胸腺五肽
五肽重复序列
外肽酶
生物活性
乙酰化
化学
蛋白水解酶
生物化学
酶
氨肽酶
蛋白质水解
寡肽
肽
氨基酸
肽水解酶类
体外
生物
蛋白酶
亮氨酸
基因
免疫学
作者
George A. Heavner,Daniel J. Kroon,Tapan Audhya,Gideon Goldstein
出处
期刊:Peptides
[Elsevier BV]
日期:1986-11-01
卷期号:7 (6): 1015-1019
被引量:24
标识
DOI:10.1016/0196-9781(86)90131-2
摘要
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-Pro2-TP5-NH2 and Aib2-TP5-NH2 retained activity and were shown to exhibit a high degree of stability when incubated in human serum.
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