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在毛细管中使用固定化pH梯度对血小板多肽进行二维凝胶电泳。

Two-dimensional gel electrophoresis of platelet polypeptides with immobilized pH gradients in capillary tubes.

作者信息

Asakawa J

机构信息

Department of Genetics, Radiation Effects Research Foundation, Hiroshima, Japan.

出版信息

Electrophoresis. 1988 Sep;9(9):562-8. doi: 10.1002/elps.1150090916.

Abstract

Two-dimensional electrophoresis (2-DE) with immobilized pH gradient (IPG) gels in capillary tubes was used in the first-dimensional isoelectric focusing (IEF) for the separation of human platelet polypeptides. Two types of IPG tube gels, pH ranges 4-8 and 7-10, containing 8 M urea, 1% Nonidet P-40 and 0.1% pH 3.5-10 Ampholine carrier ampholytes (CA) were prepared by a simple method not requiring special equipment. The addition of CA to both gel and sample solutions was essential in the tube gel IPG system. Proteins were visualized by a modification of Wray's silver-staining technique. The degree of resolution and the number of spots observed on an IPG 2-DE gel with pH 4-8 were comparable with those obtained with O'Farrell's high-resolution 2-DE. Approximately 200 basic polypeptides, which are difficult to separate by conventional CA-based IEF 2-DE or the non-equilibrium pH gradient system, were well resolved by 2-DE with a pH 7-10 IPG tube gel in the first-dimension. The gel patterns with either pH gradient 4-8 or 7-10 were highly reproducible among gels prepared and run simultaneously. These results demonstrated the potential and usefulness of the 2-DE system with IPG gels in capillary tubes.

摘要

在一维等电聚焦(IEF)中,采用毛细管中固定化pH梯度(IPG)凝胶的二维电泳(2-DE)分离人血小板多肽。通过一种无需特殊设备的简单方法制备了两种类型的IPG管凝胶,pH范围分别为4-8和7-10,含有8 M尿素、1% Nonidet P-40和0.1% pH 3.5-10两性电解质载体两性电解质(CA)。在管凝胶IPG系统中,向凝胶和样品溶液中添加CA至关重要。通过改良的Wray银染技术对蛋白质进行可视化。pH 4-8的IPG 2-DE凝胶上的分辨率和观察到的斑点数量与O'Farrell高分辨率2-DE获得的结果相当。大约200种难以通过传统基于CA的IEF 2-DE或非平衡pH梯度系统分离的碱性多肽,在一维中通过pH 7-10的IPG管凝胶2-DE得到了很好的分离。pH梯度为4-8或7-10的凝胶图谱在同时制备和运行的凝胶之间具有高度可重复性。这些结果证明了毛细管中IPG凝胶2-DE系统的潜力和实用性。

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