We propose a new approach to identify interacting proteins based on gene expression data. By using hypergeometric distribution and extensive Monte-Carlo simulations, we demonstrate that looking at synchronous expression peaks in a single time interval is a high sensitivity approach to detect co-regulation among interacting proteins. Combining gene expression and Gene Ontology similarity analyses enabled the extraction of novel interactions from microarray datasets. Applying this approach to p21-activated kinase 1, we validated alpha-tubulin and early endosome antigen 1 as its novel interactors.

A new computational approach to analyze human protein complexes and predict novel protein interactions

ZANIVAN, SARA ROSSANA;CASCONE I;MOLINERIS I;MARCHIO', Serena;CASELLE, Michele;BUSSOLINO, Federico
2007-01-01

Abstract

We propose a new approach to identify interacting proteins based on gene expression data. By using hypergeometric distribution and extensive Monte-Carlo simulations, we demonstrate that looking at synchronous expression peaks in a single time interval is a high sensitivity approach to detect co-regulation among interacting proteins. Combining gene expression and Gene Ontology similarity analyses enabled the extraction of novel interactions from microarray datasets. Applying this approach to p21-activated kinase 1, we validated alpha-tubulin and early endosome antigen 1 as its novel interactors.
2007
8
R256.1
R256.15
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246258/
systems biology; montecarlo simulation; hypergeometric distribution; vascular biology
ZANIVAN S; CASCONE I; PEYRON C; MOLINERIS I; MARCHIO S; CASELLE M; BUSSOLINO F
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/35587
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