Glycopeptide Analogues of PSGL-1 Inhibit P-Selectin In Vitro and In Vivo

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Glycopeptide Analogues of PSGL-1 Inhibit P-Selectin In Vitro and In Vivo

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Title: Glycopeptide Analogues of PSGL-1 Inhibit P-Selectin In Vitro and In Vivo
Author: Krishnamurthy, Venkata R; Sardar, Mohammed Y. R.; Yu, Ying; Song, Xuezheng; Haller, Carolyn; Dai, Erbin; Wang, Xiacong; Hanjaya-Putra, Donny; Sun, Lijun; Morikis, Vasilios; Simon, Scott I.; Woods, Robert; Cummings, Richard D.; Chaikof, Elliot L.

Note: Order does not necessarily reflect citation order of authors.

Citation: Krishnamurthy, V. R., M. Y. R. Sardar, Y. Yu, X. Song, C. Haller, E. Dai, X. Wang, et al. 2015. “Glycopeptide Analogues of PSGL-1 Inhibit P-Selectin In Vitro and In Vivo.” Nature communications 6 (1): 6387. doi:10.1038/ncomms7387. http://dx.doi.org/10.1038/ncomms7387.
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Abstract: Blockade of P-selectin/PSGL-1 interactions holds significant potential for treatment of disorders of innate immunity, thrombosis, and cancer. Current inhibitors remain limited due to low binding affinity or by the recognized disadvantages inherent to chronic administration of antibody therapeutics. Here we report an efficient approach for generating glycosulfopeptide mimics of N-terminal PSGL-1 through development of a stereoselective route for multi-gram scale synthesis of the C2 O-glycan building block and replacement of hydrolytically labile tyrosine sulfates with isosteric sulfonate analogs. Library screening afforded a compound of exceptional stability, GSnP-6, that binds to human P-selectin with nanomolar affinity (Kd ~ 22 nM). Molecular dynamics simulation defines the origin of this affinity in terms of a number of critical structural contributions. GSnP-6 potently blocks P-selectin/PSGL-1 interactions in vitro and in vivo and represents a promising candidate for the treatment of diseases driven by acute and chronic inflammation.
Published Version: doi:10.1038/ncomms7387
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423566/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:22857017
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