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通过对选定酰胺键进行临时恶唑烷保护来获取cpn 60.1 (195 - 217)难以接近的序列。

Access to the inaccessible sequence of cpn 60.1 (195-217) by temporary oxazolidine protection of selected amide bonds.

作者信息

Keller M, Miller A D

机构信息

Imperial College Genetic Therapies Centre, Department of Chemistry, Imperial College of Science, Technology and Medicine, South Kensington, UK.

出版信息

Bioorg Med Chem Lett. 2001 Mar 26;11(6):857-9. doi: 10.1016/s0960-894x(01)00085-3.

Abstract

The solid-phase peptide synthesis of a reportedly inaccessible peptide sequence of chaperonin 60.1 (195-219) is described using oxazolidine containing dipeptide building blocks ('pseudo-proline' dipeptide units). Two attempts at the synthesis of the chaperonin 60.1 sequence are outlined using one and two pseudo-proline units, respectively, and these results are compared with the outcome of an ordinary stepwise (double) coupling procedure. The only successful synthesis is that combining two pseudo-proline building blocks.

摘要

本文描述了使用含恶唑烷的二肽构建模块(“假脯氨酸”二肽单元)对伴侣蛋白60.1(195 - 219)中据报道难以合成的肽序列进行固相肽合成。分别概述了使用一个和两个假脯氨酸单元合成伴侣蛋白60.1序列的两次尝试,并将这些结果与普通逐步(双)偶联程序的结果进行了比较。唯一成功的合成是结合两个假脯氨酸构建模块的合成。

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