MOTIVATION: Cellular processes often hinge upon specific interactions among proteins, and knowledge of these processes at a system level constitutes a major goal of proteomics. In particular, a greater understanding of protein-protein interactions can be gained via a more detailed investigation of the protein domain interactions that mediate the interactions of proteins. Existing high-throughput experimental techniques assay protein-protein interactions, yet they do not provide any direct information on the interactions among domains. Inferences concerning the latter can be made by analysis of the domain composition of a set of proteins and their interaction map. This inference problem is non-trivial, however, due to the high level of noise generally present in experimental data concerning protein-protein interactions. This noise leads to contradictions, i.e. the impossibility of having a pattern of domain interactions compatible with the protein-protein interaction map. RESULTS: We formulate the problem of prediction of protein domain interactions in a form that lends itself to the application of belief propagation, a powerful algorithm for such inference problems, which is based on message passing. The input to our algorithm is an interaction map among a set of proteins, and a set of domain assignments to the relevant proteins. The output is a list of probabilities of interaction between each pair of domains. Our method is able to effectively cope with errors in the protein-protein interaction dataset and systematically resolve contradictions. We applied the method to a dataset concerning the budding yeast Saccharomyces cerevisiae and tested the quality of our predictions by cross-validation on this dataset, by comparison with existing computational predictions, and finally with experimentally available domain interactions. Results compare favourably to those by existing algorithms. AVAILABILITY: A C language implementation of the algorithm is available upon request.
MOTIVATION: Cellular processes often hinge upon specific interactions among proteins, and knowledge of these processes at a system level constitutes a major goal of proteomics. In particular, a greater understanding of protein-protein interactions can be gained via a more detailed investigation of the protein domain interactions that mediate the interactions of proteins. Existing high-throughput experimental techniques assay protein-protein interactions, yet they do not provide any direct information on the interactions among domains. Inferences concerning the latter can be made by analysis of the domain composition of a set of proteins and their interaction map. This inference problem is non-trivial, however, due to the high level of noise generally present in experimental data concerning protein-protein interactions. This noise leads to contradictions, i.e. the impossibility of having a pattern of domain interactions compatible with the protein-protein interaction map. RESULTS: We formulate the problem of prediction of protein domain interactions in a form that lends itself to the application of belief propagation, a powerful algorithm for such inference problems, which is based on message passing. The input to our algorithm is an interaction map among a set of proteins, and a set of domain assignments to the relevant proteins. The output is a list of probabilities of interaction between each pair of domains. Our method is able to effectively cope with errors in the protein-protein interaction dataset and systematically resolve contradictions. We applied the method to a dataset concerning the budding yeastSaccharomyces cerevisiae and tested the quality of our predictions by cross-validation on this dataset, by comparison with existing computational predictions, and finally with experimentally available domain interactions. Results compare favourably to those by existing algorithms. AVAILABILITY: A C language implementation of the algorithm is available upon request.
Authors: Jianhua Yang; Kim Osman; Mudassar Iqbal; Dov J Stekel; Zewei Luo; Susan J Armstrong; F Chris H Franklin Journal: Front Plant Sci Date: 2013-01-04 Impact factor: 5.753