Proteolytic ectodomain shedding of membrane proteins in mammals—hardware, concepts, and recent developments. (5th July 2018)
- Record Type:
- Journal Article
- Title:
- Proteolytic ectodomain shedding of membrane proteins in mammals—hardware, concepts, and recent developments. (5th July 2018)
- Main Title:
- Proteolytic ectodomain shedding of membrane proteins in mammals—hardware, concepts, and recent developments
- Authors:
- Lichtenthaler, Stefan F
Lemberg, Marius K
Fluhrer, Regina - Abstract:
- Abstract: Proteolytic removal of membrane protein ectodomains (ectodomain shedding) is a post‐translational modification that controls levels and function of hundreds of membrane proteins. The contributing proteases, referred to as sheddases, act as important molecular switches in processes ranging from signaling to cell adhesion. When deregulated, ectodomain shedding is linked to pathologies such as inflammation and Alzheimer's disease. While proteases of the "a disintegrin and metalloprotease" (ADAM) and "beta‐site APP cleaving enzyme" (BACE) families are widely considered as sheddases, in recent years a much broader range of proteases, including intramembrane and soluble proteases, were shown to catalyze similar cleavage reactions. This review demonstrates that shedding is a fundamental process in cell biology and discusses the current understanding of sheddases and their substrates, molecular mechanisms and cellular localizations, as well as physiological functions of protein ectodomain shedding. Moreover, we provide an operational definition of shedding and highlight recent conceptual advances in the field. While new developments in proteomics facilitate substrate discovery, we expect that shedding is not a rare exception, but rather the rule for many membrane proteins, and that many more interesting shedding functions await discovery. Abstract : This review gives an operational definition of shedding as a fundamental cell biological and (patho)physiological process,Abstract: Proteolytic removal of membrane protein ectodomains (ectodomain shedding) is a post‐translational modification that controls levels and function of hundreds of membrane proteins. The contributing proteases, referred to as sheddases, act as important molecular switches in processes ranging from signaling to cell adhesion. When deregulated, ectodomain shedding is linked to pathologies such as inflammation and Alzheimer's disease. While proteases of the "a disintegrin and metalloprotease" (ADAM) and "beta‐site APP cleaving enzyme" (BACE) families are widely considered as sheddases, in recent years a much broader range of proteases, including intramembrane and soluble proteases, were shown to catalyze similar cleavage reactions. This review demonstrates that shedding is a fundamental process in cell biology and discusses the current understanding of sheddases and their substrates, molecular mechanisms and cellular localizations, as well as physiological functions of protein ectodomain shedding. Moreover, we provide an operational definition of shedding and highlight recent conceptual advances in the field. While new developments in proteomics facilitate substrate discovery, we expect that shedding is not a rare exception, but rather the rule for many membrane proteins, and that many more interesting shedding functions await discovery. Abstract : This review gives an operational definition of shedding as a fundamental cell biological and (patho)physiological process, and summarizes our current understanding of sheddases and their substrates, mechanisms and roles. … (more)
- Is Part Of:
- EMBO journal. Volume 37:Number 15(2018)
- Journal:
- EMBO journal
- Issue:
- Volume 37:Number 15(2018)
- Issue Display:
- Volume 37, Issue 15 (2018)
- Year:
- 2018
- Volume:
- 37
- Issue:
- 15
- Issue Sort Value:
- 2018-0037-0015-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2018-07-05
- Subjects:
- matrix metalloproteases -- meprin β -- pro‐protein convertases -- rhomboids -- signal peptide peptidase‐like
Molecular biology -- Periodicals
572.805 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.15252/embj.201899456 ↗
- Languages:
- English
- ISSNs:
- 0261-4189
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3733.085000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 7149.xml