Fluorimetric probes of the individual and competitive binding of 1-anilinonaphthalene-8-sulfonate, eosine and fluorescene to bovine serum albumin

Indian J Biochem Biophys. 1994 Apr;31(2):109-14.

Abstract

Fluorescence of 1-anilinonaphthalene-8-sulfonate (ANS) is greatly enhanced on its binding to bovine serum albumin (BSA). Fluorimetric titration shows that three ANS molecules bind per BSA molecule. The enhanced fluorescence of BSA-ANS is quenched by eosine (EOS); and one EOS physically displaces one ANS bound to BSA. The enhanced fluorescence of free ANS in the hydrophobic environment of the nonionic surfactant Triton X 100 is also quenched by EOS but by an energy transfer mechanism. The dye fluorescene (FLSN) also quenches the fluorescence of BSA-bound ANS, but by the energy transfer mechanism. The binding region of ANS in BSA has been speculated.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anilino Naphthalenesulfonates
  • Binding, Competitive
  • Eosine Yellowish-(YS)
  • Fluoresceins
  • Fluorescent Dyes*
  • Kinetics
  • Serum Albumin, Bovine / chemistry*
  • Serum Albumin, Bovine / metabolism
  • Spectrometry, Fluorescence / methods

Substances

  • Anilino Naphthalenesulfonates
  • Fluoresceins
  • Fluorescent Dyes
  • Serum Albumin, Bovine
  • 1-anilino-8-naphthalenesulfonate
  • Eosine Yellowish-(YS)