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光交联小分子亲和基质作为生物活性小分子靶标鉴定的工具。

Photo-cross-linked small-molecule affinity matrix as a tool for target identification of bioactive small molecules.

机构信息

Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aza-aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan.

出版信息

Nat Prod Rep. 2016 May 4;33(5):709-18. doi: 10.1039/c5np00117j.

Abstract

Covering: up to the end of 2015A photo-cross-linked small-molecule affinity matrix is a unique platform for identifying targets for bioactive small molecules. It utilises a photogenerated carbene species to immobilise a variety of bioactive small molecules on an affinity matrix in a chemo- and site-nonselective manner. Although this platform would seem to run counter to the more typical approach of small-molecule immobilisation on an affinity matrix (i.e., selective coupling), it has been successfully utilised in the past decade to screen protein targets for many bioactive small molecules. This review describes the status of the photo-cross-linking methodology while providing a useful tutorial for academic and industrial chemical biologists who are involved or interested in drug target identification.

摘要

涵盖

截至 2015 年底 光交联小分子亲和基质是一种独特的平台,可用于鉴定生物活性小分子的靶标。它利用光生卡宾物种以化学和非选择性方式将各种生物活性小分子固定在亲和基质上。尽管该平台似乎与更典型的小分子在亲和基质上的固定方法(即选择性偶联)背道而驰,但在过去十年中,它已成功用于筛选许多生物活性小分子的蛋白质靶标。本综述描述了光交联方法的现状,同时为从事或感兴趣的药物靶标鉴定的学术和工业化学生物学家提供了有用的教程。

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