Description: Evaluation of the coarse-grained OPEP force field for protein-protein docking

This title appears in the Scientific Report : 2016

Evaluation of the coarse-grained OPEP force field for protein-protein docking

Background: Knowing the binding site of protein–protein complexes helps understand their function and shows possible regulation sites. The ultimate goal of protein–protein docking is the prediction of the three-dimensional structure of a protein–protein complex. Docking itself only produces plausibl...

Personal Name(s):	Kynast, Philipp
	Derreumaux, Philippe / Strodel, Birgit (Corresponding author)
Contributing Institute:	Strukturbiochemie; ICS-6
Published in:	BMC Biophysics, 9 (2016) 1, S. 4
Imprint:	London BioMed Central 2016
DOI:	10.1186/s13628-016-0029-y
PubMed ID:	27103992
Document Type:	Journal Article
Research Program:	Functional Macromolecules and Complexes
Link:	Get full text OpenAccess OpenAccess
	Publikationsportal JuSER

Please use the identifier: http://dx.doi.org/10.1186/s13628-016-0029-y in citations.
Please use the identifier: http://hdl.handle.net/2128/12532 in citations.

Background: Knowing the binding site of protein–protein complexes helps understand their function and shows possible regulation sites. The ultimate goal of protein–protein docking is the prediction of the three-dimensional structure of a protein–protein complex. Docking itself only produces plausible candidate structures, which must be ranked using scoring functions to identify the structures that are most likely to occur in nature. Methods: In this work, we rescore rigid body protein–protein predictions using the optimized potential for efficient structure prediction (OPEP), which is a coarse-grained force field. Using a force field based on continuous functions rather than a grid-based scoring function allows the introduction of protein flexibility during the docking procedure. First, we produce protein–protein predictions using ZDOCK, and after energy minimization via OPEP we rank them using an OPEP-based soft rescoring function. We also train the rescoring function for different complex classes and demonstrate its improved performance for an independent dataset. Results: The trained rescoring function produces a better ranking than ZDOCK for more than 50 % of targets, rising to over 70 % when considering only enzyme/inhibitor complexes. Conclusions: This study demonstrates for the first time that energy functions derived from the coarse-grained OPEP force field can be employed to rescore predictions for protein–protein complexes.