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dc.contributor.authorParcerisas, Antoni
dc.contributor.authorOrtega-Gascó, Alba
dc.contributor.authorHernaiz Llorens, Marc
dc.contributor.authorOdena Caballol, Maria Antonia
dc.contributor.authorUlloa, Fausto
dc.contributor.authorde Oliveira, Eliandre
dc.contributor.authorBosch, Miquel
dc.contributor.authorPujadas, Lluís
dc.contributor.authorSoriano, Eduardo
dc.date.accessioned2021-12-09T18:27:30Z
dc.date.available2021-12-09T18:27:30Z
dc.date.issued2021
dc.identifier.citationParcerisas, Antoni; Ortega-Gascó, Alba; Hernaiz-Llorens, Marc [et al.]. New partners identified by mass spectrometry assay reveal functions of NCAM2 in neural cytoskeleton organization. International Journal of Molecular Sciences, 2021, 22(14), 7404. Disponible en: <https://www.mdpi.com/1422-0067/22/14/7404>. Fecha de acceso: 9 dic. 2021. DOI: 10.3390/ijms22147404ca
dc.identifier.issn1422-0067ca
dc.identifier.urihttp://hdl.handle.net/20.500.12328/2998
dc.description.abstractNeuronal cell adhesion molecule 2 (NCAM2) is a membrane protein with an important role in the morphological development of neurons. In the cortex and the hippocampus, NCAM2 is essential for proper neuronal differentiation, dendritic and axonal outgrowth and synapse formation. However, little is known about NCAM2 functional mechanisms and its interactive partners during brain development. Here we used mass spectrometry to study the molecular interactome of NCAM2 in the second postnatal week of the mouse cerebral cortex. We found that NCAM2 interacts with >100 proteins involved in numerous processes, including neuronal morphogenesis and synaptogenesis. We validated the most relevant interactors, including Neurofilaments (NEFs), Microtubule-associated protein 2 (MAP2), Calcium/calmodulin kinase II alpha (CaMKIIα), Actin and Nogo. An in silico analysis of the cytosolic tail of the NCAM2.1 isoform revealed specific phosphorylation site motifs with a putative affinity for some of these interactors. Our results expand the knowledge of NCAM2 interactome and confirm the key role of NCAM2 in cytoskeleton organization, neuronal morphogenesis and synaptogenesis. These findings are of interest in explaining the phenotypes observed in different pathologies with alterations in the NCAM2 gene.en
dc.format.extent20ca
dc.language.isoengca
dc.publisherMDPIca
dc.relation.ispartofInternational Journal of Molecular Sciencesca
dc.relation.ispartofseries22;14
dc.rightsThis is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.otherNCAM2ca
dc.subject.otherEspectrometria de massesca
dc.subject.otherCitoesqueletca
dc.subject.otherMorfogènesi neuronalca
dc.subject.otherMAPA2ca
dc.subject.otherCaMKIIαca
dc.subject.otherNeurofilamentsca
dc.subject.otherNCAM2es
dc.subject.otherEspectrometría de masases
dc.subject.otherCitoesqueletoes
dc.subject.otherMorfogénesis neuronales
dc.subject.otherMAP2es
dc.subject.otherCaMKIIαes
dc.subject.otherNeurofilamentoses
dc.subject.otherNCAM2en
dc.subject.otherMass spectrometryen
dc.subject.otherCytoskeletonen
dc.subject.otherNeuronal morphogenesisen
dc.subject.otherMAP2en
dc.subject.otherCaMKIIαen
dc.subject.otherNeurofilamentsen
dc.titleNew partners identified by mass spectrometry assay reveal functions of NCAM2 in neural cytoskeleton organizationen
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.subject.udc54ca
dc.subject.udc57ca
dc.subject.udc61ca
dc.identifier.doihttps://dx.doi.org/10.3390/ijms22147404ca


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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0/
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