| Literature DB >> 28514494 |
Veronica Pessino1, Y Rose Citron1, Siyu Feng2, Bo Huang3.
Abstract
Labeling proteins with high specificity and efficiency is a fundamental prerequisite for microscopic visualization of subcellular protein structures and interactions. Although the comparatively small size of epitope tags makes them less perturbative to fusion proteins, they require the use of large antibodies that often limit probe accessibility and effective resolution. Here we use the covalent SpyTag-SpyCatcher system as an epitope-like tag for fluorescent labeling of intracellular proteins in fixed cells for both conventional and super-resolution microscopy. We also applied this method to endogenous proteins by gene editing, demonstrating its high labeling efficiency and capability for isoform-specific labeling.Entities:
Keywords: SpyTag-SpyCatcher; epitope tags; fluorescence microscopy; fluorescent probes; super-resolution microscopy
Mesh:
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Year: 2017 PMID: 28514494 PMCID: PMC5599254 DOI: 10.1002/cbic.201700177
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164