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使用铜(I)催化的叠氮化物-炔烃[3 + 2]环加成反应在体内进行基于活性的蛋白质谱分析。

Activity-based protein profiling in vivo using a copper(i)-catalyzed azide-alkyne [3 + 2] cycloaddition.

作者信息

Speers Anna E, Adam Gregory C, Cravatt Benjamin F

机构信息

The Skaggs Institute for Chemical Biology, Departments of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.

出版信息

J Am Chem Soc. 2003 Apr 23;125(16):4686-7. doi: 10.1021/ja034490h.

Abstract

Toward the goal of assigning function to the tens of thousands of protein products encoded by eukaryotic and prokaryotic genomes, the field of proteomics requires new technologies that can functionally characterize proteins within the dynamic environment of the cell, where these biomolecules are subject to myriad posttranslational modifications and the actions of endogenous activators and inhibitors. Here, we report an advanced strategy for activity-based protein profiling (ABPP) that addresses this important need. We show that several enzymes can be labeled in an activity-based manner both in vitro and in vivo by an azido-sulfonate ester probe and that these labeling events can be detected in whole proteomes by copper-catalyzed ligation with a rhodamine-alkyne reagent. This click chemistry-based strategy for ABPP represents a unique and versatile method for functional proteome analysis.

摘要

为了实现对真核生物和原核生物基因组编码的数以万计蛋白质产物进行功能指派的目标,蛋白质组学领域需要能够在细胞动态环境中对蛋白质进行功能表征的新技术,在这种环境中,这些生物分子会经历无数的翻译后修饰以及内源性激活剂和抑制剂的作用。在此,我们报告了一种基于活性的蛋白质谱分析(ABPP)的先进策略,该策略满足了这一重要需求。我们表明,几种酶可以在体外和体内通过叠氮基磺酸酯探针以基于活性的方式进行标记,并且这些标记事件可以通过与罗丹明炔试剂的铜催化连接在完整蛋白质组中检测到。这种基于点击化学的ABPP策略代表了一种独特且通用的功能蛋白质组分析方法。

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