b22精氨酸替代对胰岛素生物活性的影响。

Scientia Sinica Pub Date : 1981-02-01
S Q Zhu, T F Li, D F Cui, Q P Cao, Y S Zhang
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引用次数: 0

摘要

本文描述了一系列用b22精氨酸取代的B23-D-Ala去己肽和去己肽类似物的半合成。采用以下半合成方案:由胰岛素六甲基酯经胰蛋白酶和羧肽酶B作用制备去氨肽胰岛素五甲基酯,氨基用boc保护,被保护产物与合成肽缩合,用三氟乙酸处理和皂化去除保护基团。这些类似物的生物活性表明,B22-Arg不是必需的,可以被赖氨酸甚至Asp取代而不影响生物活性。当被缬氨酸取代时,活性降低到一半,当被Gly或D-Arg取代时,活性降低到非常低的水平。探讨了豚鼠胰岛素活性低的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of B22-arginine replacement on the biological activity of insulin.

The semisynthesis of a series of B23-D-Ala deshexapeptide and despentapeptide analogues with B22-arginine replaced are described. The following semisynthetic scheme is used: desnonapeptide insulin pentamethyl ester is prepared from insulin hexamethyl ester through the action of trypsin and carboxypeptidase B, the amino groups are protected with Boc-groups, the protected product is condensed with synthetic peptides, and the protecting groups are removed with trifluoroacetic acid treatment and by saponification. The biological activities of these analogues indicate that the B22-Arg is non-essential and can be replaced by Lys or even Asp without any influence on the biological activity. The activity is reduced to one half when it is replaced by valine or to a very low level when replaced by Gly or D-Arg. The reason for the low activity of guinea pig insulin is discussed.

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