Journal
CELL
Volume 134, Issue 3, Pages 534-545Publisher
CELL PRESS
DOI: 10.1016/j.cell.2008.07.009
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Funding
- Leukemia Research Foundation
- W. M. Keck foundation
- National Institutes of Health [R21RR023114, R01HG001715, R33CA105405, R33CA81658, R21CA113711, U54 CA011295, CA95281]
- United States Army Medical Research Acquisition Activity [W23RYX-3275-N605]
- New York State Foundation of Science, Technology
- Academic Research [C040066]
- National Science Foundation [MCB 0444818, BDI-0345474, IUAP-P6:28, UG-GOA12051401, FWO-G.0031.06]
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Many protein-protein interactions are mediated through independently folding modular domains. Proteome-wide efforts to model protein-protein interaction or interactome'' networks have largely ignored this modular organization of proteins. We developed an experimental strategy to efficiently identify interaction domains and generated a domain-based interactome network for proteins involved in C. elegans early-embryonic cell divisions. Minimal interacting regions were identified for over 200 proteins, providing important information on their domain organization. Furthermore, our approach increased the sensitivity of the two-hybrid system, resulting in amore complete interactome network. This interactome modeling strategy revealed insights into C. elegans centrosome function and is applicable to other biological processes in this and other organisms.
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