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{"title":"BioID: A Screen for Protein-Protein Interactions.","authors":"Kyle J Roux, Dae In Kim, Brian Burke, Danielle G May","doi":"10.1002/cpps.51","DOIUrl":null,"url":null,"abstract":"<p><p>BioID is a unique method to screen for physiologically relevant protein interactions that occur in living cells. This technique harnesses a promiscuous biotin ligase to biotinylate proteins based on proximity. The ligase is fused to a protein of interest and expressed in cells, where it biotinylates proximal endogenous proteins. Because it is a rare protein modification in nature, biotinylation of these endogenous proteins by BioID fusion proteins enables their selective isolation and identification with standard biotin-affinity capture. Proteins identified by BioID are candidate interactors for the protein of interest. BioID can be applied to insoluble proteins, can identify weak and/or transient interactions, and is amenable to temporal regulation. Initially applied to mammalian cells, BioID has potential application in a variety of cell types from diverse species. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":10866,"journal":{"name":"Current Protocols in Protein Science","volume":"91 ","pages":"19.23.1-19.23.15"},"PeriodicalIF":0.0000,"publicationDate":"2018-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028010/pdf/nihms952973.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Protein Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/cpps.51","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
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Abstract
BioID is a unique method to screen for physiologically relevant protein interactions that occur in living cells. This technique harnesses a promiscuous biotin ligase to biotinylate proteins based on proximity. The ligase is fused to a protein of interest and expressed in cells, where it biotinylates proximal endogenous proteins. Because it is a rare protein modification in nature, biotinylation of these endogenous proteins by BioID fusion proteins enables their selective isolation and identification with standard biotin-affinity capture. Proteins identified by BioID are candidate interactors for the protein of interest. BioID can be applied to insoluble proteins, can identify weak and/or transient interactions, and is amenable to temporal regulation. Initially applied to mammalian cells, BioID has potential application in a variety of cell types from diverse species. © 2018 by John Wiley & Sons, Inc.
BioID:蛋白质-蛋白质相互作用的筛选。
BioID是一种筛选活细胞中发生的生理相关蛋白质相互作用的独特方法。这项技术利用一种混杂的生物素连接酶,基于接近度对蛋白质进行生物素化。连接酶与感兴趣的蛋白质融合并在细胞中表达,在细胞中生物素化近端内源性蛋白质。由于这是自然界中罕见的蛋白质修饰,BioID融合蛋白对这些内源性蛋白质的生物素化使其能够通过标准的生物素亲和捕获进行选择性分离和鉴定。BioID鉴定的蛋白质是感兴趣蛋白质的候选相互作用物。BioID可以应用于不溶性蛋白质,可以识别微弱和/或短暂的相互作用,并服从时间调节。BioID最初应用于哺乳动物细胞,在来自不同物种的各种细胞类型中具有潜在应用。©2018 John Wiley&Sons,股份有限公司版权所有。
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