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通过蓝色天然聚丙烯酰胺凝胶电泳分析膜蛋白复合物

Analysis of membrane protein complexes by blue native PAGE.

作者信息

Reisinger Veronika, Eichacker Lutz Andreas

机构信息

Ludwig Maximilian University, Munich, Germany.

出版信息

Proteomics. 2006 Sep;6 Suppl 2:6-15. doi: 10.1002/pmic.200600553.

Abstract

Blue native polyacryamide gel electrophoresis is a special case of native electrophoresis for high resolution separation of enzymatically active protein complexes from tissue homogenates and cell fractions. The method is powerful between 10 and 10,000 kDa. Also membrane protein complexes are separated well after solubilization of complexes with mild neutral detergents. The separation principle relies on binding of Coomassie blue G250 which provides negative charges to the surface of the protein. During migration to the anode, protein complexes are separated according to molecular mass and/or size and high resolution is obtained by the decreasing pore size of a polyacrylamide gradient gel. The principles of 2-dimensional blue native sodium dodecyl sulfate polyacrylamide gel electrophoresis are presented here together with a practical step-by-step guide to performing the method in the laboratory.

摘要

蓝色天然聚丙烯酰胺凝胶电泳是天然电泳的一种特殊形式,用于从组织匀浆和细胞组分中高分辨率分离具有酶活性的蛋白质复合物。该方法在10至10,000 kDa范围内效果显著。在用温和的中性去污剂溶解复合物后,膜蛋白复合物也能得到很好的分离。分离原理基于考马斯亮蓝G250的结合,它为蛋白质表面提供负电荷。在向阳极迁移的过程中,蛋白质复合物根据分子量和/或大小进行分离,通过聚丙烯酰胺梯度凝胶孔径的减小可获得高分辨率。本文介绍了二维蓝色天然十二烷基硫酸钠聚丙烯酰胺凝胶电泳的原理,并提供了在实验室中进行该方法的实用分步指南。

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