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细胞核中存在肌球蛋白I的证据。

Evidence for the presence of myosin I in the nucleus.

作者信息

Nowak G, Pestic-Dragovich L, Hozák P, Philimonenko A, Simerly C, Schatten G, de Lanerolle P

机构信息

Department of Physiology and Biophysics, University of Illinois, Chicago, Illinois 60612-7246, USA.

出版信息

J Biol Chem. 1997 Jul 4;272(27):17176-81. doi: 10.1074/jbc.272.27.17176.

Abstract

We produced and affinity-purified polyclonal antibodies to adrenal myosin I. These antibodies recognize adrenal myosin I by Western blot analysis (116 kDa) and inhibit the actin-activated ATPase activity of purified adrenal myosin I. They also recognize a 120-kDa protein in extracts prepared from many different cell lines. Fluorescence microscopy demonstrated the presence of immunoreactive material in the perinuclear region, the leading edges, and the nuclei of 3T3 cells. Fluorescence microscopy also demonstrated nuclear staining in mouse oocytes at the germinal vesicle stage and in the pronuclei during fertilization. Confocal and immunoelectron microscopy confirmed the intranuclear localization. Electron microscopy also demonstrated staining of structures in nucleoli that are thought to be associated with rDNA transcription. Western blot analyses revealed the presence of the 120-kDa protein in extracts prepared from nuclei that are apparently free of cytosolic contamination. The same nuclear protein binds 125I-calmodulin and is photoaffinity labeled with [alpha-32P]ATP. The 120-kDa protein was partially purified from twice washed nuclei using ammonium sulfate fractionation and gel filtration chromatography. Column fractions containing 120-kDa protein as revealed by Western blot analysis also contain K+-EDTA ATPase activity. The 120-kDa protein was also shown to bind actin in the absence, but not the presence, of ATP. Since K+-EDTA ATPase activity, actin, and ATP binding are defining features of the members of the myosin superfamily of proteins, we propose that the 120-kDa protein is a previously undescribed myosin I isoform that is an intranuclear actin-based molecular motor.

摘要

我们制备并亲和纯化了针对肾上腺肌球蛋白I的多克隆抗体。这些抗体通过蛋白质免疫印迹分析(116 kDa)识别肾上腺肌球蛋白I,并抑制纯化的肾上腺肌球蛋白I的肌动蛋白激活的ATP酶活性。它们还能识别从许多不同细胞系制备的提取物中的一种120 kDa的蛋白质。荧光显微镜检查显示,在3T3细胞的核周区域、前缘和细胞核中存在免疫反应性物质。荧光显微镜检查还显示,在生发泡期的小鼠卵母细胞和受精过程中的原核中有核染色。共聚焦显微镜和免疫电子显微镜证实了其核内定位。电子显微镜检查还显示核仁中一些被认为与rDNA转录相关的结构有染色。蛋白质免疫印迹分析显示,从明显无胞质污染的细胞核制备的提取物中存在120 kDa的蛋白质。相同的核蛋白能结合125I-钙调蛋白,并被[α-32P]ATP进行光亲和标记。使用硫酸铵分级分离和凝胶过滤色谱法从经过两次洗涤的细胞核中部分纯化了120 kDa的蛋白质。蛋白质免疫印迹分析显示含有120 kDa蛋白质的柱级分也含有K+-EDTA ATP酶活性。还显示120 kDa的蛋白质在无ATP存在时能结合肌动蛋白,但在有ATP存在时则不能。由于K+-EDTA ATP酶活性、肌动蛋白和ATP结合是肌球蛋白超家族蛋白质成员的决定性特征,我们提出120 kDa的蛋白质是一种先前未描述的肌球蛋白I异构体,是一种基于肌动蛋白的核内分子马达。

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