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用抗肌球蛋白抗体检测应力纤维动力学。

Stress fiber dynamics as probed by antibodies against myosin.

作者信息

Höner B, Jockusch B M

机构信息

Developmental Biology Unit, University of Bielefeld/Federal Republic of Germany.

出版信息

Eur J Cell Biol. 1988 Oct;47(1):14-21.

PMID:3068056
Abstract

The dynamics of microfilament bundles (stress fibers) in tissue culture cells were studied by microinjecting an affinity-purified polyclonal antibody against chicken gizzard myosin. This antibody cross-reacted exclusively with the light chains of nonmuscle myosin and should therefore bind to the head portion of myosin molecules. When injected in high concentrations (13-26 mg/ml), it disrupted stress fibers in a high proportion (60-80%) of rat and chicken embryo fibroblasts, as well as in PtK2 cells. Myosin was found collected in large aggregates probably comprising protein: antibody precipitates, while actin and alpha-actinin were not localized in any defined structures in stress fiber depleted cells. Fibroblasts rounded up, probably because of lack of tension-generating microfilament bundles. After several hours, stress fibers were seen to regrow again in the afflicted cells, even when myosin precipitates and excess antibody were still present. The extent of stress fiber disruption and the time point of their reappearance were dependent on the concentration of the injected antibody.

摘要

通过显微注射针对鸡胗肌球蛋白的亲和纯化多克隆抗体,研究了组织培养细胞中微丝束(应力纤维)的动态变化。该抗体仅与非肌肉肌球蛋白的轻链发生交叉反应,因此应与肌球蛋白分子的头部结合。当以高浓度(13 - 26 mg/ml)注射时,它会破坏高比例(60 - 80%)的大鼠和鸡胚胎成纤维细胞以及PtK2细胞中的应力纤维。发现肌球蛋白聚集形成大的聚集体,可能包含蛋白质:抗体沉淀物,而肌动蛋白和α - 辅肌动蛋白在应力纤维缺失的细胞中未定位在任何特定结构中。成纤维细胞变圆,可能是因为缺乏产生张力的微丝束。数小时后,即使肌球蛋白沉淀物和过量抗体仍然存在,受累细胞中的应力纤维也会再次重新生长。应力纤维破坏的程度及其重新出现的时间点取决于注射抗体的浓度。

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