dc.contributor.author
Vabulas, R. Martin
dc.date.accessioned
2021-02-09T09:52:11Z
dc.date.available
2021-02-09T09:52:11Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/29562
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-29306
dc.description.abstract
Ferroptosis has been described recently as an iron-dependent cell death driven by peroxidation of membrane lipids. It is involved in the pathogenesis of a number of diverse diseases. From the other side, the induction of ferroptosis can be used to kill tumor cells as a novel therapeutic approach. Because of the broad clinical relevance, a comprehensive understanding of the ferroptosis-controlling protein network is necessary. Noteworthy, several proteins from this network are flavoenzymes. This review is an attempt to present the ferroptosis-related flavoproteins in light of their involvement in anti-ferroptotic and pro-ferroptotic roles. When available, the data on the structural stability of mutants and cofactor-free apoenzymes are discussed. The stability of the flavoproteins could be an important component of the cellular death processes.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
flavoproteins
en
dc.subject
lipid peroxidation
en
dc.subject
protein quality control
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Ferroptosis-Related Flavoproteins: Their Function and Stability
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
430
dcterms.bibliographicCitation.doi
10.3390/ijms22010430
dcterms.bibliographicCitation.journaltitle
International Journal of Molecular Sciences
dcterms.bibliographicCitation.number
1
dcterms.bibliographicCitation.originalpublishername
MDPI AG
dcterms.bibliographicCitation.volume
22
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
33406703
dcterms.isPartOf.eissn
1422-0067