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中枢神经系统膜组分中微管蛋白的特性分析。

The characterization of tubulin in CNS membrane fractions.

作者信息

Strocchi P, Brown B A, Young J D, Bonventre J A, Gilbert J M

出版信息

J Neurochem. 1981 Nov;37(5):1295-307. doi: 10.1111/j.1471-4159.1981.tb04681.x.

Abstract

Rough endoplasmic reticulum (RER), smooth endoplasmic reticulum (SER), and a plasma membrane (PM) fraction enriched in synaptic membranes were isolated from rat forebrain. The proteins in these membrane fractions were analyzed by two-dimensional gel electrophoresis (2DGE) in the isoelectric range of 5.1 to 6.0 by a modification of the O'Farrell procedure. Proteins were detected by Coomassie Brilliant Blue staining of the electrophoretograms. The results of these analyses were compared with 2DGE analysis of cytosol proteins, with particular attention given to tubulin subunits and actin. The RER contained one major protein (53K 5.4) in the beta-tubulin region with a molecular weight of 53,000 and an isoelectric point of 5.4. The SER contained at least two major proteins in the alpha-tubulin region; one with a migration identical to 53K 5.4 and other proteins with slightly higher apparent molecular weights and more acidic isoelectric points (54K, 5.4 to 5.3), identical to cytoplasmic beta-tubulin. The PM fraction also contained multiple overlapping proteins (54K, 5.4 to 5.3) in the beta-tubulin area and a trace amount of the 53K 5.4 protein. The proteins in the beta-tubulin region were removed from the 2DGE electrophoretogram and digested by Staphylococcus aureus V8 protease, and the peptides separated on one-dimensional polyacrylamide gels. The peptide patterns of 53K 5.4 protein from RER and SER were almost identical and differed significantly from the cytoplasmic beta-tubulin pattern; however, the peptide maps of the PM and SER beta-tubulin region were identical to the cytoplasmic beta-tubulin. The 2DGE analysis of RER did not contain proteins in the region of cytoplasmic alpha-tubulin. SER and PM contained proteins in the alpha-tubulin region with a similar, but not identical, peptide analysis to cytoplasmic alpha-tubulin. Significant amounts of actin were detected in 2DGE analysis of SER and PM, and the peptide analysis of the actin was identical to the cytoplasmic actin analysis. The RER fraction contained only trace amounts of actin. The cytosol and all membrane fractions contained a protein (68K 5.6) found among microtubule-associated proteins, as judged by molecular weight and isoelectric point. Several proteins present in all membrane fractions (61K 5.1 and 58K 5.1) bound to concanavalin A agarose.

摘要

从大鼠前脑分离出粗面内质网(RER)、滑面内质网(SER)以及富含突触膜的质膜(PM)组分。通过对奥法雷尔方法进行改进,在5.1至6.0的等电范围内,采用二维凝胶电泳(2DGE)对这些膜组分中的蛋白质进行分析。通过考马斯亮蓝对电泳图谱进行染色来检测蛋白质。将这些分析结果与胞质溶胶蛋白质的二维凝胶电泳分析结果进行比较,特别关注微管蛋白亚基和肌动蛋白。RER在β-微管蛋白区域含有一种主要蛋白质(53K 5.4),其分子量为53,000,等电点为5.4。SER在α-微管蛋白区域至少含有两种主要蛋白质;一种迁移情况与53K 5.4相同,其他蛋白质的表观分子量略高,等电点更偏酸性(54K,5.4至5.3),与胞质β-微管蛋白相同。PM组分在β-微管蛋白区域也含有多种重叠蛋白质(54K,5.4至5.3)以及微量的53K 5.4蛋白质。将二维凝胶电泳图谱中β-微管蛋白区域的蛋白质去除,用金黄色葡萄球菌V8蛋白酶进行消化,然后在一维聚丙烯酰胺凝胶上分离肽段。来自RER和SER的53K 5.4蛋白质的肽段图谱几乎相同,与胞质β-微管蛋白图谱有显著差异;然而,PM和SER的β-微管蛋白区域的肽图与胞质β-微管蛋白相同。RER的二维凝胶电泳分析在胞质α-微管蛋白区域不含蛋白质。SER和PM在α-微管蛋白区域含有蛋白质,其肽段分析与胞质α-微管蛋白相似但不完全相同。在SER和PM的二维凝胶电泳分析中检测到大量肌动蛋白,其肌动蛋白的肽段分析与胞质肌动蛋白分析相同。RER组分仅含有微量肌动蛋白。根据分子量和等电点判断,胞质溶胶和所有膜组分都含有一种微管相关蛋白中发现的蛋白质(68K 5.6)。所有膜组分中存在的几种蛋白质(61K 5.1和58K 5.1)与伴刀豆球蛋白A琼脂糖结合。

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