A modified Western blot protocol for enhanced sensitivity in the detection of a membrane protein

被引：60

作者：

Kaur, Jaspreet ^{[1
]}

Bachhawat, Anand K. ^{[1
]}

机构：

[1] Inst Microbial Technol, Chandigarh 160036, India

来源：

ANALYTICAL BIOCHEMISTRY | 2009年 / 384卷 / 02期

关键词：

SACCHAROMYCES-CEREVISIAE;

D O I：

10.1016/j.ab.2008.10.005

中图分类号：

Q5 [生物化学];

学科分类号：

071010 ; 081704 ;

摘要：

Membrane proteins, owing to their highly hydrophobic nature, have always posed a daunting challenge to biochemists and Structural biologists working on the characterization of these "naughty" proteins. Here we describe a problem that we encountered in the immunodetection of a hemagglutinin (HA) epitope-tagged membrane protein, Hgt1p (high-affinity glutathione transporter from the yeast Saccharomyces cerevisiae), for which little or no signal was observed on the blots with monoclonal antibody, on following the standard Western blot protocol. The introduction of a single step that involved posttransfer incubation oft be blots with sodium dodecyl Sulfate (SDS)/[beta-mercaptoethanol solution at 55 degrees C for 15 min enabled LIS to detect a strong, stable, and reproducible signal for the membrane protein. (C) 2008 Elsevier Inc. All rights reserved.

引用

页码：348 / 349

页数：2

共 8 条

[1] Conditions that allow for effective transfer of membrane proteins onto nitrocellulose membrane in Western blots [J].