Structural and functional characterization of human CXCR4 as a chemokine receptor and HIV-1 co-receptor by mutagenesis and molecular modeling studies

J Biol Chem. 2001 Nov 16;276(46):42826-33. doi: 10.1074/jbc.M106582200. Epub 2001 Sep 10.

Abstract

The human CXC chemokine receptor 4 (CXCR4) is a receptor for the chemokine stromal cell-derived factor (SDF-1alpha) and a co-receptor for the entry of specific strains of human immunodeficiency virus type I (HIV-1). CXCR4 is also recognized by an antagonistic chemokine, the viral macrophage inflammatory protein II (vMIP-II) encoded by human herpesvirus type VIII. SDF-1alpha or vMIP-II binding to CXCR4 can inhibit HIV-1 entry via this co-receptor. An approach combining protein structural modeling and site-directed mutagenesis was used to probe the structure-function relationship of CXCR4, and interactions with its ligands SDF-1alpha and vMIP-II and HIV-1 envelope protein gp120. Hypothetical three-dimensional structures were proposed by molecular modeling studies of the CXCR4.SDF-1alpha complex, which rationalize extensive biological information on the role of CXCR4 in its interactions with HIV-1 envelope protein gp120. With site-directed mutagenesis, we have identified that the amino acid residues Asp (D20A) and Tyr (Y21A) in the N-terminal domain and the residue Glu (E268A) in extracellular loop 3 (ECL3) are involved in ligand binding, whereas the mutation Y190A in extracellular loop 2 (ECL2) impairs the signaling mediated by SDF-1alpha. As an HIV-1 co-receptor, we found that the N-terminal domain, ECL2, and ECL3 of CXCR4 are involved in HIV-1 entry. These structural and mutational studies provide valuable information regarding the structural basis for CXCR4 activity in chemokine binding and HIV-1 viral entry, and could guide the design of novel targeted inhibitors.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aspartic Acid / chemistry
  • Calcium / metabolism
  • Cell Line
  • Chemokines / chemistry*
  • Flow Cytometry
  • Genes, Reporter
  • Glutamic Acid / chemistry
  • HIV-1 / metabolism*
  • Humans
  • Ligands
  • Models, Molecular
  • Mutagenesis, Site-Directed
  • Mutation
  • Plasmids / metabolism
  • Protein Binding
  • Protein Conformation
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • Receptors, CXCR4 / chemistry*
  • Receptors, CXCR4 / genetics
  • Receptors, CXCR4 / physiology*
  • Recombinant Fusion Proteins / metabolism
  • Recombinant Proteins / metabolism
  • Signal Transduction
  • Structure-Activity Relationship
  • Tyrosine / chemistry

Substances

  • Chemokines
  • Ligands
  • Receptors, CXCR4
  • Recombinant Fusion Proteins
  • Recombinant Proteins
  • Aspartic Acid
  • Glutamic Acid
  • Tyrosine
  • Calcium