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小分子的发现方法,用于监测和干扰人蛋白酶体的活性。

Methods for the discovery of small molecules to monitor and perturb the activity of the human proteasome.

机构信息

Department of Medicinal Chemistry & Molecular Pharmacology, Purdue University, 575 West Stadium Avenue, West Lafayette, IN 47907, USA.

出版信息

Future Med Chem. 2021 Jan;13(2):99-116. doi: 10.4155/fmc-2020-0288. Epub 2020 Dec 4.

Abstract

Regulating protein production and degradation is critical to maintaining cellular homeostasis. The proteasome is a key player in keeping proteins at the proper levels. However, proteasome activity can be altered in certain disease states, such as blood cancers and neurodegenerative diseases. Cancers often exhibit enhanced proteasomal activity, as protein synthesis is increased in these cells compared with normal cells. Conversely, neurodegenerative diseases are characterized by protein accumulation, leading to reduced proteasome activity. As a result, the proteasome has emerged as a target for therapeutic intervention. The potential of the proteasome as a therapeutic target has come from studies involving chemical stimulators and inhibitors, and the development of a suite of assays and probes that can be used to monitor proteasome activity with purified enzyme and in live cells.

摘要

调控蛋白质的产生和降解对于维持细胞内环境的稳定至关重要。蛋白酶体是维持蛋白质水平的关键因素。然而,在某些疾病状态下,如血液癌和神经退行性疾病,蛋白酶体的活性可能会发生改变。癌症细胞通常表现出增强的蛋白酶体活性,因为与正常细胞相比,这些细胞中的蛋白质合成增加了。相反,神经退行性疾病的特征是蛋白质堆积,导致蛋白酶体活性降低。因此,蛋白酶体已成为治疗干预的一个靶点。蛋白酶体作为治疗靶点的潜力来自于涉及化学刺激剂和抑制剂的研究,以及开发了一系列可以用于监测纯化酶和活细胞中蛋白酶体活性的测定法和探针。

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A Practical Review of Proteasome Pharmacology.蛋白酶体药理学实用综述。
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