| Literature DB >> 30058756 |
Kai Wen Teng1,2,3, Pin Ren1,2, Paul R Selvin1,2,3.
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.Entities:
Keywords: cell delivery; fluorescence microscopy; microscopy; single molecule; streptolysin O; super-resolution
Mesh:
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Year: 2018 PMID: 30058756 PMCID: PMC6097887 DOI: 10.1002/cpps.60
Source DB: PubMed Journal: Curr Protoc Protein Sci ISSN: 1934-3655