Suppr超能文献

单细胞内蛋白质水平的定量分析

Quantification of Protein Levels in Single Living Cells.

机构信息

Centre for Research in Neuroscience, Research Institute of the McGill University Health Centre, Montréal, QC H3G 1A4, Canada.

Centre for Research in Neuroscience, Research Institute of the McGill University Health Centre, Montréal, QC H3G 1A4, Canada; Departments of Medicine and Neurology and Neurosurgery, McGill University, Montréal, QC H3G 1A4, Canada.

出版信息

Cell Rep. 2015 Dec 22;13(11):2634-2644. doi: 10.1016/j.celrep.2015.11.048. Epub 2015 Dec 10.

Abstract

Accurate measurement of the amount of specific protein a cell produces is important for investigating basic molecular processes. We have developed a technique that allows for quantitation of protein levels in single cells in vivo. This protein quantitation ratioing (PQR) technique uses a genetic tag that produces a stoichiometric ratio of a fluorescent protein reporter and the protein of interest during protein translation. The fluorescence intensity is proportional to the number of molecules produced of the protein of interest and is used to determine the relative amount of protein within the cell. We use PQR to quantify protein expression of different genes using quantitative imaging, electrophysiology, and phenotype. We use genome editing to insert Protein Quantitation Reporters into endogenous genomic loci in three different genomes for quantitation of endogenous protein levels. The PQR technique will allow for a wide range of quantitative experiments examining gene-to-phenotype relationships with greater accuracy.

摘要

准确测量细胞产生的特定蛋白质的量对于研究基本分子过程非常重要。我们开发了一种技术,可用于定量测量体内单细胞中的蛋白质水平。该蛋白质定量比(PQR)技术使用一种遗传标记,该标记在蛋白质翻译过程中产生荧光蛋白报告基因与感兴趣的蛋白质的化学计量比。荧光强度与感兴趣的蛋白质的分子数成正比,并用于确定细胞内蛋白质的相对含量。我们使用 PQR 通过定量成像、电生理学和表型来量化不同基因的蛋白质表达。我们使用基因组编辑将蛋白定量报告基因插入三个不同基因组的内源性基因组位点中,以定量内源性蛋白质水平。PQR 技术将允许进行广泛的定量实验,更准确地研究基因与表型的关系。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验