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高效液相色谱分离及去污剂增溶的整体膜蛋白的完整质谱分析。

High-performance liquid chromatography separation and intact mass analysis of detergent-solubilized integral membrane proteins.

机构信息

Structural Genomics Consortium, University of Oxford, ORCRB, Roosevelt Drive, Oxford OX3 7DQ, UK.

出版信息

Anal Biochem. 2011 Mar 15;410(2):272-80. doi: 10.1016/j.ab.2010.11.008. Epub 2010 Nov 17.

Abstract

We have developed a method for intact mass analysis of detergent-solubilized and purified integral membrane proteins using liquid chromatography-mass spectrometry (LC-MS) with methanol as the organic mobile phase. Membrane proteins and detergents are separated chromatographically during the isocratic stage of the gradient profile from a 150-mm C3 reversed-phase column. The mass accuracy is comparable to standard methods employed for soluble proteins; the sensitivity is 10-fold lower, requiring 0.2-5 μg of protein. The method is also compatible with our standard LC-MS method used for intact mass analysis of soluble proteins and may therefore be applied on a multiuser instrument or in a high-throughput environment.

摘要

我们开发了一种使用甲醇作为有机流动相的液相色谱-质谱联用(LC-MS)方法,用于分析去污剂溶解和纯化的完整膜蛋白的质荷比。在梯度轮廓的等度阶段,膜蛋白和去污剂在 150-mm C3 反相柱上进行色谱分离。质荷比精度与用于可溶性蛋白的标准方法相当;灵敏度低 10 倍,需要 0.2-5 μg 的蛋白质。该方法也与我们用于可溶性蛋白完整质荷比分析的标准 LC-MS 方法兼容,因此可以在多用户仪器或高通量环境中应用。

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