| FEBS Letters | |
| Inhibition of thrombin by synthetic hirudin peptides | |
| Hermans, Jan2  Binnie, Cameron G.2  Erickson, Bruce W.1  | |
| [1] Department of Chemistry, A808 Kenan Labs., University of North Carolina, Chapel Hill, NC 27599, USA;Department of Biochemistry, 323 Faculty Laboratory Office Building Chapel Hill, NC 27599, USA | |
| 关键词: Hirudin; Thrombin; Synthetic segment; Peptide segment; | |
| DOI : 10.1016/0014-5793(90)81240-O | |
| 学科分类:生物化学/生物物理 | |
| 来源: John Wiley & Sons Ltd. | |
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【 摘 要 】
To investigate the role of different regions of hirudin in the interaction with the proteinase thrombin, segments of hirudin containing 15-51 residues were synthesized. The C-terminal segment 40-65 inhibited the fibrinogen clotting activity of thrombin but not amidolysis of tosyl-Gly-Pro-Arg-p-nitroanilide. Central peptide 15–42 was insoluble at pH 7, but peptide 15-65 inhibited fibrinogen clotting and amidolysis to an equal extent. The N-terminal loop peptide 1-15 had no inhibitory activity and did not affect the potency of peptide 15-65. These data suggest that the central region inhibits catalysis.
【 授权许可】
Unknown
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| Files | Size | Format | View |
|---|---|---|---|
| RO201912020293871ZK.pdf | 551KB |
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