通过镜像噬菌体展示发现镜像蛋白质和多肽药物

IF 19.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Chem Pub Date : 2024-08-08 DOI:10.1016/j.chempr.2024.06.004
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引用次数: 0

摘要

由 D-氨基酸组成的镜像蛋白质和肽作为诊断试剂和候选药物正受到越来越多的关注,因为与 L-氨基酸相比,它们具有更高的稳定性和更低的免疫原性。镜像噬菌体展示技术是发现原生蛋白质的镜像蛋白质和肽配体的常用策略,在噬菌体展示筛选中,L-目标的 D-对映体形式被用作诱饵。化学蛋白合成技术的进步极大地促进了这些 D 蛋白靶标的生产,而这些靶标通过重组表达技术是无法实现的。本综述将重点介绍镜像蛋白质和多肽药物的最新发展,重点是获得 D 蛋白靶标所采用的最先进合成方法,以及镜像噬菌体展示的基本工作流程和最新进展及其在药物发现中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mirror-image protein and peptide drug discovery through mirror-image phage display

Mirror-image protein and peptide drug discovery through mirror-image phage display

Mirror-image protein and peptide drug discovery through mirror-image phage display

Mirror-image proteins and peptides composed of D-amino acids are garnering increasing attention as diagnostic agents and drug candidates due to their higher stability and lower immunogenicity compared with their L-amino acid counterparts. The often-used strategy to discover mirror-image protein and peptide ligands of a native protein is the mirror-image phage display technique, in which the D-enantiomeric form of the L-target is used as the bait in phage display screening. Advancements in chemical protein synthesis have greatly facilitated the production of these D-protein targets, which are unattainable through recombinant expression technologies. This review spotlights recent developments in mirror-image protein and peptide drugs, focusing on the state-of-the-art synthetic methodologies that have been employed to acquire D-protein targets as well as the basic workflow and recent progress of mirror-image phage display and its applications to drug discovery.

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来源期刊
Chem
Chem Environmental Science-Environmental Chemistry
CiteScore
32.40
自引率
1.30%
发文量
281
期刊介绍: Chem, affiliated with Cell as its sister journal, serves as a platform for groundbreaking research and illustrates how fundamental inquiries in chemistry and its related fields can contribute to addressing future global challenges. It was established in 2016, and is currently edited by Robert Eagling.
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