A new scoring function for protein–protein docking that identifies native structures with unprecedented accuracy. Issue 4 (9th December 2014)
- Record Type:
- Journal Article
- Title:
- A new scoring function for protein–protein docking that identifies native structures with unprecedented accuracy. Issue 4 (9th December 2014)
- Main Title:
- A new scoring function for protein–protein docking that identifies native structures with unprecedented accuracy
- Authors:
- Moreira, Irina S.
Martins, João M.
Coimbra, João T. S.
Ramos, Maria J.
Fernandes, Pedro A. - Abstract:
- Abstract : Here we present a new, high accuracy, scoring method to discover the native 3D structure of protein–protein (P–P) complexes. This methodology incorporates alanine scanning experimental data previously known. The P–P interface area is also included in the scheme. Abstract : Protein–protein (P–P) 3D structures are fundamental to structural biology and drug discovery. However, most of them have never been determined. Many docking algorithms were developed for that purpose, but they have a very limited accuracy in generating native-like structures and identifying the most correct one, in particular when a single answer is asked for. With such a low success rate it is difficult to point out one docked structure as being native-like. Here we present a new, high accuracy, scoring method to identify the 3D structure of P–P complexes among a set of trial poses. It incorporates alanine scanning mutagenesis experimental data that need to be obtained a priori . The scoring scheme works by matching the computational and the experimental alanine scanning mutagenesis results. The size of the trial P–P interface area is also taken into account. We show that the method ranks the trial structures and identifies the native-like structures with unprecedented accuracy (∼94%), providing the correct P–P 3D structures that biochemists and molecular biologists need to pursue their studies. With such a success rate, the bottleneck of protein–protein docking moves from the scoring toAbstract : Here we present a new, high accuracy, scoring method to discover the native 3D structure of protein–protein (P–P) complexes. This methodology incorporates alanine scanning experimental data previously known. The P–P interface area is also included in the scheme. Abstract : Protein–protein (P–P) 3D structures are fundamental to structural biology and drug discovery. However, most of them have never been determined. Many docking algorithms were developed for that purpose, but they have a very limited accuracy in generating native-like structures and identifying the most correct one, in particular when a single answer is asked for. With such a low success rate it is difficult to point out one docked structure as being native-like. Here we present a new, high accuracy, scoring method to identify the 3D structure of P–P complexes among a set of trial poses. It incorporates alanine scanning mutagenesis experimental data that need to be obtained a priori . The scoring scheme works by matching the computational and the experimental alanine scanning mutagenesis results. The size of the trial P–P interface area is also taken into account. We show that the method ranks the trial structures and identifies the native-like structures with unprecedented accuracy (∼94%), providing the correct P–P 3D structures that biochemists and molecular biologists need to pursue their studies. With such a success rate, the bottleneck of protein–protein docking moves from the scoring to searching algorithms. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 17:Issue 4(2015)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 17:Issue 4(2015)
- Issue Display:
- Volume 17, Issue 4 (2015)
- Year:
- 2015
- Volume:
- 17
- Issue:
- 4
- Issue Sort Value:
- 2015-0017-0004-0000
- Page Start:
- 2378
- Page End:
- 2387
- Publication Date:
- 2014-12-09
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c4cp04688a ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1872.xml