Developing algorithms for predicting protein-protein interactions of homology modeled proteins.

Martin, Shawn Bryan ; Sale, Kenneth L. ; Faulon, Jean-Loup Michel ; Roe, Diana C.

Sandia National Laboratories

关键词: Solvation;    Validation Protein Folding-Computer Simulation.;    Protein Folding-Computer Simulation.;    59 Basic Biological Sciences;    Protein Binding.;   

DOI  :  10.2172/883467
RP-ID  :  SAND2005-7984
RP-ID  :  AC04-94AL85000
RP-ID  :  883467

美国|英语

来源: UNT Digital Library

【 摘 要 】

The goal of this project was to examine the protein-protein docking problem, especially as it relates to homology-based structures, identify the key bottlenecks in current software tools, and evaluate and prototype new algorithms that may be developed to improve these bottlenecks. This report describes the current challenges in the protein-protein docking problem: correctly predicting the binding site for the protein-protein interaction and correctly placing the sidechains. Two different and complementary approaches are taken that can help with the protein-protein docking problem. The first approach is to predict interaction sites prior to docking, and uses bioinformatics studies of protein-protein interactions to predict theses interaction site. The second approach is to improve validation of predicted complexes after docking, and uses an improved scoring function for evaluating proposed docked poses, incorporating a solvation term. This scoring function demonstrates significant improvement over current state-of-the art functions. Initial studies on both these approaches are promising, and argue for full development of these algorithms.