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dc.contributor.authorJaraíz-Rodríguez, Myriam
dc.contributor.authorGonzález-Sánchez, Ana
dc.contributor.authorGarcía-Vicente, Laura
dc.contributor.authorMedina, Jose M.
dc.contributor.authorTabernero, Arantxa
dc.date.accessioned2020-01-31T09:10:29Z
dc.date.available2020-01-31T09:10:29Z
dc.date.issued2017
dc.identifier.citationJaraíz-Rodríguez, M., González-Sánchez, A., García-Vicente, L., Medina, J. M., Tabernero, A. (2017). Biotinylated Cell-penetrating Peptides to Study Intracellular Protein-protein Interactions. Journal of Visualized Experiments, (130), e56457. doi:10.3791/56457es_ES
dc.identifier.issn1940-087X
dc.identifier.urihttp://hdl.handle.net/10366/140747
dc.description.abstract[EN] Here we present a protocol to study intracellular protein-protein interactions that is based on the widely used biotin-avidin pull-down system. The modification presented includes the combination of this technique with cell-penetrating sequences. We propose to design cell-penetrating baits that can be incubated with living cells instead of cell lysates and therefore the interactions found will reflect those that occur within the intracellular context. Connexin43 (Cx43), a protein that forms gap junction channels and hemichannels is down-regulated in high-grade gliomas. The Cx43 region comprising amino acids 266-283 is responsible for the inhibition of the oncogenic activity of c-Src in glioma cells. Here we use TAT as the cell-penetrating sequence, biotin as the pull-down tag and the region of Cx43 comprised between amino acids 266-283 as the target to find intracellular interactions in the hard-to-transfect human glioma stem cells. One of the limitations of the proposed method is that the molecule used as bait could fail to fold properly and, consequently, the interactions found could not be associated with the effect. However, this method can be especially interesting for the interactions involved in signal transduction pathways because they are usually carried out by intrinsically disordered regions and, therefore, they do not require an ordered folding. In addition, one of the advantages of the proposed method is that the relevance of each residue on the interaction can be easily studied. This is a modular system; therefore, other cell-penetrating sequences, other tags, and other intracellular targets can be employed. Finally, the scope of this protocol is far beyond protein-protein interaction because this system can be applied to other bioactive cargoes such as RNA sequences, nanoparticles, viruses or any molecule that can be transduced with cell-penetrating sequences and fused to pull-down tags to study their intracellular mechanism of action.es_ES
dc.format.mimetypeapplicatio/pdf
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectBiochemistryes_ES
dc.subjectIssue 130es_ES
dc.subjectTATes_ES
dc.subjectBiotin-avidines_ES
dc.subjectCell-penetrating peptideses_ES
dc.subjectPull-downes_ES
dc.subjectIntracellular interactionses_ES
dc.subjectProtein-protein interactionses_ES
dc.subjectWestern blotes_ES
dc.subject.meshIntracellular Signaling Peptides and Proteins*
dc.titleBiotinylated Cell-penetrating Peptides to Study Intracellular Protein-protein Interactionses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttp://dx.doi.org/10.3791/56457
dc.identifier.doi10.3791/56457
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1940-087X
dc.journal.titleJournal of Visualized Experimentses_ES
dc.issue.number130es_ES
dc.page.initial1es_ES
dc.page.final11es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decspéptidos y proteínas de señalización intracelular*


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internacional