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

被引:105
作者
Kustatscher, Georg [1 ]
Grabowski, Piotr [2 ,4 ]
Schrader, Tina A. [3 ]
Passmore, Josiah B. [3 ]
Schrader, Michael [3 ]
Rappsilber, Juri [1 ,2 ]
机构
[1] Univ Edinburgh, Wellcome Ctr Cell Biol, Edinburgh, Midlothian, Scotland
[2] Tech Univ Berlin, Div Bioanalyt, Inst Biotechnol, Berlin, Germany
[3] Univ Exeter, Biosci, Exeter, Devon, England
[4] AstraZeneca, R&D, Clin Pharmacol & Safety Sci, Data Sci & Artificial Intelligence, Cambridge, England
基金
英国生物技术与生命科学研究理事会; 欧盟地平线“2020”; 英国惠康基金;
关键词
GENE-COEXPRESSION NETWORK; ATP SYNTHASE; ASSOCIATION NETWORKS; RNA; EXPRESSION; DISCOVERY; DYNAMICS; MITOCHONDRIA; MICROPROTEIN; PEROXISOMES;
D O I
10.1038/s41587-019-0298-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 PEX11 beta 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.
引用
收藏
页码:1361 / +
页数:14
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