Biologically active analogs of thymopentin with enhanced enzymatic stability
Thymopentin, a synthetic pentapeptide fragment of thymopoietin (residues 32–36, Arg-Lys-Asp-Val-Tyr) is biologically active but susceptible to proteolytic digestion. Analogs were synthesized and studied for biological activity and susceptibility to peptidases. Amino acid changes were incorporated at...
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Veröffentlicht in: | Peptides (New York, N.Y. : 1980) N.Y. : 1980), 1986-11, Vol.7 (6), p.1015-1019 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Thymopentin, a synthetic pentapeptide fragment of thymopoietin (residues 32–36, Arg-Lys-Asp-Val-Tyr) is biologically active but susceptible to proteolytic digestion. Analogs were synthesized and studied for biological activity and susceptibility to peptidases. Amino acid changes were incorporated at positions known to not affect activity adversely and N-terminal acetylation and C-terminal amidation were used to increase resistance to proteolytic degradation by exopeptidases. Ac-Pro
2-TP5-NH
2 and Aib
2-TP5-NH
2 retained activity and were shown to exhibit a high degree of stability when incubated in human serum. |
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ISSN: | 0196-9781 1873-5169 |
DOI: | 10.1016/0196-9781(86)90131-2 |