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Title: Bacterial Overexpression and Denaturing Purification of VPS34-Binding Domain of Beclin 1. Author: Baek JH, Jung J, Seo J, Kim JH, Kim J. Journal: J Microbiol Biotechnol; 2016 Oct 28; 26(10):1808-1816. PubMed ID: 27363473. 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 Escherichia coli. The expression and purification conditions determined in this study successfully provided soluble and functional Vps34-BD.[Abstract] [Full Text] [Related] [New Search]