Unknown

Dataset Information

0

Contacts-based prediction of binding affinity in protein-protein complexes.


ABSTRACT: Almost all critical functions in cells rely on specific protein-protein interactions. Understanding these is therefore crucial in the investigation of biological systems. Despite all past efforts, we still lack a thorough understanding of the energetics of association of proteins. Here, we introduce a new and simple approach to predict binding affinity based on functional and structural features of the biological system, namely the network of interfacial contacts. We assess its performance against a protein-protein binding affinity benchmark and show that both experimental methods used for affinity measurements and conformational changes have a strong impact on prediction accuracy. Using a subset of complexes with reliable experimental binding affinities and combining our contacts and contact-types-based model with recent observations on the role of the non-interacting surface in protein-protein interactions, we reach a high prediction accuracy for such a diverse dataset outperforming all other tested methods.

SUBMITTER: Vangone A 

PROVIDER: S-EPMC4523921 | biostudies-literature | 2015 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

Contacts-based prediction of binding affinity in protein-protein complexes.

Vangone Anna A   Bonvin Alexandre Mjj AM  

eLife 20150720


Almost all critical functions in cells rely on specific protein-protein interactions. Understanding these is therefore crucial in the investigation of biological systems. Despite all past efforts, we still lack a thorough understanding of the energetics of association of proteins. Here, we introduce a new and simple approach to predict binding affinity based on functional and structural features of the biological system, namely the network of interfacial contacts. We assess its performance again  ...[more]

Similar Datasets

| S-EPMC3498326 | biostudies-literature
| S-EPMC6361695 | biostudies-literature
| S-EPMC8376549 | biostudies-literature
| S-EPMC8637032 | biostudies-literature
| S-EPMC8425427 | biostudies-literature
| S-EPMC6859855 | biostudies-literature
| S-EPMC6486753 | biostudies-literature
| S-EPMC1369289 | biostudies-literature