Ligand interactions with the acetylcholine receptor from Torpedo californica. Extensions of the allosteric model for cooperativity to half-of-site activity
- 24 August 1976
- journal article
- research article
- Published by American Chemical Society (ACS) in Biochemistry
- Vol. 15 (17) , 3890-3901
- https://doi.org/10.1021/bi00662a037
Abstract
The solubilized acetylcholine (ACh) receptor from T. californica showed positive cooperativity in ACh binding with a dissociation constant of 1.2 .times. 10-8 M. Blockade of ACh binding by nicotine was competitive; blockade by d-tubocurarine appeared to result from an allosteric interaction that altered half of the ACh binding sites to a lower affinity form; decamethonium blockade displayed properties of competitive and allosteric inhibition suggesting less specificity for decamethonium binding than seen with either nicotine or d-tubocurarine inhibition data were evaluated by several possible models involving either differential competitive inhibition or allosteric inhibition. The data were best described by the allosteric model.This publication has 7 references indexed in Scilit:
- Cooperativities in the binding of acetylcholine to its receptorBiochemical Pharmacology, 1973
- On the application of “a plausible model” of allosteric proteins to the receptor for acetylcholineJournal of Theoretical Biology, 1967
- ON THE COOPERATIVITY OF BIOLOGICAL MEMBRANESProceedings of the National Academy of Sciences, 1967
- On the nature of allosteric transitions: Implications of non-exclusive ligand bindingJournal of Molecular Biology, 1966
- Sulfur and selenium isologs related to acetylcholine and choline IV. Activity in the electroplax preparationBiochemical Pharmacology, 1966
- Comparison of Experimental Binding Data and Theoretical Models in Proteins Containing Subunits*Biochemistry, 1966
- A study of the ‘desensitization’ produced by acetylcholine at the motor end‐plateThe Journal of Physiology, 1957