Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Subscribe

Sci. Signal., 17 December 2013
Vol. 6, Issue 306, p. ra109
[DOI: 10.1126/scisignal.2004560]

RESEARCH ARTICLES

Integration of Protein Abundance and Structure Data Reveals Competition in the ErbB Signaling Network

Christina Kiel1,2*, Erik Verschueren1,2, Jae-Seong Yang1,2, and Luis Serrano1,2,3

1 European Molecular Biology Laboratory and Centre for Genomic Regulation Systems Biology Research Unit, Dr. Aiguader Street 88, 08003 Barcelona, Spain.
2 Universitat Pompeu Fabra, 08003 Barcelona, Spain.
3 Institució Catalana de Recerca i Estudis Avançats, Passeig Lluís Companys 23, 08010 Barcelona, Spain.

Abstract: The mechanisms of context-specific differences in signal transduction, such as those that occur among different cell types, are not fully understood. One possibility is that differences in the abundance of proteins change signaling outputs because these proteins compete for binding to hub proteins at critical network branch points. Focusing on the ErbB signaling, we created a protein interaction network that included information about protein domains and analyzed the role of competing protein interactions. By leveraging three-dimensional protein structures to infer steric interactions among binding partners for a common binding domain or linear motif (node) and including information about protein abundance and interaction affinities, we identified a large number of competitive, mutually exclusive (XOR) protein interactions. Modeling changes in protein abundance with different patterns of partner proteins and XOR nodes (XOR motifs) revealed that each motif conferred a different response. We experimentally investigated the XOR motif containing the hub protein Ras and its binding partners RIN1 (Ras and Rab interactor 1) and CRAF (v-raf–leukemia viral oncogene 1). Consistent with the computational prediction, overexpression of RIN1 in cultured cells decreased the phosphorylation of CRAF and its downstream targets. Thus, our analyses provide evidence that variation in the abundance of proteins that compete for binding to XOR nodes could contribute to context-specific signaling plasticity.

* Corresponding author. E-mail: christina.kiel{at}crg.eu

Citation: C. Kiel, E. Verschueren, J.-S. Yang, L. Serrano, Integration of Protein Abundance and Structure Data Reveals Competition in the ErbB Signaling Network. Sci. Signal. 6, ra109 (2013).

Read the Full Text


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Visualizing and Manipulating Temporal Signaling Dynamics with Fluorescence-Based Tools.
D. P. Doupe and N. Perrimon (2014)
Science Signaling 7, re1
   Abstract »    Full Text »    PDF »
2013: Signaling Breakthroughs of the Year.
J. D. Berndt and N. R. Gough (2014)
Science Signaling 7, eg1
   Abstract »    Full Text »    PDF »

To Advertise     Find Products


Science Signaling. ISSN 1937-9145 (online), 1945-0877 (print). Pre-2008: Science's STKE. ISSN 1525-8882