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Ligand‐Induced conformational changes in the lactose permease of escherichia coli : Evidence for two binding sites
Author(s) -
Wu Jianhua,
Frillingos Stathis,
Voss John,
Ronald Kaback H.
Publication year - 1994
Publication title -
protein science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.353
H-Index - 175
eISSN - 1469-896X
pISSN - 0961-8368
DOI - 10.1002/pro.5560031214
Subject(s) - lactose permease , chemistry , permease , ligand (biochemistry) , conformational change , quenching (fluorescence) , stereochemistry , fluorescence , biochemistry , escherichia coli , physics , receptor , quantum mechanics , gene
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, β,d‐galactopyranosyl 1‐thio‐β,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‐β,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 K d ≌ 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%. Finally, the EPR spectrum of nitroxide spin‐labeled Val 331 → Cys permease exhibits 2 components with different mobilities, and TDG causes the immobilized component to increase. The results provide evidence for the argument that lac permease has more than a single binding site. TDG binding to a higher affinity site quenches the fluorescence of MIANS‐labeled Val 331 → Cys permease, and occupation of a second lower affinity site causes position 331 to become more accessible from a hydrophobic environment.