Integrin β cytoplasmic domain interactions with phosphotyrosine-binding domains: A structural prototype for diversity in integrin signaling
- David A. Calderwood*,†,
- Yosuke Fujioka*,†,
- Jose M. de Pereda‡,
- Begoña García-Alvarez‡,
- Tetsuya Nakamoto*,
- Ben Margolis§,
- C. Jane McGlade¶,
- Robert C. Liddington‡, and
- Mark H. Ginsberg*,‖
- *Division of Vascular Biology, Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037; ‡Program on Cell Adhesion, The Burnham Institute, La Jolla, CA 92037; §Howard Hughes Medical Institute, Departments of Internal Medicine and Biological Chemistry, University of Michigan Medical School, Ann Arbor, MI 48109-0650; and ¶Department of Medical Biophysics and Program in Cell Biology, Hospital for Sick Children, Toronto, ON, Canada M5G 1X8
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Communicated by Richard O. Hynes, Massachusetts Institute of Technology, Cambridge, MA (received for review September 10, 2002)
Abstract
The cytoplasmic domains (tails) of heterodimeric integrin adhesion receptors mediate integrins' biological functions by binding to cytoplasmic proteins. Most integrin β tails contain one or two NPXY/F motifs that can form β turns. These motifs are part of a canonical recognition sequence for phosphotyrosine-binding (PTB) domains, protein modules that are present in a wide variety of signaling and cytoskeletal proteins. Indeed, talin and ICAP1-α bind to integrin β tails by means of a PTB domain–NPXY ligand interaction. To assess the generality of this interaction we examined the binding of a series of recombinant PTB domains to a panel of short integrin β tails. In addition to the known integrin-binding proteins, we found that Numb (a negative regulator of Notch signaling) and Dok-1 (a signaling adaptor involved in cell migration) and their isolated PTB domain bound to integrin tails. Furthermore, Dok-1 physically associated with integrin αIIbβ3. Mutations of the integrin β tails confirmed that these interactions are canonical PTB domain–ligand interactions. First, the interactions were blocked by mutation of an NPXY motif in the integrin tail. Second, integrin class-specific interactions were observed with the PTB domains of Dab, EPS8, and tensin. We used this specificity, and a molecular model of an integrin β tail–PTB domain interaction to predict critical interacting residues. The importance of these residues was confirmed by generation of gain- and loss-of-function mutations in β7 and β3 tails. These data establish that short integrin β tails interact with a large number of PTB domain-containing proteins through a structurally conserved mechanism.
Footnotes
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↵ † D.A.C. and Y.F. contributed equally to this work.
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↵ ‖ To whom correspondence should be addressed. E-mail: ginsberg{at}scripps.edu.
- Abbreviations:
- CHO,
- Chinese hamster ovary;
- PTB,
- phosphotyrosine binding;
- IRS,
- insulin receptor substrate;
- ICAP,
- integrin cytoplasmic domain-associated protein;
- PH domain,
- pleckstrin homology domain;
- Nak,
- Numb-associated kinase
- Copyright © 2003, The National Academy of Sciences





