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用于发现小分子探针和药物的无偏结合测定法。

Unbiased binding assays for discovering small-molecule probes and drugs.

机构信息

Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.

出版信息

Bioorg Med Chem. 2012 Mar 15;20(6):1979-89. doi: 10.1016/j.bmc.2011.11.071. Epub 2011 Dec 24.

Abstract

2011 marks the 10-year anniversary of milestone manuscripts describing drafts of the human genome sequence. Over the past decade, a number of new proteins have been linked to disease-many of which fall into classes that have been historically considered challenging from the perspective of drug discovery. Several of these newly associated proteins lack structural information or strong annotation with regard to function, making development of conventional in vitro functional assays difficult. A recent resurgence in the popularity of simple small molecule binding assays has led to new approaches that do not require knowledge of protein structure or function in advance. Here we briefly review selected methods for executing binding assays that have been used successfully to discover small-molecule probes or drug candidates.

摘要

2011 年标志着描述人类基因组序列草案的里程碑式手稿发表 10 周年。在过去的十年中,许多新的蛋白质与疾病有关,其中许多蛋白质属于从药物发现的角度来看历史上具有挑战性的类别。这些新关联的蛋白质中有一些缺乏结构信息或功能的强烈注释,使得传统的体外功能测定的开发变得困难。最近,简单的小分子结合测定的重新流行导致了不需要事先了解蛋白质结构或功能的新方法。在这里,我们简要回顾了成功用于发现小分子探针或药物候选物的选定结合测定方法。

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