4.1 Review

G Protein-Coupled Receptors in the Sweet Spot: Glycosylation and other Post-translational Modifications

期刊

ACS PHARMACOLOGY & TRANSLATIONAL SCIENCE
卷 3, 期 2, 页码 237-245

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsptsci.0c00016

关键词

glycosylation; tyrosine sulfation; proteolytic cleavage; G protein-coupled receptor; PTM interplay

资金

  1. Academy of Finland
  2. European Research Council [682549]
  3. Lundbeck Foundation [R242-2017-409]
  4. Novo Nordisk Foundation [NNF17OC0029222]
  5. European Research Council (ERC) [682549] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Post-translational modifications (PTMs) are a fundamental phenomenon across all classes of life and several hundred different types have been identified. PTMs contribute widely to the biological functions of proteins and greatly increase their diversity. One important class of proteins regulated by PTMs, is the cell surface expressed G protein-coupled receptors (GPCRs). While most PTMs have been shown to exert distinct biological functions, we are only beginning to approach the complexity that the potential interplay between different PTMs may have on biological functions and their regulation. Importantly, PTMs and their potential interplay represent an appealing mechanism for cell and tissue specific regulation of GPCR function and may partially contribute to functional selectivity of some GPCRs. In this review we highlight examples of PTMs located in GPCR extracellular domains, with special focus on glycosylation and the potential interplay with other close-by PTMs such as tyrosine sulfation, proteolytic cleavage, and phosphorylation.

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