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On the relationship of amino acid composition to silver staining of proteins in electrphoresis gels
Author(s) -
Gersten Douglas M.,
Wolf Pamela H.,
Ledley Robert S.,
Rodriguez Lewis V.,
Zapolski Edward J.
Publication year - 1986
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/elps.1150070708
Subject(s) - staining , reagent , silver stain , silver nitrate , amino acid , chemistry , stain , electrophoresis , chromatography , polyacrylamide gel electrophoresis , biochemistry , nuclear chemistry , biology , microbiology and biotechnology , organic chemistry , enzyme , genetics
Development of techniques for silver staining of proteins separated by polyacrylamide gel electrophoresis has increased experimental detection limits. However, the precise basis for the reaction between silver and polypeptides is still unclear and, depending upon the choice of silver reagent, may even differ. We compared protein stain intensity with silver diamine (ammoniacal silver) and silver nitrate reagents based on amino acid composition by determining the protein amount required to generate an arbitrary staining intensity and then calculating moles of each amino acid present in some representative proteins. We compared these values for each amino acid, taken singly, as well as for combinations of two and more. In no case could staining be attributed entirely to specific or classes of amino acids, thus supporting the argument that an inherent difference exists between primary reactive centers for the two staining reagents.