Mechanism of Coomassie brilliant blue G-250 binding to proteins: a hydrophobic assay for nanogram quantities of proteins

• DOI: 10.1007/s00216-008-1996-x
• Publication Date: 2008-03-07T18:05:25Z
• Authors: Christos D. Georgiou; Konstantinos Grin...; George Zervoudakis; Ioannis Papapostolou
• Keywords: 0301 basic medicine; 03 medical and health sciences; Ammonium Sulfate; Rosaniline Dyes; Animals; Proteins; Hydrogen-Ion Concentration; Trichloroacetic Acid; Hydrophobic and Hydrophilic Interactions; Sensitivity and Specificity; Protein Binding

We investigated the mechanism of Coomassie brilliant blue G-250 (CBB) binding to proteins in order to develop a protein assay with the maximum possible sensitivity. We found that the neutral ionic species of CBB binds to proteins by a combination of hydrophobic interactions and heteropolar bonding with basic amino acids. On the basis of these findings, we developed a very sensitive hydrophobic assay for proteins (at the nanogram level) using the hydrophobic reagents ammonium sulfate and trichloroacetic acid under pH conditions that increase neutral species concentration in the assay reagent in order to enhance the binding of more CBB dye molecules per protein molecule than in previous CBB-based assays.