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Peptidomimetic inhibitors targeting the membrane-binding site of the neutrophil proteinase 3

dc.abstract.enProteinase 3 (PR3), together with other serine proteases, such as neutrophil elastase (NE) and cathepsin G (CG), regulates inflammatory and immune responses. However, in comparison with NE and CG, there is increasing evidence that PR3 functions significantly differ. In particular, PR3 can bind to cell membranes and such membrane-bound PR3 (mbPR3) might be differently involved in the activation of cytokines, growth factors, cellular receptors, and in the regulation of cell apoptosis. For instance, PR3 membrane binding can block some "eat me" signals, notably, phosphatidylserine membrane lipid, and facilitate non-resolving inflammation. Based on the clear evidence that PR3 membrane binding affects the biological functions of PR3, we designed peptidomimetic inhibitors that can remove mbPR3 from the membrane surface in vitro without influencing PR3 catalytic activity. Such inhibitors, which specifically target PR3 binding to membranes, are still lacking. In particular, we found peptidomimetics that inhibit binding of PR3 to POPC:PS liposomes, which mimic the biological environment of PR3.
dc.affiliationUniwersytet Warszawski
dc.contributor.authorTrylska, Joanna
dc.contributor.authorMaximova, Ksenia
dc.contributor.authorReuter, Nathalie
dc.date.accessioned2024-01-25T16:22:52Z
dc.date.available2024-01-25T16:22:52Z
dc.date.issued2019
dc.description.financeNie dotyczy
dc.description.number8
dc.description.volume1861
dc.identifier.doi10.1016/J.BBAMEM.2019.06.009
dc.identifier.issn0005-2736
dc.identifier.urihttps://repozytorium.uw.edu.pl//handle/item/115671
dc.identifier.weblinkhttps://api.elsevier.com/content/article/PII:S0005273619301415?httpAccept=text/xml
dc.languageeng
dc.pbn.affiliationphysical sciences
dc.relation.ispartofBiochimica et Biophysica Acta - Biomembranes
dc.relation.pages1502-1509
dc.rightsClosedAccess
dc.sciencecloudnosend
dc.titlePeptidomimetic inhibitors targeting the membrane-binding site of the neutrophil proteinase 3
dc.typeJournalArticle
dspace.entity.typePublication