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合成和生物方法研究蛋白酶的底物特异性。

Synthetic and biological approaches to map substrate specificities of proteases.

机构信息

Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.

Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.

出版信息

Biol Chem. 2019 Dec 18;401(1):165-182. doi: 10.1515/hsz-2019-0332.

Abstract

Proteases are regulators of diverse biological pathways including protein catabolism, antigen processing and inflammation, as well as various disease conditions, such as malignant metastasis, viral infection and parasite invasion. The identification of substrates of a given protease is essential to understand its function and this information can also aid in the design of specific inhibitors and active site probes. However, the diversity of putative protein and peptide substrates makes connecting a protease to its downstream substrates technically difficult and time-consuming. To address this challenge in protease research, a range of methods have been developed to identify natural protein substrates as well as map the overall substrate specificity patterns of proteases. In this review, we highlight recent examples of both synthetic and biological methods that are being used to define the substrate specificity of protease so that new protease-specific tools and therapeutic agents can be developed.

摘要

蛋白酶是多种生物途径的调节剂,包括蛋白质分解代谢、抗原加工和炎症,以及各种疾病状况,如恶性转移、病毒感染和寄生虫入侵。鉴定给定蛋白酶的底物对于理解其功能至关重要,并且这些信息还可以帮助设计特定的抑制剂和活性位点探针。然而,假定的蛋白质和肽底物的多样性使得将蛋白酶与其下游底物连接在技术上具有挑战性且耗时。为了解决蛋白酶研究中的这一挑战,已经开发了一系列方法来鉴定天然蛋白质底物,并绘制蛋白酶的整体底物特异性模式。在这篇综述中,我们重点介绍了最近使用的合成和生物学方法的例子,这些方法用于定义蛋白酶的底物特异性,以便开发新的蛋白酶特异性工具和治疗剂。

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