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用于成像PAR切割蛋白酶活性的化学工具。

Chemical Tools to Image the Activity of PAR-Cleaving Proteases.

作者信息

Lee Irene Y, Tantisirivat Piyapa, Edgington-Mitchell Laura E

机构信息

Department of Biochemistry and Pharmacology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, Victoria 3052 Australia.

出版信息

ACS Bio Med Chem Au. 2023 May 27;3(4):295-304. doi: 10.1021/acsbiomedchemau.3c00019. eCollection 2023 Aug 16.

Abstract

Protease-activated receptors (PARs) comprise a family of four G protein-coupled receptors (GPCRs) that have broad functions in health and disease. Unlike most GPCRs, PARs are uniquely activated by proteolytic cleavage of their extracellular N termini. To fully understand PAR activation and function in vivo, it is critical to also study the proteases that activate them. As proteases are heavily regulated at the post-translational level, measures of total protease abundance have limited utility. Measures of protease activity are instead required to inform their function. This review will introduce several classes of chemical probes that have been developed to measure the activation of PAR-cleaving proteases. Their strengths, weaknesses, and applications will be discussed, especially as applied to image protease activity at the whole organism, tissue, and cellular level.

摘要

蛋白酶激活受体(PARs)由四个G蛋白偶联受体(GPCRs)组成的家族,在健康和疾病中具有广泛的功能。与大多数GPCRs不同,PARs通过其细胞外N端的蛋白水解切割而独特地被激活。为了全面了解PARs在体内的激活和功能,研究激活它们的蛋白酶也至关重要。由于蛋白酶在翻译后水平受到严格调控,总蛋白酶丰度的测量效用有限。相反,需要蛋白酶活性的测量来了解其功能。本综述将介绍几类已开发用于测量PAR切割蛋白酶激活的化学探针。将讨论它们的优点、缺点和应用,特别是在全生物体、组织和细胞水平上用于成像蛋白酶活性的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e4/10436261/c93dea0b3a7d/bg3c00019_0001.jpg

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