NDLI: Solution structures of the cytoplasmic tail complex from platelet integrin alpha IIb- and beta 3-subunits.

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Solution structures of the cytoplasmic tail complex from platelet integrin alpha IIb- and beta 3-subunits.

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Weljie, Aalim M. Vogel, Hans J. Hwang, Peter M.
Description	Author Affiliation: Weljie AM ( Department of Biological Sciences, University of Calgary, 2500 University Drive NW, Calgary, AB, Canada.);
Abstract	Integrin adhesion receptors constitute a cell-signaling system whereby interactions in the small cytoplasmic domains of the heterodimeric alpha- and beta-subunits provoke major functional alterations in the large extracellular domains. With two-dimensional NMR spectroscopy, we examined two synthetic peptides [alphaIIb((987)MWKVGFFKRNR) and beta3((716)KLLITIHDRKEFAKFEEERARAKWD)] encompassing the membrane-proximal regions of the cytoplasmic domain motifs from the platelet integrin complex alphaIotaIotabbeta3. These membrane-proximal regions contain two conserved motifs, represented by (989)KVGFFKR in the alphaIIb-subunit, and (716)KLLITIHDR in the beta3-subunit. The dimer interaction consists of two adjacent helices with residues V990 and F993 of the alphaIotaIotab-subunit heavily implicated in the dimer interfacial region, as is I719 of beta3. These residues are situated within the conserved motifs of their respective proteins. Further structural analysis of this unique peptide heterodimer suggests that two distinct conformers are present. The major structural difference between the two conformers is a bend in the beta3-peptide between D723 and A728, whereas the helical character in the other regions remains intact. Earlier mutational analysis has shown that a salt bridge between the side chains of alphaIotaIotab(R955) and beta3(D723) is formed. When this ion pair was modeled into both conformers, increased nuclear Overhauser effect violations suggested that the more bent structure was less able to accommodate this interaction. These results provide a molecular level rationalization for previously reported biochemical studies, as well as a basis for an atomic level understanding of the intermolecular interactions that regulate integrin activity.
ISSN	00278424
e-ISSN	10916490
Journal	Proceedings of the National Academy of Sciences of the United States of America
Issue Number	9
Volume Number	99
Language	English
Publisher	National Academy of Sciences
Publisher Date	2002-05-01
Publisher Place	United States
Access Restriction	Open
Subject Keyword	Blood Platelets Metabolism Cytoplasm Platelet Glycoprotein GPIIb-IIIa Complex Chemistry Amino Acid Motifs Amino Acid Sequence Animals Crystallography, X-Ray DNA Mutational Analysis Dimerization Magnetic Resonance Spectroscopy Models, Molecular Molecular Sequence Data Peptides Protein Conformation Protein Structure, Tertiary Sequence Homology, Amino Acid Signal Transduction Research Support, Non-U.S. Gov't Multidisciplinary
Content Type	Text
Resource Type	Article
Subject	Multidisciplinary

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