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基于活性的蛋白质组学:复杂蛋白质组中的酶活性分析

Activity-based proteomics: enzymatic activity profiling in complex proteomes.

作者信息

Schmidinger H, Hermetter A, Birner-Gruenberger R

机构信息

Department of Biochemistry, Graz University of Technology, Graz, Austria.

出版信息

Amino Acids. 2006 Jun;30(4):333-50. doi: 10.1007/s00726-006-0305-2. Epub 2006 May 15.

Abstract

In the postgenomic era new technologies are emerging for global analysis of protein function. The introduction of active site-directed chemical probes for enzymatic activity profiling in complex mixtures, known as activity-based proteomics has greatly accelerated functional annotation of proteins. Here we review probe design for different enzyme classes including serine hydrolases, cysteine proteases, tyrosine phosphatases, glycosidases, and others. These probes are usually detected by their fluorescent, radioactive or affinity tags and their protein targets are analyzed using established proteomics techniques. Recent developments, such as the design of probes for in vivo analysis of proteomes, as well as microarray technologies for higher throughput screenings of protein specificity and the application of activity-based probes for drug screening are highlighted. We focus on biological applications of activity-based probes for target and inhibitor discovery and discuss challenges for future development of this field.

摘要

在后基因组时代,用于蛋白质功能全局分析的新技术不断涌现。用于复杂混合物中酶活性谱分析的活性位点导向化学探针的引入,即基于活性的蛋白质组学,极大地加速了蛋白质的功能注释。在此,我们综述了针对不同酶类的探针设计,包括丝氨酸水解酶、半胱氨酸蛋白酶、酪氨酸磷酸酶、糖苷酶等。这些探针通常通过其荧光、放射性或亲和标签进行检测,其蛋白质靶点则使用既定的蛋白质组学技术进行分析。文中突出介绍了近期的进展,如用于蛋白质组体内分析的探针设计,以及用于蛋白质特异性高通量筛选的微阵列技术,还有基于活性的探针在药物筛选中的应用。我们重点关注基于活性的探针在靶点和抑制剂发现方面的生物学应用,并讨论该领域未来发展面临的挑战。

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