Study on the interaction mechanism of lysozyme and bromophenol blue by fluorescence spectroscopy

J Fluoresc. 2008 Jan;18(1):11-5. doi: 10.1007/s10895-007-0228-7. Epub 2007 Aug 8.

Abstract

The interaction of lysozyme with bromophenol blue (BPB) in acetate buffer (pH 6.0) was studied by fluorescence quenching method for the first time. It was found that BPB could conspicuously quench the fluorescence of lysozyme by the static quenching process, possibly due to the binding on the active site near Trp62. The binding parameters including the binding constant and the number of binding site were calculated. The thermodynamic parameters DeltaH degrees, DeltaS degrees and DeltaG degrees at different temperatures were obtained. The formation of lysozyme-BPB complex depended on the cooperation of the hydrophobic and electrostatic forces. And the binding average distance between lysozyme and BPB was determined. The effect of common metal ions on the binding constant of lysozyme-BPB was also examined.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bromphenol Blue / metabolism*
  • Energy Transfer
  • Muramidase / metabolism*
  • Protein Binding
  • Spectrometry, Fluorescence*
  • Thermodynamics

Substances

  • Bromphenol Blue
  • Muramidase