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Mol Biosyst. 2010 Dec;6(12):2351-62. doi: 10.1039/c005060c. Epub 2010 Aug 19.

Protein-protein docking tested in blind predictions: the CAPRI experiment.

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  • 1Yeast Structural Genomics, IBBMC UMR 8619, Bat. 430, Universit√© Paris-Sud 91405-Orsay, France.

Abstract

Docking algorithms build multimolecular assemblies based on the subunit structures. "Unbound" docking, which starts with the free molecules and allows for conformation changes, may be used to predict the structure of a protein-protein complex. This requires at least two steps, a rigid-body search that determines the relative position and orientation of the subunits, and a refinement step. The methods developed in the past twenty years yield native-like models in most cases, but always with many false positives that must be filtered out, and they fail when the conformation changes are large. CAPRI (Critical Assessment of PRedicted Interactions) is a community-wide experiment set up to monitor progress in the field. It offers participants the opportunity to test their methods in blind predictions that are assessed against an unpublished experimental structure. The models submitted by predictor groups are judged depending on how well they reproduce the geometry and the residue-residue contacts seen in the target structure. In nine years of CAPRI, 42 target complexes have been subjected to prediction based on the components' unbound structures. Good models have been submitted for 28 targets, and prediction has failed on 6. Both these successes and these failures have been fruitful, as they stimulated participant groups to develop new score functions to identify native-like solutions, and new algorithms that allow the molecules to be flexible during docking.

PMID:
20725658
[PubMed - indexed for MEDLINE]
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