
- HSKCCNHLWZSIDN-LZVKGNEYSA-N (2s)-2-[[(2s)-1-[(2s)-2-[[2-[[(2r)-2-[[(2s)-5-(diaminomethylideneamino)-2-[[(2s)-pyrrolidine-2-carbonyl]amino]pentanoyl]amino]-3-sulfanylpropanoyl]amino]acetyl]amino]-3-methylbutanoyl]pyrrolidine-2-carbonyl]amino]butanedioic acid Chemical compound N([C@@H](CCCN=C(N)N)C(=O)N[C@@H](CS)C(=O)NCC(=O)N[C@@H](C(C)C)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC(O)=O)C(O)=O)C(=O)[C@@H]1CCCN1 HSKCCNHLWZSIDN-LZVKGNEYSA-N 0.000 description 1
- DWNBOPVKNPVNQG-LURJTMIESA-N (2s)-4-hydroxy-2-(propylamino)butanoic acid Chemical compound CCCN[C@H](C(O)=O)CCO DWNBOPVKNPVNQG-LURJTMIESA-N 0.000 description 1
- NOUIAHOPEGZYFE-JPLJXNOCSA-N (3S)-4-[[(2S)-1-[[(1S)-1-carboxy-2-(4-hydroxyphenyl)ethyl]amino]-3-methyl-1-oxobutan-2-yl]amino]-3-[[(2S)-2,6-diaminohexanoyl]amino]-4-oxobutanoic acid Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O NOUIAHOPEGZYFE-JPLJXNOCSA-N 0.000 description 1
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 description 1
- OTEWWRBKGONZBW-UHFFFAOYSA-N 2-[[2-[[2-[(2-azaniumylacetyl)amino]-4-methylpentanoyl]amino]acetyl]amino]acetate Chemical compound NCC(=O)NC(CC(C)C)C(=O)NCC(=O)NCC(O)=O OTEWWRBKGONZBW-UHFFFAOYSA-N 0.000 description 1
- KPGXRSRHYNQIFN-UHFFFAOYSA-N 2-oxoglutaric acid Chemical compound OC(=O)CCC(=O)C(O)=O KPGXRSRHYNQIFN-UHFFFAOYSA-N 0.000 description 1
- KPGXRSRHYNQIFN-HOSYLAQJSA-N 2-oxopentanedioic acid Chemical class OC(=O)CCC(=O)[13C](O)=O KPGXRSRHYNQIFN-HOSYLAQJSA-N 0.000 description 1
- 101150070093 AG gene Proteins 0.000 description 1
- YLTKNGYYPIWKHZ-ACZMJKKPSA-N Ala-Ala-Glu Chemical compound C[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@H](C(O)=O)CCC(O)=O YLTKNGYYPIWKHZ-ACZMJKKPSA-N 0.000 description 1
- 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 1
- WQVFQXXBNHHPLX-ZKWXMUAHSA-N Ala-Ala-His Chemical compound C[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1cnc[nH]1)C(O)=O WQVFQXXBNHHPLX-ZKWXMUAHSA-N 0.000 description 1
- 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 1
- XQGIRPGAVLFKBJ-CIUDSAMLSA-N Ala-Asn-Lys Chemical compound N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)O XQGIRPGAVLFKBJ-CIUDSAMLSA-N 0.000 description 1
- KIUYPHAMDKDICO-WHFBIAKZSA-N Ala-Asp-Gly Chemical compound C[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)NCC(O)=O KIUYPHAMDKDICO-WHFBIAKZSA-N 0.000 description 1
- GWFSQQNGMPGBEF-GHCJXIJMSA-N Ala-Asp-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](C)N GWFSQQNGMPGBEF-GHCJXIJMSA-N 0.000 description 1
- ZIWWTZWAKYBUOB-CIUDSAMLSA-N Ala-Asp-Leu Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(O)=O ZIWWTZWAKYBUOB-CIUDSAMLSA-N 0.000 description 1
- BUDNAJYVCUHLSV-ZLUOBGJFSA-N Ala-Asp-Ser Chemical compound C[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(O)=O BUDNAJYVCUHLSV-ZLUOBGJFSA-N 0.000 description 1
- 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
- RXTBLQVXNIECFP-FXQIFTODSA-N Ala-Gln-Gln Chemical compound C[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O RXTBLQVXNIECFP-FXQIFTODSA-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
- XYTNPQNAZREREP-XQXXSGGOSA-N Ala-Glu-Thr Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O XYTNPQNAZREREP-XQXXSGGOSA-N 0.000 description 1
- ZVFVBBGVOILKPO-WHFBIAKZSA-N Ala-Gly-Ala Chemical compound C[C@H](N)C(=O)NCC(=O)N[C@@H](C)C(O)=O ZVFVBBGVOILKPO-WHFBIAKZSA-N 0.000 description 1
- OBVSBEYOMDWLRJ-BFHQHQDPSA-N Ala-Gly-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)CNC(=O)[C@H](C)N OBVSBEYOMDWLRJ-BFHQHQDPSA-N 0.000 description 1
- OKEWAFFWMHBGPT-XPUUQOCRSA-N Ala-His-Gly Chemical compound OC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](N)C)CC1=CN=CN1 OKEWAFFWMHBGPT-XPUUQOCRSA-N 0.000 description 1
- GSHKMNKPMLXSQW-KBIXCLLPSA-N Ala-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](C)N GSHKMNKPMLXSQW-KBIXCLLPSA-N 0.000 description 1
- RZZMZYZXNJRPOJ-BJDJZHNGSA-N Ala-Ile-Lys Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](C)N RZZMZYZXNJRPOJ-BJDJZHNGSA-N 0.000 description 1
- HHRAXZAYZFFRAM-CIUDSAMLSA-N Ala-Leu-Asn Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(O)=O HHRAXZAYZFFRAM-CIUDSAMLSA-N 0.000 description 1
- NOGFDULFCFXBHB-CIUDSAMLSA-N Ala-Leu-Cys Chemical compound C[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CS)C(=O)O)N NOGFDULFCFXBHB-CIUDSAMLSA-N 0.000 description 1
- SUMYEVXWCAYLLJ-GUBZILKMSA-N Ala-Leu-Gln Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O SUMYEVXWCAYLLJ-GUBZILKMSA-N 0.000 description 1
- CCDFBRZVTDDJNM-GUBZILKMSA-N Ala-Leu-Glu Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O CCDFBRZVTDDJNM-GUBZILKMSA-N 0.000 description 1
- MNZHHDPWDWQJCQ-YUMQZZPRSA-N Ala-Leu-Gly Chemical compound C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)NCC(O)=O MNZHHDPWDWQJCQ-YUMQZZPRSA-N 0.000 description 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
- OPZJWMJPCNNZNT-DCAQKATOSA-N Ala-Leu-Met Chemical compound C[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)O)N OPZJWMJPCNNZNT-DCAQKATOSA-N 0.000 description 1
- PMQXMXAASGFUDX-SRVKXCTJSA-N Ala-Lys-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@H](C)N)CCCCN PMQXMXAASGFUDX-SRVKXCTJSA-N 0.000 description 1
- MDNAVFBZPROEHO-UHFFFAOYSA-N Ala-Lys-Val Natural products CC(C)C(C(O)=O)NC(=O)C(NC(=O)C(C)N)CCCCN MDNAVFBZPROEHO-UHFFFAOYSA-N 0.000 description 1
- RAAWHFXHAACDFT-FXQIFTODSA-N Ala-Met-Asn Chemical compound CSCC[C@H](NC(=O)[C@H](C)N)C(=O)N[C@@H](CC(N)=O)C(O)=O RAAWHFXHAACDFT-FXQIFTODSA-N 0.000 description 1
- MAEQBGQTDWDSJQ-LSJOCFKGSA-N Ala-Met-His Chemical compound C[C@@H](C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)N MAEQBGQTDWDSJQ-LSJOCFKGSA-N 0.000 description 1
- 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 1
- YCRAFFCYWOUEOF-DLOVCJGASA-N Ala-Phe-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)C)CC1=CC=CC=C1 YCRAFFCYWOUEOF-DLOVCJGASA-N 0.000 description 1
- IHMCQESUJVZTKW-UBHSHLNASA-N Ala-Phe-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@H](C)N)CC1=CC=CC=C1 IHMCQESUJVZTKW-UBHSHLNASA-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
- CQJHFKKGZXKZBC-BPNCWPANSA-N Ala-Pro-Tyr Chemical compound C[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 CQJHFKKGZXKZBC-BPNCWPANSA-N 0.000 description 1
- OEVCHROQUIVQFZ-YTLHQDLWSA-N Ala-Thr-Ala Chemical compound C[C@H](N)C(=O)N[C@@H]([C@H](O)C)C(=O)N[C@@H](C)C(O)=O OEVCHROQUIVQFZ-YTLHQDLWSA-N 0.000 description 1
- YNOCMHZSWJMGBB-GCJQMDKQSA-N Ala-Thr-Asp Chemical compound [H]N[C@@H](C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(O)=O YNOCMHZSWJMGBB-GCJQMDKQSA-N 0.000 description 1
- 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 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
- 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 1
- XPBVBZPVNFIHOA-UVBJJODRSA-N Ala-Trp-Val Chemical compound C1=CC=C2C(C[C@@H](C(=O)N[C@@H](C(C)C)C(O)=O)NC(=O)[C@H](C)N)=CNC2=C1 XPBVBZPVNFIHOA-UVBJJODRSA-N 0.000 description 1
- BGGAIXWIZCIFSG-XDTLVQLUSA-N Ala-Tyr-Glu Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CCC(O)=O)C(O)=O BGGAIXWIZCIFSG-XDTLVQLUSA-N 0.000 description 1
- 102000013918 Apolipoproteins E Human genes 0.000 description 1
- 108010025628 Apolipoproteins E Proteins 0.000 description 1
- XPSGESXVBSQZPL-SRVKXCTJSA-N Arg-Arg-Arg Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O XPSGESXVBSQZPL-SRVKXCTJSA-N 0.000 description 1
- UXJCMQFPDWCHKX-DCAQKATOSA-N Arg-Arg-Glu Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(O)=O)C(O)=O UXJCMQFPDWCHKX-DCAQKATOSA-N 0.000 description 1
- UISQLSIBJKEJSS-GUBZILKMSA-N Arg-Arg-Ser Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CO)C(O)=O UISQLSIBJKEJSS-GUBZILKMSA-N 0.000 description 1
- GHNDBBVSWOWYII-LPEHRKFASA-N Arg-Asn-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC(=O)N)NC(=O)[C@H](CCCN=C(N)N)N)C(=O)O GHNDBBVSWOWYII-LPEHRKFASA-N 0.000 description 1
- IIABBYGHLYWVOS-FXQIFTODSA-N Arg-Asn-Ser Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(O)=O IIABBYGHLYWVOS-FXQIFTODSA-N 0.000 description 1
- XVLLUZMFSAYKJV-GUBZILKMSA-N Arg-Asp-Arg Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O XVLLUZMFSAYKJV-GUBZILKMSA-N 0.000 description 1
- OZNSCVPYWZRQPY-CIUDSAMLSA-N Arg-Asp-Glu Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(O)=O OZNSCVPYWZRQPY-CIUDSAMLSA-N 0.000 description 1
- HKRXJBBCQBAGIM-FXQIFTODSA-N Arg-Asp-Ser Chemical compound C(C[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CO)C(=O)O)N)CN=C(N)N HKRXJBBCQBAGIM-FXQIFTODSA-N 0.000 description 1
- QQJSJIBESHAJPM-IHRRRGAJSA-N Arg-Cys-Tyr Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CS)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 QQJSJIBESHAJPM-IHRRRGAJSA-N 0.000 description 1
- PTVGLOCPAVYPFG-CIUDSAMLSA-N Arg-Gln-Asp Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(O)=O PTVGLOCPAVYPFG-CIUDSAMLSA-N 0.000 description 1
- LMPKCSXZJSXBBL-NHCYSSNCSA-N Arg-Gln-Val Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C(C)C)C(O)=O LMPKCSXZJSXBBL-NHCYSSNCSA-N 0.000 description 1
- PPPXVIBMLFWNSK-BQBZGAKWSA-N Arg-Gly-Cys Chemical compound C(C[C@@H](C(=O)NCC(=O)N[C@@H](CS)C(=O)O)N)CN=C(N)N PPPXVIBMLFWNSK-BQBZGAKWSA-N 0.000 description 1
- ZATRYQNPUHGXCU-DTWKUNHWSA-N Arg-Gly-Pro Chemical compound C1C[C@@H](N(C1)C(=O)CNC(=O)[C@H](CCCN=C(N)N)N)C(=O)O ZATRYQNPUHGXCU-DTWKUNHWSA-N 0.000 description 1
- OOIMKQRCPJBGPD-XUXIUFHCSA-N Arg-Ile-Leu Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(O)=O OOIMKQRCPJBGPD-XUXIUFHCSA-N 0.000 description 1
- GMFAGHNRXPSSJS-SRVKXCTJSA-N Arg-Leu-Gln Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O GMFAGHNRXPSSJS-SRVKXCTJSA-N 0.000 description 1
- JEXPNDORFYHJTM-IHRRRGAJSA-N Arg-Leu-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CCCN=C(N)N JEXPNDORFYHJTM-IHRRRGAJSA-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
- JOTRDIXZHNQYGP-DCAQKATOSA-N Arg-Ser-Lys Chemical compound C(CCN)C[C@@H](C(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](CCCN=C(N)N)N JOTRDIXZHNQYGP-DCAQKATOSA-N 0.000 description 1
- JPAWCMXVNZPJLO-IHRRRGAJSA-N Arg-Ser-Phe Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O JPAWCMXVNZPJLO-IHRRRGAJSA-N 0.000 description 1
- RYQSYXFGFOTJDJ-RHYQMDGZSA-N Arg-Thr-Leu Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(O)=O RYQSYXFGFOTJDJ-RHYQMDGZSA-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
- AZHXYLJRGVMQKW-UMPQAUOISA-N Arg-Trp-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC1=CNC2=CC=CC=C21)NC(=O)[C@H](CCCN=C(N)N)N)O AZHXYLJRGVMQKW-UMPQAUOISA-N 0.000 description 1
- VJIQPOJMISSUPO-BVSLBCMMSA-N Arg-Trp-Tyr Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O VJIQPOJMISSUPO-BVSLBCMMSA-N 0.000 description 1
- NMTANZXPDAHUKU-ULQDDVLXSA-N Arg-Tyr-Lys Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(O)=O)CC1=CC=C(O)C=C1 NMTANZXPDAHUKU-ULQDDVLXSA-N 0.000 description 1
- WTUZDHWWGUQEKN-SRVKXCTJSA-N Arg-Val-Met Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCSC)C(O)=O WTUZDHWWGUQEKN-SRVKXCTJSA-N 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- QEYJFBMTSMLPKZ-ZKWXMUAHSA-N Asn-Ala-Val Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(O)=O QEYJFBMTSMLPKZ-ZKWXMUAHSA-N 0.000 description 1
- HUZGPXBILPMCHM-IHRRRGAJSA-N Asn-Arg-Phe Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O HUZGPXBILPMCHM-IHRRRGAJSA-N 0.000 description 1
- GOVUDFOGXOONFT-VEVYYDQMSA-N Asn-Arg-Thr Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(O)=O GOVUDFOGXOONFT-VEVYYDQMSA-N 0.000 description 1
- IOTKDTZEEBZNCM-UGYAYLCHSA-N Asn-Asn-Ile Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O IOTKDTZEEBZNCM-UGYAYLCHSA-N 0.000 description 1
- ZWASIOHRQWRWAS-UGYAYLCHSA-N Asn-Asp-Ile Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O ZWASIOHRQWRWAS-UGYAYLCHSA-N 0.000 description 1
- WQSCVMQDZYTFQU-FXQIFTODSA-N Asn-Cys-Arg Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O WQSCVMQDZYTFQU-FXQIFTODSA-N 0.000 description 1
- ZPMNECSEJXXNBE-CIUDSAMLSA-N Asn-Cys-Leu Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CS)C(=O)N[C@@H](CC(C)C)C(O)=O ZPMNECSEJXXNBE-CIUDSAMLSA-N 0.000 description 1
- DDPXDCKYWDGZAL-BQBZGAKWSA-N Asn-Gly-Arg Chemical compound NC(=O)C[C@H](N)C(=O)NCC(=O)N[C@H](C(O)=O)CCCN=C(N)N DDPXDCKYWDGZAL-BQBZGAKWSA-N 0.000 description 1
- OLVIPTLKNSAYRJ-YUMQZZPRSA-N Asn-Gly-Lys Chemical compound C(CCN)C[C@@H](C(=O)O)NC(=O)CNC(=O)[C@H](CC(=O)N)N OLVIPTLKNSAYRJ-YUMQZZPRSA-N 0.000 description 1
- RAQMSGVCGSJKCL-FOHZUACHSA-N Asn-Gly-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)CC(N)=O RAQMSGVCGSJKCL-FOHZUACHSA-N 0.000 description 1
- 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 1
- 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 1
- IBLAOXSULLECQZ-IUKAMOBKSA-N Asn-Ile-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@@H](N)CC(N)=O IBLAOXSULLECQZ-IUKAMOBKSA-N 0.000 description 1
- WIDVAWAQBRAKTI-YUMQZZPRSA-N Asn-Leu-Gly Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)NCC(O)=O WIDVAWAQBRAKTI-YUMQZZPRSA-N 0.000 description 1
- JLNFZLNDHONLND-GARJFASQSA-N Asn-Leu-Pro Chemical compound CC(C)C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CC(=O)N)N JLNFZLNDHONLND-GARJFASQSA-N 0.000 description 1
- FHETWELNCBMRMG-HJGDQZAQSA-N Asn-Leu-Thr Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O FHETWELNCBMRMG-HJGDQZAQSA-N 0.000 description 1
- NTWOPSIUJBMNRI-KKUMJFAQSA-N Asn-Lys-Tyr Chemical compound NC(=O)C[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 NTWOPSIUJBMNRI-KKUMJFAQSA-N 0.000 description 1
- LSJQOMAZIKQMTJ-SRVKXCTJSA-N Asn-Phe-Asp Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC(O)=O)C(O)=O LSJQOMAZIKQMTJ-SRVKXCTJSA-N 0.000 description 1
- QXOPPIDJKPEKCW-GUBZILKMSA-N Asn-Pro-Arg Chemical compound C1C[C@H](N(C1)C(=O)[C@H](CC(=O)N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O QXOPPIDJKPEKCW-GUBZILKMSA-N 0.000 description 1
- BYLSYQASFJJBCL-DCAQKATOSA-N Asn-Pro-Leu Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(O)=O BYLSYQASFJJBCL-DCAQKATOSA-N 0.000 description 1
- VHQSGALUSWIYOD-QXEWZRGKSA-N Asn-Pro-Val Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(O)=O VHQSGALUSWIYOD-QXEWZRGKSA-N 0.000 description 1
- GZXOUBTUAUAVHD-ACZMJKKPSA-N Asn-Ser-Glu Chemical compound NC(=O)C[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CCC(O)=O GZXOUBTUAUAVHD-ACZMJKKPSA-N 0.000 description 1
- XHTUGJCAEYOZOR-UBHSHLNASA-N Asn-Ser-Trp Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O XHTUGJCAEYOZOR-UBHSHLNASA-N 0.000 description 1
- 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 1
- FMNBYVSGRCXWEK-FOHZUACHSA-N Asn-Thr-Gly Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(O)=O FMNBYVSGRCXWEK-FOHZUACHSA-N 0.000 description 1
- DPWDPEVGACCWTC-SRVKXCTJSA-N Asn-Tyr-Ser 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](CO)C(O)=O DPWDPEVGACCWTC-SRVKXCTJSA-N 0.000 description 1
- WQAOZCVOOYUWKG-LSJOCFKGSA-N Asn-Val-Val Chemical compound CC(C)[C@@H](C(=O)N[C@@H](C(C)C)C(=O)O)NC(=O)[C@H](CC(=O)N)N WQAOZCVOOYUWKG-LSJOCFKGSA-N 0.000 description 1
- KRXIWXCXOARFNT-ZLUOBGJFSA-N Asp-Ala-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC(O)=O KRXIWXCXOARFNT-ZLUOBGJFSA-N 0.000 description 1
- XBQSLMACWDXWLJ-GHCJXIJMSA-N Asp-Ala-Ile Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O XBQSLMACWDXWLJ-GHCJXIJMSA-N 0.000 description 1
- BUVNWKQBMZLCDW-UGYAYLCHSA-N Asp-Asn-Ile Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O BUVNWKQBMZLCDW-UGYAYLCHSA-N 0.000 description 1
- KNMRXHIAVXHCLW-ZLUOBGJFSA-N Asp-Asn-Ser Chemical compound C([C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CO)C(=O)O)N)C(=O)O KNMRXHIAVXHCLW-ZLUOBGJFSA-N 0.000 description 1
- RRKCPMGSRIDLNC-AVGNSLFASA-N Asp-Glu-Tyr Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O RRKCPMGSRIDLNC-AVGNSLFASA-N 0.000 description 1
- DTNUIAJCPRMNBT-WHFBIAKZSA-N Asp-Gly-Ala Chemical compound [H]N[C@@H](CC(O)=O)C(=O)NCC(=O)N[C@@H](C)C(O)=O DTNUIAJCPRMNBT-WHFBIAKZSA-N 0.000 description 1
- KHGPWGKPYHPOIK-QWRGUYRKSA-N Asp-Gly-Phe Chemical compound [H]N[C@@H](CC(O)=O)C(=O)NCC(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O KHGPWGKPYHPOIK-QWRGUYRKSA-N 0.000 description 1
- KPNUCOPMVSGRCR-DCAQKATOSA-N Asp-His-Arg Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O KPNUCOPMVSGRCR-DCAQKATOSA-N 0.000 description 1
- OOXKFYNWRVGYFM-XIRDDKMYSA-N Asp-His-Trp Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)O)NC(=O)[C@H](CC3=CN=CN3)NC(=O)[C@H](CC(=O)O)N OOXKFYNWRVGYFM-XIRDDKMYSA-N 0.000 description 1
- SEMWSADZTMJELF-BYULHYEWSA-N Asp-Ile-Gly Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(O)=O SEMWSADZTMJELF-BYULHYEWSA-N 0.000 description 1
- AYFVRYXNDHBECD-YUMQZZPRSA-N Asp-Leu-Gly Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)NCC(O)=O AYFVRYXNDHBECD-YUMQZZPRSA-N 0.000 description 1
- CTWCFPWFIGRAEP-CIUDSAMLSA-N Asp-Lys-Asp Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(O)=O CTWCFPWFIGRAEP-CIUDSAMLSA-N 0.000 description 1
- QNIACYURSSCLRP-GUBZILKMSA-N Asp-Lys-Gln Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(O)=O QNIACYURSSCLRP-GUBZILKMSA-N 0.000 description 1
- RPUYTJJZXQBWDT-SRVKXCTJSA-N Asp-Phe-Ser Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](CC(=O)O)N RPUYTJJZXQBWDT-SRVKXCTJSA-N 0.000 description 1
- QSFHZPQUAAQHAQ-CIUDSAMLSA-N Asp-Ser-Leu Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(O)=O QSFHZPQUAAQHAQ-CIUDSAMLSA-N 0.000 description 1
- NVXLFIPTHPKSKL-UBHSHLNASA-N Asp-Trp-Asn Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@H](CC(O)=O)N)C(=O)N[C@@H](CC(N)=O)C(O)=O)=CNC2=C1 NVXLFIPTHPKSKL-UBHSHLNASA-N 0.000 description 1
- WAEDSQFVZJUHLI-BYULHYEWSA-N Asp-Val-Asp Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(O)=O WAEDSQFVZJUHLI-BYULHYEWSA-N 0.000 description 1
- GYNUXDMCDILYIQ-QRTARXTBSA-N Asp-Val-Trp Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)O)NC(=O)[C@H](CC(=O)O)N GYNUXDMCDILYIQ-QRTARXTBSA-N 0.000 description 1
- 229940126074 CDK kinase inhibitor Drugs 0.000 description 1
- 102100033210 CUGBP Elav-like family member 2 Human genes 0.000 description 1
- 101710170321 CUGBP Elav-like family member 2 Proteins 0.000 description 1
- 101100005789 Caenorhabditis elegans cdk-4 gene Proteins 0.000 description 1
- 102100023126 Cell surface glycoprotein MUC18 Human genes 0.000 description 1
- 102100022641 Coagulation factor IX Human genes 0.000 description 1
- 102100024335 Collagen alpha-1(VII) chain Human genes 0.000 description 1
- 101710157591 Cyclin-dependent kinase inhibitor 3 Proteins 0.000 description 1
- KLLFLHBKSJAUMZ-ACZMJKKPSA-N Cys-Asn-Glu Chemical compound C(CC(=O)O)[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CS)N KLLFLHBKSJAUMZ-ACZMJKKPSA-N 0.000 description 1
- YZFCGHIBLBDZDA-ZLUOBGJFSA-N Cys-Asp-Ser Chemical compound [H]N[C@@H](CS)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(O)=O YZFCGHIBLBDZDA-ZLUOBGJFSA-N 0.000 description 1
- QJUDRFBUWAGUSG-SRVKXCTJSA-N Cys-Cys-Phe Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)O)NC(=O)[C@H](CS)NC(=O)[C@H](CS)N QJUDRFBUWAGUSG-SRVKXCTJSA-N 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
- XZKJEOMFLDVXJG-KATARQTJSA-N Cys-Leu-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CS)N)O XZKJEOMFLDVXJG-KATARQTJSA-N 0.000 description 1
- YFKWIIRWHGKSQQ-WFBYXXMGSA-N Cys-Trp-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CC1=CNC2=CC=CC=C21)NC(=O)[C@H](CS)N YFKWIIRWHGKSQQ-WFBYXXMGSA-N 0.000 description 1
- 108010070977 Cytoplasmic Dyneins Proteins 0.000 description 1
- 102000005362 Cytoplasmic Dyneins Human genes 0.000 description 1
- 238000002965 ELISA Methods 0.000 description 1
- 206010014989 Epidermolysis bullosa Diseases 0.000 description 1
- 108010076282 Factor IX Proteins 0.000 description 1
- 102100024785 Fibroblast growth factor 2 Human genes 0.000 description 1
- 108090000379 Fibroblast growth factor 2 Proteins 0.000 description 1
- 102000016970 Follistatin Human genes 0.000 description 1
- 108010014612 Follistatin Proteins 0.000 description 1
- 101150082479 GAL gene Proteins 0.000 description 1
- 102100030479 Germinal center-associated signaling and motility protein Human genes 0.000 description 1
- LKUWAWGNJYJODH-KBIXCLLPSA-N Gln-Ala-Ile Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O LKUWAWGNJYJODH-KBIXCLLPSA-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
- WOACHWLUOFZLGJ-GUBZILKMSA-N Gln-Arg-Gln Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(N)=O)C(O)=O WOACHWLUOFZLGJ-GUBZILKMSA-N 0.000 description 1
- ULXXDWZMMSQBDC-ACZMJKKPSA-N Gln-Asp-Asp Chemical compound C(CC(=O)N)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)O)N ULXXDWZMMSQBDC-ACZMJKKPSA-N 0.000 description 1
- SOIAHPSKKUYREP-CIUDSAMLSA-N Gln-Asp-Met Chemical compound CSCC[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCC(=O)N)N SOIAHPSKKUYREP-CIUDSAMLSA-N 0.000 description 1
- IXFVOPOHSRKJNG-LAEOZQHASA-N Gln-Asp-Val Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(O)=O IXFVOPOHSRKJNG-LAEOZQHASA-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
- KVXVVDFOZNYYKZ-DCAQKATOSA-N Gln-Gln-Leu Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(O)=O KVXVVDFOZNYYKZ-DCAQKATOSA-N 0.000 description 1
- RBWKVOSARCFSQQ-FXQIFTODSA-N Gln-Gln-Ser Chemical compound NC(=O)CC[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CO)C(O)=O RBWKVOSARCFSQQ-FXQIFTODSA-N 0.000 description 1
- LFIVHGMKWFGUGK-IHRRRGAJSA-N Gln-Glu-Phe Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)N)N LFIVHGMKWFGUGK-IHRRRGAJSA-N 0.000 description 1
- FGYPOQPQTUNESW-IUCAKERBSA-N Gln-Gly-Leu Chemical compound CC(C)C[C@@H](C(=O)O)NC(=O)CNC(=O)[C@H](CCC(=O)N)N FGYPOQPQTUNESW-IUCAKERBSA-N 0.000 description 1
- HXOLDXKNWKLDMM-YVNDNENWSA-N Gln-Ile-Glu Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)O)NC(=O)[C@H](CCC(=O)N)N HXOLDXKNWKLDMM-YVNDNENWSA-N 0.000 description 1
- HYPVLWGNBIYTNA-GUBZILKMSA-N Gln-Leu-Ala Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(O)=O HYPVLWGNBIYTNA-GUBZILKMSA-N 0.000 description 1
- IHSGESFHTMFHRB-GUBZILKMSA-N Gln-Lys-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CCC(N)=O IHSGESFHTMFHRB-GUBZILKMSA-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
- KLKYKPXITJBSNI-CIUDSAMLSA-N Gln-Met-Ala Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](C)C(O)=O KLKYKPXITJBSNI-CIUDSAMLSA-N 0.000 description 1
- ZXGLLNZQSBLQLT-SRVKXCTJSA-N Gln-Met-Lys Chemical compound CSCC[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CCC(=O)N)N ZXGLLNZQSBLQLT-SRVKXCTJSA-N 0.000 description 1
- DFRYZTUPVZNRLG-KKUMJFAQSA-N Gln-Met-Phe Chemical compound CSCC[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)NC(=O)[C@H](CCC(=O)N)N DFRYZTUPVZNRLG-KKUMJFAQSA-N 0.000 description 1
- 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 1
- LGWNISYVKDNJRP-FXQIFTODSA-N Gln-Ser-Gln Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(O)=O LGWNISYVKDNJRP-FXQIFTODSA-N 0.000 description 1
- OKQLXOYFUPVEHI-CIUDSAMLSA-N Gln-Ser-Met Chemical compound CSCC[C@@H](C(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(=O)N)N OKQLXOYFUPVEHI-CIUDSAMLSA-N 0.000 description 1
- NHMRJKKAVMENKJ-WDCWCFNPSA-N Gln-Thr-Leu Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(O)=O NHMRJKKAVMENKJ-WDCWCFNPSA-N 0.000 description 1
- VLOLPWWCNKWRNB-LOKLDPHHSA-N Gln-Thr-Pro Chemical compound C[C@H]([C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CCC(=O)N)N)O VLOLPWWCNKWRNB-LOKLDPHHSA-N 0.000 description 1
- JKDBRTNMYXYLHO-JYJNAYRXSA-N Gln-Tyr-Leu Chemical compound NC(=O)CC[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(O)=O)CC1=CC=C(O)C=C1 JKDBRTNMYXYLHO-JYJNAYRXSA-N 0.000 description 1
- LKDIBBOKUAASNP-FXQIFTODSA-N Glu-Ala-Glu Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(O)=O LKDIBBOKUAASNP-FXQIFTODSA-N 0.000 description 1
- ZJICFHQSPWFBKP-AVGNSLFASA-N Glu-Asn-Tyr Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O ZJICFHQSPWFBKP-AVGNSLFASA-N 0.000 description 1
- QPRZKNOOOBWXSU-CIUDSAMLSA-N Glu-Asp-Arg Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(O)=O)CCCN=C(N)N QPRZKNOOOBWXSU-CIUDSAMLSA-N 0.000 description 1
- XXCDTYBVGMPIOA-FXQIFTODSA-N Glu-Asp-Glu Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(O)=O XXCDTYBVGMPIOA-FXQIFTODSA-N 0.000 description 1
- JRCUFCXYZLPSDZ-ACZMJKKPSA-N Glu-Asp-Ser Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(O)=O JRCUFCXYZLPSDZ-ACZMJKKPSA-N 0.000 description 1
- GFLQTABMFBXRIY-GUBZILKMSA-N Glu-Gln-Arg Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O GFLQTABMFBXRIY-GUBZILKMSA-N 0.000 description 1
- NUSWUSKZRCGFEX-FXQIFTODSA-N Glu-Glu-Cys Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CS)C(O)=O NUSWUSKZRCGFEX-FXQIFTODSA-N 0.000 description 1
- KASDBWKLWJKTLJ-GUBZILKMSA-N Glu-Glu-Met Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCSC)C(O)=O KASDBWKLWJKTLJ-GUBZILKMSA-N 0.000 description 1
- LYCDZGLXQBPNQU-WDSKDSINSA-N Glu-Gly-Cys Chemical compound OC(=O)CC[C@H](N)C(=O)NCC(=O)N[C@@H](CS)C(O)=O LYCDZGLXQBPNQU-WDSKDSINSA-N 0.000 description 1
- WRNAXCVRSBBKGS-BQBZGAKWSA-N Glu-Gly-Gln Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)NCC(=O)N[C@@H](CCC(N)=O)C(O)=O WRNAXCVRSBBKGS-BQBZGAKWSA-N 0.000 description 1
- VXQOONWNIWFOCS-HGNGGELXSA-N Glu-His-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CC1=CN=CN1)NC(=O)[C@H](CCC(=O)O)N VXQOONWNIWFOCS-HGNGGELXSA-N 0.000 description 1
- 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 1
- ATVYZJGOZLVXDK-IUCAKERBSA-N Glu-Leu-Gly Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)NCC(O)=O ATVYZJGOZLVXDK-IUCAKERBSA-N 0.000 description 1
- OQXDUSZKISQQSS-GUBZILKMSA-N Glu-Lys-Ala Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(O)=O OQXDUSZKISQQSS-GUBZILKMSA-N 0.000 description 1
- SJJHXJDSNQJMMW-SRVKXCTJSA-N Glu-Lys-Arg Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O SJJHXJDSNQJMMW-SRVKXCTJSA-N 0.000 description 1
- BCYGDJXHAGZNPQ-DCAQKATOSA-N Glu-Lys-Glu Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(O)=O BCYGDJXHAGZNPQ-DCAQKATOSA-N 0.000 description 1
- ILWHFUZZCFYSKT-AVGNSLFASA-N Glu-Lys-Leu Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(O)=O ILWHFUZZCFYSKT-AVGNSLFASA-N 0.000 description 1
- RBXSZQRSEGYDFG-GUBZILKMSA-N Glu-Lys-Ser Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(O)=O RBXSZQRSEGYDFG-GUBZILKMSA-N 0.000 description 1
- AQNYKMCFCCZEEL-JYJNAYRXSA-N Glu-Lys-Tyr Chemical compound OC(=O)CC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 AQNYKMCFCCZEEL-JYJNAYRXSA-N 0.000 description 1
- UMHRCVCZUPBBQW-GARJFASQSA-N Glu-Met-Pro Chemical compound CSCC[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CCC(=O)O)N UMHRCVCZUPBBQW-GARJFASQSA-N 0.000 description 1
- UCZXXMREFIETQW-AVGNSLFASA-N Glu-Tyr-Asn Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC(N)=O)C(O)=O UCZXXMREFIETQW-AVGNSLFASA-N 0.000 description 1
- HBMRTXJZQDVRFT-DZKIICNBSA-N Glu-Tyr-Val 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](C(C)C)C(O)=O HBMRTXJZQDVRFT-DZKIICNBSA-N 0.000 description 1
- LZEUDRYSAZAJIO-AUTRQRHGSA-N Glu-Val-Glu Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O LZEUDRYSAZAJIO-AUTRQRHGSA-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
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- PYTZFYUXZZHOAD-WHFBIAKZSA-N Gly-Ala-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)CN PYTZFYUXZZHOAD-WHFBIAKZSA-N 0.000 description 1
- BRFJMRSRMOMIMU-WHFBIAKZSA-N Gly-Ala-Asn Chemical compound NCC(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(O)=O BRFJMRSRMOMIMU-WHFBIAKZSA-N 0.000 description 1
- VSVZIEVNUYDAFR-YUMQZZPRSA-N Gly-Ala-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)CN VSVZIEVNUYDAFR-YUMQZZPRSA-N 0.000 description 1
- 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 1
- GRIRDMVMJJDZKV-RCOVLWMOSA-N Gly-Asn-Val Chemical compound [H]NCC(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](C(C)C)C(O)=O GRIRDMVMJJDZKV-RCOVLWMOSA-N 0.000 description 1
- KQDMENMTYNBWMR-WHFBIAKZSA-N Gly-Asp-Ala Chemical compound [H]NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(O)=O KQDMENMTYNBWMR-WHFBIAKZSA-N 0.000 description 1
- XEJTYSCIXKYSHR-WDSKDSINSA-N Gly-Asp-Gln Chemical compound C(CC(=O)N)[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)CN XEJTYSCIXKYSHR-WDSKDSINSA-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
- TZOVVRJYUDETQG-RCOVLWMOSA-N Gly-Asp-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)CN TZOVVRJYUDETQG-RCOVLWMOSA-N 0.000 description 1
- GVVKYKCOFMMTKZ-WHFBIAKZSA-N Gly-Cys-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](CS)NC(=O)CN GVVKYKCOFMMTKZ-WHFBIAKZSA-N 0.000 description 1
- YZACQYVWLCQWBT-BQBZGAKWSA-N Gly-Cys-Arg Chemical compound [H]NCC(=O)N[C@@H](CS)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O YZACQYVWLCQWBT-BQBZGAKWSA-N 0.000 description 1
- CQZDZKRHFWJXDF-WDSKDSINSA-N Gly-Gln-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CN CQZDZKRHFWJXDF-WDSKDSINSA-N 0.000 description 1
- DTRUBYPMMVPQPD-YUMQZZPRSA-N Gly-Gln-Arg Chemical compound [H]NCC(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O DTRUBYPMMVPQPD-YUMQZZPRSA-N 0.000 description 1
- BULIVUZUDBHKKZ-WDSKDSINSA-N Gly-Gln-Asn Chemical compound NCC(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O BULIVUZUDBHKKZ-WDSKDSINSA-N 0.000 description 1
- BPQYBFAXRGMGGY-LAEOZQHASA-N Gly-Gln-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)CN BPQYBFAXRGMGGY-LAEOZQHASA-N 0.000 description 1
- LJXWZPHEMJSNRC-KBPBESRZSA-N Gly-Gln-Trp Chemical compound [H]NCC(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O LJXWZPHEMJSNRC-KBPBESRZSA-N 0.000 description 1
- MOJKRXIRAZPZLW-WDSKDSINSA-N Gly-Glu-Ala Chemical compound [H]NCC(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(O)=O MOJKRXIRAZPZLW-WDSKDSINSA-N 0.000 description 1
- JSNNHGHYGYMVCK-XVKPBYJWSA-N Gly-Glu-Val Chemical compound [H]NCC(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(O)=O JSNNHGHYGYMVCK-XVKPBYJWSA-N 0.000 description 1
- XPJBQTCXPJNIFE-ZETCQYMHSA-N Gly-Gly-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)CNC(=O)CN XPJBQTCXPJNIFE-ZETCQYMHSA-N 0.000 description 1
- MVORZMQFXBLMHM-QWRGUYRKSA-N Gly-His-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)CN)CC1=CN=CN1 MVORZMQFXBLMHM-QWRGUYRKSA-N 0.000 description 1
- VIIBEIQMLJEUJG-LAEOZQHASA-N Gly-Ile-Gln Chemical compound [H]NCC(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCC(N)=O)C(O)=O VIIBEIQMLJEUJG-LAEOZQHASA-N 0.000 description 1
- PAWIVEIWWYGBAM-YUMQZZPRSA-N Gly-Leu-Ala Chemical compound NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(O)=O PAWIVEIWWYGBAM-YUMQZZPRSA-N 0.000 description 1
- YIFUFYZELCMPJP-YUMQZZPRSA-N Gly-Leu-Cys Chemical compound NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CS)C(O)=O YIFUFYZELCMPJP-YUMQZZPRSA-N 0.000 description 1
- 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 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
- CLNSYANKYVMZNM-UWVGGRQHSA-N Gly-Lys-Arg Chemical compound NCCCC[C@H](NC(=O)CN)C(=O)N[C@H](C(O)=O)CCCN=C(N)N CLNSYANKYVMZNM-UWVGGRQHSA-N 0.000 description 1
- VLIJYPMATZSOLL-YUMQZZPRSA-N Gly-Lys-Cys Chemical compound C(CCN)C[C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)CN VLIJYPMATZSOLL-YUMQZZPRSA-N 0.000 description 1
- MHXKHKWHPNETGG-QWRGUYRKSA-N Gly-Lys-Leu Chemical compound [H]NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(O)=O MHXKHKWHPNETGG-QWRGUYRKSA-N 0.000 description 1
- WDEHMRNSGHVNOH-VHSXEESVSA-N Gly-Lys-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CCCCN)NC(=O)CN)C(=O)O WDEHMRNSGHVNOH-VHSXEESVSA-N 0.000 description 1
- BBTCXWTXOXUNFX-IUCAKERBSA-N Gly-Met-Arg Chemical compound CSCC[C@H](NC(=O)CN)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O BBTCXWTXOXUNFX-IUCAKERBSA-N 0.000 description 1
- ICUTTWWCDIIIEE-BQBZGAKWSA-N Gly-Met-Asn Chemical compound CSCC[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)CN ICUTTWWCDIIIEE-BQBZGAKWSA-N 0.000 description 1
- RVGMVLVBDRQVKB-UWVGGRQHSA-N Gly-Met-His Chemical compound CSCC[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)CN RVGMVLVBDRQVKB-UWVGGRQHSA-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
- YYXJFBMCOUSYSF-RYUDHWBXSA-N Gly-Phe-Gln Chemical compound [H]NCC(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCC(N)=O)C(O)=O YYXJFBMCOUSYSF-RYUDHWBXSA-N 0.000 description 1
- IEGFSKKANYKBDU-QWHCGFSZSA-N Gly-Phe-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CC=CC=C2)NC(=O)CN)C(=O)O IEGFSKKANYKBDU-QWHCGFSZSA-N 0.000 description 1
- VDCRBJACQKOSMS-JSGCOSHPSA-N Gly-Phe-Val Chemical compound [H]NCC(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](C(C)C)C(O)=O VDCRBJACQKOSMS-JSGCOSHPSA-N 0.000 description 1
- JJGBXTYGTKWGAT-YUMQZZPRSA-N Gly-Pro-Glu Chemical compound NCC(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(O)=O JJGBXTYGTKWGAT-YUMQZZPRSA-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
- FGPLUIQCSKGLTI-WDSKDSINSA-N Gly-Ser-Glu Chemical compound NCC(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CCC(O)=O FGPLUIQCSKGLTI-WDSKDSINSA-N 0.000 description 1
- ZKJZBRHRWKLVSJ-ZDLURKLDSA-N Gly-Thr-Cys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)CN)O ZKJZBRHRWKLVSJ-ZDLURKLDSA-N 0.000 description 1
- 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 1
- GJHWILMUOANXTG-WPRPVWTQSA-N Gly-Val-Arg Chemical compound [H]NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O GJHWILMUOANXTG-WPRPVWTQSA-N 0.000 description 1
- BAYQNCWLXIDLHX-ONGXEEELSA-N Gly-Val-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)CN BAYQNCWLXIDLHX-ONGXEEELSA-N 0.000 description 1
- 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 1
- 229940121710 HMGCoA reductase inhibitor Drugs 0.000 description 1
- BIAKMWKJMQLZOJ-ZKWXMUAHSA-N His-Ala-Ala Chemical compound C[C@H](NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(O)=O BIAKMWKJMQLZOJ-ZKWXMUAHSA-N 0.000 description 1
- XINDHUAGVGCNSF-QSFUFRPTSA-N His-Ala-Ile Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](C)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O XINDHUAGVGCNSF-QSFUFRPTSA-N 0.000 description 1
- FLUVGKKRRMLNPU-CQDKDKBSSA-N His-Ala-Phe Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](C)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O FLUVGKKRRMLNPU-CQDKDKBSSA-N 0.000 description 1
- WGVPDSNCHDEDBP-KKUMJFAQSA-N His-Asp-Phe Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O WGVPDSNCHDEDBP-KKUMJFAQSA-N 0.000 description 1
- NNBWMLHQXBTIIT-HVTMNAMFSA-N His-Gln-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CC1=CN=CN1)N NNBWMLHQXBTIIT-HVTMNAMFSA-N 0.000 description 1
- PYNUBZSXKQKAHL-UWVGGRQHSA-N His-Gly-Arg Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(O)=O PYNUBZSXKQKAHL-UWVGGRQHSA-N 0.000 description 1
- FDQYIRHBVVUTJF-ZETCQYMHSA-N His-Gly-Gly Chemical compound [O-]C(=O)CNC(=O)CNC(=O)[C@@H]([NH3+])CC1=CN=CN1 FDQYIRHBVVUTJF-ZETCQYMHSA-N 0.000 description 1
- MPXGJGBXCRQQJE-MXAVVETBSA-N His-Ile-Leu Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(O)=O MPXGJGBXCRQQJE-MXAVVETBSA-N 0.000 description 1
- LVWIJITYHRZHBO-IXOXFDKPSA-N His-Leu-Thr Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O LVWIJITYHRZHBO-IXOXFDKPSA-N 0.000 description 1
- RLAOTFTXBFQJDV-KKUMJFAQSA-N His-Phe-Asp Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC(O)=O)C(O)=O)C1=CN=CN1 RLAOTFTXBFQJDV-KKUMJFAQSA-N 0.000 description 1
- SVVULKPWDBIPCO-BZSNNMDCSA-N His-Phe-Leu Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC(C)C)C(O)=O SVVULKPWDBIPCO-BZSNNMDCSA-N 0.000 description 1
- WCHONUZTYDQMBY-PYJNHQTQSA-N His-Pro-Ile Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N1CCC[C@H]1C(=O)N[C@@H]([C@@H](C)CC)C(O)=O WCHONUZTYDQMBY-PYJNHQTQSA-N 0.000 description 1
- PZAJPILZRFPYJJ-SRVKXCTJSA-N His-Ser-Leu Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(O)=O PZAJPILZRFPYJJ-SRVKXCTJSA-N 0.000 description 1
- ILUVWFTXAUYOBW-CUJWVEQBSA-N His-Ser-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC1=CN=CN1)N)O ILUVWFTXAUYOBW-CUJWVEQBSA-N 0.000 description 1
- 101000909498 Homo sapiens Collagen alpha-1(VII) chain Proteins 0.000 description 1
- 101000945639 Homo sapiens Cyclin-dependent kinase inhibitor 3 Proteins 0.000 description 1
- 101000638886 Homo sapiens Urokinase-type plasminogen activator Proteins 0.000 description 1
- DMHGKBGOUAJRHU-RVMXOQNASA-N Ile-Arg-Pro Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@@H]1C(=O)O)N DMHGKBGOUAJRHU-RVMXOQNASA-N 0.000 description 1
- 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 1
- AZEYWPUCOYXFOE-CYDGBPFRSA-N Ile-Arg-Val Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](C(C)C)C(=O)O)N AZEYWPUCOYXFOE-CYDGBPFRSA-N 0.000 description 1
- QADCTXFNLZBZAB-GHCJXIJMSA-N Ile-Asn-Ala Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](C)C(=O)O)N QADCTXFNLZBZAB-GHCJXIJMSA-N 0.000 description 1
- QIHJTGSVGIPHIW-QSFUFRPTSA-N Ile-Asn-Val Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](C(C)C)C(=O)O)N QIHJTGSVGIPHIW-QSFUFRPTSA-N 0.000 description 1
- NKRJALPCDNXULF-BYULHYEWSA-N Ile-Asp-Gly Chemical compound [H]N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(O)=O)C(=O)NCC(O)=O NKRJALPCDNXULF-BYULHYEWSA-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
- 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
- LWWILHPVAKKLQS-QXEWZRGKSA-N Ile-Gly-Met Chemical compound CC[C@H](C)[C@@H](C(=O)NCC(=O)N[C@@H](CCSC)C(=O)O)N LWWILHPVAKKLQS-QXEWZRGKSA-N 0.000 description 1
- AXNGDPAKKCEKGY-QPHKQPEJSA-N Ile-Ile-Thr Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)O)N AXNGDPAKKCEKGY-QPHKQPEJSA-N 0.000 description 1
- QZZIBQZLWBOOJH-PEDHHIEDSA-N Ile-Ile-Val Chemical compound N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C(C)C)C(=O)O QZZIBQZLWBOOJH-PEDHHIEDSA-N 0.000 description 1
- KLBVGHCGHUNHEA-BJDJZHNGSA-N Ile-Leu-Ala Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)O)N KLBVGHCGHUNHEA-BJDJZHNGSA-N 0.000 description 1
- UDBPXJNOEWDBDF-XUXIUFHCSA-N Ile-Lys-Val Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(=O)O)N UDBPXJNOEWDBDF-XUXIUFHCSA-N 0.000 description 1
- SVZFKLBRCYCIIY-CYDGBPFRSA-N Ile-Pro-Arg Chemical compound CC[C@H](C)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O SVZFKLBRCYCIIY-CYDGBPFRSA-N 0.000 description 1
- KTNGVMMGIQWIDV-OSUNSFLBSA-N Ile-Pro-Thr Chemical compound CC[C@H](C)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H]([C@@H](C)O)C(O)=O KTNGVMMGIQWIDV-OSUNSFLBSA-N 0.000 description 1
- VGSPNSSCMOHRRR-BJDJZHNGSA-N Ile-Ser-Lys Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)O)N VGSPNSSCMOHRRR-BJDJZHNGSA-N 0.000 description 1
- ZDNNDIJTUHQCAM-MXAVVETBSA-N Ile-Ser-Phe Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)N ZDNNDIJTUHQCAM-MXAVVETBSA-N 0.000 description 1
- JNLSTRPWUXOORL-MMWGEVLESA-N Ile-Ser-Pro Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CO)C(=O)N1CCC[C@@H]1C(=O)O)N JNLSTRPWUXOORL-MMWGEVLESA-N 0.000 description 1
- HXIDVIFHRYRXLZ-NAKRPEOUSA-N Ile-Ser-Val Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(=O)O)N HXIDVIFHRYRXLZ-NAKRPEOUSA-N 0.000 description 1
- 101710195119 Inner capsid protein sigma-2 Proteins 0.000 description 1
- 102000004371 Insulin-like growth factor binding protein 5 Human genes 0.000 description 1
- 108090000961 Insulin-like growth factor binding protein 5 Proteins 0.000 description 1
- 102100023424 Kinesin-like protein KIF2C Human genes 0.000 description 1
- 101710134369 Kinesin-like protein KIF2C Proteins 0.000 description 1
- FADYJNXDPBKVCA-UHFFFAOYSA-N L-Phenylalanyl-L-lysin Natural products NCCCCC(C(O)=O)NC(=O)C(N)CC1=CC=CC=C1 FADYJNXDPBKVCA-UHFFFAOYSA-N 0.000 description 1
- 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 1
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 1
- KWTVLKBOQATPHJ-SRVKXCTJSA-N Leu-Ala-Lys Chemical compound C[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CC(C)C)N KWTVLKBOQATPHJ-SRVKXCTJSA-N 0.000 description 1
- DBVWMYGBVFCRBE-CIUDSAMLSA-N Leu-Asn-Asn Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O DBVWMYGBVFCRBE-CIUDSAMLSA-N 0.000 description 1
- RFUBXQQFJFGJFV-GUBZILKMSA-N Leu-Asn-Gln Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O RFUBXQQFJFGJFV-GUBZILKMSA-N 0.000 description 1
- MDVZJYGNAGLPGJ-KKUMJFAQSA-N Leu-Asn-Phe Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 MDVZJYGNAGLPGJ-KKUMJFAQSA-N 0.000 description 1
- ZDSNOSQHMJBRQN-SRVKXCTJSA-N Leu-Asp-His Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)N ZDSNOSQHMJBRQN-SRVKXCTJSA-N 0.000 description 1
- JQSXWJXBASFONF-KKUMJFAQSA-N Leu-Asp-Phe Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O JQSXWJXBASFONF-KKUMJFAQSA-N 0.000 description 1
- DPWGZWUMUUJQDT-IUCAKERBSA-N Leu-Gln-Gly Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(O)=O DPWGZWUMUUJQDT-IUCAKERBSA-N 0.000 description 1
- 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 1
- PRZVBIAOPFGAQF-SRVKXCTJSA-N Leu-Glu-Met Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCSC)C(O)=O PRZVBIAOPFGAQF-SRVKXCTJSA-N 0.000 description 1
- 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
- VZBIUJURDLFFOE-IHRRRGAJSA-N Leu-His-Arg Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O VZBIUJURDLFFOE-IHRRRGAJSA-N 0.000 description 1
- JKSIBWITFMQTOA-XUXIUFHCSA-N Leu-Ile-Val Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C(C)C)C(O)=O JKSIBWITFMQTOA-XUXIUFHCSA-N 0.000 description 1
- ZGUMORRUBUCXEH-AVGNSLFASA-N Leu-Lys-Gln Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(O)=O ZGUMORRUBUCXEH-AVGNSLFASA-N 0.000 description 1
- LZHJZLHSRGWBBE-IHRRRGAJSA-N Leu-Lys-Val Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(O)=O LZHJZLHSRGWBBE-IHRRRGAJSA-N 0.000 description 1
- KXCMQWMNYQOAKA-SRVKXCTJSA-N Leu-Met-Gln Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCC(=O)N)C(=O)O)N KXCMQWMNYQOAKA-SRVKXCTJSA-N 0.000 description 1
- BJWKOATWNQJPSK-SRVKXCTJSA-N Leu-Met-Glu Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCC(=O)O)C(=O)O)N BJWKOATWNQJPSK-SRVKXCTJSA-N 0.000 description 1
- GSSMYQHXZNERFX-WDSOQIARSA-N Leu-Met-Trp Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)O)N GSSMYQHXZNERFX-WDSOQIARSA-N 0.000 description 1
- SYRTUBLKWNDSDK-DKIMLUQUSA-N Leu-Phe-Ile Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O SYRTUBLKWNDSDK-DKIMLUQUSA-N 0.000 description 1
- QMKFDEUJGYNFMC-AVGNSLFASA-N Leu-Pro-Arg Chemical compound CC(C)C[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(O)=O QMKFDEUJGYNFMC-AVGNSLFASA-N 0.000 description 1
- RRVCZCNFXIFGRA-DCAQKATOSA-N Leu-Pro-Asn Chemical compound [H]N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(N)=O)C(O)=O RRVCZCNFXIFGRA-DCAQKATOSA-N 0.000 description 1
- VULJUQZPSOASBZ-SRVKXCTJSA-N Leu-Pro-Glu Chemical compound [H]N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(O)=O VULJUQZPSOASBZ-SRVKXCTJSA-N 0.000 description 1
- PWPBLZXWFXJFHE-RHYQMDGZSA-N Leu-Pro-Thr Chemical compound CC(C)C[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H]([C@@H](C)O)C(O)=O PWPBLZXWFXJFHE-RHYQMDGZSA-N 0.000 description 1
- IDGZVZJLYFTXSL-DCAQKATOSA-N Leu-Ser-Arg Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CCCN=C(N)N IDGZVZJLYFTXSL-DCAQKATOSA-N 0.000 description 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
- JIHDFWWRYHSAQB-GUBZILKMSA-N Leu-Ser-Glu Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@H](C(O)=O)CCC(O)=O JIHDFWWRYHSAQB-GUBZILKMSA-N 0.000 description 1
- SBANPBVRHYIMRR-GARJFASQSA-N Leu-Ser-Pro Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CO)C(=O)N1CCC[C@@H]1C(=O)O)N SBANPBVRHYIMRR-GARJFASQSA-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
- 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
- QWWPYKKLXWOITQ-VOAKCMCISA-N Leu-Thr-Leu Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@H](C(O)=O)CC(C)C QWWPYKKLXWOITQ-VOAKCMCISA-N 0.000 description 1
- KLSUAWUZBMAZCL-RHYQMDGZSA-N Leu-Thr-Pro Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1CCC[C@H]1C(O)=O KLSUAWUZBMAZCL-RHYQMDGZSA-N 0.000 description 1
- UCRJTSIIAYHOHE-ULQDDVLXSA-N Leu-Tyr-Arg Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)N UCRJTSIIAYHOHE-ULQDDVLXSA-N 0.000 description 1
- MVJRBCJCRYGCKV-GVXVVHGQSA-N Leu-Val-Gln Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O MVJRBCJCRYGCKV-GVXVVHGQSA-N 0.000 description 1
- YQFZRHYZLARWDY-IHRRRGAJSA-N Leu-Val-Lys Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(O)=O)CCCCN YQFZRHYZLARWDY-IHRRRGAJSA-N 0.000 description 1
- VHNOAIFVYUQOOY-XUXIUFHCSA-N Lys-Arg-Ile Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O VHNOAIFVYUQOOY-XUXIUFHCSA-N 0.000 description 1
- YNNPKXBBRZVIRX-IHRRRGAJSA-N Lys-Arg-Leu Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(O)=O YNNPKXBBRZVIRX-IHRRRGAJSA-N 0.000 description 1
- GGAPIOORBXHMNY-ULQDDVLXSA-N Lys-Arg-Tyr Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)N)O GGAPIOORBXHMNY-ULQDDVLXSA-N 0.000 description 1
- 108010062166 Lys-Asn-Asp Proteins 0.000 description 1
- DEFGUIIUYAUEDU-ZPFDUUQYSA-N Lys-Asn-Ile Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O DEFGUIIUYAUEDU-ZPFDUUQYSA-N 0.000 description 1
- KPJJOZUXFOLGMQ-CIUDSAMLSA-N Lys-Asp-Asn Chemical compound C(CCN)C[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(=O)N)C(=O)O)N KPJJOZUXFOLGMQ-CIUDSAMLSA-N 0.000 description 1
- OVIVOCSURJYCTM-GUBZILKMSA-N Lys-Asp-Glu Chemical compound NCCCC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(O)=O)CCC(O)=O OVIVOCSURJYCTM-GUBZILKMSA-N 0.000 description 1
- WGCKDDHUFPQSMZ-ZPFDUUQYSA-N Lys-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)CCCCN WGCKDDHUFPQSMZ-ZPFDUUQYSA-N 0.000 description 1
- AIPHUKOBUXJNKM-KKUMJFAQSA-N Lys-Cys-Phe Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CS)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O AIPHUKOBUXJNKM-KKUMJFAQSA-N 0.000 description 1
- DZQYZKPINJLLEN-KKUMJFAQSA-N Lys-Cys-Tyr Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)O)NC(=O)[C@H](CS)NC(=O)[C@H](CCCCN)N)O DZQYZKPINJLLEN-KKUMJFAQSA-N 0.000 description 1
- QQUJSUFWEDZQQY-AVGNSLFASA-N Lys-Gln-Lys Chemical compound NCCCC[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](C(O)=O)CCCCN QQUJSUFWEDZQQY-AVGNSLFASA-N 0.000 description 1
- CKSBRMUOQDNPKZ-SRVKXCTJSA-N Lys-Gln-Met Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCSC)C(O)=O CKSBRMUOQDNPKZ-SRVKXCTJSA-N 0.000 description 1
- DCRWPTBMWMGADO-AVGNSLFASA-N Lys-Glu-Leu Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(O)=O DCRWPTBMWMGADO-AVGNSLFASA-N 0.000 description 1
- ITWQLSZTLBKWJM-YUMQZZPRSA-N Lys-Gly-Ala Chemical compound OC(=O)[C@H](C)NC(=O)CNC(=O)[C@@H](N)CCCCN ITWQLSZTLBKWJM-YUMQZZPRSA-N 0.000 description 1
- WOEDRPCHKPSFDT-MXAVVETBSA-N Lys-His-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CC1=CN=CN1)NC(=O)[C@H](CCCCN)N WOEDRPCHKPSFDT-MXAVVETBSA-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
- MYZMQWHPDAYKIE-SRVKXCTJSA-N Lys-Leu-Ala Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(O)=O MYZMQWHPDAYKIE-SRVKXCTJSA-N 0.000 description 1
- XIZQPFCRXLUNMK-BZSNNMDCSA-N Lys-Leu-Phe Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)NC(=O)[C@H](CCCCN)N XIZQPFCRXLUNMK-BZSNNMDCSA-N 0.000 description 1
- WWEWGPOLIJXGNX-XUXIUFHCSA-N Lys-Met-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)N WWEWGPOLIJXGNX-XUXIUFHCSA-N 0.000 description 1
- SKUOQDYMJFUMOE-ULQDDVLXSA-N Lys-Met-Phe Chemical compound CSCC[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O)NC(=O)[C@H](CCCCN)N SKUOQDYMJFUMOE-ULQDDVLXSA-N 0.000 description 1
- PDIDTSZKKFEDMB-UWVGGRQHSA-N Lys-Pro-Gly Chemical compound [H]N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)NCC(O)=O PDIDTSZKKFEDMB-UWVGGRQHSA-N 0.000 description 1
- LOGFVTREOLYCPF-RHYQMDGZSA-N Lys-Pro-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCCN LOGFVTREOLYCPF-RHYQMDGZSA-N 0.000 description 1
- SQXZLVXQXWILKW-KKUMJFAQSA-N Lys-Ser-Phe Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O SQXZLVXQXWILKW-KKUMJFAQSA-N 0.000 description 1
- YFQSSOAGMZGXFT-MEYUZBJRSA-N Lys-Thr-Tyr Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O YFQSSOAGMZGXFT-MEYUZBJRSA-N 0.000 description 1
- CNXOBMMOYZPPGS-NUTKFTJISA-N Lys-Trp-Ala Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](C)C(O)=O CNXOBMMOYZPPGS-NUTKFTJISA-N 0.000 description 1
- BVRNWWHJYNPJDG-XIRDDKMYSA-N Lys-Trp-Asn Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)[C@H](CCCCN)N BVRNWWHJYNPJDG-XIRDDKMYSA-N 0.000 description 1
- ZJSXCIMWLPSTMG-HSCHXYMDSA-N Lys-Trp-Ile Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O ZJSXCIMWLPSTMG-HSCHXYMDSA-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
- XABXVVSWUVCZST-GVXVVHGQSA-N Lys-Val-Gln Chemical compound NC(=O)CC[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)CCCCN XABXVVSWUVCZST-GVXVVHGQSA-N 0.000 description 1
- 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
- RIPJMCFGQHGHNP-RHYQMDGZSA-N Lys-Val-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCCN)N)O RIPJMCFGQHGHNP-RHYQMDGZSA-N 0.000 description 1
- QAHFGYLFLVGBNW-DCAQKATOSA-N Met-Ala-Lys Chemical compound CSCC[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@H](C(O)=O)CCCCN QAHFGYLFLVGBNW-DCAQKATOSA-N 0.000 description 1
- ACYHZNZHIZWLQF-BQBZGAKWSA-N Met-Asn-Gly Chemical compound CSCC[C@H](N)C(=O)N[C@@H](CC(N)=O)C(=O)NCC(O)=O ACYHZNZHIZWLQF-BQBZGAKWSA-N 0.000 description 1
- 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 1
- UZVWDRPUTHXQAM-FXQIFTODSA-N Met-Asp-Ala Chemical compound CSCC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(O)=O UZVWDRPUTHXQAM-FXQIFTODSA-N 0.000 description 1
- DNDVVILEHVMWIS-LPEHRKFASA-N Met-Asp-Pro Chemical compound CSCC[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N1CCC[C@@H]1C(=O)O)N DNDVVILEHVMWIS-LPEHRKFASA-N 0.000 description 1
- JYCQGAGDJQYEDB-GUBZILKMSA-N Met-Gln-Gln Chemical compound CSCC[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O JYCQGAGDJQYEDB-GUBZILKMSA-N 0.000 description 1
- PQPMMGQTRQFSDA-SRVKXCTJSA-N Met-Glu-His Chemical compound [H]N[C@@H](CCSC)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC1=CNC=N1)C(O)=O PQPMMGQTRQFSDA-SRVKXCTJSA-N 0.000 description 1
- MSSJHBAKDDIRMJ-SRVKXCTJSA-N Met-Lys-Gln Chemical compound [H]N[C@@H](CCSC)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(O)=O MSSJHBAKDDIRMJ-SRVKXCTJSA-N 0.000 description 1
- ILKCLLLOGPDNIP-RCWTZXSCSA-N Met-Met-Thr Chemical compound CSCC[C@H](N)C(=O)N[C@@H](CCSC)C(=O)N[C@@H]([C@@H](C)O)C(O)=O ILKCLLLOGPDNIP-RCWTZXSCSA-N 0.000 description 1
- WNJXJJSGUXAIQU-UFYCRDLUSA-N Met-Phe-Phe Chemical compound C([C@H](NC(=O)[C@@H](N)CCSC)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=CC=C1 WNJXJJSGUXAIQU-UFYCRDLUSA-N 0.000 description 1
- MQASRXPTQJJNFM-JYJNAYRXSA-N Met-Pro-Phe Chemical compound CSCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 MQASRXPTQJJNFM-JYJNAYRXSA-N 0.000 description 1
- NHXXGBXJTLRGJI-GUBZILKMSA-N Met-Pro-Ser Chemical compound [H]N[C@@H](CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(O)=O NHXXGBXJTLRGJI-GUBZILKMSA-N 0.000 description 1
- ZBLSZPYQQRIHQU-RCWTZXSCSA-N Met-Thr-Val Chemical compound CSCC[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(O)=O ZBLSZPYQQRIHQU-RCWTZXSCSA-N 0.000 description 1
- QAVZUKIPOMBLMC-AVGNSLFASA-N Met-Val-Leu Chemical compound CSCC[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(O)=O)CC(C)C QAVZUKIPOMBLMC-AVGNSLFASA-N 0.000 description 1
- 102000002151 Microfilament Proteins Human genes 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
- 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 1
- KZNQNBZMBZJQJO-UHFFFAOYSA-N N-glycyl-L-proline Natural products NCC(=O)N1CCCC1C(O)=O KZNQNBZMBZJQJO-UHFFFAOYSA-N 0.000 description 1
- 108010079364 N-glycylalanine Proteins 0.000 description 1
- 108010047562 NGR peptide Proteins 0.000 description 1
- BQVUABVGYYSDCJ-UHFFFAOYSA-N Nalpha-L-Leucyl-L-tryptophan Natural products C1=CC=C2C(CC(NC(=O)C(N)CC(C)C)C(O)=O)=CNC2=C1 BQVUABVGYYSDCJ-UHFFFAOYSA-N 0.000 description 1
- 102000009890 Osteonectin Human genes 0.000 description 1
- 108010077077 Osteonectin Proteins 0.000 description 1
- 238000012408 PCR amplification Methods 0.000 description 1
- 208000006735 Periostitis Diseases 0.000 description 1
- LSXGADJXBDFXQU-DLOVCJGASA-N Phe-Ala-Asp Chemical compound OC(=O)C[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC1=CC=CC=C1 LSXGADJXBDFXQU-DLOVCJGASA-N 0.000 description 1
- NEHSHYOUIWBYSA-DCPHZVHLSA-N Phe-Ala-Trp Chemical compound 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 NEHSHYOUIWBYSA-DCPHZVHLSA-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
- LDSOBEJVGGVWGD-DLOVCJGASA-N Phe-Asp-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H](N)CC1=CC=CC=C1 LDSOBEJVGGVWGD-DLOVCJGASA-N 0.000 description 1
- UMKYAYXCMYYNHI-AVGNSLFASA-N Phe-Gln-Asn Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC(=O)N)C(=O)O)N UMKYAYXCMYYNHI-AVGNSLFASA-N 0.000 description 1
- KAGCQPSEVAETCA-JYJNAYRXSA-N Phe-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=CC=C1)N KAGCQPSEVAETCA-JYJNAYRXSA-N 0.000 description 1
- CSDMCMITJLKBAH-SOUVJXGZSA-N Phe-Glu-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC2=CC=CC=C2)N)C(=O)O CSDMCMITJLKBAH-SOUVJXGZSA-N 0.000 description 1
- APJPXSFJBMMOLW-KBPBESRZSA-N Phe-Gly-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)CC1=CC=CC=C1 APJPXSFJBMMOLW-KBPBESRZSA-N 0.000 description 1
- SFKOEHXABNPLRT-KBPBESRZSA-N Phe-His-Gly Chemical compound N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)NCC(O)=O SFKOEHXABNPLRT-KBPBESRZSA-N 0.000 description 1
- VADLTGVIOIOKGM-BZSNNMDCSA-N Phe-His-Leu Chemical compound C([C@@H](C(=O)N[C@@H](CC(C)C)C(O)=O)NC(=O)[C@@H](N)CC=1C=CC=CC=1)C1=CN=CN1 VADLTGVIOIOKGM-BZSNNMDCSA-N 0.000 description 1
- AUJWXNGCAQWLEI-KBPBESRZSA-N Phe-Lys-Gly Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCCCN)C(=O)NCC(O)=O AUJWXNGCAQWLEI-KBPBESRZSA-N 0.000 description 1
- GRVMHFCZUIYNKQ-UFYCRDLUSA-N Phe-Phe-Val Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](C(C)C)C(O)=O GRVMHFCZUIYNKQ-UFYCRDLUSA-N 0.000 description 1
- JLLJTMHNXQTMCK-UBHSHLNASA-N Phe-Pro-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CC1=CC=CC=C1 JLLJTMHNXQTMCK-UBHSHLNASA-N 0.000 description 1
- IPFXYNKCXYGSSV-KKUMJFAQSA-N Phe-Ser-Lys Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)O)N IPFXYNKCXYGSSV-KKUMJFAQSA-N 0.000 description 1
- MRWOVVNKSXXLRP-IHPCNDPISA-N Phe-Ser-Trp Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O MRWOVVNKSXXLRP-IHPCNDPISA-N 0.000 description 1
- ZTVSVSFBHUVYIN-UFYCRDLUSA-N Phe-Tyr-Met Chemical compound C([C@@H](C(=O)N[C@@H](CCSC)C(O)=O)NC(=O)[C@@H](N)CC=1C=CC=CC=1)C1=CC=C(O)C=C1 ZTVSVSFBHUVYIN-UFYCRDLUSA-N 0.000 description 1
- FRMKIPSIZSFTTE-HJOGWXRNSA-N Phe-Tyr-Phe 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](CC1=CC=CC=C1)C(O)=O FRMKIPSIZSFTTE-HJOGWXRNSA-N 0.000 description 1
- SJRQWEDYTKYHHL-SLFFLAALSA-N Phe-Tyr-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CC=C(C=C2)O)NC(=O)[C@H](CC3=CC=CC=C3)N)C(=O)O SJRQWEDYTKYHHL-SLFFLAALSA-N 0.000 description 1
- JTKGCYOOJLUETJ-ULQDDVLXSA-N Phe-Val-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)CC1=CC=CC=C1 JTKGCYOOJLUETJ-ULQDDVLXSA-N 0.000 description 1
- 102000016462 Phosphate Transport Proteins Human genes 0.000 description 1
- 108010092528 Phosphate Transport Proteins Proteins 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- TXPUNZXZDVJUJQ-LPEHRKFASA-N Pro-Asn-Pro Chemical compound C1C[C@H](NC1)C(=O)N[C@@H](CC(=O)N)C(=O)N2CCC[C@@H]2C(=O)O TXPUNZXZDVJUJQ-LPEHRKFASA-N 0.000 description 1
- YFNOUBWUIIJQHF-LPEHRKFASA-N Pro-Asp-Pro Chemical compound C1C[C@H](NC1)C(=O)N[C@@H](CC(=O)O)C(=O)N2CCC[C@@H]2C(=O)O YFNOUBWUIIJQHF-LPEHRKFASA-N 0.000 description 1
- UPJGUQPLYWTISV-GUBZILKMSA-N Pro-Gln-Glu Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(O)=O UPJGUQPLYWTISV-GUBZILKMSA-N 0.000 description 1
- SKICPQLTOXGWGO-GARJFASQSA-N Pro-Gln-Pro Chemical compound C1C[C@H](NC1)C(=O)N[C@@H](CCC(=O)N)C(=O)N2CCC[C@@H]2C(=O)O SKICPQLTOXGWGO-GARJFASQSA-N 0.000 description 1
- LHALYDBUDCWMDY-CIUDSAMLSA-N Pro-Glu-Ala Chemical compound C[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H]1CCCN1)C(O)=O LHALYDBUDCWMDY-CIUDSAMLSA-N 0.000 description 1
- UEHYFUCOGHWASA-HJGDQZAQSA-N Pro-Glu-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H]1CCCN1 UEHYFUCOGHWASA-HJGDQZAQSA-N 0.000 description 1
- HAAQQNHQZBOWFO-LURJTMIESA-N Pro-Gly-Gly Chemical compound OC(=O)CNC(=O)CNC(=O)[C@@H]1CCCN1 HAAQQNHQZBOWFO-LURJTMIESA-N 0.000 description 1
- XFFIGWGYMUFCCQ-ULQDDVLXSA-N Pro-His-Tyr Chemical compound C1=CC(O)=CC=C1C[C@@H](C([O-])=O)NC(=O)[C@@H](NC(=O)[C@H]1[NH2+]CCC1)CC1=CN=CN1 XFFIGWGYMUFCCQ-ULQDDVLXSA-N 0.000 description 1
- XYHMFGGWNOFUOU-QXEWZRGKSA-N Pro-Ile-Gly Chemical compound OC(=O)CNC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@@H]1CCCN1 XYHMFGGWNOFUOU-QXEWZRGKSA-N 0.000 description 1
- AUQGUYPHJSMAKI-CYDGBPFRSA-N Pro-Ile-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@@H]1CCCN1 AUQGUYPHJSMAKI-CYDGBPFRSA-N 0.000 description 1
- YXHYJEPDKSYPSQ-AVGNSLFASA-N Pro-Leu-Arg Chemical compound NC(N)=NCCC[C@@H](C(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1 YXHYJEPDKSYPSQ-AVGNSLFASA-N 0.000 description 1
- RMODQFBNDDENCP-IHRRRGAJSA-N Pro-Lys-Leu Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(O)=O RMODQFBNDDENCP-IHRRRGAJSA-N 0.000 description 1
- WFIVLLFYUZZWOD-RHYQMDGZSA-N Pro-Lys-Thr Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(O)=O WFIVLLFYUZZWOD-RHYQMDGZSA-N 0.000 description 1
- AWQGDZBKQTYNMN-IHRRRGAJSA-N Pro-Phe-Asp Chemical compound C1C[C@H](NC1)C(=O)N[C@@H](CC2=CC=CC=C2)C(=O)N[C@@H](CC(=O)O)C(=O)O AWQGDZBKQTYNMN-IHRRRGAJSA-N 0.000 description 1
- FYKUEXMZYFIZKA-DCAQKATOSA-N Pro-Pro-Gln Chemical compound [H]N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(O)=O FYKUEXMZYFIZKA-DCAQKATOSA-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
- SXJOPONICMGFCR-DCAQKATOSA-N Pro-Ser-Lys Chemical compound C1C[C@H](NC1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)O SXJOPONICMGFCR-DCAQKATOSA-N 0.000 description 1
- QKDIHFHGHBYTKB-IHRRRGAJSA-N Pro-Ser-Phe Chemical compound N([C@@H](CO)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C(=O)[C@@H]1CCCN1 QKDIHFHGHBYTKB-IHRRRGAJSA-N 0.000 description 1
- CWZUFLWPEFHWEI-IHRRRGAJSA-N Pro-Tyr-Asp Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC(O)=O)C(O)=O CWZUFLWPEFHWEI-IHRRRGAJSA-N 0.000 description 1
- JXVXYRZQIUPYSA-NHCYSSNCSA-N Pro-Val-Gln Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O JXVXYRZQIUPYSA-NHCYSSNCSA-N 0.000 description 1
- 102000003946 Prolactin Human genes 0.000 description 1
- 108010057464 Prolactin Proteins 0.000 description 1
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 108700039882 Protein Glutamine gamma Glutamyltransferase 2 Proteins 0.000 description 1
- 102100038095 Protein-glutamine gamma-glutamyltransferase 2 Human genes 0.000 description 1
- 108010094028 Prothrombin Proteins 0.000 description 1
- 108091034057 RNA (poly(A)) Proteins 0.000 description 1
- 229920002684 Sepharose Polymers 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
- 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 1
- QGMLKFGTGXWAHF-IHRRRGAJSA-N Ser-Arg-Phe Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O QGMLKFGTGXWAHF-IHRRRGAJSA-N 0.000 description 1
- QVOGDCQNGLBNCR-FXQIFTODSA-N Ser-Arg-Ser Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(O)=O QVOGDCQNGLBNCR-FXQIFTODSA-N 0.000 description 1
- VAIZFHMTBFYJIA-ACZMJKKPSA-N Ser-Asp-Gln Chemical compound OC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(O)=O)CCC(N)=O VAIZFHMTBFYJIA-ACZMJKKPSA-N 0.000 description 1
- OJPHFSOMBZKQKQ-GUBZILKMSA-N Ser-Gln-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)CO OJPHFSOMBZKQKQ-GUBZILKMSA-N 0.000 description 1
- VMVNCJDKFOQOHM-GUBZILKMSA-N Ser-Gln-Lys Chemical compound C(CCN)C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CO)N VMVNCJDKFOQOHM-GUBZILKMSA-N 0.000 description 1
- BQWCDDAISCPDQV-XHNCKOQMSA-N Ser-Gln-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CO)N)C(=O)O BQWCDDAISCPDQV-XHNCKOQMSA-N 0.000 description 1
- FMDHKPRACUXATF-ACZMJKKPSA-N Ser-Gln-Ser Chemical compound OC[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CO)C(O)=O FMDHKPRACUXATF-ACZMJKKPSA-N 0.000 description 1
- HJEBZBMOTCQYDN-ACZMJKKPSA-N Ser-Glu-Asp Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(O)=O HJEBZBMOTCQYDN-ACZMJKKPSA-N 0.000 description 1
- BRGQQXQKPUCUJQ-KBIXCLLPSA-N Ser-Glu-Ile Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O BRGQQXQKPUCUJQ-KBIXCLLPSA-N 0.000 description 1
- UAJAYRMZGNQILN-BQBZGAKWSA-N Ser-Gly-Met Chemical compound [H]N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CCSC)C(O)=O UAJAYRMZGNQILN-BQBZGAKWSA-N 0.000 description 1
- CAOYHZOWXFFAIR-CIUDSAMLSA-N Ser-His-Ser Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CO)C(O)=O CAOYHZOWXFFAIR-CIUDSAMLSA-N 0.000 description 1
- IAORETPTUDBBGV-CIUDSAMLSA-N Ser-Leu-Cys Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CO)N IAORETPTUDBBGV-CIUDSAMLSA-N 0.000 description 1
- GJFYFGOEWLDQGW-GUBZILKMSA-N Ser-Leu-Gln Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](CO)N GJFYFGOEWLDQGW-GUBZILKMSA-N 0.000 description 1
- 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
- JLPMFVAIQHCBDC-CIUDSAMLSA-N Ser-Lys-Cys Chemical compound C(CCN)C[C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CO)N JLPMFVAIQHCBDC-CIUDSAMLSA-N 0.000 description 1
- OWCVUSJMEBGMOK-YUMQZZPRSA-N Ser-Lys-Gly Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)NCC(O)=O OWCVUSJMEBGMOK-YUMQZZPRSA-N 0.000 description 1
- CRJZZXMAADSBBQ-SRVKXCTJSA-N Ser-Lys-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CO CRJZZXMAADSBBQ-SRVKXCTJSA-N 0.000 description 1
- PJIQEIFXZPCWOJ-FXQIFTODSA-N Ser-Pro-Asp Chemical compound [H]N[C@@H](CO)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(O)=O)C(O)=O PJIQEIFXZPCWOJ-FXQIFTODSA-N 0.000 description 1
- QUGRFWPMPVIAPW-IHRRRGAJSA-N Ser-Pro-Phe Chemical compound OC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 QUGRFWPMPVIAPW-IHRRRGAJSA-N 0.000 description 1
- 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 1
- OZPDGESCTGGNAD-CIUDSAMLSA-N Ser-Ser-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CO OZPDGESCTGGNAD-CIUDSAMLSA-N 0.000 description 1
- XJDMUQCLVSCRSJ-VZFHVOOUSA-N Ser-Thr-Ala Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C)C(O)=O XJDMUQCLVSCRSJ-VZFHVOOUSA-N 0.000 description 1
- 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 1
- 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 1
- GSCVDSBEYVGMJQ-SRVKXCTJSA-N Ser-Tyr-Asp Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)O)NC(=O)[C@H](CO)N)O GSCVDSBEYVGMJQ-SRVKXCTJSA-N 0.000 description 1
- CAGTXGDOIFXLPC-KZVJFYERSA-N Thr-Arg-Ala Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](C)C(O)=O)CCCN=C(N)N CAGTXGDOIFXLPC-KZVJFYERSA-N 0.000 description 1
- LHUBVKCLOVALIA-HJGDQZAQSA-N Thr-Arg-Gln Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(N)=O)C(O)=O LHUBVKCLOVALIA-HJGDQZAQSA-N 0.000 description 1
- NAXBBCLCEOTAIG-RHYQMDGZSA-N Thr-Arg-Lys Chemical compound NC(N)=NCCC[C@H](NC(=O)[C@@H](N)[C@H](O)C)C(=O)N[C@@H](CCCCN)C(O)=O NAXBBCLCEOTAIG-RHYQMDGZSA-N 0.000 description 1
- SWIKDOUVROTZCW-GCJQMDKQSA-N Thr-Asn-Ala Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](C)C(=O)O)N)O SWIKDOUVROTZCW-GCJQMDKQSA-N 0.000 description 1
- 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 1
- LXWZOMSOUAMOIA-JIOCBJNQSA-N Thr-Asn-Pro Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N1CCC[C@@H]1C(=O)O)N)O LXWZOMSOUAMOIA-JIOCBJNQSA-N 0.000 description 1
- DCCGCVLVVSAJFK-NUMRIWBASA-N Thr-Asp-Gln Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCC(=O)N)C(=O)O)N)O DCCGCVLVVSAJFK-NUMRIWBASA-N 0.000 description 1
- OYTNZCBFDXGQGE-XQXXSGGOSA-N Thr-Gln-Ala Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](C)C(=O)O)N)O OYTNZCBFDXGQGE-XQXXSGGOSA-N 0.000 description 1
- VUVCRYXYUUPGSB-GLLZPBPUSA-N Thr-Gln-Glu Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCC(=O)O)C(=O)O)N)O VUVCRYXYUUPGSB-GLLZPBPUSA-N 0.000 description 1
- GUZGCDIZVGODML-NKIYYHGXSA-N Thr-Gln-His Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)N)O GUZGCDIZVGODML-NKIYYHGXSA-N 0.000 description 1
- 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 1
- FHDLKMFZKRUQCE-HJGDQZAQSA-N Thr-Glu-Arg Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O FHDLKMFZKRUQCE-HJGDQZAQSA-N 0.000 description 1
- SHOMROOOQBDGRL-JHEQGTHGSA-N Thr-Glu-Gly Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCC(O)=O)C(=O)NCC(O)=O SHOMROOOQBDGRL-JHEQGTHGSA-N 0.000 description 1
- KBLYJPQSNGTDIU-LOKLDPHHSA-N Thr-Glu-Pro Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N1CCC[C@@H]1C(=O)O)N)O KBLYJPQSNGTDIU-LOKLDPHHSA-N 0.000 description 1
- FDALPRWYVKJCLL-PMVVWTBXSA-N Thr-His-Gly Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CNC=N1)C(=O)NCC(O)=O FDALPRWYVKJCLL-PMVVWTBXSA-N 0.000 description 1
- WPAKPLPGQNUXGN-OSUNSFLBSA-N Thr-Ile-Arg Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O WPAKPLPGQNUXGN-OSUNSFLBSA-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
- VTVVYQOXJCZVEB-WDCWCFNPSA-N Thr-Leu-Glu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O VTVVYQOXJCZVEB-WDCWCFNPSA-N 0.000 description 1
- 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 1
- 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 1
- XSEPSRUDSPHMPX-KATARQTJSA-N Thr-Lys-Ser Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(O)=O XSEPSRUDSPHMPX-KATARQTJSA-N 0.000 description 1
- MCDVZTRGHNXTGK-HJGDQZAQSA-N Thr-Met-Glu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCC(O)=O)C(O)=O MCDVZTRGHNXTGK-HJGDQZAQSA-N 0.000 description 1
- NZRUWPIYECBYRK-HTUGSXCWSA-N Thr-Phe-Glu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCC(O)=O)C(O)=O NZRUWPIYECBYRK-HTUGSXCWSA-N 0.000 description 1
- MXNAOGFNFNKUPD-JHYOHUSXSA-N Thr-Phe-Thr Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)O)C(O)=O MXNAOGFNFNKUPD-JHYOHUSXSA-N 0.000 description 1
- 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 1
- NYQIZWROIMIQSL-VEVYYDQMSA-N Thr-Pro-Asn Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(N)=O)C(O)=O NYQIZWROIMIQSL-VEVYYDQMSA-N 0.000 description 1
- NDXSOKGYKCGYKT-VEVYYDQMSA-N Thr-Pro-Asp Chemical compound C[C@@H](O)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(O)=O)C(O)=O NDXSOKGYKCGYKT-VEVYYDQMSA-N 0.000 description 1
- DEGCBBCMYWNJNA-RHYQMDGZSA-N Thr-Pro-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)[C@@H](C)O DEGCBBCMYWNJNA-RHYQMDGZSA-N 0.000 description 1
- VUXIQSUQQYNLJP-XAVMHZPKSA-N Thr-Ser-Pro Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CO)C(=O)N1CCC[C@@H]1C(=O)O)N)O VUXIQSUQQYNLJP-XAVMHZPKSA-N 0.000 description 1
- AAZOYLQUEQRUMZ-GSSVUCPTSA-N Thr-Thr-Asn Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@H](C(O)=O)CC(N)=O AAZOYLQUEQRUMZ-GSSVUCPTSA-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
- BKIOKSLLAAZYTC-KKHAAJSZSA-N Thr-Val-Asn Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(N)=O)C(O)=O BKIOKSLLAAZYTC-KKHAAJSZSA-N 0.000 description 1
- FYBFTPLPAXZBOY-KKHAAJSZSA-N Thr-Val-Asp Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(O)=O FYBFTPLPAXZBOY-KKHAAJSZSA-N 0.000 description 1
- QGVBFDIREUUSHX-IFFSRLJSSA-N Thr-Val-Gln Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O QGVBFDIREUUSHX-IFFSRLJSSA-N 0.000 description 1
- AKHDFZHUPGVFEJ-YEPSODPASA-N Thr-Val-Gly Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(=O)NCC(O)=O AKHDFZHUPGVFEJ-YEPSODPASA-N 0.000 description 1
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 1
- 239000004473 Threonine Substances 0.000 description 1
- 108060008539 Transglutaminase Proteins 0.000 description 1
- BIJDDZBDSJLWJY-PJODQICGSA-N Trp-Ala-Val Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(O)=O BIJDDZBDSJLWJY-PJODQICGSA-N 0.000 description 1
- PHNBFZBKLWEBJN-BPUTZDHNSA-N Trp-Glu-Gln Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)N)C(=O)O)N PHNBFZBKLWEBJN-BPUTZDHNSA-N 0.000 description 1
- 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 1
- 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 1
- RRVUOLRWIZXBRQ-IHPCNDPISA-N Trp-Leu-Lys Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)NC(=O)[C@H](CC1=CNC2=CC=CC=C21)N RRVUOLRWIZXBRQ-IHPCNDPISA-N 0.000 description 1
- HJWLQSFTGDQSRX-BPUTZDHNSA-N Trp-Met-Ser Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(O)=O HJWLQSFTGDQSRX-BPUTZDHNSA-N 0.000 description 1
- BIBZRFIKOLGWFQ-XIRDDKMYSA-N Trp-Pro-Gln Chemical compound C1C[C@H](N(C1)C(=O)[C@H](CC2=CNC3=CC=CC=C32)N)C(=O)N[C@@H](CCC(=O)N)C(=O)O BIBZRFIKOLGWFQ-XIRDDKMYSA-N 0.000 description 1
- KBKTUNYBNJWFRL-UBHSHLNASA-N Trp-Ser-Asn Chemical compound C1=CC=C2C(C[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(O)=O)=CNC2=C1 KBKTUNYBNJWFRL-UBHSHLNASA-N 0.000 description 1
- AKFLVKKWVZMFOT-IHRRRGAJSA-N Tyr-Arg-Asn 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](CC(N)=O)C(O)=O AKFLVKKWVZMFOT-IHRRRGAJSA-N 0.000 description 1
- KDGFPPHLXCEQRN-STECZYCISA-N Tyr-Arg-Ile 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)CC)C(O)=O KDGFPPHLXCEQRN-STECZYCISA-N 0.000 description 1
- DWJQKEZKLQCHKO-SRVKXCTJSA-N Tyr-Asn-Cys Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CS)C(=O)O)N)O DWJQKEZKLQCHKO-SRVKXCTJSA-N 0.000 description 1
- AYHSJESDFKREAR-KKUMJFAQSA-N Tyr-Asn-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 AYHSJESDFKREAR-KKUMJFAQSA-N 0.000 description 1
- FXYOYUMPUJONGW-FHWLQOOXSA-N Tyr-Gln-Phe Chemical compound C([C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=C(O)C=C1 FXYOYUMPUJONGW-FHWLQOOXSA-N 0.000 description 1
- LOOCQRRBKZTPKO-AVGNSLFASA-N Tyr-Glu-Asn Chemical compound NC(=O)C[C@@H](C(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](N)CC1=CC=C(O)C=C1 LOOCQRRBKZTPKO-AVGNSLFASA-N 0.000 description 1
- CNLKDWSAORJEMW-KWQFWETISA-N Tyr-Gly-Ala Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)NCC(=O)N[C@@H](C)C(O)=O CNLKDWSAORJEMW-KWQFWETISA-N 0.000 description 1
- PMDWYLVWHRTJIW-STQMWFEESA-N Tyr-Gly-Arg Chemical compound NC(N)=NCCC[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1 PMDWYLVWHRTJIW-STQMWFEESA-N 0.000 description 1
- FBHBVXUBTYVCRU-BZSNNMDCSA-N Tyr-His-Leu Chemical compound C([C@@H](C(=O)N[C@@H](CC(C)C)C(O)=O)NC(=O)[C@@H](N)CC=1C=CC(O)=CC=1)C1=CN=CN1 FBHBVXUBTYVCRU-BZSNNMDCSA-N 0.000 description 1
- BSCBBPKDVOZICB-KKUMJFAQSA-N Tyr-Leu-Asp 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(O)=O)C(O)=O BSCBBPKDVOZICB-KKUMJFAQSA-N 0.000 description 1
- DWAMXBFJNZIHMC-KBPBESRZSA-N Tyr-Leu-Gly Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC(C)C)C(=O)NCC(O)=O DWAMXBFJNZIHMC-KBPBESRZSA-N 0.000 description 1
- NSGZILIDHCIZAM-KKUMJFAQSA-N Tyr-Leu-Ser Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)N NSGZILIDHCIZAM-KKUMJFAQSA-N 0.000 description 1
- CWVHKVVKAQIJKY-ACRUOGEOSA-N Tyr-Lys-Phe Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC2=CC=C(C=C2)O)N CWVHKVVKAQIJKY-ACRUOGEOSA-N 0.000 description 1
- YYLHVUCSTXXKBS-IHRRRGAJSA-N Tyr-Pro-Ser Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(O)=O YYLHVUCSTXXKBS-IHRRRGAJSA-N 0.000 description 1
- XGZBEGGGAUQBMB-KJEVXHAQSA-N Tyr-Pro-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC2=CC=C(C=C2)O)N)O XGZBEGGGAUQBMB-KJEVXHAQSA-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
- QFHRUCJIRVILCK-YJRXYDGGSA-N Tyr-Thr-Cys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CS)C(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)O)N)O QFHRUCJIRVILCK-YJRXYDGGSA-N 0.000 description 1
- AKRHKDCELJLTMD-BVSLBCMMSA-N Tyr-Trp-Arg Chemical compound C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)NC(=O)[C@H](CC3=CC=C(C=C3)O)N AKRHKDCELJLTMD-BVSLBCMMSA-N 0.000 description 1
- AFWXOGHZEKARFH-ACRUOGEOSA-N Tyr-Tyr-His Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CC=1NC=NC=1)C(O)=O)C1=CC=C(O)C=C1 AFWXOGHZEKARFH-ACRUOGEOSA-N 0.000 description 1
- 101150074732 U gene Proteins 0.000 description 1
- 102100031358 Urokinase-type plasminogen activator Human genes 0.000 description 1
- IZFVRRYRMQFVGX-NRPADANISA-N Val-Ala-Gln Chemical compound C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](C(C)C)N IZFVRRYRMQFVGX-NRPADANISA-N 0.000 description 1
- YFOCMOVJBQDBCE-NRPADANISA-N Val-Ala-Glu Chemical compound C[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)O)NC(=O)[C@H](C(C)C)N YFOCMOVJBQDBCE-NRPADANISA-N 0.000 description 1
- ZLFHAAGHGQBQQN-AEJSXWLSSA-N Val-Ala-Pro Chemical compound C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](C(C)C)N ZLFHAAGHGQBQQN-AEJSXWLSSA-N 0.000 description 1
- ZLFHAAGHGQBQQN-GUBZILKMSA-N Val-Ala-Pro Natural products CC(C)[C@H](N)C(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(O)=O ZLFHAAGHGQBQQN-GUBZILKMSA-N 0.000 description 1
- SLLKXDSRVAOREO-KZVJFYERSA-N Val-Ala-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](C(C)C)N)O SLLKXDSRVAOREO-KZVJFYERSA-N 0.000 description 1
- COYSIHFOCOMGCF-WPRPVWTQSA-N Val-Arg-Gly Chemical compound CC(C)[C@H](N)C(=O)N[C@H](C(=O)NCC(O)=O)CCCN=C(N)N COYSIHFOCOMGCF-WPRPVWTQSA-N 0.000 description 1
- COYSIHFOCOMGCF-UHFFFAOYSA-N Val-Arg-Gly Natural products CC(C)C(N)C(=O)NC(C(=O)NCC(O)=O)CCCN=C(N)N COYSIHFOCOMGCF-UHFFFAOYSA-N 0.000 description 1
- IVXJODPZRWHCCR-JYJNAYRXSA-N Val-Arg-Phe Chemical compound CC(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 IVXJODPZRWHCCR-JYJNAYRXSA-N 0.000 description 1
- DCOOGDCRFXXQNW-ZKWXMUAHSA-N Val-Asn-Cys Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CS)C(=O)O)N DCOOGDCRFXXQNW-ZKWXMUAHSA-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
- OGNMURQZFMHFFD-NHCYSSNCSA-N Val-Asn-Lys Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CCCCN)C(=O)O)N OGNMURQZFMHFFD-NHCYSSNCSA-N 0.000 description 1
- ISERLACIZUGCDX-ZKWXMUAHSA-N Val-Asp-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](C(C)C)N ISERLACIZUGCDX-ZKWXMUAHSA-N 0.000 description 1
- QHDXUYOYTPWCSK-RCOVLWMOSA-N Val-Asp-Gly Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)NCC(=O)O)N QHDXUYOYTPWCSK-RCOVLWMOSA-N 0.000 description 1
- QHFQQRKNGCXTHL-AUTRQRHGSA-N Val-Gln-Glu Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(O)=O QHFQQRKNGCXTHL-AUTRQRHGSA-N 0.000 description 1
- ZXAGTABZUOMUDO-GVXVVHGQSA-N Val-Glu-Lys Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)O)N ZXAGTABZUOMUDO-GVXVVHGQSA-N 0.000 description 1
- BEGDZYNDCNEGJZ-XVKPBYJWSA-N Val-Gly-Gln Chemical compound CC(C)[C@H](N)C(=O)NCC(=O)N[C@H](C(O)=O)CCC(N)=O BEGDZYNDCNEGJZ-XVKPBYJWSA-N 0.000 description 1
- CHWRZUGUMAMTFC-IHRRRGAJSA-N Val-His-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)C(C)C)CC1=CNC=N1 CHWRZUGUMAMTFC-IHRRRGAJSA-N 0.000 description 1
- XTDDIVQWDXMRJL-IHRRRGAJSA-N Val-Leu-His Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)[C@H](C(C)C)N XTDDIVQWDXMRJL-IHRRRGAJSA-N 0.000 description 1
- 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 1
- VPGCVZRRBYOGCD-AVGNSLFASA-N Val-Lys-Val Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(O)=O VPGCVZRRBYOGCD-AVGNSLFASA-N 0.000 description 1
- FMQGYTMERWBMSI-HJWJTTGWSA-N Val-Phe-Ile Chemical compound CC[C@H](C)[C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)[C@H](C(C)C)N FMQGYTMERWBMSI-HJWJTTGWSA-N 0.000 description 1
- ZEBRMWPTJNHXAJ-JYJNAYRXSA-N Val-Phe-Met Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCSC)C(=O)O)N ZEBRMWPTJNHXAJ-JYJNAYRXSA-N 0.000 description 1
- SSYBNWFXCFNRFN-GUBZILKMSA-N Val-Pro-Ser Chemical compound CC(C)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(O)=O SSYBNWFXCFNRFN-GUBZILKMSA-N 0.000 description 1
- DEGUERSKQBRZMZ-FXQIFTODSA-N Val-Ser-Ala Chemical compound CC(C)[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(O)=O DEGUERSKQBRZMZ-FXQIFTODSA-N 0.000 description 1
- 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 1
- VBTFUDNTMCHPII-UHFFFAOYSA-N Val-Trp-Tyr Natural products C=1NC2=CC=CC=C2C=1CC(NC(=O)C(N)C(C)C)C(=O)NC(C(O)=O)CC1=CC=C(O)C=C1 VBTFUDNTMCHPII-UHFFFAOYSA-N 0.000 description 1
- WHNSHJJNWNSTSU-BZSNNMDCSA-N Val-Val-Trp Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)C(C)C)C(O)=O)=CNC2=C1 WHNSHJJNWNSTSU-BZSNNMDCSA-N 0.000 description 1
- 102100028885 Vitamin K-dependent protein S Human genes 0.000 description 1
- 101710193896 Vitamin K-dependent protein S Proteins 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 102100021377 Zinc finger protein 18 Human genes 0.000 description 1
- 101710160445 Zinc finger protein 18 Proteins 0.000 description 1
- VVBXXVAFSPEIJQ-CVIPOMFBSA-N [(2r)-3-[[(2r)-1-[[(2s,5r,8r,11r,12s,15s,18s,21s)-15-[3-(diaminomethylideneamino)propyl]-21-hydroxy-5-[(4-hydroxyphenyl)methyl]-4,11-dimethyl-2-(2-methylpropyl)-3,6,9,13,16,22-hexaoxo-8-propan-2-yl-10-oxa-1,4,7,14,17-pentazabicyclo[16.3.1]docosan-12-yl]am Chemical compound C([C@@H]1C(=O)N[C@@H](C(=O)O[C@H](C)[C@@H](C(N[C@@H](CCCN=C(N)N)C(=O)N[C@H]2CC[C@H](O)N(C2=O)[C@@H](CC(C)C)C(=O)N1C)=O)NC(=O)[C@H](NC(=O)[C@H](O)COS(O)(=O)=O)CC(C)C)C(C)C)C1=CC=C(O)C=C1 VVBXXVAFSPEIJQ-CVIPOMFBSA-N 0.000 description 1
- 108010024078 alanyl-glycyl-serine Proteins 0.000 description 1
- 108010045023 alanyl-prolyl-tyrosine Proteins 0.000 description 1
- 108010041407 alanylaspartic acid Proteins 0.000 description 1
- 108010087924 alanylproline Proteins 0.000 description 1
- 108010070783 alanyltyrosine 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
- 150000001413 amino acids Chemical group 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 230000000890 antigenic effect Effects 0.000 description 1
- 101150010487 are gene Proteins 0.000 description 1
- 108010013835 arginine glutamate Proteins 0.000 description 1
- 108010072041 arginyl-glycyl-aspartic acid Proteins 0.000 description 1
- 108010009111 arginyl-glycyl-glutamic acid Proteins 0.000 description 1
- 108010091092 arginyl-glycyl-proline Proteins 0.000 description 1
- 108010069926 arginyl-glycyl-serine Proteins 0.000 description 1
- 108010060035 arginylproline Proteins 0.000 description 1
- 108010038633 aspartylglutamate Proteins 0.000 description 1
- 108010092854 aspartyllysine Proteins 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 244000309466 calf Species 0.000 description 1
- 230000005859 cell recognition Effects 0.000 description 1
- 210000002230 centromere Anatomy 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 210000001612 chondrocyte Anatomy 0.000 description 1
- 230000000875 corresponding effect Effects 0.000 description 1
- 210000004748 cultured cell Anatomy 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 239000002875 cyclin dependent kinase inhibitor Substances 0.000 description 1
- 229940043378 cyclin-dependent kinase inhibitor Drugs 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 108010054813 diprotin B Proteins 0.000 description 1
- 235000015177 dried meat Nutrition 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- ZMMJGEGLRURXTF-UHFFFAOYSA-N ethidium bromide Chemical compound [Br-].C12=CC(N)=CC=C2C2=CC=C(N)C=C2[N+](CC)=C1C1=CC=CC=C1 ZMMJGEGLRURXTF-UHFFFAOYSA-N 0.000 description 1
- 229960005542 ethidium bromide Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 238000000684 flow cytometry Methods 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 description 1
- 108010055341 glutamyl-glutamic acid Proteins 0.000 description 1
- 108010073628 glutamyl-valyl-phenylalanine Proteins 0.000 description 1
- 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 1
- 108010027668 glycyl-alanyl-valine Proteins 0.000 description 1
- 108010026364 glycyl-glycyl-leucine Proteins 0.000 description 1
- 108010038983 glycyl-histidyl-lysine Proteins 0.000 description 1
- 108010079413 glycyl-prolyl-glutamic acid Proteins 0.000 description 1
- 108010082286 glycyl-seryl-alanine Proteins 0.000 description 1
- 108010045126 glycyl-tyrosyl-glycine Proteins 0.000 description 1
- 108010010147 glycylglutamine Proteins 0.000 description 1
- 108010015792 glycyllysine Proteins 0.000 description 1
- 108010081551 glycylphenylalanine Proteins 0.000 description 1
- 108010077515 glycylproline Proteins 0.000 description 1
- 210000003958 hematopoietic stem cell Anatomy 0.000 description 1
- 108010040030 histidinoalanine Proteins 0.000 description 1
- 108010045383 histidyl-glycyl-glutamic acid Proteins 0.000 description 1
- 108010036413 histidylglycine Proteins 0.000 description 1
- 108010025306 histidylleucine Proteins 0.000 description 1
- 108010018006 histidylserine Proteins 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 108010027338 isoleucylcysteine Proteins 0.000 description 1
- 210000002415 kinetochore Anatomy 0.000 description 1
- 108010053037 kyotorphin Proteins 0.000 description 1
- 108010073472 leucyl-prolyl-proline Proteins 0.000 description 1
- 108010003700 lysyl aspartic acid Proteins 0.000 description 1
- 108010017391 lysylvaline Proteins 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 108010022588 methionyl-lysyl-proline Proteins 0.000 description 1
- 108010068488 methionylphenylalanine Proteins 0.000 description 1
- 210000003632 microfilament Anatomy 0.000 description 1
- 210000000214 mouth Anatomy 0.000 description 1
- 210000002894 multi-fate stem cell Anatomy 0.000 description 1
- 210000004165 myocardium Anatomy 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 230000004072 osteoblast differentiation Effects 0.000 description 1
- 230000001582 osteoblastic effect Effects 0.000 description 1
- 210000004409 osteocyte Anatomy 0.000 description 1
- 210000003460 periosteum Anatomy 0.000 description 1
- 108010084525 phenylalanyl-phenylalanyl-glycine Proteins 0.000 description 1
- 108010024654 phenylalanyl-prolyl-alanine Proteins 0.000 description 1
- 108010024607 phenylalanylalanine Proteins 0.000 description 1
- 108010012581 phenylalanylglutamate Proteins 0.000 description 1
- 108010073101 phenylalanylleucine Proteins 0.000 description 1
- 108010051242 phenylalanylserine Proteins 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 108010025488 pinealon Proteins 0.000 description 1
- 230000008488 polyadenylation Effects 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 229940097325 prolactin Drugs 0.000 description 1
- 108010020755 prolyl-glycyl-glycine Proteins 0.000 description 1
- 108010014614 prolyl-glycyl-proline Proteins 0.000 description 1
- 108010079317 prolyl-tyrosine Proteins 0.000 description 1
- 108010004914 prolylarginine Proteins 0.000 description 1
- 108010070643 prolylglutamic acid Proteins 0.000 description 1
- 108010090894 prolylleucine Proteins 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 150000003180 prostaglandins Chemical class 0.000 description 1
- 235000019419 proteases Nutrition 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000010839 reverse transcription Methods 0.000 description 1
- 108010048818 seryl-histidine Proteins 0.000 description 1
- 108010071207 serylmethionine Proteins 0.000 description 1
- 210000002027 skeletal muscle Anatomy 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 108010033670 threonyl-aspartyl-tyrosine Proteins 0.000 description 1
- 102000003601 transglutaminase Human genes 0.000 description 1
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 1
- 229940038773 trisodium citrate Drugs 0.000 description 1
- 108010035534 tyrosyl-leucyl-alanine Proteins 0.000 description 1
- 108010051110 tyrosyl-lysine Proteins 0.000 description 1
- 108010003137 tyrosyltyrosine Proteins 0.000 description 1
- IBIDRSSEHFLGSD-UHFFFAOYSA-N valinyl-arginine Natural products CC(C)C(N)C(=O)NC(C(O)=O)CCCN=C(N)N IBIDRSSEHFLGSD-UHFFFAOYSA-N 0.000 description 1
- 108010000998 wheylin-2 peptide Proteins 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
- C12N15/1138—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against receptors or cell surface proteins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6881—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for tissue or cell typing, e.g. human leukocyte antigen [HLA] probes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/158—Expression markers
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Wood Science & Technology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Biotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Physics & Mathematics (AREA)
- Immunology (AREA)
- Analytical Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Plant Pathology (AREA)
- Toxicology (AREA)
- Gastroenterology & Hepatology (AREA)
- Cell Biology (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Peptides Or Proteins (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
本发明提供一种用于检测、分离识别间充质干细胞的标记以及采用该标记检测、分离识别间充质干细胞的方法。序列表所示基因在间充质干细胞中特异表达。该基因构成作为检测间充质干细胞的标记。尤其是,本发明含有用于检测该间充质干细胞标记基因的探针,以及在检测该间充质干细胞基因标记时扩增被检细胞所述基因的PCR所使用的引物,还含有本发明的间充质干细胞标记基因表达的多肽构成的用于检测间充质干细胞的多肽标记、用于检测该多肽标记的与该多肽标记特异结合的抗体,尤其是含有一种采用用于检测间充质干细胞标记基因的探针、与多肽标记特异结合的抗体对间充质干细胞进行识别、分离的方法。
Description
本申请是以下申请的分案申请:
原案申请号:200480007550.0(国际申请号:PCT/JP2004/002457);
原案申请日:2004年02月27日;
原案发明创造名称:检测间充质干细胞的标记和采用该标记识别间充质干细胞的方法
技术领域
本发明涉及检测、分离识别间充质干细胞、尤其是涉及在检测、分离识别间充质干细胞中使用的用于检测间充质干细胞的基因标记和多肽标记,以及用所述标记检测、识别间充质干细胞的方法。
背景技术
众所周知,间充质干细胞是存在于哺乳类的骨髓等处,分化为脂肪细胞、软骨细胞、骨细胞的多能性干细胞。由于其分化的多能性,间充质干细胞作为以再生医疗为的目的多种组织的移植材料正受到人们关注(《基因医学》第4卷第2期(2000)p58-61)。最近,发表了关于间充质干细胞研究现状与展望的综述,作出了关于间充质干细胞的收集与培养的报告(实验医学、第19卷第3期(2月号)2001、p350-356)。此外,已有报道间充质干细胞也存在于脂肪组织中(Tissue Engineering,P.A.Zuk et al.,Multilineage cells from human adipose tissue:implications for cell-based therapies.7:211-228,2001)。
近年,一些专利申请公开了关于间充质干细胞的培养、分化等内容。例如,特表平11-506610号公报中公开了关于在无血清环境下维持人间充质前体细胞生存的组和物及其方法,在特表平10-512756号公报中公开了关于为了诱导间充质干细胞的分化将其与由前列腺素、抗坏血酸、胶原细胞外基质等组成的骨诱导因子、分化付随因子、软骨诱导因子等生物活性因子相接触的方法,在特开2000-217576号公报中公开了关于在催乳激素或其等效物共存下培养多能性间充质细胞,使间充质细胞分化成脂肪细胞的方法。
首先,本发明人公开了一种通过在基底膜细胞外基质存在条件下或是在含有成纤维细胞增殖因子(FGF)等物质的培养基中培养间充质干细胞,使得间充质干细胞得以显著的增殖,并且发现能够维持其分化能力,与以前的培养方法相比获得了效果显著的间充质干细胞的培养方法(特开2003-52360号公报)。并且,公开了一种为了在采集间充质干细胞时在采集母体以安全并且容易方式进行采集,从口腔组织中分离采集间充质干细胞的方法(特开2003-52365号公报)。
近年,随着再生医疗的进展,由于其分化多能性,人们正关注于将间充质干细胞作为骨、软骨、肌肉、脂肪、齿周组织等多种组织的再生医疗性的移植材料。为了在组织的再生医疗中利用间充质细胞,首先,从活体组织中采集所述干细胞,使其增殖,尤其是必需使其分化增殖,从而进行组织的制备。间充质干细胞存在于骨髓或骨膜中,为了能在组织再生医疗中实现实用化,首先,必须要开发出能够安全地从所述组织中采集间充质干细胞的方法。而且,为了间充质干细胞在组织再生医疗中实现实用化,必须要开发出足以确保干细胞数量的技术。为了实现上述目的,重要的是开发出仍能维持所采集的间充质干细胞的分化能力的培养增殖技术。
通过上述内容,本发明人开发出一种实现在采集间充质干细胞时从采集母体中以安全且容易的方式采集的分离采集的方法。尤其是,本发明人开发了一种通过在基底膜细胞外基质存在条件下或是在含有成纤维细胞增殖因子(FGF)等物质的培养基中培养间充质干细胞,以维持其的分化能力的形式大量增殖间充质干细胞的方法(特开2003-52360号公報)。但是,为了使增殖培养的间充质干细胞在再生医疗中实用化,必须确认所培养的细胞是间充质干细胞,必须开发出检测、识别该间充质干细胞的方法。以前,在间充质干细胞中,无法对该细胞的特征标记基因进行鉴定。因此、为了使间充质干细胞在再生医疗中实现实用化解决的重要课题是必须要开发出鉴定间充质干细胞的标记基因,从而检测分离识别间充质干细胞的方法。
本发明提供了用于检测识别间充质干细胞的间充质干细胞检测用基因标记和间充质干细胞检测用多肽标记,用于检测该基因标记的PCR扩增用引物,以及采用该标记和该引物检测、识别间充质干细胞的方法。本发明人为了发现检测间充质干细胞用的标记基因,对间充质干细胞中的各种基因的表达进行了比较,对构成标记的基因进行研究,结果发现,与序列表所示的13个基因相关的间充质干细胞与成纤维细胞之间的表达量存在差异,间充质干细胞中
特异表达,发现这些基因是间充质干细胞检测用的标记,从而完成本发明。本发明含有用于检测该间充质干细胞标记基因的探针,和在检测该间充质干细胞标记基因时用于扩增被检细胞的该基因子的PCR所用引物。此外,本发明还含有本发明的间充质干细胞标记基因表达的多肽构成的用于检测间充质干细胞的多肽标记、用于检测该多肽标记的与该多肽标记特异结合的抗体。更优选本发明含有一种采用用于检测间充质干细胞标记基因的探针、与多肽标记特异结合的抗体的间充质干细胞识别方法和分离方法。
下面对完成本发明的过程进行说明,在各种干细胞中,间充质干细胞在骨、软骨、肌肉、脂肪、骨骼肌、心肌、血管、神经等许多组织中保持了分化能力,因此间充质干细胞作为再生用细胞有很大前景。但是,迄今为止未有过对间充质干细胞特征标记基因鉴定的描述。因此,本发明人为了确定间充质干细胞的特征标记基因,进行了积极地研究。也就是,本发明人首次开发,通过在FGF等存在下培养间充质干细胞,采用仍维持其分化能力的快速增殖方法,增殖间充质干细胞,在FGF等存在下培养由该方法获得的间充质干细胞与人成纤维细胞,从培养细胞中抽提mRNA,以该mRNA为模板,以DNA芯片(インサイト社insit公司)作为探针,通过DNA微阵列法对人源间充质干细胞与成纤维细胞中表达的基因进行比较。
9400个基因中有63个基因在间充质干细胞中显著高表达,141个基因显著低表达。其中87个基因表达差别达3倍以上(29个基因在间充质干细胞中高表达、58个基因低表达)。从来源于三个个体的间充质干细胞以及来源于三个个体的成纤维细胞中抽提全RNA,以它们为模板,通过半定量的RT-PCR法对上述87个基因的表达量进行调查。其结果是大多数基因的表达量未发现差异。此外,由于不同个体的间充质干细胞,或成纤维细胞之间也存在表达量的差异,认为由个体差异引起表达差异的情形也是很多的。
根据RT-PCR,经确认间充质干细胞中高表达的是3个基因(组织因子途径抑制剂2(tissue factor pathway inhibitor 2),2类主要组织相容性复合体DR β3(majorhistocompatibility complex class2 DR beta 3),丝氨酸(或半胱氨酸)蛋白酶抑制剂)、经确认低表达的基因有10种(基质金属蛋白酶(matrix metalloprotease)1,XV-α型胶原酶(collagenase type XV alpha),CUG三联体重叠RNA结合蛋白(CUG triplet repeat RNAbinding protein),皮肤桥蛋白,蛋白质酪氨酸激酶7(蛋白tyrosine激酶7),异柠檬酸脱氢酶2,Sam68样磷酸酪氨酸蛋白(Sam68样phosphotyrosine protein),C-型凝集素超家族成员2,肾上腺髓质素,载脂蛋白D)。通过测定这13个基因的表达量,使得在短时间内便宜地对难以识别的间充质干细胞进行鉴定成为可能。尤其是,本发明中,进行基因检索的结果是,确认了在间充质干细胞或成纤维细胞中表达量存在差异的许多基因。由于这些基因构成了用于检测间充质干细胞的基因表记物,其通过构建成检测基因用探针,以微阵列或DNA芯片等形式能够用于检测间充质干细胞。
发明内容
本发明具体的是由下列物质构成的:用于检测间充质干细胞的基因标记,特征在于其具有序列表1、2、4、6、7、9、10、11、12、14、15、17、19或46所示的碱基序列的基因、和用于检测间充质干细胞的基因标记,其特征在于其为整联蛋白,ALPHA6(ITGA6)基因,MRNA(NM_000210);溶质载体家族20(PHOSPHATE TRANSPORTER)、成员1(NM_005415)基因;核糖核苷酸还原酶M2多肽(RRM2),MRNA(NM_001034)基因;滤泡素抑制素(FOLLISTATIN)(FST),转录变异体FST317,MRNA基因(NM_006350);SPROUTY(DROSOPHILA)HOMOLOG2(SPRY2),MRNA(NM_005842);RAB3B,成员RAS ONCOGENE FAMILY(RAB3B),MRNA(NM_002867)基因;溶质载体家族2(FACILITATED GLUCOSE TRANSPORTER)(NM_006516)基因;白介素13受体,ALPHA2(IL13RA2),MRNA(NM_000640)基因;丝氨酸/苏氨酸激酶12(STK12),MRNA(NM_004217)基因;MINICHROMOSOME MAINTENANCE DEFICIENT(S.CEREVISIAE)5(CE)(NM_006739)基因;甲状腺激素受体中间子INTERACTOR 13(TRIP13),MRNA(NM_004237)基因;类驱动蛋白6(有丝分裂着丝粒相关驱动蛋白)(K)(NM_006845)基因;细胞周期蛋白依赖性激酶抑制因子3(CDK2-ASSOCIATEDDUAL(NM_005192)基因;染色体凝缩蛋白G(HCAP-G),MRNA(NM_022346)基因;CDC28蛋白激酶1(CKS1),MRNA(NM_001826)基因;胞质分裂蛋白质调节子1(PRC1),MRNA(NM_003981)基因;细胞增殖周期2,G1→S→G2→M(CDC2),MRNA(NM_001786)基因;CDC20(细胞增殖周期20,酿酒酵母,同源基因)(CD)(NM_001255)基因;LIKELY ORTHOLOG OF MATERNAL EMBRYONICLEUCINE ZIPPER KINAS(NM_014791)基因;微染色体维持缺陷蛋白(酿酒酵母)7(M)(NM_005916)基因;细胞周期蛋白A2(CCNA2),MRNA(NM_001237)基因;胸苷激酶1,SOLUBLE(TK1),MRNA(NM_003258)基因;和细胞周期蛋白依赖性激酶抑制因子2A(黑色素瘤,p16,抑制CDK4)(CDKN2A),mRNA基因(NM_000077)(权利要求2)、和用于检测间充质干细胞的基因标记,其特征在于其为EGF-containing fibulin-like细胞外基质蛋白1(NM_018894)基因;人胰岛素样生长因子结合蛋白5(IGFBP5)mRNA(AU132011)基因;人克隆24775 mRNA序列(AA402981)基因;蛋白聚糖1,分泌颗粒(AV734015)基因;人胰岛素样生长因子结合蛋白5(AA374325)基因;溶质载体家族21(有机阴离子转运蛋白),成员3(AF085224)基因;谷氨酰胺转移酶2(C多肽,蛋白质-谷氨酰胺-γ-谷酰基转移酶)(AL552373)基因;抗血友病因子II(凝血酶)受体(M62424);纤维蛋白溶酶原活化因子,鸟激酶(NM_002658)基因;金属蛋白酶3组织抑制剂(Sorsby fundus dystrophy,pseudoinflammatory)(W96324)基因;基质Gla蛋白(BF668572)基因;B-cell CLL/淋巴瘤1(Z23022)基因;CD74抗原(主要组织相容性复合体的不变多肽,II类相关抗原)(BG333618)基因;内收蛋白(adducin)3(γ)(AL135243)基因;溶质载体家族16(一元羧酸传送子),成员4(NM_004696)基因;S蛋白(α)(NM_000313)基因;磷脂酰肌醇(4,5)二磷酸5-磷酸酶同系物;磷脂酰肌醇多聚磷酸5-磷酸酶IV型(AF187891)基因;孕酮膜结合蛋白质(BE858855)基因;脑源性神经营养因子(X60201)基因;或者载脂蛋白E(BF967316)基因(权利要求3)、和用于检测间充质干细胞的基因标记,特征在于其是人WNT抑制因子-1(WIF-1),MRNA(NM_007191)基因;人假拟蛋白(HYPOTHETICAL PROTEIN)FLJ11175(FLJ11175),MRNA(NM_018349)基因;人RHO GDP解离抑止剂(GDI)β(ARHGDIB),MRNA(NM_001175)基因;人钾中间体/少量电导的钙活化(SMALL CONDUCTANCECALCIUM-ACTIVATE)(NM_021614)基因;人核因子(红细胞衍生物2)-类似物3(NFE2L3),MRNA(NM_004289基因;人GS3955蛋白(GS3955),MRNA(NM_021643)基因;人CDNA3′端与糖蛋白相类似的MUC18(AA302605)基因;人假拟蛋白(HYPOTHETICAL PROTEIN)FLJ21841(FLJ21841),MRNA(NM_024609)基因;人锌指蛋白185(LIM区域)(ZNF185),MRNA(NM_007150)基因;细胞周期控制中涉及的SC1=假定的转移-活化因子[人,MRNA,24](S53374)基因;人NADH酶(辅酶Q)1α子复合体,8(19K)(NM_014222)基因;酵母YEAST MCM10的人同系物;假拟蛋白(HYPOTHETICAL PROTEIN)PRO2249(PRRO2)(NM_018518)基因;人胶原,VII型,α1(大疱性表皮松解症,DYSTRO(NM_000094)基因;人自分泌运动因子受体(AMFR),MRNA(NM_001144)基因;人克隆24421 MRNA序列/CDS=未知/GB=AF070641/GI=3283914/UG=(AF070641)基因;人MRNA基因;CDNA DKFZP586E1621(源自DKFZP586E1621克隆)/CDS=未知/GB(AL080235)基因(权利要求4)、和用于检测间充质干细胞的基因标记,特征在于其是人RESERVED(KCNK12),MRNA(NM_022055)基因;人泛素结合酶E2C(UBE2C),MRNA(NM_007019)基因;人CDNA FLJ10517 FIS,克隆NT2RP2000812/CDS=(61,918)/GB=AK001379/G(AK001379)基因;人软骨连接蛋白1(CRTL1),MRNA(NM_001884)基因;人MRNA基因;CDNA DKFZP434F2322(由克隆DKFZP434F2322获得)/CDS=未知/GB(AL133105);人,克隆MGC:9549IMAGE:3857382,MRNA,完整CDS/CDS=(92,1285)/G(BC012453)基因;人假拟蛋白(HYPOTHETICAL PROTEIN)DKFZP586J1119(DKFZP586J1119),MRNA(NM_032270)基因;人GLIA成熟因子,γ(GMFG),MRNA(NM_004877)基因人CDNA:FLJ23095 FIS,克隆LNG07413/CDS=未知/GB=AK026748/GI=10(AK026748)基因;人假拟蛋白(HYPOTHETICAL PROTEIN)DKFZP762E1312(DKFZP762E1312),MRNA(NM_018410)基因;人IROQUOIS类同源域蛋白(IRX-2A),MRNA(NM_005853)基因;或者人假拟蛋白(HYPOTHETICAL PROTEIN)FLJ10540(FLJ10540),MRNA(NM_018131)基因(权利要求5)、和用于检测间充质干细胞的基因标记,特征在于其是人MRNA;CDNA DKFZP434C1915(由克隆DKFZP434C1915获得)基因;PARTIAL CDS/C(AL137698);人微染色体维持缺陷型(酿酒酵母(S.CEREVISIAE))7(M)(NM_005916)基因;人动力蛋白,细胞质的,中间体多肽1(DNCI1),M(NM_004411)基因;蛋白质基因产物的人MRNA(PGP)9.5.(X04741)基因;人RAD51-相互作用蛋白(PIR51),MRNA(NM_006479)基因;人含有杆状病毒IAP重复序列的5(SURVIVIN)(BIRC5),MR(NM_001168)基因;人UDP-N-乙酰基-ALPHA-D-半乳糖胺:多肽N-乙酰基GAL(NM 004482)基因;人细胞周期蛋白B1(CCNB1),MRNA(NM_031966)基因;人FLAP结构特异性内切酶1(FEN1),MRNA基因(NM_004111);人丝氨酸/苏氨酸激酶15(STK15),MRNA基因(NM_003600);人MAD2(有丝分裂抑止缺陷型,酵母,同系物)-类似物1(MA)基因(NM_002358);人核仁蛋白ANKT(ANKT),MRNA基因(NM_018454);人与泛素结合酶类似的HSPC150蛋白(H)基因(NM_014176);人细胞色素P450类维生素A代谢蛋白(P450RAI-2)基因,(NM_019885);人NIMA(从未有丝分裂基因A)相关激酶2(NEK2),MR基因(NM_002497);人骨形态生成蛋白4(BMP4),MRNA基因(NM_001202);人CDNAFLJ10674 FIS,克隆NT2RP2006436/CDS=未知/GB=AK001536/GI(AK001536)基因;或者人着丝粒蛋白A(17KD)(CENPA),MRNA(NM_001809)基因(权利要求6)、和用于检测间充质干细胞的基因标记基因,特征在于其是人MRNA;CDNA DKFZP564P116(FROM克隆DKFZP564P116)/CDS=未知/GB=A(AL049338);人TTK蛋白质激酶(TTK),MRNA(NM_003318)基因;人KARYOPHERINα2(RAG COHORT1,IMPORTINα1)基因(KPNA(NM_002266);人聚合酶(DNA导向的),θ(POLQ),MRNA(NM_006596)基因;人ETS变异体基因5(ETS相关分子)(ETV5),MRNA基因(NM_004454);人含转化酸性卷曲螺旋蛋白(TRANSFORMING,ACIDIC COILED-COILCONTAINING蛋白)3(TAC)(NM_006342)基因;人驱动蛋白类似物1(KNSL1),MRNA基因(NM_004523);人着丝粒蛋白E(312KD)(CENPE),MRNA基因(NM_001813);人CDNA,3′END/克隆=IMAGE:1651289/克隆_END=3′/GB=AI12(AI123815)基因;人DISTAL-LESS HOMEO BOX 5(DLX5),MRNA基因(NM_005221);人V-MYB禽成髓细胞性白血病病毒癌基因同系物类似物2基因(NM_002466);或者人血清剥夺反应(磷脂酰丝氨酸结合PRO(NM_004657)基因(权利要求7)、和用于检测间充质干细胞的基因标记,特征在于其是人假拟蛋白(HYPOTHETICAL PROTEIN)FLJ10604(FLJ10604),MRNA基因(NM_018154);人核糖核酸酶HI基因,大亚基(RNASEHI),MRNA(NM_006397);人ANILLIN(果蝇SCRAPS同系物),肌动蛋白结合蛋白基因(NM_018685);人H4组蛋白家族,成员G(H4FG)基因,MRNA(NM_003542);人G蛋白连结受体37(内皮缩血管肽受体B型-(NM_005302)人泛素载体蛋白(E2-EPF),MRNA基因(NM_014501);人,类似于肿瘤差别表达1,克隆IMAGE:3639252,(BC007375)基因;人假拟蛋白(HYPOTHETICALPROTEIN)MGC2577(MGC2577),MRNA(NM_031299)基因;人假拟蛋白(HYPOTHETICAL PROTEIN)FLJ13912(FLJ13912),MRNA基因(NM_022770);人ANNEXIN A3(ANXA3),MRNA(NM_005139)基因;人STATHMIN 1/ONCO蛋白18(STMN1),MRNA基因(NM_005563)人,与核糖体蛋白L39类似,克隆MGC:20168IMAGE:4555759,M(BC012328);人POLO(果蝇)类似物激酶(PLK),MRNA基因(NM_005030)(权利要求8)、和用于检测间充质干细胞的基因标记,特征在于其是人蛋白酶复合体(PROSOME,MACROPAIN)26S亚基,ATP酶,5(PS)基因(NM_002805);人真核翻译起始因子4γ,2(EIF4G)基因(NM_001418);人二氢嘧啶酶-LIKE 3(DPYSL3)基因,MRNA)(NM_001387);人ADAPTOR相关蛋白复合体1,SIGMA 2亚基(AP1S2)基因(NM_003916);人网蛋白1,中间丝结合蛋白,500KD(P)基因(NM_000445);人异种核蛋白U(SCAFFOLD ATTAC(NM_031844)基因;人假拟蛋白(HYPOTHETICAL PROTEIN)MGC5306(MGC5306),MRNA基因(NM_024116);人MHC I类多肽相关序列A(MICA),MRNA基因(NM_000247);人PRK1相关蛋白(AWP1),MRNA基因(NM_019006);人孕酮受体膜成分2(PGRMC2),MRNA基因(NM_006320);人多聚谷氨酸结合蛋白1(PQBP1),MRNA基因(NM_005710);人S-腺苷甲硫氨酸脱羧酶1(AMD1),MRNA基因(NM_001634);人干扰素诱导的C型肝炎相关MICROTUBULARAG(NM_006417)基因;人蛋白激酶,AMP-活化的,γ1非催化性亚基(NON-CATALYTIC SUBUN)基因(NM_002733);人前胶原-脯氨酸,2-OXOGLUTARATE 4-DIOXYGENASE(脯氨酸(NM_004199);人血管内皮分化,溶血磷脂酸G-PROTE基因(NM 012152);或人KIAA0127基因产物(KIAA0127),MRNA基因(NM_014755)(权利要求9)、和具有与权利要求1-9中任一记载的用于检测间充质干细胞的基因标记在严谨条件下杂交的D N A序列的用于检测间充质干细胞基因标记的探针(权利要求10)、和由上述任一记载的碱基序列的反义链的全部或者部分构成的权利要求10记载的用于检测间充质干细胞基因标记的探针(权利要求11)、和用于检测间充质干细胞基因标记的微阵列或D N A芯片,特征在于其固定有至少一个及一个以上的权利要求10或11记载的D N A(权利要求12)、和上述的用于检测间充质干细胞标记基因的微阵列或D N A芯片,特征在于其固定有具有序列表序列号1、2、4、6、7、9、10、11、12、14、15、17、19或46所示碱基序列基因组、和检测出权利要求2-9中任一记载的基因组的2个以上基因的探针(权利要求13)、和用于检测间充质干细胞的多肽标记,特征在于其是具有序列表的序列3、5、8、13、16或18所示的氨基酸序列的多肽(权利要求14)、和一种抗体,特征在于其受权利要求14记载的多肽诱导、与该多肽特异性结合(权利要求15)、和权利要求15记载的抗体,其特征在于抗体是单克隆抗体(权利要求16)和权利要求15记载的抗体,其特征在于抗体是多克隆抗体(权利要求17)。
此外,本发明还由下列物质组成:识别间充质干细胞的方法,特征在于从被检细胞中检测出权利要求1-9中任一项记载的间充质干细胞标记基因表达(权利要求18)、和权利要求18记载的间充质干细胞的识别方法,其特征是采用RNA印迹法检测间充质干细胞标记基因的表达(权利要求19)、和权利要求18记载的间充质干细胞的识别方法,其特征是采用用于检测权利要求10或11记载的间充质干细胞标记基因的探针对间充质干细胞标记基因的表达进行检测(权利要求20)、和权利要求18记载的间充质干细胞的识别方法,其特征是采用用于检测权利要求12或13记载的间充质干细胞标记基因的微阵列或DNA芯片对间充质干细胞标记基因的表达进行检测(权利要求21)、和识别间充质干细胞的方法,其特征是权利要求18-21中任一记载的间充质干细胞标记基因表达的检测包括定量或半定量的PCR的使用(权利要求22)、和权利要求22记载的间充质干细胞的识别方法,其特征是其使用的定量的或半定量的PCR是RT-PCR法(权利要求23)。
此外,本发明还由以下物质组成:由具有序列表的序列号20所示的碱基序列的正义引物以及具有序列表的序列号21所示的碱基序列的反义引物、具有序列表的序列号22所示的碱基序列的正义引物和具有序列表的序列号23所示的碱基序列的反义引物、具有序列表的序列号24所示的碱基序列的正义引物和具有序列表的序列号25所示的碱基序列的反义引物、具有序列表的序列号26所示的碱基序列的正义引物和具有序列表的序列号27所示的碱基序列的反义引物、具有序列表的序列号28所示的碱基序列的正义引物和具有序列表的序列号29所示的碱基序列的反义引物、具有序列表的序列号30所示的碱基序列的正义引物和具有序列表的序列号31所示的碱基序列的反义引物、具有序列表的序列号32所示的碱基序列的正义引物和具有序列表的序列号33所示的碱基序列的反义引物、具有序列表的序列号34所示的碱基序列的正义引物和具有序列表的序列号35所示的碱基序列的反义引物、具有序列表的序列号36所示的碱基序列的正义引物和具有序列表的序列号37所示的碱基序列的反义引物、具有序列表的序列号38所示的碱基序列的正义引物和具有序列表的序列号39所示的碱基序列的反义引物、具有序列表的序列号40所示的碱基序列的正义引物和具有序列表的序列号41所示的碱基序列的反义引物、具有序列表的序列号42所示的碱基序列的正义引物和具有序列表的序列号43所示的碱基序列的反义引物、或具有序列表的序列号44所示的碱基序列的正义引物和具有序列表的序列号45所示的碱基序列的反义引物构成的用于扩增间充质干细胞的RT-PCR用引物(权利要求24)、和由具有序列表的序列号47所示的碱基序列的正义引物和具有序列表的序列号48所示的碱基序列的反义引物、具有序列表的序列号49所示的碱基序列的正义引物和具有序列表的序列号50所示的碱基序列的反义引物、具有序列表的序列号51所示的碱基序列的正义引物和具有序列表的序列号52所示的碱基序列的反义引物、具有序列表的序列号53所示的碱基序列的正义引物和具有序列表的序列号54所示的碱基序列的反义引物、具有序列表的序列号55所示的碱基序列的正义引物和具有序列表的序列号56所示的碱基序列的反义引物、具有序列表的序列号57所示的碱基序列的正义引物和具有序列表的序列号58所示的碱基序列的反义引物、具有序列表的序列号59所示的碱基序列的正义引物和具有序列表的序列号60所示的碱基序列的反义引物、具有序列表的序列号61所示的碱基序列的正义引物和具有序列表的序列号62所示的碱基序列的反义引物、具有序列表的序列号63所示的碱基序列的正义引物和具有序列表的序列号64所示的碱基序列的反义引物、具有序列表的序列号65所示的碱基序列的正义引物和具有序列表的序列号66所示的碱基序列的反义引物、具有序列表的序列号67所示的碱基序列的正义引物和具有序列表的序列号68所示的碱基序列的反义引物、或具有序列表的序列号69所示的碱基序列的正义引物和具有序列表的序列号70所示的碱基序列的反义引物构成的扩增间充质干细胞标记基因的实时P C R所使用的引物(权利要求25)、和具有序列表的序列号71所示的碱基序列的正义引物和具有序列表的序列号72所示的碱基序列的反义引物、具有序列表的序列号73所示的碱基序列的正义引物和具有序列表的序列号74所示的碱基序列的反义引物、具有序列表的序列号75所示的碱基序列的正义引物和具有序列表的序列号76所示的碱基序列的反义引物、具有序列表的序列号77所示的碱基序列的正义引物和具有序列表的序列号78所示的碱基序列的反义引物、具有序列表的序列号79所示的碱基序列的正义引物和具有序列表的序列号80所示的碱基序列的反义引物、具有序列表的序列号81所示的碱基序列的正义引物和具有序列表的序列号82所示的碱基序列的反义引物、具有序列表的序列号83所示的碱基序列的正义引物和具有序列表的序列号84所示的碱基序列的反义引物、具有序列表的序列号85所示的碱基序列的正义引物和具有序列表的序列号86所示的碱基序列的反义引物、具有序列表的序列号87所示的碱基序列的正义引物和具有序列表的序列号88所示的碱基序列的反义引物、具有序列表的序列号89所示的碱基序列的正义引物和具有序列表的序列号90所示的碱基序列的反义引物、具有序列表的序列号91所示的碱基序列的正义引物和具有序列表的序列号92所示的碱基序列的反义引物、具有序列表的序列号93所示的碱基序列的正义引物和具有序列表的序列号94所示的碱基序列的反义引物、具有序列表的序列号95所示的碱基序列的正义引物和具有序列表的序列号96所示的碱基序列的反义引物、具有序列表的序列号97所示的碱基序列的正义引物和具有序列表的序列号98所示的碱基序列的反义引物、具有序列表的序列号99所示的碱基序列的正义引物和具有序列表的序列号100所示的碱基序列的反义引物、具有序列表的序列号101所示的碱基序列的正义引物和具有序列表的序列号102所示的碱基序列的反义引物、具有序列表的序列号103所示的碱基序列的正义引物和具有序列表的序列号104所示的碱基序列的反义引物、具有序列表的序列号105所示的碱基序列的正义引物和具有序列表的序列号106所示的碱基序列的反义引物、具有序列表的序列号107所示的碱基序列的正义引物和具有序列表的序列号108所示的碱基序列的反义引物、具有序列表的序列号109所示的碱基序列的正义引物和具有序列表的序列号110所示的碱基序列的反义引物、具有序列表的序列号111所示的碱基序列的正义引物和具有序列表的序列号112所示的碱基序列的反义引物、具有序列表的序列号113所示的碱基序列的正义引物和具有序列表的序列号114所示的碱基序列的反义引物、或具有序列表的序列号115所示的碱基序列的正义引物和具有序列表的序列号116所示的碱基序列的反义引物构成的用于扩增间充质干细胞标记基因的RT-PCR所使用的引物(权利要求26)。
此外,本发明还由以下物质组成:权利要求1-8记载的间充质干细胞的识别方法,其特征是采用权利要求10或11中记载的间充质干细胞标记基因检测用探针对被检细胞中的基因、用权利要求24-26其中之一记载的正义引物以及反义引物中至少一对以上的引物扩增的基因进行检测(权利要求27)、和间充质干细胞的识别方法,其特征是采用权利要求15-17其中之一记载的抗体对被检细胞中的间充质干细胞标记多肽的表达进行检测(权利要求28)、和间充质干细胞的识别方法,其特征是将被检细胞中由序列表的序列号1、11和19构成的间充质干细胞标记基因组成的组中一个以上基因的表达以及由序列表的序列号2、4、6、7、9、10、12、14、15和17构成的间充质干细胞标记基因组成的组中一个以上基因的表达组合起来,进行评价(权利要求29)、和间充质干细胞的识别分离方法,其特征是采用权利要求10或权利要求11记载的间充质干细胞标记基因检测用探针和/或权利要求15-17中任一记载的抗体对被检细胞中间充质干细胞检测用标记基因和/或间充质干细胞检测用标记多肽的表达进行检测、对识别出的间充质干细胞进行分离(权利要求30)、和权利要求30记载的间充质干细胞的识别分离方法,其特征是通过采用权利要求15-17中任一记载的抗体的荧光抗体法将被检细胞中的间充质干细胞进行标识、分离经标识的间充质干细胞(权利要求31)、和用于识别间充质干细胞的试剂盒,其中装备有权利要求10或11记载的用于检测间充质干细胞标记基因的探针、固定有该探针的权利要求12或13记载的用于检测间充质干细胞标记基因的微阵列或D N A芯片、和权利要求15-17中任一记载的抗体中至少一个以上的抗体(权利要求32)。
附图说明
图1.表示的是本发明的实施例中,由半定量RT-PCR法获得的人间充质干细胞或人成纤维细胞间由个体(的不同)产生差异很大的基因。
图2.表示的是本发明的实施例中,由半定量RT-PCR法获得的MSC中高表达的基因。
图3.表示的是本发明的实施例中,由半定量RT-PCR法获得的MSC中低表达的基因。
图4.表示的是对于确认了间充质干细胞中高/低表达的13个基因,从来源于7个个体的间充质干细胞和来源于4个个体的成纤维细胞中抽提全部RNA,以其为模板通过RT-PCR法,对它们的表达量进行确认的结果。
图5.表示的是本发明的实施例中,间充质干细胞和成纤维细胞中本发明的标记基因表达状况的试验结果。
图6.表示的是本发明的实施例中,间充质干细胞和成骨细胞中各标记基因的差别基因表达的状况。
图7.表示的是本发明的实施例中,间充质干细胞和成骨细胞中各标记基因的差别基因表达的状况。
图8.表示的是本发明的实施例中,间充质干细胞和成骨细胞中各标记基因的差别基因表达的状况。
图9.表示的是本发明的实施例中,各个标记基因在间充质干细胞和人成纤维细胞中基因的表达状况。
图10.表示的是本发明的实施例中,各个标记基因在间充质干细胞和人成纤维细胞中基因的表达状况。
图11.表示的是本发明的实施例中,采用流式细胞仪对人细胞中间充质干细胞DR的表达的测定结果。
图12.表示的是本发明的实施例中,对在间充质干细胞向成骨细胞分化诱导中各个基因的表达状况的测定结果。
图13.表示的是本发明的实施例中,各标记基因在骨分化诱导的第4天-28天之间基因表达的变化。
图14表示的是本发明的实施例中,各标记基因在骨分化诱导的第4天-28天之间基因表达的变化。
图15.表示的是本发明的实施例中,各标记基因在骨分化诱导的第4天-28天之间基因表达的变化。
图16.表示的是本发明的实施例中,各标记基因在骨分化诱导的第4天-28天之间基因表达的变化。
具体实施方式
本发明由对间充质干细胞中的特异性表达的用于检测间充质干细胞的标记基因或用于检测间充质干细胞的标记多肽的表达进行检测,识别间充质干细胞构成。本发明中,用于检测间充质干细胞的基因标记构成的基因是具有序列表中序列号1、2、4、6、7、9、10、11、12、14、15、17或19所示的碱基序列的基因。
此外,在本发明中用于检测间充质干细胞的多肽标记构成的多肽是具有序列表中序列号3、5、8、13、16或18所示氨基酸序列的多肽。
序列表中序列号1所示的基因是“丝氨酸(或半胱氨酸)蛋白酶抑制剂”基因,序列表中序列号2所示的基因是“肾上腺髓质素”基因,序列表中序列号4所示的基因是“载脂蛋白D(apolopoprotein D)”基因,序列表中序列号6所示的基因是“XV-α1型胶原酶(collagenase type XV alpha 1)”基因,序列表中序列号7所示的基因是“CUG三联体重复RNA结合蛋白2(CUG triplet repeat RNA binding protein2)”基因,序列表中序列号9所示的基因是“皮肤桥蛋白”基因,序列表中序列号10所示的基因是“异柠檬酸脱氢酶2”基因,序列表中序列号11所示的基因是“2类主要组织相容性复合体DRβ3(majorhistocompatibility complex class2,DR beta 3)”基因,序列表中序列号12所示的基因是“蛋白质酪氨酸激酶7(protein tyrosine kinase 7)”基因,序列表中序列号14所示的基因是“Sam68样磷酸酪氨酸蛋白(Sam68-like phosphotyrosine protein)”基因,序列表中序列号15所示的基因是“C-型凝集素超家族(C-type lectin superfamily)成员2”基因,序列表中序列号17所示的基因是“基质金属酶1(matrix metalloprotease 1)”基因,和序列表中序列号19所示的基因是“组织因子途径抑制剂2(tissue factor pathway inhibitor2)”基因,序列表中序列号46所示的基因是“主要组织相容性复合体DRα(major histocompatibilitycomplex DR alpha)”基因。
可以通过NCBI的基因数据库中、各个登陆号:AI133613(序列号1)、NM_001124(序列号2)、NM_001647(序列号4)、L01697(序列号6)、U69546(序列号7)、AW016451(序列号9)、AL545953(序列号10)、BF732822(序列号11)、AL157486(序列号12)、AA112001(序列号14)、XM_006626(序列号15)、NM_002421(序列号17)、AL550357(序列号19)、和BF795929(序列号46)获得本发明的用于检测间充质干细胞的标记基因的DNA序列的信息。
进而,经确认本发明中,与成纤维细胞相比在间充质干细胞中表达量更多的基因列举为如下基因:整联蛋白,α6(ITGA6),MRNA基因(NM_000210);溶质载体家族20(PHOSPHATE TRANSPORTER)、成员1基因(NM_005415);核苷酸还原酶M2多肽(RRM2),MRNA基因(NM_001034);卵泡抑制素(FST),转录变异型FST317,MRNA基因(NM_006350);SPROUTY(果蝇)同源基因2(SPRY2),MRNA基因(NM_005842);RAB3B,成员RAS癌基因家族成员(RAB3B),MRNA基因(NM_002867);溶质载体家族2(FACILITATED GLUCOSE TRANSPORTER)基因(NM_006516);白介素13受体,ALPHA 2(IL13RA2),MRNA基因(NM_000640);丝氨酸(或苏氨酸)蛋白酶抑制剂12(STK12),MRNA基因(NM_004217);微染色体维持缺陷蛋白(酿酒酵母)5(CE)基因(NM_006739);甲状腺激素受体中间子13(TRIP13),MRNA基因(NM_004237);类驱动蛋白6(MITOTIC CENTROMERE-ASSOCIATED KINESIN)(K)基因(NM_006845);细胞周期蛋白依赖性抑止剂3(细胞周期蛋白依赖性抑止剂3(CYCLIN-DEPENDENT KINASE INHIBITOR 3))(CDK2-ASSOCIATED DUAL基因(NM_005192);染色体凝集蛋白G(HCAP-G),MRNA基因(NM_022346);CDC28蛋白激酶(CKS1),MRNA基因(NM_001826);胞质分裂的蛋白质调节子1(PRC1),MRNA基因(NM_003981);细胞分裂周期2,G1→S→G2→M(CDC2),MRNA基因(NM_001786);CDC20(CDC20细胞分裂周期20,酿酒酵母同源基因)(CD)基因(NM_001255);LIKELY ORTHOLOG OF MATERNAL EMBRYONIC LEUCINEZIPPER KINAS基因(NM_014791);微染色体维持缺陷蛋白(酿酒酵母)7(M)基因(NM_005916);细胞周期蛋白A2(CCNA2),MRNA基因(NM_001237);胸苷激酶1,可溶性(TK1),MRNA基因(NM_003258);或细胞周期蛋白依赖性激酶抑止剂2A(cyclin-dependent kinase inhibitor 2A)(黑色素瘤,p16,抑止CDK4)(CDKN2A),mRNA基因(NM_000077)。
含EGF的细胞微丝(fibulin)样细胞外基质蛋白1基因(NM_018894);人胰岛素样生长因子结合蛋白5(IGFBP5)mRNA基因(AU132011);人克隆24775 mRNA序列基因(AA402981);蛋白聚糖1,分泌颗粒(AV734015);胰岛素样生长因子结合蛋白质5(insulin-like growth factor binding protein 5)基因(AA374325);基因溶质载体家族21(有机阴离子转运蛋白),成员3(AF085224);谷氨酰胺转移酶2(C多肽,蛋白质-谷氨酰胺-γ-谷酰基转移酶)(AL552373)基因;血友病因子II(凝血酶)受体基因(M62424);纤维蛋白溶酶原活化因子,鸟激酶(NM_002658)基因;金属蛋白酶组织抑制因子3(Sorsby fundus dystrophy,pseudoinflammatory)(W96324)基因;基质Gla蛋白(BF668572)基因;B-cell CLL/淋巴瘤1(Z23022)基因;CD74抗原(主要组织相容性复合体的不变多肽,II类相关抗原)(BG333618)基因;内收蛋白3(γ)(AL135243)基因;溶质载体家族16(一元羧酸传送子),成员4(NM_004696)基因;S蛋白(α)(NM_000313)基因;磷脂酰肌醇(4,5)二磷酸5-磷酸酶同系物;磷脂酰肌醇多聚磷酸5-磷酸酶IV型(AF187891)基因;孕酮膜结合蛋白质(BE858855)基因;脑源性神经营养因子(X60201)基因;或者载脂蛋白E(BF967316)基因。
人WNT抑止因子-1(WIF-1),MRNA(NM_007191)基因;人假拟蛋白(HYPOTHETICAL PROTEIN)FLJ11175(FLJ11175),MRNA基因(NM_018349);人RHO GDP解离抑止剂(GDI)β(ARHGDIB),MRNA基因(NM_001175);人钾中间体/少量电导的钙活化(SMALL CONDUCTANCE CALCIUM-ACTIVATE)基因(NM_021614);人核因子(红细胞衍生物2)-类似物3(NFE2L3),MRNA基因(NM_004289);人GS3955蛋白(GS3955),MRNA基因(NM_021643);人CDNA 3′END与糖蛋白相类似的MUC18基因(AA302605);人假拟蛋白(HYPOTHETICALPROTEIN)FLJ21841(FLJ21841),MRNA基因(NM_024609);人ZINC FINGER蛋白185(LIM域)(ZNF185),MRNA基因(NM_007150);SC1=假定的转移-活化因子,细胞周期控制中涉及的[人,MRNA,24](S53374)基因;人NADH脱氢酶(辅酶Q)1α子复合体,8(19K)基因(NM_014222);人酵母MCM10的同系物基因;假拟蛋白(HYPOTHETICAL PROTEIN)PRO2249(PRO2)(NM_018518);人XV-α1型胶原酶(COLLAGEN,TYPE VII,ALPHA1)(大疱性表皮松解症,DYSTRO基因(NM_000094);人自分泌运动因子受体(AMFR),MRNA基因(NM_001144);人克隆24421 MRNA序列/CDS=未知/GB=AF070641/GI=3283914/UG=(AF070641)基因;人MRNA基因;CDNA DKFZP586E1621(FROM克隆DKFZP586E1621)/CDS=未知/GB(AL080235)基因。
人保留(KCNK12),MRNA(NM_022055)基因;人泛素结合酶E2C(UBE2C),MRNA基因(NM_007019);人CDNA FLJ10517 FIS,克隆NT2RP2000812/CDS=(61,918)/GB=AK001379/G基因(AK001379);人骨连接蛋白1(CRTL1),MRNA基因(NM_001884);人MRNA;CDNA DKFZP434F2322(FROM克隆DKFZP434F2322)/CDS=未知/GB(AL133105)基因;人,克隆MGC:9549IMAGE:3857382,MRNA,完整CDS/CDS=(92,1285)/G(BC012453)基因;人假拟蛋白(HYPOTHETICAL PROTEIN)DKFZP586J1119(DKFZP586J1119),MRNA(NM_032270)基因;人神经胶质成熟因子,γ(GMFG),MRNA基因(NM_004877);人CDNA:FLJ23095 FIS,克隆LNG07413/CDS=未知/GB=AK026748/GI=10(AK026748)基因;人假拟蛋白(HYPOTHETICAL PROTEIN)DKFZP762E1312(DKFZP762E1312),MRNA基因(NM_018410);人IROQUOIS类同源域蛋白(IRX-2A),MRNA基因(NM_005853);或人假拟蛋白(HYPOTHETICAL PROTEIN)FLJ10540(FLJ10540),MRNA基因(NM_018131)。
人MRNA基因;CDNA DKFZP434C1915(FROM克隆DKFZP434C1915);PARTIAL CDS/C(AL137698);人微染色体维持缺陷型(酿酒酵母(S.CEREVISIAE))7(M)(NM_005916)基因;人动力蛋白,细胞质的,中间体多肽1(DNCI1),M基因(NM_004411);蛋白质基因产物的人MRNA(PGP)9.5.(X04741)基因;人RAD51-相互作用蛋白(PIR51),MRNA基因(NM_006479);人含有杆状病毒IAP重复序列的5(SURVIVIN)(BIRC5),MR基因(NM_001168);人UDP-N-乙酰基-ALPHA-D-半乳糖胺:多肽N-乙酰基GAL基因(NM_004482);人细胞周期蛋白B1(CCNB1),MRNA基因(NM_031966);人FLAP结构特异性内切酶1(FEN1),MRNA基因(NM_004111);人丝氨酸/苏氨酸激酶15(STK15),MRNA基因(NM_003600);人MAD2(有丝分裂抑止缺陷型,酵母,同系物)-类似物1(MA)基因(NM_002358);人核仁蛋白ANKT(ANKT),MRNA基因(NM_018454);人与泛素结合酶类似的HSPC150蛋白(H)基因(NM_014176);人细胞色素P450类维生素A代谢蛋白(P450RAI-2),(NM_019885)基因;人NIMA(从未有丝分裂基因A)相关激酶2(NEK2),MR基因(NM_002497);人骨形态生成蛋白4(BMP4),MRNA基因(NM_001202);人CDNA FLJ10674 FIS,克隆NT2RP2006436/CDS=未知/GB=AK001536/G基因I(AK001536);或人着丝粒蛋白A(17KD)(CENPA),MRNA基因(NM_001809)。
人MRNA基因;CDNADKFZP564P116(来自克隆DKFZP564P116)/CDS=未知/GB=A(AL049338);人TTK蛋白质激酶(TTK),MRNA基因(NM_003318);人KARYOPHERINα2(RAG COHORT1,IMPORTINα1)(KPNA基因(NM_002266);人聚合酶(DNA导向的),θ(POLQ),MRNA基因(NM_006596);人ETS变异体基因5(ETS相关分子)(ETV5),MRNA基因(NM_004454);人含转化酸性卷曲螺旋蛋白(TRANSFORMING,ACIDIC COILED-COIL CONTAINING蛋白)3(TAC)基因(NM_006342);人驱动蛋白类似物1(KNSL1),MRNA基因(NM_004523);人着丝粒蛋白E(312KD)(CENPE),MRNA基因(NM_001813);人CDNA,3′END/克隆=IMAGE:1651289/克隆END=3′/GB=AI12(AI123815);基因人DISTAL-LESSHOMEO BOX 5(DLX5),MRNA基因(NM_005221);人V-MYB禽成髓细胞性白血病病毒癌基因同系物类似物2基因(NM_002466);或人血清剥夺反应(磷脂酰丝氨酸结合PRO(NM_004657)基因。
用于检测间充质干细胞的基因标记,特征在于其是人假拟蛋白(HYPOTHETICAL PROTEIN)FLJ10604(FLJ10604),MRNA基因(NM_018154);人核糖核酸酶HI,大亚基(RNASEHI),MRNA(NM_006397)基因;人ANILLIN(果蝇SCRAPS同系物),肌动蛋白结合蛋白基因(NM_018685);人H4组蛋白家族,成员G(H4FG),MRNA基因(NM_003542);人G蛋白连结受体37(内皮缩血管肽受体B型-(NM_005302)人泛素载体蛋白(E2-EPF),MRNA(NM_014501)基因;人,类似于肿瘤差别表达1,克隆IMAGE:3639252,(BC007375)基因;人假拟蛋白(HYPOTHETICAL PROTEIN)MGC2577(MGC2577),MRNA基因(NM_031299);人假拟蛋白(HYPOTHETICAL PROTEIN)FLJ13912(FLJ13912),MRNA基因(NM_022770);人ANNEXIN A3(ANXA3),MRNA基因NM_005139);人STATHMIN 1/ONCO蛋白18(STMN1),MRNA基因(NM_005563)人,与核糖体蛋白L39类似,克隆MGC:20168 IMAGE:4555759,M(BC012328);人POLO(果蝇)类似物激酶(PLK),MRNA基因(NM_005030)。
同时,本发明中经确认的、与纤维母细胞相比较、在间充质细胞中不表达或表达量的基因是,如下列举的基因:
用于检测间充质干细胞的基因标记,特征在于人蛋白酶体(PROSOME,MACROPAIN)26S亚基,ATP酶,5(PS)基因(NM_002805);人真核翻译起始因子4γ,2(EIF4G)基因(NM_001418);人二氢嘧啶酶类似物3(DPYSL3),MRNA)基因(NM_001387);人ADAPTOR相关蛋白复合体1,σ2亚基(AP1S2)基因(NM_003916);人网蛋白1,中间丝结合蛋白,500KD(P)基因(NM_000445);人异种核蛋白U基因(SCAFFOLD ATTAC(NM_031844);人假拟蛋白(HYPOTHETICAL PROTEIN)MGC5306(MGC5306),MRNA基因(NM_024116);人MHCI类多肽相关序列A(MICA),MRNA基因(NM_000247);人PRK1相关蛋白(AWP1),MRNA基因(NM_019006);人孕酮受体膜成分2(PGRMC2),MRNA基因(NM_006320);人多聚谷氨酸结合蛋白1(PQBP1),MRNA基因(NM_005710);人S-腺苷甲硫氨酸脱羧酶1(AMD1),MRNA基因(NM_001634);人干扰素诱导的C型肝炎相关MICROTUBULAR AG基因(NM_006417);人蛋白质激酶,AMP-活化的,γ1非催化性亚基(NON-CATALYTIC SUBUN)基因(NM_002733);人前胶原-脯氨酸,2-氧代戊二酸盐4-加双氧酶(脯氨酸(NM_004199)基因;人血管内皮分化,溶血磷脂酸G-PROTE基因(NM_012152);或人KIAA0127基因产物(KIAA0127),MRNA基因(NM_014755)
本发明中,对本发明的间充质干细胞标记基因表达进行的检测中可以采用公知的基因表达检测方法。例如,为了检测本发明的间充质干细胞标记基因的表达,可以采用RNA印迹法(northern blot)。此外,为了通过本发明的基因标记,检测识别间充质干细胞,可以采用具有与本发明的间充质干细胞基因标记的DNA序列在严谨条件下杂交的DNA序列的探针。在采用该探针检测间充质干细胞中,可采用公知方法采取相应措施。例如,由序列表所示基因标记DNA序列制备出适应长度的DNA探针,给探针加上合适的荧光标记等标记,通过将其与被检体杂交,从而对间充质干细胞进行检测。该DNA探针可以采用由序列表所示的本发明的基因标记的碱基序列的反义链的全部或部分构成的用于检测间充质干细胞标记基因的探针。或者,也可以采用固定有至少1个以上所述探针的用于检测标记基因的微阵列或DNA芯片。
此外,在制备上述DNA探针时,本发明的碱基序列中,所谓“与用于检测间充质干细胞的标记基因的DNA序列在严谨条件下杂交”是指,例如42℃下的杂交,以及在42℃下通过含有1×SSC(0.15M NaCl、0.015M柠檬酸钠)、0.1%SDS(十二烷基硫酸钠)的缓冲液进行冲洗,最为理想的是65℃下的杂交,以及在65℃下通过含有1×SSC、0.1%SDS的缓冲液进行冲洗。此外,影响杂交的严谨度的因素除上述温度条件以外还存在各种因素,如果本领域技术人员对各种因素进行组合,就可能实现与上述列举的杂交的严谨性等同的严谨度。
尤其是,本发明中检测本发明的用于检测间充质干细胞的多肽标记时,可以使用由该蛋白质的多肽诱导,与该多肽特异性结合的抗体。该抗体可以是例如多克隆抗体和单克隆抗体。作为本发明的多肽标记的抗体,该抗体可以通过常规方法制得。采用本发明的抗体,在对被检细胞中用于检测间充质干细胞的标记多肽的表达进行检测中,可以实施采用公知抗体的免疫学测定法。所述免疫学测定法可以是例如RIA法、ELISA法、荧光抗体发等公知的免疫学测定法。
本发明可通过采用本发明的用于检测间充质干细胞的探针和/或本发明的用于检测间充质干细胞的抗体,对被检细胞中用于检测间充质干细胞的标记基因和/或用于检测间充质干细胞的标记多肽的表达进行检测,对识别出的间充质干细胞进行分离得以实现。在对被检细胞中用于检测间充质干细胞的标记基因检测时,为了扩增被检细胞的基因,可采用定量或半定量的PCR。所述PCR可采用RT-PCR(逆转录PCR)。进行所述PCR时,采用用于扩增用于检测间充质干细胞的标记基因的正义引物和反义引物组成的引物。
用于扩增本发明的用于检测间充质干细胞的标记基因的引物举例如下:具有序列表的序列号20所示的碱基序列的正义引物以及具有序列表的序列号21所示的碱基序列的反义引物、具有序列表的序列号22所示的碱基序列的正义引物和具有序列表的序列号23所示的碱基序列的反义引物、具有序列表的序列号24所示的碱基序列的正义引物和具有序列表的序列号25所示的碱基序列的反义引物、具有序列表的序列号26所示的碱基序列的正义引物和具有序列表的序列号27所示的碱基序列的反义引物、具有序列表的序列号28所示的碱基序列的正义引物和具有序列表的序列号29所示的碱基序列的反义引物、具有序列表的序列号30所示的碱基序列的正义引物和具有序列表的序列号31所示的碱基序列的反义引物、具有序列表的序列号32所示的碱基序列的正义引物和具有序列表的序列号33所示的碱基序列的反义引物、具有序列表的序列号34所示的碱基序列的正义引物和具有序列表的序列号35所示的碱基序列的反义引物、具有序列表的序列号36所示的碱基序列的正义引物和具有序列表的序列号37所示的碱基序列的反义引物、具有序列表的序列号38所示的碱基序列的正义引物和具有序列表的序列号39所示的碱基序列的反义引物、具有序列表的序列号40所示的碱基序列的正义引物和具有序列表的序列号41所示的碱基序列的反义引物、具有序列表的序列号42所示的碱基序列的正义引物和具有序列表的序列号43所示的碱基序列的反义引物、或具有序列表的序列号44所示的碱基序列的正义引物和具有序列表的序列号45所示的碱基序列的反义引物。
尤其是,用于扩增本发明的用于检测间充质干细胞的标记基因的引物举例如下:由具有序列表的序列号47所示的碱基序列的正义引物和具有序列表的序列号48所示的碱基序列的反义引物、具有序列表的序列号49所示的碱基序列的正义引物和具有序列表的序列号50所示的碱基序列的反义引物、具有序列表的序列号51所示的碱基序列的正义引物和具有序列表的序列号52所示的碱基序列的反义引物、具有序列表的序列号53所示的碱基序列的正义引物和具有序列表的序列号54所示的碱基序列的反义引物、具有序列表的序列号55所示的碱基序列的正义引物和具有序列表的序列号56所示的碱基序列的反义引物、具有序列表的序列号57所示的碱基序列的正义引物和具有序列表的序列号58所示的碱基序列的反义引物、具有序列表的序列号59所示的碱基序列的正义引物和具有序列表的序列号60所示的碱基序列的反义引物、具有序列表的序列号61所示的碱基序列的正义引物和具有序列表的序列号62所示的碱基序列的反义引物、具有序列表的序列号63所示的碱基序列的正义引物和具有序列表的序列号64所示的碱基序列的反义引物、具有序列表的序列号65所示的碱基序列的正义引物和具有序列表的序列号66所示的碱基序列的反义引物、具有序列表的序列号67所示的碱基序列的正义引物和具有序列表的序列号68所示的碱基序列的反义引物、或具有序列表的序列号69所示的碱基序列的正义引物和具有序列表的序列号70所示的碱基序列的反义引物构成的扩增间充质干细胞标记基因的实时P C R所使用的引物。
进而,用于扩增本发明的用于检测间充质干细胞的标记基因的引物列举如下:由具有序列表的序列号71所示的碱基序列的正义引物和具有序列表的序列号72所示的碱基序列的反义引物、具有序列表的序列号73所示的碱基序列的正义引物和具有序列表的序列号74所示的碱基序列的反义引物、具有序列表的序列号75所示的碱基序列的正义引物和具有序列表的序列号76所示的碱基序列的反义引物、具有序列表的序列号77所示的碱基序列的正义引物和具有序列表的序列号78所示的碱基序列的反义引物、具有序列表的序列号79所示的碱基序列的正义引物和具有序列表的序列号80所示的碱基序列的反义引物、具有序列表的序列号81所示的碱基序列的正义引物和具有序列表的序列号82所示的碱基序列的反义引物、具有序列表的序列号83所示的碱基序列的正义引物和具有序列表的序列号84所示的碱基序列的反义引物、具有序列表的序列号85所示的碱基序列的正义引物和具有序列表的序列号86所示的碱基序列的反义引物、具有序列表的序列号87所示的碱基序列的正义引物和具有序列表的序列号88所示的碱基序列的反义引物、具有序列表的序列号89所示的碱基序列的正义引物和具有序列表的序列号90所示的碱基序列的反义引物、具有序列表的序列号91所示的碱基序列的正义引物和具有序列表的序列号92所示的碱基序列的反义引物、具有序列表的序列号93所示的碱基序列的正义引物和具有序列表的序列号94所示的碱基序列的反义引物、具有序列表的序列号95所示的碱基序列的正义引物和具有序列表的序列号96所示的碱基序列的反义引物、具有序列表的序列号97所示的碱基序列的正义引物和具有序列表的序列号98所示的碱基序列的反义引物、具有序列表的序列号99所示的碱基序列的正义引物和具有序列表的序列号100所示的碱基序列的反义引物、具有序列表的序列号101所示的碱基序列的正义引物和具有序列表的序列号102所示的碱基序列的反义引物、具有序列表的序列号103所示的碱基序列的正义引物和具有序列表的序列号104所示的碱基序列的反义引物、具有序列表的序列号105所示的碱基序列的正义引物和具有序列表的序列号106所示的碱基序列的反义引物、具有序列表的序列号107所示的碱基序列的正义引物和具有序列表的序列号108所示的碱基序列的反义引物、具有序列表的序列号109所示的碱基序列的正义引物和具有序列表的序列号110所示的碱基序列的反义引物、具有序列表的序列号111所示的碱基序列的正义引物和具有序列表的序列号112所示的碱基序列的反义引物、具有序列表的序列号113所示的碱基序列的正义引物和具有序列表的序列号114所示的碱基序列的反义引物、或具有序列表的序列号115所示的碱基序列的正义引物和具有序列表的序列号116所示的碱基序列的反义引物构成的用于扩增间充质干细胞标记基因的RT-PCR所使用的引物。
本发明中,对间充质干细胞的识别是以下述方式进行:在被检细胞中以上述正义引物和反义引物的至少一对以上的引物进行扩增,采用用于检测本发明的间充质干细胞的标记基因的探针对扩增出的基因进行检测。
本发明的用于检测间充质干细胞的标记基因是在间充质干细胞中特异性高表达的基因和特异性低表达的基因,通过以组合方式检测这些基因表达,能够提高间充质干细胞检测的精确度。因此,作为在间充质干细胞中特异性高表达的基因,可例举为序列表的序列号1、11和19构成的间充质干细胞标记基因,作为在间充质干细胞中特异性低表达的基因,可例举为序列号2、4、6、7、9、10、12、14、15、17和46构成的间充质干细胞标记基因。进而,可以列举出本发明中经证实的间充质干细胞标记基因。因此,通过对各个基因的组合中的一个以上基因的表达进行组合,可以以更高的检测精确度对间充质干细胞进行识别。
在通过采用利用本发明的抗体的荧光抗体法,对被检细胞中的间充质干细胞标记多肽的表达进行检测,从而识别分离间充质干细胞的过程中可通过公知的方法对间充质干细胞进行标记、分离。所述标记方法,可举例为如荧光抗体法。在通过荧光抗体法对未分化的造血细胞进行标记中,对与本发明的用于检测间充质干细胞的多肽标记特异性结合的抗体进行荧光标记,通过与表达所述抗原的间充质干细胞结合,标记间充质干细胞(直接荧光抗体法),或在表达抗原的间充质干细胞与未标记的本发明的特异抗体结合后,对与标记的二次抗体结合的间充质干细胞标记(间接荧光抗体法)、对所述经标记的间充质干细胞分离,收集。
本发明的间充质干细胞的检测识别中所使用的用于检测间充质干细胞标记基因的探针,固定有该探针的用于检测间充质干细胞标记基因的微阵列或DNA芯片以及本发明的用于检测间充质干细胞的抗体可以以装备有上述物质的用于识别间充质干细胞的试剂盒制品化形式存放。
下面,通过实施例更为具体地对本发明进行说明,本发明的技术范围不受其实施例所举例的内容限制。
实施例1【材料和方法】
(细胞)
在Dalbecco’s modified Eagle’s medium(低葡萄糖)(Sigma公司制造)中添加了10%胎牛血清、1ng/ml bFGF的培养基中在37℃对人间充质干细胞(human mesenchymal stemcell)和人成纤维细胞(human fibroblast)进行培养。
(DNA微阵列)
用TRIZOL试剂(Invitrogen公司制造)从一个10cm皿的各个细胞中抽提全部RNA,用micro poly(A)purist(Ambion公司制造)提取mRNA,进行DNA微阵列(IncyteGenomics公司:Kurabo Life Array analysis servis;Lot.No.KL01081)。并且,DNA微阵列分析委托Kurabo公司进行。
(半定量RT-PCR)
用TRIZOL试剂(Invitrogen公司制造)从各个细胞中抽提全部RNA后,以各个1mg全部RNA为模板,采用用于RT-PCR的SuperScript first-strand合成系统(Invitrogen公司),42℃下进行50分钟逆转录反应从而合成cDNA。以合成的cDNA为模板采用Advantage 2 PCR enzyme system(Clontech公司制造)对各个基因进行扩增。94℃下变性30秒,68℃下1分钟内退火30个循环。用于扩增各个基因的引物序列汇集在表1中。通过采用1%琼脂糖凝胶的电泳分离扩增出的基因,通过溴乙锭染色进行检测。
实施例2【检测结果】
(DNA微阵列)
DNA微阵列的结果表明,9400个基因中,与在成纤维细胞中相比63个基因在间充质干细胞中的显著表达更高,141个基因表达较低。此外,还看出了除这些基因之外的其它基因的显著差异。其中,发现存在3倍以上差异的87个基因中,在间充质干细胞中高表达的基因为29个基因,低表达的基因为58个基因。
(半定量RT-PCR)
从源于3个个体的间充质干细胞和源于3个个体的成纤维细胞中抽提全长RNA,以其为模板,通过半定量RT-PCR法就上述87个基因的表达量进行调查。其结果是表达量未发现差异的基因最多。此外,不同个体的间充质干细胞或成纤维细胞间表达量存在差异,认为由个体不同产生的表达差异也很大(图1)。
经RT-PCR证实在间充质干细胞中高表达的基因是丝氨酸(或半胱氨酸)蛋白酶抑止剂(序列表的序列号1)、2类主要组织相容性复合体DR β3(序列号11)、和组织因子途径抑制物2(序列号19)这三个基因(图2)。
此外,经证实低表达的基因是(序列号2)、载脂蛋白D(序列号4)、XV-α型胶原酶(collagenase type XV alpha 1)(序列号6)、CUG三联体重叠RNA结合蛋白(CUGtriplet repeat RNA binding protein)(序列号7)、皮肤桥蛋白(序列号9)、异柠檬酸脱氢酶2(序列号10)、酪氨酸激酶7(序列号12)、Sam68样磷酸酪氨酸蛋白(序列号14)、C-型凝集素超家族成员2(序列号15)、和基质金属酶1(matrix metalloprotease 1)(序列号17)这10个基因(图3)。并且,通过半定量RT-PCR法对这13个基因的表达量进行证实,所述半定量RT-PCR法是以从源于7个个体的间充质干细胞和4个个体成纤维细胞中抽提的全长RNA作为模板的(图4)。
实施例3【间充质干细胞中各个基因的表达量的测定I】
以与实施例1相同方法,对本发明的基因标记在人间充质干细胞和人成纤维细胞中的表达进行测定。所使用的RT-PCR和实时PCR的引物和实时PCR所用探针示于表2中。
间充质干细胞和成纤维细胞中的mRNA水平的表达状况示于图5。此外,间充质干细胞和成纤维细胞中相对的mRNA水平的表达状况示于图6、7、8。
实施例4【间充质干细胞中各个基因的表达量的测定II】
以与实施例1相同方法,对本发明的各个基因标记在人间充质干细胞和人成纤维细胞中的表达进行测定。所使用的RT-PCR的正义及反义引物如序列表的序列号71-116的序列所示。间充质干细胞和成纤维细胞中的mRNA的表达状况示于图9和图10。此外,间充质干细胞/成纤维细胞的表达之比示于表3。
表3
MSC/成纤维细胞 | 基因名称 |
11.6 | NTEGRIN,ALPHA 6(ITGA6),MRNA |
8.7 | 溶质载体家族20(磷酸盐转运蛋白),成员1 |
7.8 | 核苷酸还原酶M2多肽(RRM2),MRNA |
7.6 | 滤泡素抑制素(FOLLISTATIN) (FST),转录物变异体FST317,MRNA |
7.3 | SPROUTY(果蝇)同系物2(SPRY2),MRNA |
6.9 | RAB3B,成员RAS癌基因家族(RAB3B),MRNA |
6.5 | 溶质载体家族2(促进葡萄糖转运蛋白(FACILITATEDGLUCOSE TRANSPORTER)) |
6.1 | 白介素13受体,ALPHA 2(IL13RA2),MRNA |
5.9 | 丝氨酸/苏氨酸激酶12(STK12),MRNA |
5.7 | 微染色体维持缺陷型(酿酒酵母(S.CEREVISIAE)) |
5.6 | 甲状腺激素受体中间子13(TRIP13),MRNA |
5.5 | 驱动蛋白类似物6(有丝分裂着丝粒相关驱动蛋白(MITOTIC CENTROMERE相关KINESIN)) |
5.5 | 细胞周期蛋白依赖性抑止剂3(细胞周期蛋白依赖性激酶抑止剂3) |
5.4 | 染色体凝缩蛋白G(HCAP-G),MRNA |
5.2 | CDC28蛋白质激酶1(CKS1),MRNA |
5.2 | 胞质分裂蛋白调节子1(PRC1),MRNA |
5.2 | 细胞分裂周期2,G1→S→G2→M(CDC2),MRNA |
5.2 | CDC20(细胞分裂周期20,酿酒酵母(S.CEREVISIAE),同系物)(CD |
5.1 | LIKELY ORTHOLOG OF MATERNAL EMBRYONICLEUCINE ZIPPER KINAS |
5.1 | 微染色体维持缺陷型(酿酒酵母(S.CEREVISIAE))7 |
4.9 | YCLIN A2(CCNA2),MRNA |
3.6 | 胸苷激酶1,可溶性(TK1),MRNA |
0.6 | 细胞周期蛋白依赖性激酶抑止剂2A(黑色素瘤,p16,抑止CDK4)(CDKN2A),mRNA |
实施例5【间充质干细胞中各个基因的表达量的测定III】
以与实施例1相同方法,对本发明的各个基因标记在人源间充质干细胞和人成纤维细胞中的表达进行测定。间充质干细胞/成纤维细胞的表达之比示于表4。
(表4)
(间充质干细胞/成纤维细胞) (基因名称)
8.9 含EGF的fibulin样细胞外基质蛋白1
8.4 人胰岛素样生长因子结合蛋白质5(IGFBP5)mRNA
7.7 人克隆24775 mRNA序列
7 ″蛋白聚糖1,分泌颗粒″
6.8 人胰岛素样生长因子结合蛋白质5
6.7 ″溶质载体家族21(有机阴离子转运蛋白),成员3″
6.5 ″转谷氨酰胺酶2(C多肽,蛋白质氨酰胺酶-γ-氨酰胺酶 转移酶)″
5.8 凝集因子II(凝血酶)受体
5.6 ″纤溶酶原激活物,uro激酶″
5.5 ″金属蛋白酶3组织抑止剂(Sorsby fundus dystrophy,
pseudoinflammatory)″
5.1 基质Gla蛋白
4.6 B-cell CLL/淋巴瘤1
4.6 ″CD74抗原(主要组织相容性复合体的不变多肽,II类抗原相
关)″
4.2 内收蛋白3(γ)
4.2 ″溶质载体家族16(一元羧酸转运蛋白),成员4″
3.4 蛋白S(α)
3.3 ″磷脂酰肌醇(4,5)二磷酸5-磷酸酶同系物;磷脂酰肌醇多聚磷
酸5-磷酸酶IV型″
3.2 孕酮膜结合蛋白质
3.2 脑源性神经营养因子
3 载脂蛋白E
38.5 ″GI|6005949|REF|NM_007191.1|人WNT抑止因子-1(WIF-1),
MRNA″
12.7 ″GI|8922916|REF|NM_018349.1|人假拟蛋白(HYPOTHETICAL
PROTEIN)FLJ11175(FLJ11175),MRNA″
11.2 ″GI|10835001|REF|NM_001175.1|人RHO GDP解离抑止剂
(GDI)β(ARHGDIB),MRNA″
10.3 ″GI|11055973|REF|NM_021614.1|人钾中间体/少量电导的钙活
化(SMALL CONDUCTANCE CALCIUM-ACTIVATE)″
8.7 ″GI|5731346|REF|NM_004289.3|人核因子(红细胞衍生物2)-类
似物3(NFE2L3),MRNA″
7.6 ″GI|11056053|REF|NM_021643.1|人GS3955蛋白(GS3955),
MRNA″
7.5 ″EST10324脂肪组织,白色I人CDNA 3′端与糖蛋白相类似
的MUC18,″
6.6 ″GI|13375818|REF|NM_024609.1|人假拟蛋白(HYPOTHETICAL
PROTEIN)FLJ21841(FLJ21841),MRNA″
6.5 ″GI|6005971|REF|NM_007150.1|人ZINC FINGER
蛋白185(LIM域)(ZNF185),MRNA″
6.5 ″细胞周期控制中涉及的GNL|UG|HS#S2334464 SC1=假定的转
移-活化因子[人,MRNA,24″
6.4 ″GI|7657368|REF|NM_014222.1 |人NADH脱氢酶(辅酶Q)1α
子复合体,8(19K″
6.3 ″GI|8924142|REF|NM_018518.1|F酵母MCM10的人同系物;假
拟蛋白(HYPOTHETICAL PROTEIN)PRO2249(PRO2″
6.2 ″GI|4502960|REF|NM_000094.1|人VII-α1型胶原蛋白1(大疱性
表皮松解症,DYSTRO″
6.2 ″GI|4502074|REF|NM_001144.1|人自分泌运动因子受体
(AMFR),MRNA″
6.2 GNL|UG|HS#S1090551人克隆24421 MRNA序列/CDS=未知
/GB=AF070641/GI=3283914/UG=
6.2 GNL|UG|HS#S1570341人MRNA;CDNA DKFZP586E1621(源自
克隆DKFZP586E1621)/CDS=未知/GB
6.1 ″GI|11545760|REF|NM_022055.1|人保性(KCNK12),MRNA″
6.0 ″GI|5902145|REF|NM_007019.1|人泛素结合酶E2C(UBE2C),
MRNA″
5.9 ″GNL|UG|HS#S1970614人 CDNA FLJ10517 FIS,克隆
NT2RP2000812/CDS=(61,918)/GB=AK001379/G″
5.8 ″GI|4503052|REF|NM_001884.1|人软骨连接蛋白1(CRTL1),
MRNA″
5.8 GNL|UG|HS#S1972520人 MRNA;CDNA DKFZP434F2322
(FROM克隆DKFZP434F2322)/CDS=未知/GB
5.7 ″GNL|UG|HS#S3837475人,克隆MGC:9549 IMAGE:3857382,
MRNA,完整CDS/CDS=(92,1285)/G″
5.4 ″GI|14150008|REF|NM_032270.1|人 假 拟 蛋 白
(HYPOTHETICAL PROTEIN) DKFZP586J1119
(DKFZP586J1119),MRNA″
5.4 ″GI|4758439|REF|NM_004877.1|人神经胶质成熟因子,γ(GMFG),
MRNA″
5.4 ″GNL|UG|HS#S2654530人 CDNA:FLJ23095 FIS,克隆
LNG07413/CDS=未知/GB=AK026748/GI=10″
5.3 ″GI|8922180|REF|NM_018410.1|人假拟蛋白(HYPOTHETICAL
PROTEIN)DKFZP762E1312(DKFZP762E1312),MRNA″
5.3 ″GI|5031806|REF|NM_005853.1|人IROQUOIS类同源域蛋白
(IRX-2A),MRNA″
5.2 ″GI|8922501|REF|NM_018131.1|人假拟蛋白(HYPOTHETICAL
PROTEIN)FLJ10540(FLJ10540),MRNA″
5.1 ″GNL|UG|HS#S1972896人MRNA;CDNA DKFZP434C1915
(FROM克隆DKFZP434C1915);PARTIAL CDS/C″
5.1 ″GI|14149622|REF|NM_005916.1|人微染色体维持缺陷型(酿
酒酵母(S.CEREVISIAE))7(M″
5.0 ″GI|4758177|REF|NM_004411.1|人动力蛋白,细胞质的,中间
体多肽1(DNCI1),M″
5.0 蛋白质基因产物的人MRNA(PGP)9.5.
5.0 ″GI|5453903|REF|NM_006479.1|人RAD51-相互作用蛋白
(PIR51),MRNA″
4.9 ″GI|4502144|REF|NM_001168.1|人含有杆状病毒IAP重复序列
的5(SURVIVIN)(BIRC5),MR″
4.9 ″GI|9945386|REF|NM_004482.2|人UDP-N-乙酰基-ALPHA
-D-半乳糖胺:多肽N-乙酰基GAL″
4.9 ″GI|14327895|REF|NM_031966.1|人细胞周期蛋白B1
(CCNB1),MRNA″
4.8 ″GI|6325465|REF|NM_004111.3|人FLAP结构特异性内切酶1
(FEN1),MRNA″
4.8 ″GI|4507274|REF|NM_003600.1|人丝氨酸/苏氨酸激酶15
(STK15),MRNA″
4.8 ″GI|6466452|REF|NM_002358.2|人MAD2(有丝分裂抑止缺陷
型,酵母,同系物)-类似物1(MA″
4.7 ″GI|15421859|REF|NM_018454.2|人核仁蛋白ANKT(ANKT),
MRNA″
4.7 ″GI|7661807|REF|NM_014176.1|人与泛素结合酶类似的
HSPC150蛋白(H″
4.7 ″GI|9845284|REF|NM_019885.1|人细胞色素P450类维生素A
代谢蛋白(P450RAI-2),″
4.7 ″GI|4505372|REF|NM_002497.1|人NIMA(从未有丝分裂基因A)
相关激酶2(NEK2),MR″
4.7 ″GI|4502422|REF|NM_001202.1|人骨形态生成蛋白4(BMP4),
MRNA″
4.7 ″GNL|UG|HS#S1970775人 CDNA FLJ10674 FIS,克隆
NT2RP2006436/CDS=未知/GB=AK001536/GI″
4.7 ″GI|4585861|REF|NM_001809.2|人着丝粒蛋白A(17KD)
(CENPA),MRNA″
4.6 GNL|UG|HS#S1368141人 MRNA;CDNA DKFZP564P116
(FROM克隆DKFZP564P116)/CDS=未知/GB=A
4.6 ″GI|4507718|REF|NM_003318.1|人TTK蛋白质激酶(TTK),
MRNA″
4.6 ″GI|4504896|REF|NM_002266.1|人KARYOPHERIN ALPHA 2
(RAG COHORT1,IMPORTIN ALPHA1)(KPNA″
4.6 ″GI|5729983|REF|NM_006596.1|人聚合酶(DNA导向的),
THETA(POLQ),MRNA″
4.5 ″GI|4758315|REF|NM_004454.1|人ETS变异体基因5(ETS相
关分子)(ETV5),MRNA″
4.5 ″人含转化酸性卷曲螺旋蛋白(TRANSFORMING,ACIDIC
COILED-COIL CONTAINING PROTEIN)3(TAC″
4.5 ″人驱动蛋白类似物1(KNSL1),MRNA″
4.5 ″人着丝粒蛋白E(312KD)(CENPE),MRNA″
4.5 ″人CDNA,3′END/克隆=IMAGE:1651289/克隆_END=3′
/GB=AI12″
4.4 ″人DISTAL-LESS HOMEO BOX 5(DLX5),MRNA″
4.4 ″人V-MYB禽成髓细胞性白血病病毒癌基因同系物类似物2″
4.4 ″人血清剥夺反应(磷脂酰丝氨酸结合PRO″
4.4 ″人假拟蛋白(HYPOTHETICAL PROTEIN)FLJ10604(FLJ10604),
MRNA″
4.4 ″人核糖核酸酶HI,大亚基(RNASEHI),MRNA
4.4 ″人ANILLIN(果蝇SCRAPS同系物),肌动蛋白结合蛋白″
4.4 ″人H4组蛋白家族,成员G(H4FG),MRNA″
4.3 ″人G蛋白连结受体37(内皮缩血管肽受体B型-″
4.3 ″人泛素载体蛋白(E2-EPF),MRNA″
4.3 ″人,类似于肿瘤差别表达1,克隆IMAGE:3639252,″
4.2 ″人 假拟蛋白(HYPOTHETICAL PROTEIN)MGC2577
(MGC2577),MRNA″
4.2 ″人假拟蛋白(HYPOTHETICAL PROTEIN)FLJ13912(FLJ13912),
MRNA″
4.2 ″人ANNEXIN A3(ANXA3),MRNA″
4.2 ″人STATHMIN1/ONCO蛋白18(STMN1),MRNA″
4.2 ″GNL|UG|HS#S3837587人,与核糖体蛋白L39类似,克隆
MGC:20168 IMAGE:4555759,M″
4.2 ″人POLO(果蝇)类似物激酶(PLK),MRNA″
实施例6【间充质干细胞中各个基因的表达量的测定IV】
以与实施例1相同方法,对本发明的各个基因标记在人源间充质干细胞和人成纤维细胞中的表达进行测定。间充质干细胞/成纤维细胞的表达之比示于表5。表中的-表示的是在间充质干细胞中基因不表达或极少量表达。
表5
(间充质干细胞/成纤维细胞) (基因名称)
-53.576 ″人蛋白酶复合体(PROSOME,MACROPAIN)26S亚基,ATP
酶,5(PS″
-45.692 ″人真核翻译起始因子4γ,2(EIF4G″
-27.6354 ″人二氢嘧啶酶类似物3(DPYSL3),MRNA″
-20.5446 ″人ADAPTOR相关蛋白复合体1,SIGMA2亚基(AP1S2)″
-19.5809 ″人网蛋白1,中间丝结合蛋白,500KD P″
-16.9025 ″人异种核蛋白U(SCAFFOLD ATTAC″
-14.97 ″人假拟蛋白(HYPOTHETICAL PROTEIN)MGC5306
(MGC5306),MRNA″
-14.6106 ″人MHCI类多肽相关序列A(MICA),MRNA″
-13.8886 ″人PRK1相关蛋白(AWP1),MRNA″
-13.6578 ″人孕酮受体膜成分2(PGRMC2),MRNA″
-11.4783 ″人多聚谷氨酸结合蛋白1(PQBP1),MRNA″
-10.2392 ″人S-腺苷甲硫氨酸脱羧酶1(AMD1),MRNA″
-9.9506 ″人干扰素诱导的C型肝炎相关MICROTUBULAR AG″
-9.2594 ″人蛋白激酶,AMP-活化的,γ1非催化性亚基
(NON-CATALYTIC SUBUN)″
-7.518 ″人前胶原-脯氨酸,2-OXOGLUTARATE 4-DIOXYGENASE(脯
氨酸″
-6.0365 ″人血管内皮分化,溶血磷脂酸G-PROTE″
-5.4442 ″人KIAA0127基因产物(KIAA0127),MRNA″″″
实施例7【人细胞中间充质干细胞DR的表达的测定】
采用流式细胞仪测定人细胞中间充质干细胞DR的表达。结果示于图11中。
实施例8【在间充质干细胞的分化诱导中个基因的表达的变化】
以与实施例1相同方式进行RT-PCR,测定间充质干细胞的分化诱导中各基因表达的表化。成骨细胞的分化诱导中各基因的表达示于图12-16中。
产业上利用的可能性
近年来,随着再生医疗的发展,间充质干细胞作为可用于多种组织的再生医疗的移植材料受到人们关注。为了将间充质干细胞利用于组织的再生医疗中,必须要开发出确保间充质干细胞有足够数量的技术,同时还必须证实所培养的细胞是间充质干细胞,重要的是检测、分离该间充质干细胞的方法。此外,采用抗体等从多种类型的细胞集团中分离间充质干细胞也是有用的。根据本发明,通过对间充质细胞的特征标记基因进行指示,就可能容易且确实地检测识别间充质干细胞,故而可期待为将间充质干细胞在再生医疗中实用化作出重大贡献。
序列表
<110>独立行政法人科学技术振兴机构(Japan Science and Technology Agency)
加藤幸夫(Yukio KATO)
智再如股份公司(Two Cells Co.,Ltd.)
<120>检测间充质干细胞的标记和采用该标记识别间充质干细胞的方法
<130>V320P006US(PCT)
<150>JP2003-63077
<151>2000-03-10
<160>116
<170>PatentIn version 3.1
<210>1
<211>652
<212>DNA
<213>人
<400>1
gaattgccaa ttccttgttt gtgcaaaatg gatttcatgt caatgaggag tttttgcaaa 60
tgatgaaaaa atattttaat gcagcagtaa atcatgtgga cttcagtcaa aatgtagccg 120
tggccaacta catcaataag tgggtggaga ataacacaaa caatctggtg aaagatttgg 180
tatccccaag ggattttgat gctgccactt atctggccct cattaatgct gtctatttca 240
aggggaactg gaagtcgcag tttaggcctg aaaatactag aaccttttct ttcactaaag 300
atgatgaaag tgaagtccaa attccaatga tgtatcagca aggagaattt tattatgggg 360
aatttagtga tggctccaat gaagctggtg gtatctacca agtcctagaa ataccatatg 420
aaggagatga aataagcatg atgctggtgc tgtccagaca ggaagttcct cttgctactc 480
tggagccatt agtcaaagca cagctggttg aagaatgggc aaactctgtg aagaagcaaa 540
aagtagaagt atacctgccc aggttcacag tggaacagga aattgattta aaagatgttt 600
tgaaggctct tggaataact gaaaattttc atcaaagatg caaattttga ca 652
<210>2
<211>1450
<212>DNA
<213>人
<400>2
ctggatagaa cagctcaagc cttgccactt cgggcttctc actgcagctg ggcttggact 60
tcggagtttt gccattgcca gtgggacgtc tgagactttc tccttcaagt acttggcaga 120
tcactctctt agcagggtct gcgcttcgca gccgggatga agctggtttc cgtcgccctg 180
atgtacctgg gttcgctcgc cttcctaggc gctgacaccg ctcggttgga tgtcgcgtcg 240
gagtttcgaa agaagtggaa taagtgggct ctgagtcgtg ggaagaggga actgcggatg 300
tccagcagct accccaccgg gctcgctgac gtgaaggccg ggcctgccca gacccttatt 360
cggccccagg acatgaaggg tgcctctcga agccccgaag acagcagtcc ggatgccgcc 420
cgcatccgag tcaagcgcta ccgccagagc atgaacaact tccagggcct ccggagcttt 480
ggctgccgct tcgggacgtg cacggtgcag aagctggcac accagatcta ccagttcaca 540
gataaggaca aggacaacgt cgcccccagg agcaagatca gcccccaggg ctacggccgc 600
cggcgccggc gctccctgcc cgaggccggc ccgggtcgga ctctggtgtc ttctaagcca 660
caagcacacg gggctccagc ccccccgagt ggaagtgctc cccactttct ttaggattta 720
ggcgcccatg gtacaaggaa tagtcgcgca agcatcccgc tggtgcctcc cgggacgaag 780
gacttcccga gcggtgtggg gaccgggctc tgacagccct gcggagaccc tgagtccggg 840
aggcaccgtc cggcggcgag ctctggcttt gcaagggccc ctccttctgg gggcttcgct 900
tccttagcct tgctcaggtg caagtgcccc agggggcggg gtgcagaaga atccgagtgt 960
ttgccaggct taaggagagg agaaactgag aaatgaatgc tgagaccccc ggagcagggg 1020
tctgagccac agccgtgctc gcccacaaac tgatttctca cggcgtgtca ccccaccagg 1080
gcgcaagcct cactattact tgaactttcc aaaacctaaa gaggaaaagt gcaatgcgtg 1140
ttgtacatac agaggtaact atcaatattt aagtttgttg ctgtcaagat tttttttgta 1200
acttcaaata tagagatatt tttgtacgtt atatattgta ttaagggcat tttaaaagca 1260
attatattgt cctcccccta ttttaagacg tgaatgtctc agcgaggtgt aaagttgttc 1320
gccgcgtgga atgtgagtgt gtttgtgtgc atgaaagaga aagactgatt acctcctgtg 1380
tggaagaagg aaacaccgag tctctgtata atctatttac ataaaatggg tgatatgcga 1440
acagcaaacc 1450
<210>3
<211>185
<212>PRT
<213>人
<400>3
Met Lys Leu Val Ser Val Ala Leu Met Tyr Leu Gly Ser Leu Ala Phe
1 5 10 15
Leu Gly Ala Asp Thr Ala Arg Leu Asp Val Ala Ser Glu Phe Arg Lys
20 25 30
Lys Trp Asn Lys Trp Ala Leu Ser Arg Gly Lys Arg Glu Leu Arg Met
35 40 45
Ser Ser Ser Tyr Pro Thr Gly Leu Ala Asp Val Lys Ala Gly Pro Ala
50 55 60
Gln Thr Leu Ile Arg Pro Gln Asp Met Lys Gly Ala Ser Arg Ser Pro
65 70 75 80
Glu Asp Ser Ser Pro Asp Ala Ala Arg Ile Arg Val Lys Arg Tyr Arg
85 90 95
Gln Ser Met Asn Asn Phe Gln Gly Leu Arg Ser Phe Gly Cys Arg Phe
100 105 110
Gly Thr Cys Thr Val Gln Lys Leu Ala His Gln Ile Tyr Gln Phe Thr
115 120 125
Asp Lys Asp Lys Asp Asn Val Ala Pro Arg Ser Lys Ile Ser Pro Gln
130 135 140
Gly Tyr Gly Arg Arg Arg Arg Arg Ser Leu Pro Glu Ala Gly Pro Gly
145 150 155 160
Arg Thr Leu Val Ser Ser Lys Pro Gln Ala His Gly Ala Pro Ala Pro
165 170 175
Pro Ser Gly Ser Ala Pro His Phe Leu
180 185
<210>4
<211>809
<212>DNA
<213>人
<400>4
atgcctgtct tcatcttgaa agaaaagctc caggtccctt ctccagccac ccagccccaa 60
gatggtgatg ctgctgctgc tgctttccgc actggctggc ctcttcggtg cggcagaggg 120
acaagcattt catcttggga agtgccccaa tcctccggtg caggagaatt ttgacgtgaa 180
taagtatctc ggaagatggt acgaaattga gaagatccca acaacctttg agaatggacg 240
ctgcatccag gccaactact cactaatgga aaacggaaag atcaaagtgt taaaccagga 300
gttgagagct gatggaactg tgaatcaaat cgaaggtgaa gccaccccag ttaacctcac 360
agagcctgcc aagctggaag ttaagttttc ctggtttatg ccatcggcac cgtactggat 420
cctggccacc gactatgaga actatgccct cgtgtattcc tgtacctgca tcatccaact 480
ttttcacgtg gattttgctt ggatcttggc aagaaaccct aatctccctc cagaaacagt 540
ggactctcta aaaaatatcc tgacttctaa taacattgat gtcaagaaaa tgacggtcac 600
agaccaggtg aactgcccca agctctcgta accaggttct acagggaggc tgcacccact 660
ccatgttact tctgcttcgc tttcccctac cccacccccc cccataaaga caaaccaatc 720
aaccacgaca aaggaagttg acctaaacat gtaaccatgc cctaccctgt taccttgcta 780
gctgcaaaat aaacttgttg ctgacctgc 809
<210>5
<211>189
<212>PRT
<213>人
<400>5
Met Val Met Leu Leu Leu Leu Leu Ser Ala Leu Ala Gly Leu Phe Gly
1 5 10 15
Ala Ala Glu Gly Gln Ala Phe His Leu Gly Lys Cys Pro Asn Pro Pro
20 25 30
Val Gln Glu Asn Phe Asp Val Asn Lys Tyr Leu Gly Arg Trp Tyr Glu
35 40 45
Ile Glu Lys Ile Pro Thr Thr Phe Glu Asn Gly Arg Cys Ile Gln Ala
50 55 60
Asn Tyr Ser Leu Met Glu Asn Gly Lys Ile Lys Val Leu Asn Gln Glu
65 70 75 80
Leu Arg Ala Asp Gly Thr Val Asn Gln Ile Glu Gly Glu Ala Thr Pro
85 90 95
Val Asn Leu Thr Glu Pro Ala Lys Leu Glu Val Lys Phe Ser Trp Phe
100 105 110
Met Pro Ser Ala Pro Tyr Trp Ile Leu Ala Thr Asp Tyr Glu Asn Tyr
115 120 125
Ala Leu Val Tyr Ser Cys Thr Cys Ile Ile Gln Leu Phe His Val Asp
130 135 140
Phe Ala Trp Ile Leu Ala Arg Asn Pro Asn Leu Pro Pro Glu Thr Val
145 150 155 160
Asp Ser Leu Lys Asn Ile Leu Thr Ser Asn Asn Ile Asp Val Lys Lys
165 170 175
Met Thr Val Thr Asp Gln Val Asn Cys Pro Lys Leu Ser
180 185
<210>6
<211>2127
<212>DNA
<213>人
<400>6
gaaagatgga tcactccagc tcaaagagaa catgtgggaa tgaaaggaca ggctgggccc 60
aaaggagaaa agggtgatgc tggggaggag cttcctggcc ctcctgaacc ttctgggcct 120
gttggaccca cggcaggagc agaagcagag ggctctggcc taggctgggg ctcggacgtc 180
ggctctggct ctggtgacct ggtgggcagt gagcagctgc tgagaggtcc tccaggaccc 240
ccagggccac ctggcttacc tgggattcca ggaaaaccag gaactgatgt tttcatggga 300
ccccctggat ctcctggaga ggatggacct gctggtgaac ctgggccccc gggccctgag 360
ggacagcctg gagttgatgg agccaccggc cttcccggga tgaaagggga gaagggagca 420
agagggccta atggctcagt tggtgaaaag ggtgaccctg gcaacagagg cttacctgga 480
cccccgggga aaaagggaca agctggccct cctggggtca tgggaccccc agggcctcct 540
ggaccccctg ggcccccagg ccctggatgc acaatgggac ttggattcga ggataccgaa 600
ggctctggaa gcacccagct attgaatgaa cccaaactct ccagaccaac ggctgcaatt 660
ggtctcaaag gagagaaagg agaccgggga cccaagggag aaagggggat ggatggagcc 720
agtattgtgg gaccccctgg gccgagaggg ccacctgggc acatcaaggt cttgtctaat 780
tccttgatca atatcaccca tggattcatg aatttctcgg acattcctga gctggtgggg 840
cctccggggc cggacgggtt gcctgggctg ccaggatttc caggtcctag aggaccaaaa 900
ggtgacactg gtttacctgg ctttccagga ctaaaaggag aacagggcga gaagggagag 960
ccgggtgcca tcctgacaga ggacattcct ctggaaaggc tgatggggaa aaagggtgaa 1020
cctggaatgc atggagcccc aggaccaatg gggcccaaag gaccaccagg acataaagga 1080
gaatttggcc ttcccgggcg acctggtcgc ccaggactga atggcctcaa gggtaccaaa 1140
ggagdtccag gggtcattat gcagggccca cctggcttac ctggccctcc aggcccccct 1200
gggccacctg gagctgtgat taacatcaaa ggagccattt tcccaatacc cgtccgacca 1260
cactgcaaaa tgccagttga tactgctcat cctgggagtc cagagctcat cacttttcac 1320
ggtgttaaag gagagaaagg atcctggggt cttcctggct caaagggaga aaaaggcgac 1380
cagggagccc agggaccacc aggtcctcca cttgatctag cttacctgag acactttctg 1440
aacaacttga agggggagaa tggagacaag gggttcaaag gtgaaaaagg agaaaaagga 1500
gacattaatg gcagcttcct tatgtctggg cctccaggcc tgcccggaaa tccaggcccg 1560
gctggccaaa aaggggagac agtcgttggg ccccaaggac ccccaggtgc tcctggtctg 1620
cctgggccac ctggctttgg aagacctggt gatcctgggc caccggggcc cccggggcca 1680
ccaggacctc cagctatcct gggagcagct gtggcccttc caggtccccc tggccctcca 1740
ggacagccag ggcttcccgg atccagaaac ctggtcacag cattcagcaa catggatgac 1800
atgctgcaga aagcgcattt ggttatagaa ggaacattca tctacctgag ggacagcact 1860
gagtttttca ttcgtgttag agatggctgg aaaaaattac agctgggaga actgatcccc 1920
attcctgccg acagccctcc accccctgcg ctttccagca acccacatca gcttctgcct 1980
ccaccaaacc ctatttcaag tgccaattat gagaagcctg ctctgcattt ggctgctctg 2040
aacatgccat tttctgggga cattcgagct gattttcagt gcttcaagca ggccagagct 2100
gcaggactgt tgtccaccta ccgagca 2127
<210>7
<211>2384
<212>DNA
<213>人
<400>7
cctgctcgtt cctgacagaa ttaacggcac agccaacaag atgaacggag ctttggatca 60
ctcagaccaa ccagacccag atgccattaa gatgtttgtc ggacagatcc cccggtcatg 120
gtcggaaaag gagctgaaag aactttttga gccttacgga gccgtctacc agatcaacgt 180
cctccgggac cggagtcaga accctccgca gagtaaaggt tgttgtttcg taacatttta 240
tacaagaaaa gctgcacttg aggcccagaa tgcactgcac aatattaaaa ctttacctgg 300
gatgcatcat cccattcaga tgaaacctgc agatagtgaa aagtccaacg ctgtggaaga 360
cagaaaattg ttcataggaa tggtttcgaa gaaatgtaat gagaacgaca tcagggtgat 420
gttctctcca tttggccaga tagaagaatg ccggatcctc cggggacctg atgggctgag 480
tcgaggctgt gcgtttgtca cattttctac aagggcaatg gcacagaatg caatcaaagc 540
catgcatcag tctcagacca tggagggctg ctcttcacct atcgtggtga agtttgctga 600
cactcagaag gacaaagagc aaaggcgcct ccagcagcag ctcgctcagc agatgcagca 660
gctcaacact gccacctggg ggaacctgac agggctgggc ggactgaccc cacagtatct 720
ggcgctcctg cagcaggcca cctcctccag caacctgggt gcgttcagcg gcattcaaca 780
aatggcaggc atgaatgctt tacagttgca gaacctggcg acgctggctg ctgctgcagc 840
tgcggcccag acctcagcca ccagcaccaa tgcaaaccct ctctctacca cgagcagcgc 900
cctgggagcc ctcacgagtc ccgtggctgc ttcaaccccc aactccactg ctggtgcagc 960
catgaactcc ttgacctctc tcgggactct gcaaggactg gctggagcca ctgttggact 1020
gaataatatt aatgcactag cagttgctca aatgctctca ggtatggcgg ctctgaatgg 1080
aggacttggc gccacaggct tgacgaatgg cacggctggc accatggacg ccctcaccca 1140
ggcctactca ggaattcaac agtacgcagc cgccgcgctg cccactctgt acagccagag 1200
cctgctgcag cagcagagcg ctgcaggcag ccagaaggaa ggtccagagg gggcaaacct 1260
ctttatttac caccttccac aggaatttgg agaccagcac attctgcaga tgttcatgcc 1320
ttttggaaat gttatctctg ctaaagtctt cattgacaaa cagaccaatc tgagcaagtg 1380
ctttggtttt gttagctacg acaatccagt ctctgcacaa gctgctatcc aagctatgaa 1440
tggctttcag atcggcatga aacgcttgaa ggtgcagctg aagcgttcca aaaacgacag 1500
caaaccttac tgatcctaac cccagaggct ccctgctctc attttagctt tcttaggaca 1560
tcttcatgcc cgttagttca tcgtttgcct agcatgtccc tgtggcgtct caaaaaaaag 1620
tttcatcgtc ccgtcattgt ttctgatgtc tttctgacct cacatcatat ttggttctcc 1680
tactgacctt tgatctagtt tgacctttga aatttgcatg tgacctcatc tagctatgaa 1740
ttctgggaag tcaatgtgaa aaacattgct gcattcatgc aagactgaaa tttattatta 1800
gacaaattca ttatagaaaa aacctgtggc aaaaacgttt ctttcttatt ttttttcttt 1860
tcctaaaaca gacttgaaag tattatacag ggattggcat tcttcccggt cactggtaac 1920
aatagcaata tgtgtccagg gacacagaat gttggtttct aacagactac ttccaaaaac 1980
agtttgagaa aaaaactgtc tgattttaag tctctagagg tctgtaatag tttttacatt 2040
tttcaggcag tgtaaagttt tttgataagg ccattttagg tggctcactt tctcattaag 2100
atatatatat agaaccactt tttgtagatt agtataagaa aaatatttac cctgttttgg 2160
ggcaaatgct acctatttgt gtcacctttt gctgaactca cagttagaca atccatggtt 2220
taatgcacat gaaattacct atattttata ctgtttcaat gtacaggaga aaggttactg 2280
taaactgtgt tatgttggtg cttctgtgaa ttaagttgtg gtttcatcat gagtcttaat 2340
gttctttgtt gataagacaa gtttagaatt ggtttactta atac 2384
<210>8
<211>490
<212>PRT
<213>人
<400>8
Met Asn Gly Ala Leu Asp His Ser Asp Gln Pro Asp Pro Asp Ala Ile
1 5 10 15
Lys Met Phe Val Gly Gln Ile Pro Arg Ser Trp Ser Glu Lys Glu Leu
20 25 30
Lys Glu Leu Phe Glu Pro Tyr Gly Ala Val Tyr Gln Ile Asn Val Leu
35 40 45
Arg Asp Arg Ser Gln Asn Pro Pro Gln Ser Lys Gly Cys Cys Phe Val
50 55 60
Thr Phe Tyr Thr Arg Lys Ala Ala Leu Glu Ala Gln Asn Ala Leu His
65 70 75 80
Asn Ile Lys Thr Leu Pro Gly Met His His Pro Ile Gln Met Lys Pro
85 90 95
Ala Asp Ser Glu Lys Ser Asn Ala Val Glu Asp Arg Lys Leu Phe Ile
100 105 110
Gly Met Val Ser Lys Lys Cys Asn Glu Asn Asp Ile Arg Val Met Phe
115 120 125
Ser Pro Phe Gly Gln Ile Glu Glu Cys Arg Ile Leu Arg Gly Pro Asp
130 135 140
Gly Leu Ser Arg Gly Cys Ala Phe Val Thr Phe Ser Thr Arg Ala Met
145 150 155 160
Ala Gln Asn Ala Ile Lys Ala Met His Gln Ser Gln Thr Met Glu Gly
165 170 175
Cys Ser Ser Pro Ile Val Val Lys Phe Ala Asp Thr Gln Lys Asp Lys
180 185 190
Glu Gln Arg Arg Leu Gln Gln Gln Leu Ala Gln Gln Met Gln Gln Leu
195 200 205
Asn Thr Ala Thr Trp Gly Asn Leu Thr Gly Leu Gly Gly Leu Thr Pro
210 215 220
Gln Tyr Leu Ala Leu Leu Gln Gln Ala Thr Ser Ser Ser Asn Leu Gly
225 230 235 240
Ala Phe Ser Gly Ile Gln Gln Met Ala Gly Met Asn Ala Leu Gln Leu
245 250 255
Gln Asn Leu Ala Thr Leu Ala Ala Ala Ala Ala Ala Ala Gln Thr Ser
260 265 270
Ala Thr Ser Thr Asn Ala Asn Pro Leu Ser Thr Thr Ser Ser Ala Leu
275 280 285
Gly Ala Leu Thr Ser Pro Val Ala Ala Ser Thr Pro Asn Ser Thr Ala
290 295 300
Gly Ala Ala Met Asn Ser Leu Thr Ser Leu Gly Thr Leu Gln Gly Leu
305 310 315 320
Ala Gly Ala Thr Val Gly Leu Asn Asn Ile Asn Ala Leu Ala Val Ala
325 330 335
Gln Met Leu Ser Gly Met Ala Ala Leu Asn Gly Gly Leu Gly Ala Thr
340 345 350
Gly Leu Thr Asn Gly Thr Ala Gly Thr Met Asp Ala Leu Thr Gln Ala
355 360 365
Tyr Ser Gly Ile Gln Gln Tyr Ala Ala Ala Ala Leu Pro Thr Leu Tyr
370 375 380
Ser Gln Ser Leu Leu Gln Gln Gln Ser Ala Ala Gly Ser Gln Lys Glu
385 390 395 400
Gly Pro Glu Gly Ala Asn Leu Phe Ile Tyr His Leu Pro Gln Glu Phe
405 410 415
Gly Asp Gln His Ile Leu Gln Met Phe Met Pro Phe Gly Asn Val Ile
420 425 430
Ser Ala Lys Val Phe Ile Asp Lys Gln Thr Asn Leu Ser Lys Cys Phe
435 440 445
Gly Phe Val Ser Tyr Asp Asn Pro Val Ser Ala Gln Ala Ala Ile Gln
450 455 460
Ala Met Asn Gly Phe Gln Ile Gly Met Lys Arg Leu Lys Val Gln Leu
465 470 475 480
Lys Arg Ser Lys Asn Asp Ser Lys Pro Tyr
485 490
<210>9
<211>419
<212>DNA
<213>人
<400>9
tttttttttt tttttttcag catagtgaac gttaatattt ttatttcttt tgtaatgaag 60
agtacaaatg gttgggagca ggacatcaca ggaggaggaa agatagcgcc atctctgcag 120
aagaactcct gagccacaca cagaaggaaa gttgatcccc agggcagcct ttcccaccaa 180
aaaaatcagg cccaatccag gagagtttgc cagtagctcc ccagggttcc agggtgtctg 240
ccagccttcc taggaatcgt gggcaggctt ctaggtgcca gtgactcaaa ctcctttttc 300
cacttcccag ttcaacctgg tcactctcat ccccacaagt tcccaatctg aatcccattc 360
tctgaccatt ctctgcttcc ttgtttttaa tctcatttga gagtgatcct cacgggttc 419
<210>10
<211>762
<212>DNA
<213>人
<400>10
gccgggagga gcggcgcgcg ctcggacctc tcccgccctg ctcgttcgct ctccagcttg 60
ggatggccgg ctacctgcgg gtcgtgcgct cgctctgcag agcctcaggc tcgcggccgg 120
cctgggcgcc ggcggccctg acagccccca cctcgcaaga gcagccgcgg cgccactatg 180
ccgacaaaag gatcaaggtg gcgaagccgt ggtggagatg gatggtgatg agatgacccg 240
tattatctgg cagttcatca aggagaagct catcctgccc cacgtggaca tccagctaaa 300
gtattttgac ctcgggctcc caaaccgtga ccagactgat gaccaggtca ccattgactc 360
tgcactggcc acccagaagt acagtgtggc tgtcaagtgt gccaccatca cccctgatga 420
ggcccgtgtg gaagagttca agctgaagaa gatgtggaaa agtcccaatg gaactatccg 480
gaacatcctg ggggggactg tcttccggga gcccatcatc tgcaaaaaca tcccacgcct 540
agtccctggc tggaccaagc ccatcaccat tggcaggcac gcccatggcg accagtacaa 600
ggccacagac tttgtggcag accgggccgg cactttcaaa atggtcttca ccccaaaaga 660
tggcagtggt gtcaaggagt gggaagtgta caacttcccc gcaggcgcgc gtgggcatgg 720
gcatgtacma caccgacgag tccatctcag gttttgcgca ca 762
<210>11
<211>689
<212>DNA
<213>人
<400>11
aactccatct ttgaaaaaca tttaataatg taatgtgttt gtggtacagg gtgagtacag 60
atgcacagga ggccataggg tttaggcaaa ggggagcaca aaagttgaag atgaggcgct 120
gccatcaatg ctgggacttc aggccaaggg caggaactga ggaagccaca agggaggaca 180
ttttctgcag ttgctgaacc agtagcaact aggtcctgag aaagccctct ctcgtggaag 240
aataacagcc aggcgggaaa gcttttcatc ctgcaaagct ggggaagaag attcttcctt 300
aaattgtcat ctgcacttca gctcaggaat cctgttggct gaagtccaga gtgtcctttc 360
tgattcctga agtagatgaa cagcccggcc ccaaggaaga gcaggcccag cacaaagccc 420
ccgactccac tcagcatctt gctctgtgca gattcagacc gtgcactcca ttccactgtg 480
agagggctcg ttacgcttgg gtgctccact tggcaggtgt aaacctctcc actccgagga 540
actgtttcta gcatcaccag ggtctggaat gtccagtctc cattctggat caggcgcgtg 600
gacaccaccc cagccttctc ttcctgcccg ttccggaacc agctgacttc aatgctgcct 660
ggatagaaac cactcacaga gcagaccag 689
<210>12
<211>1959
<212>DNA
<213>人
<400>12
gggagcacgc gggagtccgg ctgcccaccc atggcagggt ctaccagaag ggccacgagc 60
tggtgttggc caatattgct gaaagtgatg ctggtgtcta cacctgccac gcggccaacc 120
tggctggtca gcggagacag gatgtcaaca tcactgtggc cactgtgccc tcctggctga 180
agaagcccca agacagccag ctggaggagg gcaaacccgg ctacttggat tgcctgaccc 240
aggccacacc aaaacctaca gttgtctggt acagaaacca gatgctcatc tcagaggact 300
cacggttcga ggtgttcctg gcaaaggctc agggcttgga ggagggagtg gcagagaccc 360
tggtacttgt gaagagcctg cagagcaagg atgagcagca gcagctggac ttccggaggg 420
agttggagat gtttgggaag ctgaaccacg ccaacgtggt gcggctcctg gggctgtgcc 480
gggaggctga gccccactac atggtgctgg aatatgtgga tctgggagac ctcaagcagt 540
tcctgaggat ttccaagagc aaggatgaaa aattgaagtc acagcccctc agcaccaagc 600
agaaggtggc cctatgcacc caggtagccc tgggcatgga gcacctgtcc aacaaccgct 660
ttgtgcataa ggacttggct gcgcgtaact gcctggtcag tgcccagaga caagtgaagg 720
tgtctgccct gggcctcagc aaggatgtgt acaacagtga gtactaccac ttccgccagg 780
cctgggtgcc gctgcgctgg atgtcccccg aggccatcct ggagggtgac ttctctacca 840
agtctgatgt ctgggccttc ggtgtgctga tgtgggaagt gtttacacat ggagagatgc 900
cccatggtgg gcaggcagat gatgaagtac tggcagattt gcaggctggg aaggctagac 960
ttcctcagcc cgagggctgc ccttccaaac tctatcggct gatgcagcgc tgctgggccc 1020
tcagccccaa ggaccggccc tccttcagtg agattgccag cgccctggga gacagcaccg 1080
tggacagcaa gccgtgagga gggagcccgc tcaggatggc ctgggcaggg gaggacatct 1140
ctagagggaa gctcacagca tgatgggcaa gatccctgtc ctcctgggcc ctgaggcccc 1200
tgccctagtg caacaggcat tgctgaggtc tgagcagggc ctggcctttc ctcctcttcc 1260
tcaccctcat cctttgggag gctgacttgg acccaaactg ggcgactagg gctttgagct 1320
gggcagtttt ccctgccacc tcttcctcta tcagggacag tgtgggtgcc acaggtaacc 1380
ccaatttctg gccttcaact tctccccttg accgggtcca actctgccac tcatctgcca 1440
actttgcctg gggagggcta ggcttgggat gagctgggtt tgtggggagt tccttaatat 1500
tctcaagttc tgggcacaca gggttaatga gtctcttggc ccactggtcc cacttggggg 1560
tctagaccag gattatagag gacacagcaa gtgagtcctc cccactctgg gcttgtgcac 1620
actgacccag acccacgtct tccccaccct tctctccttt cctcatccta agtgcctggc 1680
agatgaagga gttttcagga gcttttgaca ctatataaac cgcccttttt gtatgcacca 1740
cgggcggctt ttatatgtaa ttgcagcgtg gggtgggtgg gcatgggagg taggggtggg 1800
ccctggagat gaggagggtg ggccatcctt accccacact tttattgttg tcgttttttg 1860
tttgttttgt ttttttgttt ttgtttttgt ttttacactc gctgctctca ataaataagc 1920
cttttttaca aaaaaaaaaa aaaaaaaaaa aaaaaaaaa 1959
<210>13
<211>364
<212>PRT
<213>人
<400>13
Glu His Ala Gly Val Arg Leu Pro Thr His Gly Arg Val Tyr Gln Lys
1 5 10 15
Gly His Glu Leu Val Leu Ala Asn Ile Ala Glu Ser Asp Ala Gly Val
20 25 30
Tyr Thr Cys His Ala Ala Asn Leu Ala Gly Gln Arg Arg Gln Asp Val
35 40 45
Asn Ile Thr Val Ala Thr Val Pro Ser Trp Leu Lys Lys Pro Gln Asp
50 55 60
Ser Gln Leu Glu Glu Gly Lys Pro Gly Tyr Leu Asp Cys Leu Thr Gln
65 70 75 80
Ala Thr Pro Lys Pro Thr Val Val Trp Tyr Arg Asn Gln Met Leu Ile
85 90 95
Ser Glu Asp Ser Arg Phe Glu Val Phe Leu Ala Lys Ala Gln Gly Leu
100 105 110
Glu Glu Gly Val Ala Glu Thr Leu Val Leu Val Lys Ser Leu Gln Ser
115 120 125
Lys Asp Glu Gln Gln Gln Leu Asp Phe Arg Arg Glu Leu Glu Met Phe
130 135 140
Gly Lys Leu Asn His Ala Asn Val Val Arg Leu Leu Gly Leu Cys Arg
145 150 155 160
Glu Ala Glu Pro His Tyr Met Val Leu Glu Tyr Val Asp Leu Gly Asp
165 170 175
Leu Lys Gln Phe Leu Arg Ile Ser Lys Ser Lys Asp Glu Lys Leu Lys
180 185 190
Ser Gln Pro Leu Ser Thr Lys Gln Lys Val Ala Leu Cys Thr Gln Val
195 200 205
Ala Leu Gly Met Glu His Leu Ser Asn Asn Arg Phe Val His Lys Asp
210 215 220
Leu Ala Ala Arg Asn Cys Leu Val Ser Ala Gln Arg Gln Val Lys Val
225 230 235 240
Ser Ala Leu Gly Leu Ser Lys Asp Val Tyr Asn Ser Glu Tyr Tyr His
245 250 255
Phe Arg Gln Ala Trp Val Pro Leu Arg Trp Met Ser Pro Glu Ala Ile
260 265 270
Leu Glu Gly Asp Phe Ser Thr Lys Ser Asp Val Trp Ala Phe Gly Val
275 280 285
Leu Met Trp Glu Val Phe Thr His Gly Glu Met Pro His Gly Gly Gln
290 295 300
Ala Asp Asp Glu Val Leu Ala Asp Leu Gln Ala Gly Lys Ala Arg Leu
305 310 315 320
Pro Gln Pro Glu Gly Cys Pro Ser Lys Leu Tyr Arg Leu Met Gln Arg
325 330 335
Cys Trp Ala Leu Ser Pro Lys Asp Arg Pro Ser Phe Ser Glu Ile Ala
340 345 350
Ser Ala Leu Gly Asp Ser Thr Val Asp Ser Lys Pro
355 360
<210>14
<211>430
<212>DNA
<213>人
<400>14
ggttgatgtt tcaacaaagt agttttaagt tccatccatt cagattttaa gcattttgat 60
ttatttaaaa agggattgtt catagaaaaa aattactttg aacagtatac aggactggtg 120
gagattggct atttcacaac atcagacagt acaatcagta tctgccatat ggctggtctc 180
tgtagacgcc ctttgctgtc ctcgctgaag gtgccttgtg tcttgagtta gtccactctt 240
cttgcccgta ggaatcataa gtctcctcac tgagtccatg tccgtaatca tagtaatcag 300
caccactttg ggctggggtg ctatagctgt tatcatagga atcataactc tgttcatcat 360
aagcagtgcc atatccatca tcatagtcat attctccata agtctcttgg tgtcgggggt 420
ggcggtggaa 430
<210>15
<211>616
<212>DNA
<213>人
<400>15
ggtatgatga ccaaacataa aaagtgtttt ataattgttg gtgttttaat aacaactaat 60
attattactc tgatagttaa actaactcga gattctcaga gtttatgccc ctatgattgg 120
attggtttcc aaaacaaatg ctattatttc tctaaagaag aaggagattg gaattcaagt 180
aaatacaact gttccactca acatgccgac ctaactataa ttgacaacat agaagaaatg 240
aattttctta ggcggtataa atgcagttct gatcactgga ttggactgaa gatggcaaaa 300
aatcgaacag gacaatgggt agatggagct acatttacca aatcgtttgg catgagaggg 360
agtgaaggat gtgcctacct cagcgatgat ggtgcagcaa cagctagatg ttacaccgaa 420
agaaaatgga tttgcaggaa aagaatacac taagttaatg tctaagataa tggggaaaat 480
agaaaataac attattaagt gtaaaaccag caaagtactt ttttaattaa acaaagttcg 540
agttttgtac ctgtctggtt aattctgctt acgtgtcagg ctacacataa aagccacttc 600
aaagattggc aaaaaa 616
<400>16
Met Met Thr Lys His Lys Lys Cys Phe Ile Ile Val Gly Val Leu Ile
1 5 10 15
Thr Thr Asn Ile Ile Thr Leu Ile Val Lys Leu Thr Arg Asp Ser Gln
20 25 30
Ser Leu Cys Pro Tyr Asp Trp Ile Gly Phe Gln Asn Lys Cys Tyr Tyr
35 40 45
Phe Ser Lys Glu Glu Gly Asp Trp Asn Ser Ser Lys Tyr Asn Cys Ser
50 55 60
Thr Gln His Ala Asp Leu Thr Ile Ile Asp Asn Ile Glu Glu Met Asn
65 70 75 80
Phe Leu Arg Arg Tyr Lys Cys Ser Ser Asp His Trp Ile Gly Leu Lys
85 90 95
Met Ala Lys Asn Arg Thr Gly Gln Trp Val Asp Gly Ala Thr Phe Thr
100 105 110
Lys Ser Phe Gly Met Arg Gly Ser Glu Gly Cys Ala Tyr Leu Ser Asp
115 120 125
Asp Gly Ala Ala Thr Ala Arg Cys Tyr Thr Glu Arg Lys Trp Ile Cys
130 135 140
Arg Lys Arg Ile His
145
<210>17
<211>1973
<212>DNA
<213>人
<400>17
gggatattgg agtagcaaga ggctgggaag ccatcactta ccttgcactg agaaagaaga 60
caaaggccag tatgcacagc tttcctccac tgctgctgct gctgttctgg ggtgtggtgt 120
ctcacagctt cccagcgact ctagaaacac aagagcaaga tgtggactta gtccagaaat 180
acctggaaaa atactacaac ctgaagaatg atgggaggca agttgaaaag cggagaaata 240
gtggcccagt ggttgaaaaa ttgaagcaaa tgcaggaatt ctttgggctg aaagtgactg 300
ggaaaccaga tgctgaaacc ctgaaggtga tgaagcagcc cagatgtgga gtgcctgatg 360
tggctcagtt tgtcctcact gaggggaacc ctcgctggga gcaaacacat ctgacctaca 420
ggattgaaaa ttacacgcca gatttgccaa gagcagatgt ggaccatgcc attgagaaag 480
ccttccaact ctggagtaat gtcacacctc tgacattcac caaggtctct gagggtcaag 540
cagacatcat gatatctttt gtcaggggag atcatcggga caactctcct tttgatggac 600
ctggaggaaa tcttgctcat gcttttcaac caggcccagg tattggaggg gatgctcatt 660
ttgatgaaga tgaaaggtgg accaacaatt tcagagagta caacttacat cgtgttgcgg 720
ctcatgaact cggccattct cttggactct cccattctac tgatatcggg gctttgatgt 780
accctagcta caccttcagt ggtgatgttc agctagctca ggatgacatt gatggcatcc 840
aagccatata tggacgttcc caaaatcctg tccagcccat cggcccacaa accccaaaag 900
cgtgtgacag taagctaacc tttgatgcta taactacgat tcggggagaa gtgatgttct 960
ttaaagacag attctacatg cgcacaaatc ccttctaccc ggaagttgag ctcaatttca 1020
tttctgtttt ctggccacaa ctgccaaatg ggcttgaagc tgcttacgaa tttgccgaca 1080
gagatgaagt ccggtttttc aaagggaata agtactgggc tgttcaggga cagaatgtgc 1140
tacacggata ccccaaggac atctacagct cctttggctt ccctagaact gtgaagcata 1200
tcgatgctgc tctttctgag gaaaacactg gaaaaaccta cttctttgtt gctaacaaat 1260
actggaggta tgatgaatat aaacgatcta tggatccagg ttatcccaaa atgatagcac 1320
atgactttcc tggaattggc cacaaagttg atgcagtttt catgaaagat ggatttttct 1380
atttctttca tggaacaaga caatacaaat ttgatcctaa aacgaagaga attttgactc 1440
tccagaaagc taatagctgg ttcaactgca ggaaaaattg aacattacta atttgaatgg 1500
aaaacacatg gtgtgagtcc aaagaaggtg ttttcctgaa gaactgtcta ttttctcagt 1560
catttttaac ctctagagtc actgatacac agaatataat cttatttata cctcagtttg 1620
catatttttt tactatttag aatgtagccc tttttgtact gatataattt agttccacaa 1680
atggtgggta caaaaagtca agtttgtggc ttatggattc atataggcca gagttgcaaa 1740
gatcttttcc agagtatgca actctgacgt tgatcccaga gagcagcttc agtgacaaac 1800
atatcctttc aagacagaaa gagacaggag acatgagtct ttgccggagg aaaagcagct 1860
caagaacaca tgtgcagtca ctggtgtcac cctggatagg caagggataa ctcttctaac 1920
acaaaataag tgttttatgt ttggaataaa gtcaaccttg tttctactgt ttt 1973
<210>18
<211>469
<212>PRT
<213>人
<400>18
Met His Ser Phe Pro Pro Leu Leu Leu Leu Leu Phe Trp Gly Val Val
1 5 10 15
Ser His Ser Phe Pro Ala Thr Leu Glu Thr Gln Glu Gln Asp Val Asp
20 25 30
Leu Val Gln Lys Tyr Leu Glu Lys Tyr Tyr Asn Leu Lys Asn Asp Gly
35 40 45
Arg Gln Val Glu Lys Arg Arg Asn Ser Gly Pro Val Val Glu Lys Leu
50 55 60
Lys Gln Met Gln Glu Phe Phe Gly Leu Lys Val Thr Gly Lys Pro Asp
65 70 75 80
Ala Glu Thr Leu Lys Val Met Lys Gln Pro Arg Cys Gly Val Pro Asp
85 90 95
Val Ala Gln Phe Val Leu Thr Glu Gly Asn Pro Arg Trp Glu Gln Thr
100 105 110
His Leu Thr Tyr Arg Ile Glu Asn Tyr Thr Pro Asp Leu Pro Arg Ala
115 120 125
Asp Val Asp His Ala Ile Glu Lys Ala Phe Gln Leu Trp Ser Asn Val
130 135 140
Thr Pro Leu Thr Phe Thr Lys Val Ser Glu Gly Gln Ala Asp Ile Met
145 150 155 160
Ile Ser Phe Val Arg Gly Asp His Arg Asp Asn Ser Pro Phe Asp Gly
165 170 175
Pro Gly Gly Asn Leu Ala His Ala Phe Gln Pro Gly Pro Gly Ile Gly
180 185 190
Gly Asp Ala His Phe Asp Glu Asp Glu Arg Trp Thr Asn Asn Phe Arg
195 200 205
Glu Tyr Asn Leu His Arg Val Ala Ala His Glu Leu Gly His Ser Leu
210 215 220
Gly Leu Ser His Ser Thr Asp Ile Gly Ala Leu Met Tyr Pro Ser Tyr
225 230 235 240
Thr Phe Ser Gly Asp Val Gln Leu Ala Gln Asp Asp Ile Asp Gly Ile
245 250 255
Gln Ala Ile Tyr Gly Arg Ser Gln Asn Pro Val Gln Pro Ile Gly Pro
260 265 270
Gln Thr Pro Lys Ald Cys Asp Ser Lys Leu Thr Phe Asp Ala Ile Thr
275 280 285
Thr Ile Arg Gly Glu Val Met Phe Phe Lys Asp Arg Phe Tyr Met Arg
290 295 300
Thr Asn Pro Phe Tyr Pro Glu Val Glu Leu Asn Phe Ile Ser Val Phe
305 310 315 320
Trp Pro Gln Leu Pro Asn Gly Leu Glu Ala Ala Tyr Glu Phe Ala Asp
325 330 335
Arg Asp Glu Val Arg Phe Phe Lys Gly Asn Lys Tyr Trp Ala Val Gln
340 345 350
Gly Gln Asn Val Leu His Gly Tyr Pro Lys Asp Ile Tyr Ser Ser Phe
355 360 365
Gly Phe Pro Arg Thr Val Lys His Ile Asp Ala Ala Leu Ser Glu Glu
370 375 380
Asn Thr Gly Lys Thr Tyr Phe Phe Val Ala Asn Lys Tyr Trp Arg Tyr
385 390 395 400
Asp Glu Tyr Lys Arg Ser Met Asp Pro Gly Tyr Pro Lys Met Ile Ala
405 410 415
His Asp Phe Pro Gly Ile Gly His Lys Val Asp Ala Val Phe Met Lys
420 425 430
Asp Gly Phe Phe Tyr Phe Phe His Gly Thr Arg Gln Tyr Lys Phe Asp
435 440 445
Pro Lys Thr Lys Arg Ile Leu Thr Leu Gln Lys Ala Asn Ser Trp Phe
450 455 460
Asn Cys Arg Lys Asn
465
<210>19
<211>1141
<212>DNA
<213>人
<400>19
ccgccaggcg ctttctcgga cgccttgccc agcgggccgc ccgaccccct gcaccatgga 60
ccccgctcgc cccctggggc tgtcgattct gctgcttttc ctgacggagg ctgcactggg 120
cgatgctgct caggagccaa caggaaataa cgcggagatc tgtctcctgc ccctagacta 180
cggaccctgc cgggccctac ttctccgtta ctactacgac aggtacacgc agagctgccg 240
ccagttcctg tacgggggct gcgagggcaa cgccaacaat ttctacacct gggaggcttg 300
cgacgatgct tgctggagga tagaaaaagt tcccaaagtt tgccggctgc aagtgagtgt 360
ggacgaccag tgtgaggggt ccacagaaaa gtatttcttt aatctaagtt ccatgacatg 420
tgaaaaattc ttttccggtg ggtgtcaccg gaaccggatt gagaacaggt ttccagatga 480
agctacttgt atgggcttct gcgcaccaaa gaaaattcca tcattttgct acagtccaaa 540
agatgaggga ctgtgctctg ccaatgtgac tcgctattat tttaatccaa gatacagaac 600
ctgtgatgct ttcacctata ctggctgtgg agggaatgac aataactttg ttagcaggga 660
ggattgcaaa cgtgcatgtg caaaagcttt gaaaaagaaa aagaagatgc caaagcttcg 720
ctttgccagt agaatccgga aaattcggaa gaagcaattt taaacattct taatatgtca 780
tcttgtttgt ctttatggct tatttgcctt tatggttgta tctgaagaat aatatgacag 840
catgaggaaa caaatcattg gtgatttatt caccagtttt tattaataca agtcactttt 900
taaaaaattt ggattttttt atatataact agctgctatt caaatgtgag tctaccattt 960
ttaatttatg gttcaactgt ttgtgagact gaattcttgc aatgcataag atataaaagc 1020
aaatatgact cactcatttc ttggggtcgt attcctgatt tcagaagagg atcataactg 1080
aaacaacata agacaatata atcatgtgct tttaacatat ttgagaataa aaaggactag 1140
c 1141
<210>20
<211>22
<212>DNA
<213>人工系列
<220>
<223>序列:丝氨酸(或半胱氨酸)蛋白酶抑制因子正义引物
<400>20
ccaaactttg aaagccaagg tg
<210>21
<211>21
<212>DNA
<213>人工系列
<220>
<223>丝氨酸(或半胱氨酸)蛋白酶抑制因子反义引物
<400>21
tgcacttcaa agaccagcag g 21
<210>22
<211>21
<212>DNA
<213>人工序列
<220>
<223>肾上腺髓质素正义引物
<400>22
aggaatagtc gcgcaagcat c 21
<210>23
<211>22
<212>DNA
<213>人工系列
<220>
<223>肾上腺髓质素反义引物
<400>23
cacgcattgc acttttcctc tt 22
<210>24
<211>21
<212>DNA
<213>人工系列
<220>
<223>载脂蛋白D正义引物
<400>24
tgaagccacc ccagttaacc t 21
<210>25
<211>23
<212>DNA
<213>人工系列
<220>
<223>载脂蛋白D反义引物
<400>25
ggtcaacttc ctttgtgcgt ggt 23
<210>26
<211>22
<212>DNA
<213>人工系列
<220>
<223>a-1 XV型胶原蛋白正义引物
<400>26
accaaaccct atttcaagtg cc 22
<210>27
<211>21
<212>DNA
<212>DNA
<213>人工系列
<220>
<223>a-1XV型胶原蛋白反义引物
<400>27
tagttatcca caaggcggac g 21
<210>28
<211>21
<212>DNA
<213>人工系列
<220>
<223>CUG三联体重复RNA结合蛋白2正义引物
<400>28
atgtttgtcg gacagatccc c 21
<210>29
<211>21
<212>DNA
<213>人工系列
<220>
<223>CUG三联体重复RNA结合蛋白2反义引物
<400>29
atgtgacaaa cgcacagcct c 21
<210>30
<211>20
<212>DNA
<213>人工系列
<220>
<223>皮肤桥蛋白正义引物
<400>30
atttgaaccg gcaaggcttc 20
<210>31
<211>21
<212>DNA
<213>人工系列
<220>
<223>皮肤桥蛋白反义引物
<400>31
aagtggttgt tgctcctcgg a 21
<210>32
<211>20
<212>DNA
<213>人工系列
<220>
<223>异柠檬酸脱氢酶正义引物
<400>32
tgccatccag aagaaatggc 20
<210>33
<211>19
<212>DNA
<213>人工系列
<220>
<223>异柠檬酸脱氢酶反义引物
<400>33
aggcaaagat gctggcgat 19
<210>34
<211>22
<212>DNA
<213>人工系列
<220>
<223>MHC II类DR β3正义引物
<400>34
tagctgtgga caaagccaac ct 22
<210>35
<211>22
<212>DNA
<213>人工系列
<220>
<223>MHC II类DR β3反义引物
<400>35
ggcacacacc acgttctctg ta 22
<210>36
<211>22
<212>DNA
<213>人工系列
<220>
<223>蛋白质酪氨酸激酶7正义引物
<400>36
tggaaccaga gcgtacgact gt 22
<210>37
<211>19
<212>DNA
<213>人工系列
<220>
<223>蛋白质酪氨酸激酶7反义引物
<400>37
tggctttgca gcgcttctt 19
<210>38
<211>22
<212>DNA
<213>人工系列
<220>
<223>类Sam68磷酸化酪氨酸蛋白质,T-STAR正义引物
<400>38
aggagaaggc aaggatgaag aa 22
<210>39
<211>22
<212>DNA
<213>人工系列
<220>
<223>类Sam68磷酸化酪氨酸蛋白质,T-STAR反义引物
<400>39
tgttaactcc tggagctgtg ct 22
<210>40
<211>22
<212>DNA
<213>人工系列
<220>
<223>C-型凝集素超家族成员2正义引物
<400>40
gcccctatga ttggattggt tt 22
<210>41
<211>22
<212>DNA
<213>人工系列
<220>
<223>C-型凝集素超家族成员2反义引物
<400>41
catccttcac tccctctcat gc 22
<210>42
<211>25
<212>DNA
<213>人工系列
<220>
<223>MMP(基质金属蛋白酶)1正义引物
<400>42
cgactctaga aacacaagag caaga 25
<210>43
<211>25
<212>DNA
<213>人工系列
<220>
<223>MMP(基质金属蛋白酶)1反义引物
<400>43
aaggttagct tactgtcaca cgctt 25
<210>44
<211>17
<212>DNA
<213>人工系列
<220>
<223>TFPI(组织因子途径抑制物)2正义引物
<400>44
gtcgattctg cttttcc 17
<210>45
<211>20
<212>DNA
<213>人工系列
<220>
<223>TFPI(组织因子途径抑制物)2反义引物
<400>45
atggaatttt ctttggtgcg 20
<210>46
<211>1045
<212>DNA
<212>人
<400>46
ctcccgagct ctactgactc ccaacagagc gcccaagcaa gaaaatggcc ataagtggag 60
tccctgtgct aggatttttc atcatagctg tgctgatgag cgctcaggaa tcatgggcta 120
tcaaagaaga acatgtgatc atccaggccg agttctatct gaatcctgac caatcaggcg 180
agtttatgtt tgactttgat ggtgatgaga ttttccatgt ggatatggca aagaaggaga 240
cggtctggcg gcttgaagaa tttggacgat ttgccagctt tgaggctcaa ggtgcattgg 300
ccaacatagc tgtggacaaa gccaacctgg aaatcatgac aaagcgctcc aactatactc 360
cgatcaccaa tgtacctcca gaggtaactg tgctcacgaa cagccctgtg gaactgagag 420
agcccaacgt cctcatctgt ttcatcgaca agttcacccc accagtggtc aatgtcacgt 480
ggcttcgaaa tggaaaacct gtcaccacag gagtgtcaga gacagtcttc ctgcccaggg 540
aagaccacct tttccgcaag ttccactatc tccccttcct gccctcaact gaggacgttt 600
acgactgcag ggtggagcac tggggcttgg actgagcctc ttctcaagca ctgggaggtt 660
gatgctccaa gcccgtctcc agagacttac gagacgtggt gtgtgccctg gggctgactg 720
tgggtctggt cgggcttcct ttgggaccct ctttcatcat ccacggcgag tgcgccaaaa 780
gcattgccca gaaacccagg gggccctctg taaggcctgt gcgggggcag aacggtccct 840
taaaaagaag aacctcgtgg gcaaaacctg gcgcaagacg tcatacaaag ggggggcata 900
taacacgcgt gccccagaac gaccgcactc agggctcgcc gcctataaca ccccggtgtg 960
gtacccccaa ggcgcgctaa aactaaacag cgcgcacata gtagctcagg cgatacacca 1020
ctcacatata taatagcacc gctaa 1045
<210>47
<211>18
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的肾上腺髓质素引物
<400>47
ggtttccgtc gccctgat 18
<210>48
<211>24
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的肾上腺髓质素引物
<400>48
gagcccactt attccacttc tttc 24
<210>49
<211>22
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的基质金属蛋白酶1引物
<400>49
gatggacctg gaggaaatct tg 22
<210>50
<211>24
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的基质金属蛋白酶1引物
<400>50
ccgcaacacg atgtaagttg tact 24
<210>51
<211>21
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的组织因子途径抑制物2引物
<400>51
ggcaacgcca acaatttcta c 21
<210>52
<211>26
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的组织因子途径抑制物2引物
<400>52
caaactttgg gaactttttc tatcct 26
<210>53
<211>23
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的丝氨酸(或半胱氨酸)蛋白酶抑止因子引物
<400>53
tgggtggaga ataacacaaa caa 23
<210>54
<211>22
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的丝氨酸(或半胱氨酸)蛋白酶抑止因子引物
<400>54
ccagataagt ggcagcatca aa 22
<210>55
<211>28
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的蛋白质酪氨酸激酶7引物
<400>55
gggagttcct taatattctc aagttctg 28
<210>56
<211>27
<212>DNA
<213>人工系列
<220>
<223>蛋白质酪氨酸激酶7
<400>56
gctgtgtcct ctgtaatcct ggtctag 27
<210>57
<211>20
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的胶原蛋白,XV型,α1引物
<400>57
ccagcaaccc acatcagctt 20
<210>58
<211>23
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的胶原蛋白,XV型,α1引物
<400>58
atgcagagca ggcttctcat aat 23
<210>59
<211>29
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的类Sam68磷酸化酪氨酸蛋白质引物
<400>59
tcacaacatc agacagtaca atcagtatc 29
<210>60
<211>22
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的类Sam68磷酸化酪氨酸蛋白质引物
<400>60
acgggcaaga agagtggact aa 22
<210>61
<211>23
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的载脂蛋白D引物
<400>61
tgagaagatc ccaacaacct ttg 23
<210>62
<211>24
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的载脂蛋白D引物
<400>62
tgatctttcc gttttccatt agtg 24
<210>63
<211>22
<212>DNA
<213>人工系列
<220>
<223>主要组织相容性复合体DRβ
<400>63
ggctgaagtc cagagtgtcc tt 22
<210>64
<211>18
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的主要组织相容性复合体DR β引物
<400>64
gctgggcctg ctcttcct 18
<210>65
<211>19
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的主要组织相容性复合体DR α引物
<400>65
gcccagggaa gaccacctt 19
<210>66
<211>23
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的主要组织相容性复合体DR α引物
<400>66
cagtcgtaaa cgtcctcagt tga 23
<210>67
<211>27
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的C型凝集素引物
<400>67
atccattttc tttcggtgta acatcta 27
<210>68
<211>23
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的C型凝集素引物
<400>68
catgagaggg agtgaaggat gtg 23
<210>69
<211>24
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的CUG三联体重复RNA结合蛋白2引物
<400>69
catgaatgct ttacagttgc agaa 24
<210>70
<211>19
<212>DNA
<213>人工系列
<220>
<223>用于RT-PCR的CUG三联体重复RNA结合蛋白2引物
<400>70
gcgctgctcg tggtagaga 19
<210>71
<211>22
<212>DNA
<213>人工系列
<220>
<223>整联蛋白,α6(ITGA6),MRNA
<400>71
gatgacagtg ttccccgata cc 22
<210>72
<211>20
<212>DNA
<213>人工系列
<220>
<223>整联蛋白,α6(ITGA6),MRNA
<400>72
tgtaagtcag ccacgccaaa 20
<210>73
<211>21
<212>DNA
<213>人工系列
<220>
<223>溶质运载蛋白家族20(磷酸盐转运)成员1
<400>73
aatggagaag ctgacatggc c 21
<210>74
<211>21
<212>DNA
<213>人工系列
<220>
<223>溶质运载蛋白家族20(磷酸盐转运)成员1
<400>74
ccaaacccac agaccaacac a 21
<210>75
<211>21
<212>DNA
<213>人工系列
<220>
<223>核苷酸还原酶M2多肽(RRM2)MRNA
<400>75
tccaaggaca ttcagcactg g 21
<210>76
<211>19
<212>DNA
<213>人工系列
<220>
<223>核苷酸还原酶M2多肽(RRM2)MRNA
<400>76
atcgacgcaa aagaaccgg 19
<210>77
<211>22
<212>DNA
<213>人工系列
<220>
<223>卵泡抑制素转录变异型FST317,MRNA
<400>77
ggaagtccag taccaaggca ga 22
<210>78
<211>19
<212>DNA
<213>人工系列
<220>
<223>卵泡抑制素转录变异型FST317,MRNA
<400>78
tggcattgtc actggcaca 19
<210>79
<211>20
<212>DNA
<213>人工系列
<220>
<223>SPROUTY(果蝇)同源基因2(SPRY2),MRNA
<400>79
gccatccgaa acaccaatga 20
<210>80
<211>22
<212>DNA
<213>人工系列
<220>
<223>SPROUTY(果蝇)同源基因2(SPRY2),MRNA
<400>80
tgccacagtc ctcacacctg ta 22
<210>81
<211>21
<212>DNA
<213>人工系列
<220>
<223>RAB3B,癌基因家族成员RAS,MRNA
<400>81
atgctgatga cacgttcacc c 21
<210>82
<211>22
<212>DNA
<213>人工系列
<220>
<223>RAB3B,癌基因家族成员RAS,MRNA
<400>82
ggcctgcctt acactgatgt tc 22
<210>83
<211>21
<212>DNA
<213>人工系列
<220>
<223>溶质运载蛋白家族2(利于葡萄糖转运)
<400>83
gccttttcgt taaccgcttt g 21
<210>84
<211>19
<212>DNA
<213>人工系列
<220>
<223>溶质运载蛋白家族2(利于葡萄糖转运)
<400>84
tcctcgttgc ggttgatga 19
<210>85
<211>21
<212>DNA
<213>人工系列
<220>
<223>白介素13受体,α2(IL13RA2),MRNA
<400>85
tgaaggctat ttgaagtcgc c 21
<210>86
<211>19
<212>DNA
<213>人工系列
<220>
<223>白介素13受体,α2(IL13RA2),MRNA
<400>86
cttcgcttca atgcccttg 19
<210>87
<211>21
<212>DNA
<213>人工系列
<220>
<223>丝氨酸/苏氨酸激酶12(STK12),MRNA
<400>87
tggaaacgtg tacttggctc g 21
<210>88
<211>21
<212>DNA
<213>人工系列
<220>
<223>丝氨酸/苏氨酸激酶12(STK12),MRNA
<400>88
accagccgaa gtcagcaatc t 21
<210>89
<211>22
<212>DNA
<213>人工系列
<220>
<223>微染色体维持缺陷蛋白(啤酒酵母)5
<400>89
aagtttggcc tgactaccag ca 22
<210>90
<211>22
<212>DNA
<213>人工系列
<220>
<223>微染色体维持缺陷蛋白(啤酒酵母)5
<400>90
ccagacgtgt ataccccaat gg 22
<210>91
<211>22
<212>DNA
<213>人工系列
<220>
<223>甲状腺激素受体中间子13(TRIP13),MRNA
<400>91
cctgtgtaaa gcgttagccc ag 22
<210>92
<211>22
<212>DNA
<213>人工系列
<220>
<223>甲状腺激素受体中间子13(TRIP13),MRNA
<400>92
gtggcccaat gtactgcttg at 22
<210>93
<211>22
<212>DNA
<213>人工系列
<220>
<223>类驱动蛋白6(KINESIN-LIKE 6)
<400>93
ccagctttaa cgaagccatg ac 22
<210>94
<211>22
<212>DNA
<213>人工系列
<220>
<223>类驱动蛋白6(KINESIN-LIKE 6)
<400>94
gcatttacca gaacctgtcc ca 22
<210>95
<211>22
<212>DNA
<213>人工系列
<220>
<223>细胞周期蛋白依赖性激酶抑制物3
<400>95
tcggtttatg tgctcttcca gg 22
<210>96
<211>22
<212>DNA
<213>人工系列
<220>
<223>细胞周期蛋白依赖性激酶抑制物3
<400>96
atcctcttag gtctcgcagg ct 22
<210>97
<211>22
<212>DNA
<213>人工系列
<220>
<223>染色体凝集蛋白G(HCAP-G),MRNA
<400>97
gctcgccaga aattcgagtc ta 22
<210>98
<211>22
<212>DNA
<213>人工系列
<220>
<223>染色体凝集蛋白G(HCAP-G),MRNA
<400>98
catgatcact ttcagagtcg gc 22
<210>99
<211>21
<212>DNA
<213>人工系列
<220>
<223>CDC28蛋白激酶1(CKS1),MRNA
<400>99
gcccactacc caagaaacca a 21
<210>100
<211>22
<212>DNA
<213>人工系列
<220>
<223>CDC28蛋白激酶1(CKS1),MRNA
<400>100
cataaatccg caagtcacca ca 22
<210>101
<211>20
<212>DNA
<213>人工系列
<220>
<223>胞质分裂的蛋白质调节子1(PRC1),MRNA
<400>101
cccaagtgga attgatgcga 20
<210>102
<211>22
<212>DNA
<213>人工系列
<220>
<223>胞质分裂的蛋白质调节子1(PRC1),MRNA
<400>102
cccctcacac actgcttcat tt 22
<210>103
<211>21
<212>DNA
<213>人工系列
<220>
<223>细胞分裂循环2,G1→S→G2→M(CDC2),MRNA
<400>103
ctgattttgg ccttgccaga g 21
<210>104
<211>22
<212>DNA
<213>人工系列
<220>
<223>细胞分裂循环2,G1→S→G2→M(CDC2),MRNA
<400>104
ggatgattca gtgccatttt gc 22
<210>105
<211>21
<212>DNA
<213>人工系列
<220>
<223>CDC20细胞分裂周期20,酿酒酵母,同源基因
<400>105
acagttcgcg ttcgagagtg a 21
<210>106
<211>21
<212>DNA
<213>人工系列
<220>
<223>CDC20细胞分裂周期20,酿酒酵母,同源基因
<400>106
ttccactgag ccgaaggatc t 21
<210>107
<211>22
<212>DNA
<213>人工系列
<220>
<223>LIKELY ORTHOLOG OF MATERNAL EMBRYONIC LEUCINE ZIPPER KINAS
<400>107
tggctctctc ccagtagcat tc 22
<210>108
<211>21
<212>DNA
<213>人工系列
<220>
<223>LIKELY ORTHOLOG OF MATERNAL EMBRYONIC LEUCINE ZIPPER KINAS
<400>108
tcacttgcgg tcacatcttc c 21
<210>109
<211>22
<212>DNA
<213>人工系列
<220>
<223>微染色体维持缺陷蛋白(啤酒酵母)7
<400>109
agagaacaca aggattgccc ag 22
<210>110
<211>22
<212>DNA
<213>人工系列
<220>
<223>微染色体维持缺陷蛋白(啤酒酵母)7
<400>110
atgacaggag ctgagacttg gc 22
<210>111
<211>22
<212>DNA
<213>人工系列
<220>
<223>细胞周期蛋白A2(CCNA2),MRNA
<400>111
ggcactgctg ctatgctgtt ag 22
<210>112
<211>21
<212>DNA
<213>人工系列
<220>
<223>细胞周期蛋白A2(CCNA2),MRNA
<400>112
tgaaggtcca tgagacaagg c 21
<210>113
<211>19
<212>DNA
<213>人工系列
<220>
<223>胸苷激酶1,可溶性(TK1),MRNA
<400>113
ggcgcaatga gctgcatta 19
<210>114
<211>22
<212>DNA
<213>人工系列
<220>
<223>胸苷激酶1,可溶性(TK1),MRNA
<400>114
aaatggcttc ctctggaagg tc 22
<210>115
<211>21
<212>DNA
<213>人工系列
<220>
<223>细胞周期蛋白依赖性激酶抑制物2A(黑素瘤,p16,inhibits CDK4)
(CDKN2A),mRNA
<400>115
tccccgattg aaagaaccag a 21
<210>116
<211>22
<212>DNA
<213>人工系列
<220>
<223>细胞周期蛋白依赖性激酶抑止剂2A(cyclin-dependent kinase inhibitor
2A)(黑色素瘤p16,抑止CDK 4)(CDKN2A),mRNA
<400>116
aagagaagcc agtaaccccc ct 22
Claims (6)
1.体外系统识别间充质干细胞的方法,其特征在于对被检细胞中编码蛋白质的间充质干细胞标记基因的表达进行检测,该间充质干细胞标记基因包括有以下基因中的一个或多个:人骨形态生成蛋白4(BMP4),MRNA基因(NM_001202);人克隆24775mRNA序列基因/钾通道结构域12(KCTD:AA402981);基质Gla蛋白(MGP:BF668572)基因;蛋白聚糖1,分泌颗粒基因(PRG1:AV734015);种族同系物2(TRIB2:NM_021643)基因;人动力蛋白,细胞质的,中间体多肽1(DYNC1I1),M(NM_004411)基因;脑源性神经营养因子(BDNF:X60201)基因。
2.根据权利要求1记载的间充质干细胞的识别方法,其特征是,采用探针对间充质干细胞标记基因的表达进行检测,该探针具有的DNA序列能与基因数据库登录号为NM_001202,AA402981,BF668572,AV734015,NM_021643,NM_004411或X60201所示的碱基序列的间充质干细胞基因杂交。
3.根据权利要求1记载的间充质干细胞的识别方法,其特征是采用具有基因数据库登录号为NM_001202,AA402981,BF668572,AV734015,NM_021643,NM_004411或X60201所示碱基序列的基因的微阵列或DNA芯片对间充质干细胞标记基因的表达进行检测。
4.根据权利要求1记载的识别间充质干细胞的方法,其特征是,对间充质干细胞标记基因表达的检测包括定量或半定量PCR的使用。
5.根据权利要求4记载的识别间充质干细胞的方法,其特征是其使用的定量的或半定量的PCR是RT-PCR法或实时PCR法。
6.一种体外系统识别分离间充质干细胞的方法,特征在于,通过使用检测间充质干细胞基因标记的探针对用于检测间充质干细胞的标记基因和/或标记多肽的表达进行检测、对识别出的间充质干细胞进行分离;该探针具有的DNA系列能与基因数据库登录号为NM_001202,AA402981,BF668572,AV734015,NM_021643,NM_004411或者X60201所示碱基序列的间充质干细胞标记基因杂交。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003-63077 | 2003-03-10 | ||
JP2003063077 | 2003-03-10 |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNA2004800075500A Division CN1761749A (zh) | 2003-03-10 | 2004-02-27 | 检测间充质干细胞的标记和采用该标记识别间充质干细胞的方法 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN101265503A true CN101265503A (zh) | 2008-09-17 |
Family
ID=32984419
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNA200810081304XA Pending CN101265503A (zh) | 2003-03-10 | 2004-02-27 | 检测间充质干细胞的标记和采用该标记识别间充质干细胞的方法 |
CNA2004800075500A Pending CN1761749A (zh) | 2003-03-10 | 2004-02-27 | 检测间充质干细胞的标记和采用该标记识别间充质干细胞的方法 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNA2004800075500A Pending CN1761749A (zh) | 2003-03-10 | 2004-02-27 | 检测间充质干细胞的标记和采用该标记识别间充质干细胞的方法 |
Country Status (9)
Country | Link |
---|---|
US (1) | US20060166214A1 (zh) |
EP (2) | EP1605044A4 (zh) |
JP (1) | JP2004290189A (zh) |
KR (1) | KR100818689B1 (zh) |
CN (2) | CN101265503A (zh) |
AT (1) | ATE488588T1 (zh) |
AU (1) | AU2004219820B2 (zh) |
DE (1) | DE602004030172D1 (zh) |
WO (1) | WO2004081174A2 (zh) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102732633A (zh) * | 2012-07-06 | 2012-10-17 | 广州好芝生物科技有限公司 | 人idh基因突变的检测引物和试剂盒 |
CN102925579A (zh) * | 2012-11-16 | 2013-02-13 | 上海赛安生物医药科技有限公司 | Idh2基因突变的快速检测方法 |
CN104844705A (zh) * | 2015-01-30 | 2015-08-19 | 暨南大学 | Kctd12蛋白在细胞周期调控中新应用 |
CN111533796A (zh) * | 2017-04-10 | 2020-08-14 | 伊玛提克斯生物技术有限公司 | 用于癌症免疫治疗的肽及其肽组合物 |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5190654B2 (ja) * | 2005-03-31 | 2013-04-24 | 国立大学法人広島大学 | 分子マーカーを用いた間葉系幹細胞の識別方法及びその利用 |
WO2006112390A1 (ja) * | 2005-04-14 | 2006-10-26 | Japan As Represented By General Director Of Agency Of National Cardiovascular Center | 脂肪由来前駆細胞およびその利用 |
US20060246498A1 (en) * | 2005-04-28 | 2006-11-02 | Ramot At Tel Aviv University Ltd. | HNRPLL polypeptides, polynucleotides encoding same and compositions and methods of using same |
JP4958094B2 (ja) * | 2005-09-22 | 2012-06-20 | 国立大学法人広島大学 | 間葉系幹細胞の均質性識別方法、その方法を利用して得られる均質間葉系幹細胞 |
CN101360761B (zh) | 2005-12-08 | 2012-09-12 | 米德列斯公司 | 抗蛋白质酪氨酸激酶7(ptk7)的人单克隆抗体及其用途 |
CN100475836C (zh) * | 2005-12-09 | 2009-04-08 | 中国人民解放军军事医学科学院野战输血研究所 | 间充质干细胞亲和肽的筛选与用途 |
WO2007085266A1 (en) * | 2006-01-30 | 2007-08-02 | Dako Denmark A/S | High-speed quantification of antigen specific t-cells in whole blood by flow cytometry |
JP2008092919A (ja) * | 2006-10-16 | 2008-04-24 | Hiroshima Univ | 病変間葉系幹細胞の検出マーカーの利用 |
CA2677000A1 (en) * | 2007-01-30 | 2008-08-07 | Pharmacyclics, Inc. | Methods for determining cancer resistance to histone deacetylase inhibitors |
EP2361930A3 (en) | 2007-03-26 | 2011-10-26 | Dako Denmark A/S | Multimers of MHC-peptide complexes and uses thereof in Borrelia infectious diseases |
KR100888924B1 (ko) | 2007-06-04 | 2009-03-16 | 주식회사 제이비줄기세포연구소 | 인간 제대혈 유래 중간엽 줄기세포와 섬유아세포 분별방법 |
EP2167536A1 (en) * | 2007-07-03 | 2010-03-31 | Dako Denmark A/S | Mhc multimers, methods for their generation, labeling and use |
US10611818B2 (en) | 2007-09-27 | 2020-04-07 | Agilent Technologies, Inc. | MHC multimers in tuberculosis diagnostics, vaccine and therapeutics |
US20090305905A1 (en) * | 2007-12-13 | 2009-12-10 | Robert Bradbury | Compositions and methods relating to characterization and therapeutic application of pristine stem cells |
US10968269B1 (en) | 2008-02-28 | 2021-04-06 | Agilent Technologies, Inc. | MHC multimers in borrelia diagnostics and disease |
US10722562B2 (en) * | 2008-07-23 | 2020-07-28 | Immudex Aps | Combinatorial analysis and repair |
GB0817244D0 (en) * | 2008-09-20 | 2008-10-29 | Univ Cardiff | Use of a protein kinase inhibitor to detect immune cells, such as T cells |
US11992518B2 (en) | 2008-10-02 | 2024-05-28 | Agilent Technologies, Inc. | Molecular vaccines for infectious disease |
US10369204B2 (en) | 2008-10-02 | 2019-08-06 | Dako Denmark A/S | Molecular vaccines for infectious disease |
JP2010189302A (ja) * | 2009-02-17 | 2010-09-02 | Hiroshima Univ | 病変間葉系幹細胞が関連する疾患の治療剤および間葉系幹細胞の検出マーカーの利用 |
PE20120570A1 (es) * | 2009-07-14 | 2012-05-19 | Irm Llc | Diferenciacion de celulas madre mesenquimales |
EP2625577B1 (en) | 2010-10-08 | 2019-06-26 | Terumo BCT, Inc. | Customizable methods and systems of growing and harvesting cells in a hollow fiber bioreactor system |
ES2384790B1 (es) * | 2010-12-10 | 2013-05-20 | Instituto De Salud Carlos Iii | Células madre mesenquimales aisladas a partir de sangre periférica. |
JP5997131B2 (ja) | 2011-03-16 | 2016-09-28 | 国立大学法人東北大学 | 生体組織分析用プローブ及びその利用法 |
WO2013042993A2 (ko) | 2011-09-23 | 2013-03-28 | 가톨릭대학교 산학협력단 | 고해상도 mica 대립유전자 검출용 sprex-dna 칩 키트 |
BR112014019328A8 (pt) * | 2012-02-17 | 2017-07-11 | The Schepens Eye Res Institute | Perfil de fenótipo de células progenitoras retinais humanas |
CN104254602A (zh) * | 2012-04-24 | 2014-12-31 | 克瑞奥埃斯塔麦诺健康与技术股份有限公司 | 用于心脏组织保护的干细胞的组合物和方法 |
CA2898601C (en) | 2013-02-01 | 2021-05-18 | Tohoku University | Method for separating cell from biological tissue |
GB201310354D0 (en) * | 2013-06-11 | 2013-07-24 | Ge Healthcare Uk Ltd | Method for cell differentiation |
JP6633522B2 (ja) | 2013-11-16 | 2020-01-22 | テルモ ビーシーティー、インコーポレーテッド | バイオリアクターにおける細胞増殖 |
JP6339814B2 (ja) * | 2014-02-05 | 2018-06-06 | 株式会社島津製作所 | がん転移マーカー及びその分析方法 |
WO2015148704A1 (en) | 2014-03-25 | 2015-10-01 | Terumo Bct, Inc. | Passive replacement of media |
WO2016049421A1 (en) | 2014-09-26 | 2016-03-31 | Terumo Bct, Inc. | Scheduled feed |
WO2016086403A1 (en) * | 2014-12-05 | 2016-06-09 | Meridigen Biotech Co., Ltd. | Method of distinguishing mesenchymal stem cells |
CN104655857B (zh) * | 2015-02-10 | 2017-05-31 | 南京大学 | 一种微生物细胞内多聚磷酸盐的定量检测方法 |
US10539553B2 (en) | 2015-03-17 | 2020-01-21 | National Institute Of Advanced Industrial Science And Technology | Method and kit for detecting stem cell |
WO2017004592A1 (en) | 2015-07-02 | 2017-01-05 | Terumo Bct, Inc. | Cell growth with mechanical stimuli |
CN105018524B (zh) * | 2015-07-13 | 2020-03-27 | 广州赛琅生物技术有限公司 | 一种细胞寿命延长及成血管能力增强的人干细胞的制备方法及其试剂盒 |
US11965175B2 (en) | 2016-05-25 | 2024-04-23 | Terumo Bct, Inc. | Cell expansion |
US11685883B2 (en) | 2016-06-07 | 2023-06-27 | Terumo Bct, Inc. | Methods and systems for coating a cell growth surface |
US11104874B2 (en) | 2016-06-07 | 2021-08-31 | Terumo Bct, Inc. | Coating a bioreactor |
CN106771256B (zh) * | 2017-01-23 | 2019-02-01 | 福建医科大学 | 骨骼肌组织冰冻切片肌球蛋白三磷酸腺苷酶染色方法 |
WO2018159431A1 (ja) | 2017-03-03 | 2018-09-07 | ロート製薬株式会社 | 間葉系幹細胞及び肝疾患治療剤 |
US11624046B2 (en) | 2017-03-31 | 2023-04-11 | Terumo Bct, Inc. | Cell expansion |
EP3656841A1 (en) | 2017-03-31 | 2020-05-27 | Terumo BCT, Inc. | Cell expansion |
PL241520B1 (pl) * | 2020-03-27 | 2022-10-17 | Polski Bank Komorek Macierzystych Spolka Akcyjna | Zastosowanie panelu genów do określania potencjału teratogennego komórek mezenchymalnych i pochodzenia perinatalnego |
US12043823B2 (en) | 2021-03-23 | 2024-07-23 | Terumo Bct, Inc. | Cell capture and expansion |
EP4408979A1 (en) * | 2021-09-30 | 2024-08-07 | Polski Bank Komórek Macierzystych S.A. | Expression analysis of a specific gene pool to determine whether the population of adipose tissue-derived mesenchymal cells (at-msc) selected for clinical application can undergo a transformation into neoplastic cells |
CN114622019A (zh) * | 2022-03-23 | 2022-06-14 | 新乡医学院 | Birc5基因作为人骨髓间充质干细胞成骨分化抑制剂的应用 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5340739A (en) * | 1988-07-13 | 1994-08-23 | Brigham & Women's Hospital | Hematopoietic cell specific transcriptional regulatory elements of serglycin and uses thereof |
US5965436A (en) * | 1996-11-15 | 1999-10-12 | Osiris Therapeutics, Inc. | Method of isolating mesenchymal stem cells associated with isolated megakaryocytes by isolating megakaryocytes |
AU2180799A (en) * | 1998-02-13 | 1999-08-30 | Peter Sonderegger | Neuroserpin |
ATE328067T1 (de) * | 2000-04-28 | 2006-06-15 | Childrens Medical Center | Isolierung von mesenchymalen stammzellen und deren verwendung |
WO2001094629A2 (en) * | 2000-06-05 | 2001-12-13 | Avalon Pharmaceuticals | Cancer gene determination and therapeutic screening using signature gene sets |
WO2002028999A2 (en) * | 2000-10-03 | 2002-04-11 | Gene Logic, Inc. | Gene expression profiles in granulocytic cells |
JP2003052365A (ja) * | 2001-08-20 | 2003-02-25 | Japan Science & Technology Corp | 哺乳動物からの間葉系幹細胞の分離及びその利用方法 |
EP1288293A1 (en) * | 2001-08-30 | 2003-03-05 | Norio Sakuragawa | Human neural stem cells originated from human amniotic mesenchymal cell layer |
-
2004
- 2004-02-27 AU AU2004219820A patent/AU2004219820B2/en not_active Ceased
- 2004-02-27 US US10/548,681 patent/US20060166214A1/en not_active Abandoned
- 2004-02-27 EP EP04715524A patent/EP1605044A4/en not_active Withdrawn
- 2004-02-27 KR KR1020057016952A patent/KR100818689B1/ko not_active IP Right Cessation
- 2004-02-27 AT AT07017847T patent/ATE488588T1/de not_active IP Right Cessation
- 2004-02-27 DE DE602004030172T patent/DE602004030172D1/de not_active Expired - Lifetime
- 2004-02-27 CN CNA200810081304XA patent/CN101265503A/zh active Pending
- 2004-02-27 EP EP07017847A patent/EP1860186B1/en not_active Expired - Lifetime
- 2004-02-27 WO PCT/JP2004/002457 patent/WO2004081174A2/ja not_active Application Discontinuation
- 2004-02-27 CN CNA2004800075500A patent/CN1761749A/zh active Pending
- 2004-03-10 JP JP2004067037A patent/JP2004290189A/ja active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102732633A (zh) * | 2012-07-06 | 2012-10-17 | 广州好芝生物科技有限公司 | 人idh基因突变的检测引物和试剂盒 |
CN102732633B (zh) * | 2012-07-06 | 2014-02-26 | 广州好芝生物科技有限公司 | 人idh基因突变的检测引物和试剂盒 |
CN102925579A (zh) * | 2012-11-16 | 2013-02-13 | 上海赛安生物医药科技有限公司 | Idh2基因突变的快速检测方法 |
CN102925579B (zh) * | 2012-11-16 | 2014-12-17 | 上海赛安医学检验所有限公司 | Idh2基因突变的快速检测方法 |
CN104844705A (zh) * | 2015-01-30 | 2015-08-19 | 暨南大学 | Kctd12蛋白在细胞周期调控中新应用 |
CN104844705B (zh) * | 2015-01-30 | 2018-08-03 | 暨南大学 | Kctd12蛋白在细胞周期调控中的应用 |
CN111533796A (zh) * | 2017-04-10 | 2020-08-14 | 伊玛提克斯生物技术有限公司 | 用于癌症免疫治疗的肽及其肽组合物 |
Also Published As
Publication number | Publication date |
---|---|
CN1761749A (zh) | 2006-04-19 |
WO2004081174A2 (ja) | 2004-09-23 |
EP1860186B1 (en) | 2010-11-17 |
AU2004219820A1 (en) | 2004-09-23 |
ATE488588T1 (de) | 2010-12-15 |
AU2004219820B2 (en) | 2008-06-12 |
EP1860186A3 (en) | 2008-03-12 |
WO2004081174A3 (ja) | 2004-12-02 |
KR100818689B1 (ko) | 2008-04-02 |
JP2004290189A (ja) | 2004-10-21 |
EP1605044A4 (en) | 2006-12-06 |
US20060166214A1 (en) | 2006-07-27 |
KR20050115278A (ko) | 2005-12-07 |
EP1860186A2 (en) | 2007-11-28 |
DE602004030172D1 (de) | 2010-12-30 |
EP1605044A2 (en) | 2005-12-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101265503A (zh) | 检测间充质干细胞的标记和采用该标记识别间充质干细胞的方法 | |
Kass et al. | The U3 small nucleolar ribonucleoprotein functions in the first step of preribosomal RNA processing | |
Hughes et al. | Temporally modular gene expression during cotyledon development. | |
Kruppa et al. | Nhp6, an HMG1 protein, functions in SNR6 transcription by RNA polymerase III in S. cerevisiae | |
Zhao et al. | Quantitation of matrix Gla protein mRNA by competitive polymerase chain reaction using glyceraldehyde-3-phosphate dehydrogenase as an internal control | |
CN111183233A (zh) | 使用靶基因表达的数学建模评估Notch细胞信号传导途径活性 | |
Lee et al. | Identification of differentially expressed genes related to intramuscular fat development in the early and late fattening stages of hanwoo steers | |
Mozdy et al. | Multiple yeast genes, including Paf1 complex genes, affect telomere length via telomerase RNA abundance | |
Mandal et al. | S100A7 (psoriasin) influences immune response genes in human breast cancer | |
Mortensen et al. | Reduced expression of the DOG1 gene in Arabidopsis mutant seeds lacking the transcript elongation factor TFIIS | |
JP2008289476A (ja) | 骨分化状態を測定する組成物および骨分化を調節する組成物 | |
CN101760462A (zh) | 植物抗病基因的克隆 | |
Monticone et al. | Gene expression profile of human bone marrow stromal cells determined by restriction fragment differential display analysis | |
Roland et al. | Identification of hypoxia‐responsive messengers expressed in human microvascular endothelial cells using differential display RT‐PCR | |
Li et al. | The C2H2-type zinc-finger regulator AoKap5 is required for the growth and kojic acid synthesis in Aspergillus oryzae | |
Wang et al. | Involvement of fission yeast Pdc2 in RNA degradation and P-body function | |
KR101603633B1 (ko) | EGF 또는 bFGF를 포함하는 배지에서 배양한 지방유래 줄기세포의 증식 및 치료능력 탐지 마커 및 이의 용도 | |
Seo et al. | Identification of calcium-induced genes in HaCaT keratinocytes by polymerase chain reaction-based subtractive hybridization | |
JP4540948B2 (ja) | 分別マーカーを用いた間葉系幹細胞の識別・分離方法 | |
Stephan et al. | Sin3 is involved in cell size control at Start in Saccharomyces cerevisiae | |
Moser et al. | cis-acting mutations that affect rop protein control of plasmid copy number. | |
Wang et al. | Identification and characterization of mouse Gas6 promoter | |
CN101514340B (zh) | 人自吞噬基因Beclin 1启动子序列及其应用 | |
CN109402289B (zh) | 海州常山不同组织的荧光定量内参基因及其引物和应用 | |
KR20150019320A (ko) | EGF 또는 bFGF를 포함하는 배지에서 배양한 지방유래 줄기세포의 증식 및 치료능력 탐지 마커 및 이의 용도 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
AD01 | Patent right deemed abandoned |
Effective date of abandoning: 20080917 |
|
C20 | Patent right or utility model deemed to be abandoned or is abandoned |