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Status: Bibliographieeintrag

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Verfasst von:Lichtenthaler, Stefan [VerfasserIn]   i
 Lemberg, Marius [VerfasserIn]   i
 Fluhrer, Regina [VerfasserIn]   i
Titel:Proteolytic ectodomain shedding of membrane proteins in mammals
Titelzusatz:hardware, concepts, and recent developments
Verf.angabe:Stefan F Lichtenthaler, Marius K Lemberg, Regina Fluhrer
E-Jahr:2018
Jahr:5 July 2018
Umfang:24 S.
Illustrationen:Illustrationen
Fussnoten:Gesehen am 18.02.2020
Titel Quelle:Enthalten in: European Molecular Biology OrganizationThe EMBO journal
Ort Quelle:Heidelberg : EMBO Press, 1982
Jahr Quelle:2018
Band/Heft Quelle:37 (2018,15) Artikel-Nummer e99456, Seite 1-24, 24 Seiten
ISSN Quelle:1460-2075
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.
DOI:doi:10.15252/embj.201899456
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.15252/embj.201899456
 Volltext: https://www.embopress.org/doi/full/10.15252/embj.201899456
 DOI: https://doi.org/10.15252/embj.201899456
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:matrix metalloproteases
 meprin β
 pro-protein convertases
 rhomboids
 signal peptide peptidase-like
K10plus-PPN:1690291281
Verknüpfungen:→ Zeitschrift

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