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一种体外活性完全保留的短效胰岛素。

A shortened insulin with full in vitro potency.

作者信息

Fischer W H, Saunders D, Brandenburg D, Wollmer A, Zahn H

出版信息

Biol Chem Hoppe Seyler. 1985 May;366(5):521-5. doi: 10.1515/bchm3.1985.366.1.521.

Abstract

Des[(B26-30)-pentapeptide]insulin-B25-amide was prepared from protected des-[(B23-30)-octapeptide]insulin (pig) and H-Gly-Phe-Phe-NH2 by trypsin-mediated semisynthesis in a yield of 9% (based on insulin). The analogue was characterized with respect to chemistry, biological function and CD spectroscopy. While des[(B26-30)-pentapeptide]insulin with free carboxylate group exhibited a typical insulin activity of only 25% in vitro, des[(B26-30)-pentapeptide]insulinamide was fully active. Therefore des[(B26-30)-pentapeptide]insulin meets all structural and dynamic requirements for recognition and binding of the receptor as well as exertion of the biological effect, provided that the negative charge in the hydrophobic environment of PheB25 is neutralized.

摘要

去[(B26 - 30)-五肽]胰岛素 - B25 -酰胺是由受保护的去[(B23 - 30)-八肽]胰岛素(猪)和H - Gly - Phe - Phe - NH₂通过胰蛋白酶介导的半合成制备而成,产率为9%(基于胰岛素)。对该类似物进行了化学、生物学功能和圆二色光谱表征。虽然具有游离羧基的去[(B26 - 30)-五肽]胰岛素在体外仅表现出25%的典型胰岛素活性,但去[(B26 - 30)-五肽]胰岛素酰胺具有完全活性。因此,只要苯丙氨酸B25疏水环境中的负电荷被中和,去[(B26 - 30)-五肽]胰岛素就满足受体识别、结合以及发挥生物学效应的所有结构和动力学要求。

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