Complete Topological Mapping of a Cellular Protein Interactome Reveals Bow-Tie Motifs as Ubiquitous Connectors of Protein Complexes

Kristoffer Niss, Cristina Gomez-Casado, Jessica X. Hjaltelin, Thorsten Joeris, William W. Agace, Kirstine G. Belling, Søren Brunak*

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

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Abstract

The network topology of a protein interactome is shaped by the function of each protein, making it a resource of functional knowledge in tissues and in single cells. Today, this resource is underused, as complete network topology characterization has proved difficult for large protein interactomes. We apply a matrix visualization and decoding approach to a physical protein interactome of a dendritic cell, thereby characterizing its topology with no prior assumptions of structure. We discover 294 proteins, each forming topological motifs called “bow-ties” that tie together the majority of observed protein complexes. The central proteins of these bow-ties have unique network properties, display multifunctional capabilities, are enriched for essential proteins, and are widely expressed in other cells and tissues. Collectively, the bow-tie motifs are a pervasive and previously unnoted topological trend in cellular interactomes. As such, these results provide fundamental knowledge on how intracellular protein connectivity is organized and operates. Niss et al. show that topological motifs called bow-ties create a scaffold within the cellular protein interactome that connects a majority of protein complexes. The central proteins of these motifs are found to be associated with multifunctionality and cellular essentiality, display unique network properties, and are expressed widely across cells and tissues.
Original languageEnglish
Article number107763
JournalCell Reports
Volume31
Issue number11
Number of pages16
ISSN2211-1247
DOIs
Publication statusPublished - 2020

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