| Literature DB >> 22840778 |
Alison E Ondrus1, Hsiao-lu D Lee, Shigeki Iwanaga, William H Parsons, Brian M Andresen, W E Moerner, J Du Bois.
Abstract
A desire to better understand the role of voltage-gated sodium channels (Na(V)s) in signal conduction and their dysregulation in specific disease states motivates the development of high precision tools for their study. Nature has evolved a collection of small molecule agents, including the shellfish poison (+)-saxitoxin, that bind to the extracellular pore of select Na(V) isoforms. As described in this report, de novo chemical synthesis has enabled the preparation of fluorescently labeled derivatives of (+)-saxitoxin, STX-Cy5, and STX-DCDHF, which display reversible binding to Na(V)s in live cells. Electrophysiology and confocal fluorescence microscopy studies confirm that these STX-based dyes function as potent and selective Na(V) labels. The utility of these probes is underscored in single-molecule and super-resolution imaging experiments, which reveal Na(V) distributions well beyond the optical diffraction limit in subcellular features such as neuritic spines and filopodia.Entities:
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Year: 2012 PMID: 22840778 PMCID: PMC3731772 DOI: 10.1016/j.chembiol.2012.05.021
Source DB: PubMed Journal: Chem Biol ISSN: 1074-5521