Chemical Biology Framework to Illuminate Proteostasis.

IF 12.1 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Annual review of biochemistry Pub Date : 2020-06-20 Epub Date: 2020-02-25 DOI:10.1146/annurev-biochem-013118-111552
Rebecca M Sebastian, Matthew D Shoulders
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引用次数: 20

Abstract

Protein folding in the cell is mediated by an extensive network of >1,000 chaperones, quality control factors, and trafficking mechanisms collectively termed the proteostasis network. While the components and organization of this network are generally well established, our understanding of how protein-folding problems are identified, how the network components integrate to successfully address challenges, and what types of biophysical issues each proteostasis network component is capable of addressing remains immature. We describe a chemical biology-informed framework for studying cellular proteostasis that relies on selection of interesting protein-folding problems and precise researcher control of proteostasis network composition and activities. By combining these methods with multifaceted strategies to monitor protein folding, degradation, trafficking, and aggregation in cells, researchers continue to rapidly generate new insights into cellular proteostasis.

阐明蛋白质静止的化学生物学框架。
细胞中的蛋白质折叠是由超过1000个伴侣、质量控制因子和运输机制组成的广泛网络介导的,这些网络统称为蛋白质静止网络。虽然该网络的组成和组织通常都很完善,但我们对如何识别蛋白质折叠问题,网络组件如何整合以成功解决挑战,以及每个蛋白质平衡网络组件能够解决哪些类型的生物物理问题的理解仍然不成熟。我们描述了一个化学生物学的框架来研究细胞蛋白质平衡,它依赖于选择有趣的蛋白质折叠问题和精确的研究人员控制蛋白质平衡网络的组成和活动。通过将这些方法与多方面的策略相结合来监测细胞中的蛋白质折叠、降解、运输和聚集,研究人员继续快速地对细胞蛋白质静止产生新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annual review of biochemistry
Annual review of biochemistry 生物-生化与分子生物学
CiteScore
33.90
自引率
0.00%
发文量
31
期刊介绍: The Annual Review of Biochemistry, in publication since 1932, sets the standard for review articles in biological chemistry and molecular biology. Since its inception, these volumes have served as an indispensable resource for both the practicing biochemist and students of biochemistry.
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