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Community-wide evaluation of methods for predicting the effect of mutations on protein-protein interactions

Authors :
Moretti, Rocco
Fleishman, Sarel J
Agius, Rudi
Torchala, Mieczyslaw
Bates, Paul A
Kastritis, Panagiotis L
Garcia Lopes Maia Rodrigues, João
Trellet, Mikaël
Bonvin, Alexandre M J J
Cui, Meng
Rooman, Marianne
Gillis, Dimitri
Dehouck, Yves
Moal, Iain
Romero-Durana, Miguel
Perez-Cano, Laura
Pallara, Chiara
Jimenez, Brian
Fernandez-Recio, Juan
Flores, Samuel
Pacella, Michael
Praneeth Kilambi, Krishna
Gray, Jeffrey J
Popov, Petr
Grudinin, Sergei
Esquivel-Rodríguez, Juan
Kihara, Daisuke
Zhao, Nan
Korkin, Dmitry
Zhu, Xiaolei
Demerdash, Omar N A
Mitchell, Julie C
Kanamori, Eiji
Tsuchiya, Yuko
Nakamura, Haruki
Lee, Hasup
Park, Hahnbeom
Seok, Chaok
Sarmiento, Jamica
Liang, Shide
Teraguchi, Shusuke
Standley, Daron M
Shimoyama, Hiromitsu
Terashi, Genki
Takeda-Shitaka, Mayuko
Iwadate, Mitsuo
Umeyama, Hideaki
Beglov, Dmitri
Hall, David R
Kozakov, Dima
Vajda, Sandor
Pierce, Brian G
Hwang, Howook
Vreven, Thom
Weng, Zhiping
Huang, Yangyu
Li, Haotian
Yang, Xiufeng
Ji, Xiaofeng
Liu, Shiyong
Xiao, Yi
Zacharias, Martin
Qin, Sanbo
Zhou, Huan-Xiang
Huang, Sheng-You
Zou, Xiaoqin
Velankar, Sameer
Janin, Joël
Wodak, Shoshana J
Baker, David
Sub NMR Spectroscopy
NMR Spectroscopy
Source :
Proteins: Structure function and bioinformatics, 81(11), 1980. Wiley-Liss Inc.
Publication Year :
2013

Abstract

Community-wide blind prediction experiments such as CAPRI and CASP provide an objective measure of the current state of predictive methodology. Here we describe a community-wide assessment of methods to predict the effects of mutations on protein-protein interactions. Twenty-two groups predicted the effects of comprehensive saturation mutagenesis for two designed influenza hemagglutinin binders and the results were compared with experimental yeast display enrichment data obtained using deep sequencing. The most successful methods explicitly considered the effects of mutation on monomer stability in addition to binding affinity, carried out explicit side-chain sampling and backbone relaxation, evaluated packing, electrostatic, and solvation effects, and correctly identified around a third of the beneficial mutations. Much room for improvement remains for even the best techniques, and large-scale fitness landscapes should continue to provide an excellent test bed for continued evaluation of both existing and new prediction methodologies.

Details

Language :
English
ISSN :
08873585
Database :
OpenAIRE
Journal :
Proteins: Structure function and bioinformatics, 81(11), 1980. Wiley-Liss Inc.
Accession number :
edsair.narcis........48dd790babd9095358783fe118b31074