G protein-coupled receptor modulation with pepducins: moving closer to the clinic.

Autor: Dimond, Patricia, Carlson, Kenneth, Bouvier, Michel, Gerard, Craig, Xu, Lei, Covic, Lidija, Agarwal, Anika, Ernst, Oliver P., Janz, Jay M., Schwartz, Thue W., Gardella, Thomas J., Milligan, Graeme, Kuliopulos, Athan, Sakmar, Thomas P., Hunt III, Stephen W.
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Zdroj: Annals of the New York Academy of Sciences; May2011, Vol. 1226 Issue 1, p34-49, 16p, 1 Color Photograph, 4 Diagrams, 1 Graph
Abstrakt: At the 2nd Pepducin Science Symposium held in Cambridge, Massachusetts, on November 4-5, 2010, investigators working in G protein-coupled receptor (GPCR) research convened to discuss progress since last year's inaugural conference. This year's symposium focused on increasing knowledge of the structure and function of this ubiquitous superfamily of membrane receptors and their potential modulation for disease treatment. Presentations also focused on how GPCR mechanisms might be exploited to treat diseases with pepducins, novel synthetic lipopeptide pharmacophores that modulate heptahelical GPCR activity. While the multiple roles of GPCRs in physiological and pathophysiological processes offer significant opportunities for novel drug development, the global nature of their activity challenges drug-specific and validated target identification. This year's conference highlighted advances in understanding of GPCR agonist and antagonist ligand-binding motifs, their ligand-independent functions, structure-activity relationships (SARs), and evolving unique methods to probe GPCR structure and function. Study results summarized at the meeting also provided evidence for evolving views of how signaling mechanisms work through these receptors. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index
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