Succination of protein thiols in human brain aging

dc.contributor.author
Jové Font, Mariona
dc.contributor.author
Pradas Barriga, Irene
dc.contributor.author
Mota Martorell, Natàlia
dc.contributor.author
Cabré Cucó, Rosanna
dc.contributor.author
Ayala Jové, Ma. Victoria (Maria Victoria)
dc.contributor.author
Ferrer, Isidre
dc.contributor.author
Pamplona Gras, Reinald
dc.date.accessioned
2024-12-05T21:42:29Z
dc.date.available
2024-12-05T21:42:29Z
dc.date.issued
2021-02-15T11:24:58Z
dc.date.issued
2021-02-15T11:24:58Z
dc.date.issued
2020-03-06
dc.date.issued
2021-02-15T11:24:58Z
dc.identifier
https://doi.org/10.3389/fnagi.2020.00052
dc.identifier
1663-4365
dc.identifier
http://hdl.handle.net/10459.1/70516
dc.identifier.uri
http://hdl.handle.net/10459.1/70516
dc.description.abstract
Human brain evolution toward complexity has been achieved with increasing energy supply as the main adaptation in brain metabolism. Energy metabolism, like other biochemical reactions in aerobic cells, is under enzymatic control and strictly regulated. Nevertheless, physiologically uncontrolled and deleterious reactions take place. It has been proposed that these reactions constitute the basic molecular mechanisms that underlie the maintenance or loss-of-function of neurons and, by extension, cerebral functions during brain aging. In this review article, we focus attention on the role of the nonenzymatic and irreversible adduction of fumarate to the protein thiols, which leads to the formation of S-(2-succino)cysteine (2SC; protein succination) in the human brain. In particular, we first offer a brief approach to the succination reaction, features related to the specificity of protein succination, methods for their detection and quantification, the bases for considering 2SC as a biomarker of mitochondrial stress, the succinated proteome, the cross-regional differences in 2SC content, and changes during brain aging, as well as the potential regulatory significance of fumarate and 2SC. We propose that 2SC defines cross-regional differences of metabolic mitochondrial stress in the human brain and that mitochondrial stress is sustained throughout the healthy adult lifespan in order to preserve neuronal function and survival.
dc.description.abstract
Research by the authors was supported by the Spanish Ministry of Economy and Competitiveness, Institute of Health Carlos III (FIS grants PI13/00584 and PI14/00328), the Spanish Ministry of Science, Innovation, and Universities (Ministerio de Ciencia, Innovación y Universidades, RTI2018-099200-B-I00), and the Generalitat of Catalonia, Agency for Management of University and Research Grants (2017SGR696) and Department of Health (SLT002/16/00250) to RP. This study has been co-financed by FEDER funds from the European Union (“A way to build Europe”). IRBLleida is a CERCA Programme/Generalitat of Catalonia. IP was supported by a University of Lleida Predoctoral Fellowship. RC and NM-M were supported by a Generalitat of Catalonia Predoctoral Fellowship. MJ is a “Serra Húnter” Fellow.
dc.format
application/pdf
dc.language
eng
dc.publisher
Frontiers Media
dc.relation
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-099200-B-I00/ES/NEUROLIPIDOMICA DEL ENVEJECIMIENTO CEREBRAL HUMANO/
dc.relation
Reproducció del document publicat a: https://doi.org/10.3389/fnagi.2020.00052
dc.relation
Frontiers In Aging Neuroscience, 2020, vol. 12, núm. 52, p. 1-9
dc.rights
cc-by (c) Jové Font, Mariona et al., 2020
dc.rights
info:eu-repo/semantics/openAccess
dc.rights
http://creativecommons.org/licenses/by/3.0/es
dc.subject
Cysteine
dc.subject
Fumarate
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Loss-of-function
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Mitochondrial stress
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Posttranslational modification (PTM)
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2-(S-succino)cysteine (2SC)
dc.subject
Tthiol groups
dc.title
Succination of protein thiols in human brain aging
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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