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

一种分析人类蛋白质复合物并预测新型蛋白质相互作用的新计算方法

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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.

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