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贝林1的VPS34结合结构域的细菌过表达及变性纯化

Bacterial Overexpression and Denaturing Purification of VPS34-Binding Domain of Beclin 1.

作者信息

Baek Jong-Hyuk, Jung Juneyoung, Seo Jeongbin, Kim Jeong Hee, Kim Joungmok

机构信息

Department of Life and Nanopharmaceutical Sciences, Graduate School, Kyung Hee University, Seoul 02447, Republic of Korea.

Department of Oral Biochemistry and Molecular biology, School of Dentistry, Kyung Hee University, Seoul 02447, Republic of Korea.

出版信息

J Microbiol Biotechnol. 2016 Oct 28;26(10):1808-1816. doi: 10.4014/jmb.1604.04085.

Abstract

As a scaffolding subunit of the PIK3C3/VPS34 complex, Beclin 1 recruits a variety of proteins to class III phosphatidylinositol-3-kinase (VPS34), resulting in the formation of a distinct PIK3C3/VPS34 complex with a specific function. Therefore, the investigation of a number of Beclin 1 domains required for the protein-protein interactions will provide important clues to understand the PIK3C3/VPS34 complex, of which Beclin1-VPS34 interaction is the core unit. In the present study, we have designed a bacterial overexpression system for the Beclin 1 domain corresponding to VPS34 binding (Vps34-BD) and set up the denaturing purification protocol due to the massive aggregation of Vps34-BD in . The expression and purification conditions determined in this study successfully provided soluble and functional Vps34-BD.

摘要

作为PIK3C3/VPS34复合物的支架亚基,Beclin 1募集多种蛋白质至III类磷脂酰肌醇-3激酶(VPS34),从而形成具有特定功能的独特PIK3C3/VPS34复合物。因此,对蛋白质-蛋白质相互作用所需的多个Beclin 1结构域进行研究,将为理解PIK3C3/VPS34复合物提供重要线索,其中Beclin1-VPS34相互作用是核心单元。在本研究中,我们设计了一种用于与VPS34结合的Beclin 1结构域(Vps34-BD)的细菌过表达系统,并由于Vps34-BD在……中大量聚集而建立了变性纯化方案。本研究确定的表达和纯化条件成功提供了可溶性且具有功能的Vps34-BD。

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