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蛋白酶:功能蛋白质组学的关键点

Proteases: Pivot Points in Functional Proteomics.

作者信息

Verhamme Ingrid M, Leonard Sarah E, Perkins Ray C

机构信息

Department of Pathology, Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, TN, USA.

Chemical and Biomolecular Engineering, University of Illinois Champaign-Urbana School of Chemical Sciences, Champaign, IL, USA.

出版信息

Methods Mol Biol. 2019;1871:313-392. doi: 10.1007/978-1-4939-8814-3_20.

DOI:10.1007/978-1-4939-8814-3_20
PMID:30276748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6472488/
Abstract

Proteases drive the life cycle of all proteins, ensuring the transportation and activation of newly minted, would-be proteins into their functional form while recycling spent or unneeded proteins. Far from their image as engines of protein digestion, proteases play fundamental roles in basic physiology and regulation at multiple levels of systems biology. Proteases are intimately associated with disease and modulation of proteolytic activity is the presumed target for successful therapeutics. "Proteases: Pivot Points in Functional Proteomics" examines the crucial roles of proteolysis across a wide range of physiological processes and diseases. The existing and potential impacts of proteolysis-related activity on drug and biomarker development are presented in detail. All told the decisive roles of proteases in four major categories comprising 23 separate subcategories are addressed. Within this construct, 15 sets of subject-specific, tabulated data are presented that include identification of proteases, protease inhibitors, substrates, and their actions. Said data are derived from and confirmed by over 300 references. Cross comparison of datasets indicates that proteases, their inhibitors/promoters and substrates intersect over a range of physiological processes and diseases, both chronic and pathogenic. Indeed, "Proteases: Pivot Points …" closes by dramatizing this very point through association of (pro)Thrombin and Fibrin(ogen) with: hemostasis, innate immunity, cardiovascular and metabolic disease, cancer, neurodegeneration, and bacterial self-defense.

摘要

蛋白酶驱动着所有蛋白质的生命周期,确保新合成的、潜在的蛋白质被运输并激活为其功能形式,同时回收已消耗或不需要的蛋白质。与它们作为蛋白质消化引擎的形象大相径庭的是,蛋白酶在基础生理学和系统生物学多个层面的调节中发挥着重要作用。蛋白酶与疾病密切相关,调节蛋白水解活性被认为是成功治疗的靶点。《蛋白酶:功能蛋白质组学的关键点》探讨了蛋白水解在广泛的生理过程和疾病中的关键作用。详细介绍了蛋白水解相关活性对药物和生物标志物开发的现有及潜在影响。总共阐述了蛋白酶在包括23个独立子类别的四大类中的决定性作用。在此框架内,呈现了15组特定主题的列表数据,包括蛋白酶、蛋白酶抑制剂、底物及其作用的鉴定。这些数据源自300多篇参考文献并得到其证实。数据集的交叉比较表明,蛋白酶及其抑制剂/促进剂和底物在一系列生理过程以及慢性和致病性疾病中相互交叉。事实上,《蛋白酶:关键点……》通过将凝血酶原和纤维蛋白原与止血、先天免疫、心血管和代谢疾病、癌症、神经退行性变以及细菌自我防御联系起来,戏剧性地强调了这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7397/6472488/9958b5e5ddaa/nihms-1006950-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7397/6472488/054c67d8a6ce/nihms-1006950-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7397/6472488/9958b5e5ddaa/nihms-1006950-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7397/6472488/054c67d8a6ce/nihms-1006950-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7397/6472488/9958b5e5ddaa/nihms-1006950-f0002.jpg

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