| Literature DB >> 24133216 |
Manuela Gellert1, Simone Venz, Jessica Mitlöhner, Catherine Cott, Eva-Maria Hanschmann, Christopher Horst Lillig.
Abstract
Vertebrate-specific glutaredoxin 2 (Grx2) is expressed in at least two isoforms, mitochondrial Grx2a and cytosolic Grx2c. We have previously shown that cytosolic Grx2 is essential for embryonic development of the brain. In particular, we identified collapsin response mediator protein 2 (CRMP2/DPYSL2), a mediator of the semaphorin-plexin signaling pathway, as redox-regulated target of Grx2c and demonstrated that this regulation is required for normal axonal outgrowth. In this study, we demonstrate the molecular mechanism of this regulation, a specific and reversible intermolecular Cys-504-Cys-504 dithiol-disulfide switch in homotetrameric CRMP2. This switch determines two conformations of the quaternary CRMP2 complex that controls axonal outgrowth and thus neuronal development.Entities:
Keywords: CRMP2; Disulfide; Glutaredoxin; Neurodifferentiation; Neuronal Differentiation; Redox Regulation; Redox Signaling; Redox Switch; Thiol
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Year: 2013 PMID: 24133216 PMCID: PMC3853263 DOI: 10.1074/jbc.M113.521443
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157