LOV结构域作为蛋白表达的体内荧光报告者

John M. Christie
{"title":"LOV结构域作为蛋白表达的体内荧光报告者","authors":"John M. Christie","doi":"10.1002/9780470089941.et1301s06","DOIUrl":null,"url":null,"abstract":"<p>Chromophore-binding domains from plant and bacterial photoreceptors have received increasing interest as new sources of genetically encoded fluorescent proteins (FPs). In particular, FPs based on the flavin-binding LOV (Light, Oxygen, or Voltage sensing) domain offer advantages over green fluorescent protein (GFP) owing to their smaller size and utility under anaerobic conditions. Recombinant expression of LOV domains in <i>Escherichia coli</i> (<i>E. coli</i>) is fast, easy to detect, and inexpensive given the innate ability of LOV domains to acquire their ubiquitous organic cofactor from the cellular environment. This manuscript describes the strategies and variables to consider when expressing and purifying LOV-domain protein fusions from liquid cultures of <i>E. coli</i>. Strategies for expressing and visualizing LOV-domain fusion proteins in <i>E. coli</i> grown on agar medium are also described. <i>Curr. Protoc. Essential Lab. Tech</i>. 6:13.1.1-13.1.11. © 2012 by John Wiley &amp; Sons, Inc.</p>","PeriodicalId":500994,"journal":{"name":"Current Protocols Essential Laboratory Techniques","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2012-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/9780470089941.et1301s06","citationCount":"3","resultStr":"{\"title\":\"LOV Domains as In Vivo Fluorescent Reporters of Protein Expression\",\"authors\":\"John M. Christie\",\"doi\":\"10.1002/9780470089941.et1301s06\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Chromophore-binding domains from plant and bacterial photoreceptors have received increasing interest as new sources of genetically encoded fluorescent proteins (FPs). In particular, FPs based on the flavin-binding LOV (Light, Oxygen, or Voltage sensing) domain offer advantages over green fluorescent protein (GFP) owing to their smaller size and utility under anaerobic conditions. Recombinant expression of LOV domains in <i>Escherichia coli</i> (<i>E. coli</i>) is fast, easy to detect, and inexpensive given the innate ability of LOV domains to acquire their ubiquitous organic cofactor from the cellular environment. This manuscript describes the strategies and variables to consider when expressing and purifying LOV-domain protein fusions from liquid cultures of <i>E. coli</i>. Strategies for expressing and visualizing LOV-domain fusion proteins in <i>E. coli</i> grown on agar medium are also described. <i>Curr. Protoc. Essential Lab. Tech</i>. 6:13.1.1-13.1.11. © 2012 by John Wiley &amp; Sons, Inc.</p>\",\"PeriodicalId\":500994,\"journal\":{\"name\":\"Current Protocols Essential Laboratory Techniques\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/9780470089941.et1301s06\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Protocols Essential Laboratory Techniques\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/9780470089941.et1301s06\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols Essential Laboratory Techniques","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/9780470089941.et1301s06","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

摘要

作为遗传编码荧光蛋白(FPs)的新来源,植物和细菌光感受器的发色团结合域受到越来越多的关注。特别是基于黄素结合LOV(光、氧或电压传感)结构域的FPs,由于其更小的尺寸和在厌氧条件下的实用性,比绿色荧光蛋白(GFP)具有优势。考虑到LOV结构域从细胞环境中获得无处不在的有机辅因子的先天能力,在大肠杆菌中重组表达LOV结构域是快速、容易检测和廉价的。本文描述了从大肠杆菌液体培养物中表达和纯化lov结构域蛋白融合物时要考虑的策略和变量。还描述了在琼脂培养基上生长的大肠杆菌中表达和可视化lov结构域融合蛋白的策略。咕咕叫。Protoc。基本的实验室。科技,6:13.1.1-13.1.11。©2012 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
LOV Domains as In Vivo Fluorescent Reporters of Protein Expression

Chromophore-binding domains from plant and bacterial photoreceptors have received increasing interest as new sources of genetically encoded fluorescent proteins (FPs). In particular, FPs based on the flavin-binding LOV (Light, Oxygen, or Voltage sensing) domain offer advantages over green fluorescent protein (GFP) owing to their smaller size and utility under anaerobic conditions. Recombinant expression of LOV domains in Escherichia coli (E. coli) is fast, easy to detect, and inexpensive given the innate ability of LOV domains to acquire their ubiquitous organic cofactor from the cellular environment. This manuscript describes the strategies and variables to consider when expressing and purifying LOV-domain protein fusions from liquid cultures of E. coli. Strategies for expressing and visualizing LOV-domain fusion proteins in E. coli grown on agar medium are also described. Curr. Protoc. Essential Lab. Tech. 6:13.1.1-13.1.11. © 2012 by John Wiley & Sons, Inc.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信