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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, Christopher; Kiermaier, Eva; Gabel Eissens, Skylar; Gillitzer, Miranda; Lippner, David; Disilvio, Frank; Mueller, Casey; Wantuch, Paeton; Chaffee, Gary; Famiglietti, Michael; Zgoba, Danielle; Bailey, Asha; Bah, Yaya; Engebretson, Samantha; Graupner, David; Lackner, Emily; Larosa, Vincent; Medeiros, Tysha; Olson, Michael; Phillips, Andrew; Pyles, Harley; Richard, Amanda; Schoeller, Scott; Touzeau, Boris; Williams, Larry; Sixt, Michael K; Peterson, Francis
Source: Veldkamp C, Kiermaier E, Gabel Eissens S, et al. Solution structure of CCL19 and identification of overlapping CCR7 and PSGL-1 binding sites. Biochemistry . 2015;54(27):4163-4166. doi: 10.1021/acs.biochem.5b00560
Publisher Information: American Chemical Society
Publication Year: 2015
Collection: IST Austria Research Explorer (Institute of Science and Technology)
Description: 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.
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/wos/000358105100001; info:eu-repo/semantics/altIdentifier/pmid/26115234
Availability: https://research-explorer.ista.ac.at/record/1618
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.967FD6EB
Database: BASE