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Solution Structure of CCL19 and Identification of Overlapping CCR7 and PSGL-1 Binding Sites.

Title: Solution Structure of CCL19 and Identification of Overlapping CCR7 and PSGL-1 Binding Sites.
Authors: Veldkamp CT; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; ‡Department of Biochemistry, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, Wisconsin 53226, United States.; Kiermaier E; §IST Austria (Institute for Science and Technology Austria), 3400 Klosterneuburg, Austria.; Gabel-Eissens SJ; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Gillitzer ML; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Lippner DR; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; DiSilvio FA; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Mueller CJ; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Wantuch PL; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Chaffee GR; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Famiglietti MW; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Zgoba DM; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Bailey AA; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Bah Y; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Engebretson SJ; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Graupner DR; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Lackner ER; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; LaRosa VD; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Medeiros T; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Olson ML; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Phillips AJ; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Pyles H; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Richard AM; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Schoeller SJ; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Touzeau B; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Williams LG; †Department of Chemistry, University of Wisconsin-Whitewater, 800 West Main Street, Whitewater, Wisconsin 53190, United States.; Sixt M; §IST Austria (Institute for Science and Technology Austria), 3400 Klosterneuburg, Austria.; Peterson FC; ‡Department of Biochemistry, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, Wisconsin 53226, United States.
Source: Biochemistry [Biochemistry] 2015 Jul 14; Vol. 54 (27), pp. 4163-6. Date of Electronic Publication: 2015 Jul 06.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Language: English
Journal Info: Publisher: American Chemical Society Country of Publication: United States NLM ID: 0370623 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1520-4995 (Electronic) Linking ISSN: 00062960 NLM ISO Abbreviation: Biochemistry Subsets: MEDLINE
Imprint Name(s): Original Publication: Washington, American Chemical Society.
MeSH Terms: Chemokine CCL19/*chemistry ; Chemokine CCL19/*metabolism ; Membrane Glycoproteins/*metabolism ; Receptors, CCR7/*metabolism; Binding Sites ; Humans ; Models, Molecular ; Protein Conformation
Abstract: CCL19 and CCL21 are chemokines involved in the trafficking of immune cells, particularly within the lymphatic system, through activation of CCR7. Concurrent expression of PSGL-1 and CCR7 in naive T-cells enhances recruitment of these cells to secondary lymphoid organs by CCL19 and CCL21. Here the solution structure of CCL19 is reported. It contains a canonical chemokine domain. Chemical shift mapping shows the N-termini of PSGL-1 and CCR7 have overlapping binding sites for CCL19 and binding is competitive. Implications for the mechanism of PSGL-1's enhancement of resting T-cell recruitment are discussed.
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Grant Information: 281556 International ERC_ European Research Council; R15 CA159202 United States CA NCI NIH HHS; 1R15CA159202-01 United States CA NCI NIH HHS
Molecular Sequence: PDB 2MP1
Substance Nomenclature: 0 (CCR7 protein, human); 0 (Chemokine CCL19); 0 (Membrane Glycoproteins); 0 (P-selectin ligand protein); 0 (Receptors, CCR7)
Entry Date(s): Date Created: 20150627 Date Completed: 20151001 Latest Revision: 20250529
Update Code: 20260130
PubMed Central ID: PMC4809050
DOI: 10.1021/acs.biochem.5b00560
PMID: 26115234
Database: MEDLINE

Journal Article; Research Support, N.I.H., Extramural