Ligand-induced conformational changes in the lactose permease of Escherichia coli: evidence for two binding sites

Protein Sci. 1994 Dec;3(12):2294-301. doi: 10.1002/pro.5560031214.

Abstract

By using a lactose permease mutant containing a single Cys residue in place of Val 331 (helix X), conformational changes induced by ligand binding were studied. With right-side-out membrane vesicles containing Val 331-->Cys permease, lactose transport is inactivated by either N-ethylmaleimide (NEM) or 7-diethylamino-3-(4'-maleimidylphenyl)-4-methylcoumarin (CPM). Remarkably, beta,D-galactopyranosyl 1-thio-beta,D-galactopyranoside (TDG) enhances the rate of inactivation by CPM, a hydrophobic sulfhydryl reagent, whereas NEM inactivation is attenuated by the ligand. Val 331-->Cys permease was then purified and studied in dodecyl-beta,D-maltoside by site-directed fluorescence spectroscopy. The reactivity of Val 331-->Cys permease with 2-(4'-maleimidylanilino)-naphthalene-6-sulfonic acid (MIANS) is not changed over a low range of TDG concentrations (< 0.8 mM), but the fluorescence of the MIANS-labeled protein is quenched in a saturable manner (apparent Kd approximately equal to 0.12 mM) without a change in emission maximum. In contrast, over a higher range of TDG concentrations (1-10 mM), the reactivity of Val 331-->Cys permease with MIANS is enhanced and the emission maximum of MIANS-labeled permease is blue shifted by 3-7 nm. Furthermore, the fluorescence of MIANS-labeled Val 331 -->Cys permease is quenched by both acrylamide and iodide, but the former is considerably more effective. A low concentration of TDG (0.2 mM) does not alter quenching by either compound, whereas a higher concentration of ligand (10 mM) decreases the quenching constant for iodide by about 50% and for acrylamide by about 20%.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Anilino Naphthalenesulfonates / pharmacology
  • Bacterial Proteins / antagonists & inhibitors
  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Binding Sites
  • Coumarins / pharmacology
  • Cysteine / chemistry
  • Electron Spin Resonance Spectroscopy
  • Escherichia coli / enzymology*
  • Escherichia coli / genetics
  • Escherichia coli Proteins*
  • Ethylmaleimide / pharmacology
  • Isopropyl Thiogalactoside / pharmacology
  • Lactose / metabolism*
  • Ligands
  • Membrane Transport Modulators
  • Membrane Transport Proteins / antagonists & inhibitors
  • Membrane Transport Proteins / chemistry*
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism
  • Molecular Sequence Data
  • Monosaccharide Transport Proteins*
  • Mutagenesis, Site-Directed
  • Protein Conformation / drug effects*
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / metabolism
  • Spectrometry, Fluorescence
  • Spin Labels
  • Symporters*
  • Thiogalactosides / pharmacology
  • Valine / chemistry

Substances

  • Anilino Naphthalenesulfonates
  • Bacterial Proteins
  • Coumarins
  • Escherichia coli Proteins
  • LacY protein, E coli
  • Ligands
  • Membrane Transport Modulators
  • Membrane Transport Proteins
  • Monosaccharide Transport Proteins
  • Recombinant Fusion Proteins
  • Spin Labels
  • Symporters
  • Thiogalactosides
  • Isopropyl Thiogalactoside
  • 2-(4'-maleimidylanilino)naphthalene-6-sulfonic acid
  • N-(4-(7-diethylamino-4-methylcoumarin-3-yl)phenyl)maleimide
  • thiodigalactoside
  • lactose permease
  • Valine
  • Lactose
  • Cysteine
  • Ethylmaleimide