Large-scale de novo prediction of physical protein-protein association

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Antigoni Elefsinioti - , Biotechnology Center (BIOTEC), Max Delbrück Center for Molecular Medicine (MDC) (Author)
  • Ömer Sinan Saraç - , TUD Dresden University of Technology (Author)
  • Anna Hegele - , Max Planck Institute for Molecular Genetics (Author)
  • Conrad Plake - , TUD Dresden University of Technology (Author)
  • Nina C Hubner - , Max Planck Institute of Biochemistry, University Medical Center (UMC) Utrecht (Author)
  • Ina Poser - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Mihail Sarov - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Anthony Hyman - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Matthias Mann - , Max Planck Institute of Biochemistry (Author)
  • Michael Schroeder - , Chair of Bioinformatics (Author)
  • Ulrich Stelzl - , Max Planck Institute for Molecular Genetics (Author)
  • Andreas Beyer - , Cellular networks and systems biology, Center for Regenerative Therapies Dresden (Author)

Abstract

Information about the physical association of proteins is extensively used for studying cellular processes and disease mechanisms. However, complete experimental mapping of the human interactome will remain prohibitively difficult in the near future. Here we present a map of predicted human protein interactions that distinguishes functional association from physical binding. Our network classifies more than 5 million protein pairs predicting 94,009 new interactions with high confidence. We experimentally tested a subset of these predictions using yeast two-hybrid analysis and affinity purification followed by quantitative mass spectrometry. Thus we identified 462 new protein-protein interactions and confirmed the predictive power of the network. These independent experiments address potential issues of circular reasoning and are a distinctive feature of this work. Analysis of the physical interactome unravels subnetworks mediating between different functional and physical subunits of the cell. Finally, we demonstrate the utility of the network for the analysis of molecular mechanisms of complex diseases by applying it to genome-wide association studies of neurodegenerative diseases. This analysis provides new evidence implying TOMM40 as a factor involved in Alzheimer's disease. The network provides a high-quality resource for the analysis of genomic data sets and genetic association studies in particular. Our interactome is available via the hPRINT web server at: www.print-db.org.

Details

Original languageEnglish
Article numberM111.010629
JournalMolecular and Cellular Proteomics
Volume10
Issue number11
Publication statusPublished - Nov 2011
Peer-reviewedYes

External IDs

PubMed 21836163
PubMedCentral PMC3226409
Scopus 80555146675
ORCID /0000-0003-2848-6949/work/141543416

Keywords

Sustainable Development Goals

Keywords

  • Algorithms, Animals, Bayes Theorem, Computer Simulation, HeLa Cells, Humans, Mice, Models, Molecular, Neurodegenerative Diseases/genetics, Protein Interaction Domains and Motifs, Protein Interaction Mapping/methods, Protein Interaction Maps, Proteome/genetics, ROC Curve, Recombinant Proteins/metabolism, Statistics, Nonparametric