Co-regulation map of the human proteome enables identification of protein functions

Assigning functions to the vast array of proteins present in eukaryotic cells remains challenging. To identify relationships between proteins, and thereby enable functional annotation of proteins, we determined changes in abundance of 10,323 human proteins in response to 294 biological perturbations...

Full description

Saved in:
Bibliographic Details
Published inNature biotechnology Vol. 37; no. 11; pp. 1361 - 1371
Main Authors Kustatscher, Georg, Grabowski, Piotr, Schrader, Tina A., Passmore, Josiah B., Schrader, Michael, Rappsilber, Juri
Format Journal Article
LanguageEnglish
Published New York Nature Publishing Group US 01.11.2019
Nature Publishing Group
Subjects
Online AccessGet full text
ISSN1087-0156
1546-1696
1546-1696
DOI10.1038/s41587-019-0298-5

Cover

More Information
Summary:Assigning functions to the vast array of proteins present in eukaryotic cells remains challenging. To identify relationships between proteins, and thereby enable functional annotation of proteins, we determined changes in abundance of 10,323 human proteins in response to 294 biological perturbations using isotope-labeling mass spectrometry. We applied the machine learning algorithm treeClust to reveal functional associations between co-regulated human proteins from ProteomeHD, a compilation of our own data and datasets from the Proteomics Identifications database. This produced a co-regulation map of the human proteome. Co-regulation was able to capture relationships between proteins that do not physically interact or colocalize. For example, co-regulation of the peroxisomal membrane protein PEX11β with mitochondrial respiration factors led us to discover an organelle interface between peroxisomes and mitochondria in mammalian cells. We also predicted the functions of microproteins that are difficult to study with traditional methods. The co-regulation map can be explored at www.proteomeHD.net . Human protein co-regulation map is derived from a large set of quantitative proteomics experiments.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
Present address: Data Sciences and Artificial Intelligence, Clinical Pharmacology & Safety Sciences, IMED Biotech Unit, AstraZeneca, Cambridge CB4 0WG, UK
ISSN:1087-0156
1546-1696
1546-1696
DOI:10.1038/s41587-019-0298-5