Proteomics

Dataset Information

0

The social and structural architecture of the yeast protein interactome


ABSTRACT: Nearly all cellular functions are mediated by protein-protein interactions and mapping the interactome provides fundamental insights into the regulation and structure of biological systems. In principle, affinity purification coupled to mass spectrometry (APMS) is an ideal and scalable tool, however, it has been difficult to identify low copy number complexes, membrane complexes and those disturbed by protein-tagging. As a result, our current knowledge of the interactome is far from complete, and assessing the reliability of reported interactions is challenging. Here we develop a sensitive, high-throughput, and highly reproducible AP-MS technology combined with a quantitative two-dimensional analysis strategy for comprehensive interactome mapping of Saccharomyces cerevisiae. We reduced required cell culture volumes thousand-fold and employed 96-well formats throughout, allowing replicate analysis of the endogenous green fluorescent protein (GFP) tagged library covering the entire expressed yeast proteome. The 4159 pull-downs generated a highly structured network of 3,909 proteins connected by 29,710 interactions. Compared to previous large-scale studies, we double the number of proteins (nodes in the network) and triple the number of reliable interactions (edges), including very low abundant epigenetic complexes, organellar membrane complexes and non-taggable complexes interfered by abundance correlation. This nearly saturated interactome reveals that the vast majority of yeast proteins are highly connected, with an average of 15 interactors, the majority of them unreported so far. Similar to social networks between humans, the average shortest distance is 4.2 interactions. A web portal (www.yeastinteractome.org) enables exploration of our dataset by the network and biological communities and variations of our AP-MS technology can be employed in any organism or dynamic conditions.

INSTRUMENT(S): timsTOF Pro

ORGANISM(S): Saccharomyces Cerevisiae (baker's Yeast)

SUBMITTER: Mario Oroshi  

LAB HEAD: Matthias Mann

PROVIDER: PXD031940 | Pride | 2023-09-11

REPOSITORIES: Pride

altmetric image

Publications

The social and structural architecture of the yeast protein interactome.

Michaelis André C AC   Brunner Andreas-David AD   Zwiebel Maximilian M   Meier Florian F   Strauss Maximilian T MT   Bludau Isabell I   Mann Matthias M  

Nature 20231115 7990


Cellular functions are mediated by protein-protein interactions, and mapping the interactome provides fundamental insights into biological systems. Affinity purification coupled to mass spectrometry is an ideal tool for such mapping, but it has been difficult to identify low copy number complexes, membrane complexes and complexes that are disrupted by protein tagging. As a result, our current knowledge of the interactome is far from complete, and assessing the reliability of reported interaction  ...[more]

Similar Datasets

2022-03-14 | PXD024909 | Pride
2016-06-23 | E-GEOD-65849 | biostudies-arrayexpress
2023-10-24 | PXD031094 | Pride
2021-10-29 | PXD025410 | Pride
2016-06-23 | E-GEOD-61489 | biostudies-arrayexpress
2015-09-03 | E-MTAB-3381 | biostudies-arrayexpress
2015-03-27 | E-GEOD-67330 | biostudies-arrayexpress
2016-01-20 | E-MTAB-3478 | biostudies-arrayexpress
2018-10-24 | PXD006338 | Pride
2015-10-28 | PXD002829 | Pride