INVESTIGADORES
BOUZAT Cecilia Beatriz
artículos
Título:
Nicotinic Receptor Fourth Transmembrane Domain. Hydrogen Bonding by conserved threonine contributes to channel gating kinetics
Autor/es:
BOUZAT, C.; BARRANTES, F.J.; SINE, S.M.
Revista:
JOURNAL OF GENERAL PHYSIOLOGY
Editorial:
ROCKEFELLER UNIV PRESS
Referencias:
Año: 2000 vol. 115 p. 663 - 672
ISSN:
0022-1295
Resumen:
The fourth transmembrane domain (M4) of the nicotinic acetylcholine receptor (AChR) contributes to the kinetics of activation, yet its close association with the lipid bilayer makes it the outermost of the transmembrane domains. To investigate mechanistic and structural contributions of M4 to AChR activation, we systematically mutated alphaT422, a conserved residue that has been labeled by hydrophobic probes, and evaluated changes in rate constants underlying ACh binding and channel gating steps. Aromatic and nonpolar mutations of alphaT422 selectively affect the channel gating step, slowing the rate of opening two- to sevenfold, and speeding the rate of closing four- to ninefold. Additionally, kinetic modeling shows a second doubly liganded open state for  aromatic and nonpolar mutations. In contrast, serine and asparagine mutations of alphaT422 largely preserve the kinetics of the wild-type AChR. Thus, rapid and efficient gating of the AChR channel depends on a hydrogen bond involving the side chain at position 422 of the M4 transmembrane domain.