» Articles » PMID: 6933499

Direct Spectroscopic Studies of Cation Translocation by Torpedo Acetylcholine Receptor on a Time Scale of Physiological Relevance

Overview
Specialty Science
Date 1980 Aug 1
PMID 6933499
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

The kinetics of carbamoylcholine-mediated cation transport across the membrane of vesicles containing acetylcholine receptor have been measured on the physiologically relevant time scale of a few milliseconds. The stopped-flow spectroscopic approach utilizes thallium(I) as the cation transported into sealed vesicles containing a water-soluble fluorophore. Upon entry of thallium(I), fluorescence quenching occurs by a heavy atom effect. Rapid thallium translocation into the vesicles is mediated by cholinergic agonists and is blocked by antagonists and neurotoxins and by desensitization. The kinetics of thallium transport are used to demonstrate that the four polypeptides known to comprise the receptor are the only protein components necessary for cation translocation. The kinetics of thallium(I) transport at saturating agonist concentrations are also used to calculate the apparent ion transport rate for a single receptor. The minimal value obtained is close to that for a single activated channel determined in vivo. This demonstrates that the physiological receptor has been isolated in intact form.

Citing Articles

Screening for bilayer-active and likely cytotoxic molecules reveals bilayer-mediated regulation of cell function.

Peyear T, Andersen O J Gen Physiol. 2023; 155(4).

PMID: 36763053 PMC: 9948646. DOI: 10.1085/jgp.202213247.


Synthetic Analogues of the Snail Toxin 6-Bromo-2-mercaptotryptamine Dimer (BrMT) Reveal That Lipid Bilayer Perturbation Does Not Underlie Its Modulation of Voltage-Gated Potassium Channels.

Dockendorff C, Gandhi D, Kimball I, Eum K, Rusinova R, Ingolfsson H Biochemistry. 2018; 57(18):2733-2743.

PMID: 29616558 PMC: 6007853. DOI: 10.1021/acs.biochem.8b00292.


Stopped-Flow Fluorometric Ion Flux Assay for Ligand-Gated Ion Channel Studies.

Posson D, Rusinova R, Andersen O, Nimigean C Methods Mol Biol. 2017; 1684:223-235.

PMID: 29058195 PMC: 5971093. DOI: 10.1007/978-1-4939-7362-0_17.


Exchange of Gramicidin between Lipid Bilayers: Implications for the Mechanism of Channel Formation.

Lum K, Ingolfsson H, Koeppe 2nd R, Andersen O Biophys J. 2017; 113(8):1757-1767.

PMID: 29045870 PMC: 5647621. DOI: 10.1016/j.bpj.2017.08.049.


Clinical concentrations of chemically diverse general anesthetics minimally affect lipid bilayer properties.

Herold K, Sanford R, Lee W, Andersen O, Hemmings Jr H Proc Natl Acad Sci U S A. 2017; 114(12):3109-3114.

PMID: 28265069 PMC: 5373365. DOI: 10.1073/pnas.1611717114.


References
1.
Lester H . The response to acetylcholine. Sci Am. 1977; 236(2):106-16, 118. DOI: 10.1038/scientificamerican0277-106. View

2.
Elliott J, Blanchard S, Wu W, Miller J, Strader C, Hartig P . Purification of Torpedo californica post-synaptic membranes and fractionation of their constituent proteins. Biochem J. 1980; 185(3):667-77. PMC: 1161444. DOI: 10.1042/bj1850667. View

3.
Anderson C, Stevens C . Voltage clamp analysis of acetylcholine produced end-plate current fluctuations at frog neuromuscular junction. J Physiol. 1973; 235(3):655-91. PMC: 1350786. DOI: 10.1113/jphysiol.1973.sp010410. View

4.
Nickel E, Potter L . Ultrastructure of isolated membranes of Torpedo electric tissue. Brain Res. 1973; 57(2):508-17. DOI: 10.1016/0006-8993(73)90158-3. View

5.
Quast U, Schimerlik M, RAFTERY M . Ligand-induced changes in membrane-bound acetylcholine receptor observed by ethidium fluorescence. 2. Stopped-flow studies with agonists and antagonists. Biochemistry. 1979; 18(10):1891-901. DOI: 10.1021/bi00577a007. View