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肌动蛋白丝网络的力学性质取决于肌动蛋白单体的制备、聚合条件和储存情况。

Mechanical properties of actin filament networks depend on preparation, polymerization conditions, and storage of actin monomers.

作者信息

Xu J, Schwarz W H, Käs J A, Stossel T P, Janmey P A, Pollard T D

机构信息

Department of Biophysics and Biophysical Chemistry, School of Medicine, Johns Hopkins University, Baltimore, Maryland 21205, USA.

出版信息

Biophys J. 1998 May;74(5):2731-40. doi: 10.1016/S0006-3495(98)77979-2.

Abstract

This study investigates possible sources for the variance of more than two orders of magnitude in the published values for the shear moduli of purified actin filaments. Two types of forced oscillatory rheometers used in some of our previous work agree within a factor of three for identical samples. Polymers assembled in EGTA and Mg2+ from fresh, gel-filtered ATP-actin at 1 mg/ml typically have an elastic storage modulus (G') of approximately 1 Pa at a deformation frequency of 0.1-1 Hz. G' is slightly higher when actin is polymerized in KCl with Ca2+ and Mg2+. Gel filtration removes minor contaminants from actin but has little effect on G' for most preparations of actin from acetone powder. Storage of actin monomers without frequent changes of buffer containing fresh ATP and dithiothreitol can result in changes that increase the G' of filaments by more than a factor of 10. Frozen storage can preserve the properties of monomeric actin, but care is necessary to prevent protein denaturation or aggregation due to freezing or thawing.

摘要

本研究调查了纯化肌动蛋白丝剪切模量已发表值中超过两个数量级变化的可能来源。在我们之前的一些工作中使用的两种类型的强迫振荡流变仪,对于相同的样品,其测量结果相差不超过三倍。在1 mg/ml的新鲜、经凝胶过滤的ATP-肌动蛋白中,于EGTA和Mg2+中组装的聚合物,在0.1 - 1 Hz的变形频率下,其弹性储能模量(G')通常约为1 Pa。当肌动蛋白在含有Ca2+和Mg2+的KCl中聚合时,G'略高。凝胶过滤可去除肌动蛋白中的微量污染物,但对于大多数从丙酮粉末制备的肌动蛋白制剂,对G'影响不大。在不频繁更换含有新鲜ATP和二硫苏糖醇的缓冲液的情况下储存肌动蛋白单体,可能会导致变化,使细丝的G'增加超过10倍。冷冻保存可保留单体肌动蛋白的特性,但必须小心防止因冷冻或解冻导致蛋白质变性或聚集。

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本文引用的文献

1
G-actin:preparation by gel filtration and evidence for a double stranded structure.
Biochem Biophys Res Commun. 1963 Jul 10;12:34-8. doi: 10.1016/0006-291x(63)90409-1.
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