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Specificity of the Rat Vesicular Acetylcholine Transporter
Authors:Kim  Myung-Hee  Lu   Mei  Rogers   Gary  Parsons   Stanley  Hersh   Louis B.
Affiliation:(1) Department of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, Kentucky, 40536-0084;(2) Department of Chemistry, University of California at Santa Barbara, Santa Barbara, California, 93106;(3) Department of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, Kentucky, 40536-0084
Abstract:
The protein kinase A–deficient PC12 cell line PC12A123.7 lacks both choline acetyltransferase and the vesicular acetylcholine transporter. This cell line has been used to establish a stably transfected cell line expressing recombinant rat vesicular acetylcholine transporter that is appropriately trafficked to small synaptic vesicles. Acetylcholine is transported by the rat vesicular acetylcholine transporter at a maximal rate of 1.45 nmol acetylcholine/min/mg protein and exhibits a Km for transport of 2.5 mM. The transporter binds vesamicol with a Kd of 7.5 nM. The ability of structural analogs of acetylcholine to inhibit both acetylcholine uptake and vesamicol binding was measured. The results demonstrate that like Torpedo vesicular acetylcholine transporter, the mammalian transporter can bind a diverse group of acetylcholine analogs.
Keywords:Vesicular acetylcholine transporter  acetylcholine transport  vesamicol binding  acetylcholine analogs  inhibition  kinetics
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