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血管加压素异受体功能分子大小的测定

Determination of the functional molecular size of vasopressin isoreceptors.

作者信息

Crause P, Boer R, Fahrenholz F

出版信息

FEBS Lett. 1984 Oct 1;175(2):383-6. doi: 10.1016/0014-5793(84)80773-5.

Abstract

The molecular size of vasopressin receptors in the intact membrane-bound state was determined by radiation inactivation (target size analysis). For the V1 receptor in rat liver a molecular size of (76 +/- 8) kDa was determined. For the V2 receptor in rat kidney and bovine kidney molecular sizes of (95 +/- 4) and (108 +/- 11) kDa were found. Statistical analysis gave evidence for size differences between rat liver and rat kidney receptors or differences between rat liver and bovine kidney receptors, but not between kidney receptors from different species. The results suggest that V1 and V2 receptors can be distinguished by functional properties as well as by their size.

摘要

通过辐射失活(靶大小分析)确定完整膜结合状态下血管加压素受体的分子大小。对于大鼠肝脏中的V1受体,确定其分子大小为(76±8)kDa。对于大鼠肾脏和牛肾脏中的V2受体,分子大小分别为(95±4)kDa和(108±11)kDa。统计分析表明大鼠肝脏和大鼠肾脏受体之间存在大小差异,或大鼠肝脏和牛肾脏受体之间存在差异,但不同物种的肾脏受体之间不存在差异。结果表明,V1和V2受体可通过功能特性及其大小来区分。

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