Elucidating essential kinases of endothelin signalling by logic modelling of phosphoproteomics data


Date

2019-08-01

Publication Type

Journal Article

ETH Bibliography

yes

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Abstract

Endothelins (EDN) are peptide hormones that activate a GPCR signalling system and contribute to several diseases, including hypertension and cancer. Current knowledge about EDN signalling is fragmentary, and no systems level understanding is available. We investigated phosphoproteomic changes caused by endothelin B receptor (ENDRB) activation in the melanoma cell lines UACC257 and A2058 and built an integrated model of EDNRB signalling from the phosphoproteomics data. More than 5,000 unique phosphopeptides were quantified. EDN induced quantitative changes in more than 800 phosphopeptides, which were all strictly dependent on EDNRB. Activated kinases were identified based on high confidence EDN target sites and validated by Western blot. The data were combined with prior knowledge to construct the first comprehensive logic model of EDN signalling. Among the kinases predicted by the signalling model, AKT, JNK, PKC and AMP could be functionally linked to EDN‐induced cell migration. The model contributes to the system‐level understanding of the mechanisms underlying the pleiotropic effects of EDN signalling and supports the rational selection of kinase inhibitors for combination treatments with EDN receptor antagonists.

Publication status

published

Editor

Book title

Volume

15 (8)

Pages / Article No.

Publisher

EMBO Press

Event

Edition / version

Methods

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Geographic location

Date collected

Date created

Subject

Endothelin; GPCR; Melanoma; Molecular modelling; Phosphoproteomics

Organisational unit

03663 - Aebersold, Rudolf (emeritus) / Aebersold, Rudolf (emeritus) check_circle

Notes

Funding

670821 - Proteomics 4D: The proteome in context (EC)
115766 - Unrestricted Leveraging of Targets for Research Advancement and Drug Discovery (EC)

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