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化学生物学框架阐明蛋白质稳态。

Chemical Biology Framework to Illuminate Proteostasis.

机构信息

Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA; email:

出版信息

Annu Rev Biochem. 2020 Jun 20;89:529-555. doi: 10.1146/annurev-biochem-013118-111552. Epub 2020 Feb 25.

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.

摘要

细胞中的蛋白质折叠是由一个庞大的网络介导的,这个网络包括超过 1000 种伴侣蛋白、质量控制因子和运输机制,这些都被统称为蛋白质稳态网络。虽然这个网络的组成和组织通常已经得到很好的确立,但我们对于如何识别蛋白质折叠问题、网络组件如何整合以成功应对挑战以及每个蛋白质稳态网络组件能够解决哪些类型的物理问题的理解仍然不成熟。我们描述了一种基于化学生物学的细胞蛋白质稳态研究框架,该框架依赖于选择有趣的蛋白质折叠问题和对蛋白质稳态网络组成和活性的精确研究人员控制。通过将这些方法与多方面的策略结合起来,监测细胞中蛋白质折叠、降解、运输和聚集,研究人员继续快速获得对细胞蛋白质稳态的新见解。

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