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大鼠囊泡乙酰胆碱转运体的特异性

Specificity of the rat vesicular acetylcholine transporter.

作者信息

Kim Myung-Hee, Lu Mei, Rogers Gary, Parsons Stanley, Hersh Louis B

机构信息

Department of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, Kentucky 40536-0084, USA.

出版信息

Neurochem Res. 2003 Apr;28(3-4):473-6. doi: 10.1023/a:1022804903088.

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.

摘要

蛋白激酶A缺陷型PC12细胞系PC12A123.7既缺乏胆碱乙酰转移酶,也缺乏囊泡乙酰胆碱转运体。该细胞系已被用于建立稳定转染的细胞系,该细胞系表达重组大鼠囊泡乙酰胆碱转运体,该转运体可被正确转运至小突触囊泡。大鼠囊泡乙酰胆碱转运体转运乙酰胆碱的最大速率为1.45 nmol乙酰胆碱/分钟/毫克蛋白,其转运的Km值为2.5 mM。该转运体与vesamicol结合的解离常数(Kd)为7.5 nM。测定了乙酰胆碱结构类似物抑制乙酰胆碱摄取和vesamicol结合的能力。结果表明,与电鳐囊泡乙酰胆碱转运体一样,哺乳动物的转运体也能结合多种乙酰胆碱类似物。

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