Molecular Basis of Antiangiogenic Thrombospondin-1 Type 1 Repeat Domain Interactions With CD36
Author(s) -
Philip A. Klenotic,
Richard C. Page,
Wei Li,
Joseph Amick,
Saurav Misra,
Roy L. Silverstein
Publication year - 2013
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.113.301523
Subject(s) - cd36 , thrombospondin , thrombospondin 1 , biology , angiogenesis , microbiology and biotechnology , chemistry , biochemistry , receptor , genetics , metalloproteinase , enzyme
Antiangiogenic activity of thrombospondin-1 and related proteins is mediated by interactions between thrombospondin type 1 repeat (TSR) domains and the CD36, LIMP-2, Emp sequence homology (CLESH) domain of the endothelial cell receptor CD36. We sought to characterize key molecular determinants of the interaction between thrombospondin-1 TSR domains and the CD36 CLESH domain.
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