Silver staining of proteins on electroblotting membranes and intensification of silver staining of proteins separated by polyacrylamide gel electrophoresis

被引:47
|
作者
Sorensen, BK
Hojrup, P
Ostergård, E
Jorgensen, CS
Enghild, J
Ryder, LR
Houen, G
机构
[1] Statens Serum Inst, Dept Res & Dev, DK-2300 Copenhagen S, Denmark
[2] Univ Southern Denmark, Dept Biochem & Mol Biol, DK-5230 Odense, Denmark
[3] Aarhus Univ, Dept Mol & Struct Biol, DK-8000 Aarhus C, Denmark
关键词
proteins; electrophoresis; silver intensification; mass spectrometry; Gallyas' stain;
D O I
10.1006/abio.2001.5604
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A fast and convenient method for silver staining of proteins on electroblotting membranes was developed based on Gallyas' histochemical intensifier and applied to human endothelial cell proteins separated by one- and two-dimensional electrophoresis and electroblotted to polyvinyl difluoride membranes. The method allowed detection of proteins on membranes with a sensitivity equal to the sensitivity of the most sensitive silver-staining protocols for electrophoresis gels. Also, the method was compatible with preceding immunostaining on the same membrane. Furthermore, an intensifying method for proteins in silver-stained SDS-PAGE gels was developed based on Gallyas' histochemical intensifier. This method was applied to proteins separated by one- and two-dimensional gel electrophoresis and visualized by one of several silver-staining methods. Maximal intensification was achieved for the less sensitive but fast acidic silver-staining protocols, but even for the very sensitive alkaline protocols a significant increase in signal to noise ratio was obtained. In particular, negatively stained or invisible proteins on the silver-stained gets were found to be visualized by the Gallyas stain. Proteins from silver-stained and Gallyas-stained gels were identified by mass spectrometry, and the intensification procedure was fully compatible with mass spectrometry. (C) 2002 Elsevier Science (USA).
引用
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页码:33 / 41
页数:9
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