在低盐缓冲液中,由摩尔过量的ATP引起的肌动蛋白聚合。

T Ikkai, H Kondo
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引用次数: 1

摘要

通过稀释引起的肌动蛋白聚合先前有报道,当肌动蛋白在低盐缓冲液a (0.1 mM ATP, 0.1 mM CaCl2, 2 mM Tris-HCl, pH 8.0, 5 mM 2-巯基乙醇,1 mM NaN3)中稀释到4.0微克/毫升时,导致ATP超过肌动蛋白1000倍的摩尔过量。在缓冲液B (0.1 mM CaCl2, 2 mM Tris-HCl, pH 8.0, 1 mM NaN3)中加入超过肌动蛋白1000倍摩尔量的ATP形成细丝,然后通过凝胶过滤分离。当使用Dowex-1从这些细丝中去除ATP时,发生解聚。因此,肌动蛋白稀释或加入ATP引起的可逆聚合可归因于ATP在肌动蛋白低亲和力位点的结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polymerization of actin induced by a molar excess of ATP in a low salt buffer.

The polymerization of actin induced by dilution has previously been reported, where a 1000-fold molar excess of ATP over actin resulted when actin was diluted to 4.0 micrograms/ml in low salt buffer A (0.1 mM ATP, 0.1 mM CaCl2, 2 mM Tris-HCl, pH 8.0, 5 mM 2-mercaptoethanol, 1 mM NaN3). Filaments formed by the addition of ATP to a 1000-fold molar excess over actin in buffer B (0.1 mM CaCl2, 2 mM Tris-HCl, pH 8.0, 1 mM NaN3) were then separated by gel-filtration. When ATP was removed from these filaments using Dowex-1, depolymerization occurred. Thus, the reversible polymerization induced by the dilution of actin or by addition of ATP can be ascribed to the binding of ATP at the low affinity site of actin.

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