下载PDF
{"title":"Bioluminescence Resonance Energy Transfer (BRET)-Based Synthetic Sensor Platform for Drug Discovery.","authors":"Jongchan Woo, Jason Hong, Savithramma P Dinesh-Kumar","doi":"10.1002/cpps.30","DOIUrl":null,"url":null,"abstract":"<p><p>Bioluminescence resonance energy transfer (BRET) is a technique that analyzes protein-protein interactions (PPIs). The unique feature of BRET delineates that the resonance energy is generated by the resonance energy donor, Renilla luciferase by the oxidative decarboxylation of coelenterazine substrate. BRET is superior to FRET where issues such as autofluorescence, photobleaching, and light scattering can occur. Recently, BRET has been applied to design synthetic biosensors for monitoring autophagy in vivo and in vitro. Here, we report the methods for constructing a biosensor of human HsLC3a as a probe for autophagy biogenesis and the optimization of the intramolecular BRET assay that allows for high-throughput screening of chemical modulators of autophagy. User-friendly working interface with the BRET-based synthetic sensor of HsLC3a makes drug discovery easy and amenable for high-throughput. The BRET protocol described here could be easily applicable to generate other biosensors for monitoring PPIs by measurement of intermolecular BRET. © 2017 by John Wiley & Sons, Inc.</p>","PeriodicalId":10866,"journal":{"name":"Current Protocols in Protein Science","volume":"88 ","pages":"19.30.1-19.30.12"},"PeriodicalIF":0.0000,"publicationDate":"2017-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpps.30","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Protein Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/cpps.30","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}
引用次数: 2
引用
批量引用
Abstract
Bioluminescence resonance energy transfer (BRET) is a technique that analyzes protein-protein interactions (PPIs). The unique feature of BRET delineates that the resonance energy is generated by the resonance energy donor, Renilla luciferase by the oxidative decarboxylation of coelenterazine substrate. BRET is superior to FRET where issues such as autofluorescence, photobleaching, and light scattering can occur. Recently, BRET has been applied to design synthetic biosensors for monitoring autophagy in vivo and in vitro. Here, we report the methods for constructing a biosensor of human HsLC3a as a probe for autophagy biogenesis and the optimization of the intramolecular BRET assay that allows for high-throughput screening of chemical modulators of autophagy. User-friendly working interface with the BRET-based synthetic sensor of HsLC3a makes drug discovery easy and amenable for high-throughput. The BRET protocol described here could be easily applicable to generate other biosensors for monitoring PPIs by measurement of intermolecular BRET. © 2017 by John Wiley & Sons, Inc.
基于生物发光共振能量转移(BRET)的药物发现合成传感器平台。
生物发光共振能量转移(BRET)是一种分析蛋白质-蛋白质相互作用(PPIs)的技术。BRET的独特之处在于共振能是由共振能供体Renilla luciferase通过coelenterazine底物氧化脱羧产生的。BRET优于FRET的问题,如自身荧光,光漂白,光散射可能发生。最近,BRET已被应用于设计用于监测体内和体外自噬的合成生物传感器。在这里,我们报道了构建人类HsLC3a生物传感器作为自噬生物发生探针的方法,以及优化分子内BRET测定方法,该方法允许高通量筛选自噬的化学调节剂。用户友好的工作界面与基于bret的HsLC3a合成传感器,使药物发现容易,适合高通量。这里描述的BRET协议可以很容易地应用于生成其他生物传感器,通过测量分子间BRET来监测ppi。©2017 by John Wiley & Sons, Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。