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{"title":"Delivery of Fluorescent Probes Using Streptolysin O for Fluorescence Microscopy of Living Cells","authors":"Kai Wen Teng, Pin Ren, Paul R. Selvin","doi":"10.1002/cpps.60","DOIUrl":null,"url":null,"abstract":"<p>Methods to efficiently deliver fluorophores across the cell membrane are crucial for imaging the dynamics of intracellular proteins using fluorescence. Here we describe a simple protocol for permeabilizing living cells using streptolysin O, a bacterial toxin, which allows transient uptake of fluorescent probes for labeling specific intracellular proteins. The technique is applicable for delivering different classes of fluorescent probes with a molecular weight of <150 kDa, and it is also applicable to a variety of different cell lines. The technique enables the utilization of a broad range of fluorophores for live cell imaging of intracellular proteins. Extended observation of intracellular fluorescence bound to specific proteins is now possible through super-resolution microscopy by using fluorophores that are photostable in “cell-friendly” deoxygenating and reducing conditions. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":10866,"journal":{"name":"Current Protocols in Protein Science","volume":"93 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpps.60","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Protein Science","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpps.60","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
Methods to efficiently deliver fluorophores across the cell membrane are crucial for imaging the dynamics of intracellular proteins using fluorescence. Here we describe a simple protocol for permeabilizing living cells using streptolysin O, a bacterial toxin, which allows transient uptake of fluorescent probes for labeling specific intracellular proteins. The technique is applicable for delivering different classes of fluorescent probes with a molecular weight of <150 kDa, and it is also applicable to a variety of different cell lines. The technique enables the utilization of a broad range of fluorophores for live cell imaging of intracellular proteins. Extended observation of intracellular fluorescence bound to specific proteins is now possible through super-resolution microscopy by using fluorophores that are photostable in “cell-friendly” deoxygenating and reducing conditions. © 2018 by John Wiley & Sons, Inc.
利用链溶素O递送荧光探针用于活细胞荧光显微镜
有效地传递细胞膜上的荧光团的方法是至关重要的成像细胞内蛋白质的动态使用荧光。在这里,我们描述了一种简单的方案,通过使用链溶素O(一种细菌毒素)渗透活细胞,它允许荧光探针的瞬时摄取来标记特定的细胞内蛋白质。该技术适用于输送分子量为150 kDa的不同种类的荧光探针,也适用于多种不同细胞系。该技术能够利用广泛的荧光团对细胞内蛋白质进行活细胞成像。通过使用在“细胞友好”脱氧和还原条件下光稳定的荧光团,现在可以通过超分辨率显微镜对与特定蛋白质结合的细胞内荧光进行扩展观察。©2018 by John Wiley &儿子,Inc。
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