PMID:12885249

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Citation

Sondej, M, Vázquez-Ibar, JL, Farshidi, A, Peterkofsky, A and Kaback, HR (2003) Characterization of a lactose permease mutant that binds IIAGlc in the absence of ligand. Biochemistry 42:9153-9

Abstract

Enzyme IIA(Glc) of the Escherichia coli phosphoenolpyruvate:glucose phosphotransferase system plays a direct role in regulating inducible transport systems. Dephosphorylated IIA(Glc) binds directly to lactose permease in a reaction that requires binding of a galactosidic substrate. A double-Cys mutation (Ile129 --> Cys/Lys131 --> Cys) was introduced into helix IV of the permease near the IIA(Glc) binding site in cytoplasmic loop IV/V and in the vicinity of the galactoside binding site at the interface of helices IV, V, and VIII. The mutant no longer requires galactoside for IIA(Glc) binding as demonstrated by both a [(125)I]IIA(Glc) binding assay and a newly developed fluorescence anisotropy assay. Further characterization of the mutant shows that it binds substrate with high affinity, but is almost completely defective in all modes of translocation across the cytoplasmic membrane. The data are consistent with the interpretation that the double mutant is locked in an inward-facing conformation.

Links

PubMed Online version:10.1021/bi034406a

Keywords

Amino Acid Substitution/genetics; Binding Sites/genetics; Cysteine/genetics; Escherichia coli/genetics; Escherichia coli/growth & development; Escherichia coli/metabolism; Escherichia coli Proteins/chemistry; Escherichia coli Proteins/genetics; Escherichia coli Proteins/metabolism; Fluorescence Polarization; Galactosides/metabolism; Iodine Radioisotopes/metabolism; Ligands; Lysine/genetics; Membrane Transport Proteins/chemistry; Membrane Transport Proteins/genetics; Membrane Transport Proteins/metabolism; Monosaccharide Transport Proteins; Mutagenesis, Insertional; Phosphoenolpyruvate Sugar Phosphotransferase System/metabolism; Protein Binding/genetics; Protein Transport/genetics; Substrate Specificity/genetics; Symporters

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