Fluorescent saxitoxins for live cell imaging of single voltage-gated sodium ion channels beyond the optical diffraction limit

Chem Biol. 2012 Jul 27;19(7):902-12. doi: 10.1016/j.chembiol.2012.05.021.

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dose-Response Relationship, Drug
  • Electrophysiology
  • Fluorescence*
  • Fluorescent Dyes / chemical synthesis
  • Fluorescent Dyes / chemistry
  • Fluorescent Dyes / pharmacology*
  • Microscopy, Confocal
  • Models, Molecular
  • Molecular Structure
  • PC12 Cells
  • Rats
  • Saxitoxin / analogs & derivatives
  • Saxitoxin / chemistry
  • Saxitoxin / pharmacology*
  • Sodium Channels / chemistry
  • Sodium Channels / metabolism*
  • Structure-Activity Relationship

Substances

  • Fluorescent Dyes
  • Sodium Channels
  • Saxitoxin