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肾髓质提取物中微管蛋白的体外聚合研究。

Studies on in vitro polymerization of tubulin from renal medullary extracts.

作者信息

Barnes L D, Engel A G, Dousa T P

出版信息

Biochim Biophys Acta. 1975 Oct 20;405(2):422-33. doi: 10.1016/0005-2795(75)90107-5.

Abstract

Previous in vivo studies showed that microtubules are involved in the cellular action of vasopressin. In order to analyze the role of renal medullary microtubules, a system was developed which would allow the study of the assembly of tubulin in renal medulla extracts into microtubules in vitro. The assembly of tubulin into microtubules occurred in renal medullary cytosol (100 000 times g supernatant) under specific conditions which include pre-concentration of cytosol by ultrafiltration, the presence of ethylene glycol bis(2-aminoethyl)ether tetraacetic acid (EGTA) and 4 M glycerol, and warming at 37 degrees C. Formation of microtubules, which sedimented at 100 000 times g, was proved by (a) an increase in the apparent [3H]colchicine-binding activity of depolymerized pellets, (b) appearance of typical microtubules as shown by electron microscopy, and (c) by the increase in the quantity of microtubular protein analyzed by polyacrylamide gel electrophoresis. Vinblastine at a concentrationof 10(-6) M completely blocked formation of microtubules. A slight increase of ionized calcium in the polymerization mixture also prevented microtubule assembly; this inhibitory effect of ionized calcium was present at concentrations as low as 10(-4) M. Blockade of microtubule assembly by the increase in concentration of ionized calcium or by vinblastine may be the basis of known inhibitory effect of these two agents upon the hydroosmotic effect of vasopressin in vivo.

摘要

以往的体内研究表明,微管参与了抗利尿激素的细胞作用。为了分析肾髓质微管的作用,开发了一种系统,该系统可用于研究肾髓质提取物中的微管蛋白在体外组装成微管的过程。在特定条件下,微管蛋白在肾髓质胞质溶胶(100000倍重力离心后的上清液)中组装成微管,这些条件包括通过超滤对胞质溶胶进行预浓缩、存在乙二醇双(2-氨基乙基)醚四乙酸(EGTA)和4M甘油,以及在37℃下加热。通过以下方法证明了在100000倍重力下沉淀的微管的形成:(a)解聚沉淀的表观[3H]秋水仙碱结合活性增加;(b)电子显微镜显示典型微管的出现;(c)通过聚丙烯酰胺凝胶电泳分析微管蛋白数量的增加。浓度为10^(-6)M的长春花碱完全阻断了微管的形成。聚合混合物中离子钙的轻微增加也阻止了微管组装;离子钙的这种抑制作用在低至10^(-4)M的浓度下就存在。离子钙浓度增加或长春花碱对微管组装的阻断可能是这两种药物在体内对抗利尿激素的水渗透作用产生已知抑制作用的基础。

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