dc.creatorTrombetta, E. Sergio
dc.creatorParodi, Armando José A.
dc.date.accessioned2018-04-19T17:47:23Z
dc.date.accessioned2018-11-06T11:39:43Z
dc.date.available2018-04-19T17:47:23Z
dc.date.available2018-11-06T11:39:43Z
dc.date.created2018-04-19T17:47:23Z
dc.date.issued2005-04
dc.identifierTrombetta, E. Sergio; Parodi, Armando José A.; Glycoprotein reglucosylation; Academic Press Inc Elsevier Science; Methods; 35; 4; 4-2005; 328-337
dc.identifier1046-2023
dc.identifierhttp://hdl.handle.net/11336/42692
dc.identifier1095-9130
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1857101
dc.description.abstractProteins following the secretory pathway acquire their proper tertiary and in certain cases also quaternary structures in the endoplasmic reticulum (ER). Incompletely folded species are retained in the ER and eventually degraded. One of the molecular mechanisms by which cells achieve this conformational sorting is based on monoglucosylated N-glycans (Glc1Man5-9GlcNAc2) present on nascent glycoproteins in the ER. This chapter discusses two of the steps that regulate the abundance of such N-glycan structures, including glycoprotein deglucosylation (by glucosidase II) and reglucosylation (by the UDP-Glc:glycoprotein glucosyltransferase), as well as an overview of methods to evaluate the N-glycans prevalent during glycoprotein biogenesis in the ER.
dc.languageeng
dc.publisherAcademic Press Inc Elsevier Science
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S1046202304002300
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.ymeth.2004.10.004
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectGLYCOPROTEINS
dc.titleGlycoprotein reglucosylation
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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