1. Site-directed mutagenesis of CCR2 identified amino acid residues in transmembrane helices 1, 2, and 7 important for MCP-1 binding and biological functions.
- Author
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Gavrilin MA, Gulina IV, Kawano T, Dragan S, Chakravarti L, and Kolattukudy PE
- Subjects
- Adenylyl Cyclase Inhibitors, Adenylyl Cyclases metabolism, Amino Acid Sequence, Amino Acids genetics, Calcium metabolism, Cell Line, Cell Membrane chemistry, Chemokine CCL2 pharmacology, Chemotaxis drug effects, Chemotaxis genetics, Cytoskeleton drug effects, Cytoskeleton genetics, Cytoskeleton metabolism, Gene Expression Regulation, Humans, Microscopy, Confocal, Molecular Sequence Data, Protein Binding, Protein Structure, Secondary, Pseudopodia drug effects, Pseudopodia genetics, Pseudopodia metabolism, Receptors, CCR2, Receptors, Chemokine genetics, Signal Transduction, Amino Acids metabolism, Cell Membrane metabolism, Chemokine CCL2 metabolism, Mutagenesis, Site-Directed genetics, Receptors, Chemokine chemistry, Receptors, Chemokine metabolism
- Abstract
Monocyte chemotactic protein-1 (MCP-1) binds its G-protein-coupled seven transmembrane (TM) receptor, CCR2B, and causes infiltration of monocytes/macrophages into areas of injury, infection or inflammation. To identify functionally important amino acid residues in CCR2B, we made specific mutations of nine residues selected on the basis of conservation in chemokine receptors and located TM1 (Tyr(49)), TM2 (Leu(95)), TM3 (Thr(117) and Tyr(120)), and TM7 (Ala(286), Thr(290), Glu(291), and His(297)) and in the extracellular loop 3 (Glu(278)). MCP-1 binding was drastically affected only by mutations in TM7. Reversing the charge at Glu(291) (E291K) and at His(297) (H297D) prevented MCP binding although substitution with Ala at either site had little effect, suggesting that Glu(291) and His(297) probably stabilize TM7 by their ionic interaction. E291A elicited normal Ca(2+) influx. H297A, Y49F in TM1 and L95A in TM2 that showed normal MCP-1 binding did not elicit Ca(2+) influx and elicited no adenylate cyclase inhibition at any MCP-1 concentration. MCP-1 treatment of HEK293 cells caused lamellipodia formation only when they expressed CCR2B. The mutants that showed no Ca(2+) influx and adenylate cyclase inhibition by MCP-1 treatment showed lamellipodia formation and chemotaxis. Our results show that induction of lamellipodia formation, but not Ca(2+) influx and adenylate cyclase inhibition, is necessary for chemotaxis.
- Published
- 2005
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