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十三载肽合成:固相肽合成和酰胺键形成的关键进展在肽连接中的应用。

Thirteen decades of peptide synthesis: key developments in solid phase peptide synthesis and amide bond formation utilized in peptide ligation.

机构信息

Department of Chemistry, Faculty of Science, Al-Balqa Applied University, P.O. Box 19117, Al-Salt, Jordan.

出版信息

Amino Acids. 2018 Jan;50(1):39-68. doi: 10.1007/s00726-017-2516-0. Epub 2017 Nov 28.

Abstract

A historical overview of peptide chemistry from T. Curtius to E. Fischer to M. Bergmann and L. Zervas is first presented. Next, the fundamentals of peptide synthesis with a focus on solid phase peptide synthesis by R. B. Merrifield are described. Immobilization strategies to attach the first amino acid to the resin, coupling strategies in stepwise peptide chain elongation, and approaches to synthesize difficult peptide sequences are also shown. A brief comparison between tert-butyloxycarbonyl (Boc)/benzyl (Bzl) strategy and 9-fluorenylmethoxycarbonyl (Fmoc)/tert-butyl (t -Bu) strategy utilized in solid phase peptide synthesis is given with an emphasis on the latter. Finally, the review focuses on the discovery and development of peptide ligation and the latest advances in this field including native amide bond formation strategies, these include the native chemical ligation, α-ketoacid-hydroxylamine ligation, and serine/threonine ligation which are the most commonly used chemoselective ligation methods that provide amide bond at the ligation site. This review provides an overview of the literature concerning the most important advances in the chemical synthesis of proteins and peptides covering the period from 1882 to 2017.

摘要

首先介绍了从 T. Curtius 到 E. Fischer 再到 M. Bergmann 和 L. Zervas 的肽化学历史概述。接下来,描述了重点是 R. B. Merrifield 的固相肽合成的肽合成基础。还展示了将第一个氨基酸固定在树脂上的固定化策略、逐步肽链延伸中的偶联策略以及合成困难肽序列的方法。简要比较了固相肽合成中使用的叔丁氧羰基(Boc)/苄基(Bzl)策略和 9-芴甲氧羰基(Fmoc)/叔丁基(t -Bu)策略,并强调了后者。最后,综述重点介绍了肽连接的发现和发展以及该领域的最新进展,包括天然酰胺键形成策略,其中包括天然化学连接、α-酮酸-羟胺连接和丝氨酸/苏氨酸连接,它们是最常用的选择性化学连接方法,可在连接位点形成酰胺键。本文综述了 1882 年至 2017 年期间蛋白质和肽化学合成最重要进展的文献综述。

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