Counting bungarotoxin binding sites of nicotinic acetylcholine receptors in mammalian cells with high signal/noise ratios. Academic Article uri icon

Overview

abstract

  • Nicotinic acetylcholine receptors are some of the most studied synaptic proteins; however, many questions remain that can only be answered using single molecule approaches. Here we report our results from single α7 and neuromuscular junction type nicotinic acetylcholine receptors in mammalian cell membranes. By labeling the receptors with fluorophore-labeled bungarotoxin, we can image individual receptors and count the number of bungarotoxin-binding sites in receptors expressed in HEK 293 cells. Our results indicate that there are two bungarotoxin-binding sites in neuromuscular junction receptors, as expected, and five in α7 receptors, clarifying previous uncertainty. This demonstrates a valuable technique for counting subunits in membrane-bound proteins at the single molecule level, with nonspecialized optics and with higher signal/noise ratios than previous fluorescent protein-based techniques.

publication date

  • November 17, 2010

Research

keywords

  • Bungarotoxins
  • Receptors, Nicotinic

Identity

PubMed Central ID

  • PMC2980733

Scopus Document Identifier

  • 78549242357

Digital Object Identifier (DOI)

  • 10.1016/j.bpj.2010.08.076

PubMed ID

  • 21081055

Additional Document Info

volume

  • 99

issue

  • 10