大鼠和人谷氨酸转运蛋白GLAST1的稳定异源表达、生化和功能表征。

Biological chemistry Hoppe-Seyler Pub Date : 1995-08-01
W Stoffel, R Blau
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引用次数: 0

摘要

在巨细胞病毒启动子的控制下,通过电穿孔将GLAST1(高亲和力、Na(+)依赖性、cns特异性的l -谷氨酸转运蛋白)转移到人胚胎肾细胞系(HEK293),并永久地表达人和大鼠GLAST1。转染的HEKh GLAST1(人)和HEKrGLAST1(大鼠)细胞系强烈表达谷氨酸摄取系统,该系统具有瞬时表达爪蟾卵母细胞系统中除K+依赖性外的所有生化和电生理特性。这些细胞系为进一步研究这种最重要的兴奋性神经递质摄取系统的生化、生理和药理学研究提供了有价值的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rat and human glutamate transporter GLAST1 stable heterologous expression, biochemical and functional characterization.

Human embryonic kidney cell lines (HEK293) which express heterologously and permanently the human and rat GLAST1 (high affinity, Na(+)-dependent, CNS-specific L-glutamate transporter) have been established by the transfer of the two minigenes under the control of the cytomegalovirus promoter by electroporation. The transfected HEKh GLAST1 (human) and HEKrGLAST1 (rat) cell lines strongly express the glutamate uptake system which exhibits all biochemical and electrophysiological properties determined so far in the transiently expressing Xenopus oocyte system except the K+ dependence. These cell lines are a valuable tool for further biochemical, physiological, and pharmacological studies on this uptake system of the most important excitatory neurotransmitter.

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