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固相蛋白质化学合成

Solid phase protein chemical synthesis.

作者信息

Raibaut Laurent, El Mahdi Ouafâa, Melnyk Oleg

机构信息

Institut Pasteur de Lille, UMR CNRS 8161, Université de Lille, 59021, Lille, France.

出版信息

Top Curr Chem. 2015;363:103-54. doi: 10.1007/128_2014_609.

Abstract

The chemical synthesis of peptides or small proteins is often an important step in many research projects and has stimulated the development of numerous chemical methodologies. The aim of this review is to give a substantial overview of the solid phase methods developed for the production or purification of polypeptides. The solid phase peptide synthesis (SPPS) technique has facilitated considerably the access to short peptides (<50 amino acids). However, its limitations for producing large homogeneous peptides have stimulated the development of solid phase covalent or non-covalent capture purification methods. The power of the native chemical ligation (NCL) reaction for protein synthesis in aqueous solution has also been adapted to the solid phase by the combination of novel linker technologies, cysteine protection strategies and thioester or N,S-acyl shift thioester surrogate chemistries. This review details pioneering studies and the most recent publications related to the solid phase chemical synthesis of large peptides and proteins.

摘要

肽或小蛋白质的化学合成在许多研究项目中往往是重要的一步,并且推动了众多化学方法的发展。本综述的目的是对为多肽的生产或纯化而开发的固相方法进行全面概述。固相肽合成(SPPS)技术极大地促进了短肽(<50个氨基酸)的获取。然而,其在生产大型均一肽方面的局限性推动了固相共价或非共价捕获纯化方法的发展。通过新型连接技术、半胱氨酸保护策略以及硫酯或N,S-酰基转移硫酯替代化学的结合,水溶液中蛋白质合成的天然化学连接(NCL)反应的强大功能也已应用于固相。本综述详细介绍了与大型肽和蛋白质的固相化学合成相关的开创性研究和最新出版物。

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