Aviso: para depositar documentos, por favor, inicia sesión e identifícate con tu cuenta de correo institucional de la UCM con el botón MI CUENTA UCM. No emplees la opción AUTENTICACIÓN CON CONTRASEÑA
 

The deletion of residues 268-292 of E1 impairs the ability of HCV envelope proteins to induce pore formation

dc.contributor.authorLombana, Laura
dc.contributor.authorOrtega Atienza, Sara
dc.contributor.authorGómez Gutiérrez, Julián
dc.contributor.authorYélamos, Belén
dc.contributor.authorPeterson, Darrell
dc.contributor.authorGavilanes, Francisco
dc.date.accessioned2023-06-18T06:50:45Z
dc.date.available2023-06-18T06:50:45Z
dc.date.issued2016-03-06
dc.description.abstractWe have obtained a chimeric protein containing the ectodomains of hepatitis C virus (HCV) envelope proteins but lacking the region 268-292 of E1. All its structural properties are coincident with those of the corresponding full length chimera. The deleted and entire chimeras were compared in terms of their membrane destabilizing properties. No differences were found in their ability to induce vesicle aggregation and lipid mixing but the deleted chimera showed a reduced capacity to promote leakage. The role of the deletion was also studied by obtaining HCV pseudoparticles (HCVpp). Both E1 and E2, and also the E1 deleted mutant, were incorporated into HCVpp to a similar level. However, HCVpp containing the E1 deleted protein are almost unable to infect Huh7 cells. These results point to the involvement of the region 268-292 in the formation of pores in the membrane necessary for the complete fusion of the membranes.
dc.description.departmentDepto. de Bioquímica y Biología Molecular
dc.description.facultyFac. de Ciencias Químicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (MINECO)
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/36213
dc.identifier.doi10.1016/j.virusres.2016.02.009
dc.identifier.issn1872-7492 (Online), 0168-1702 (print)
dc.identifier.officialurlhttp://www.sciencedirect.com/science/article/pii/S0168170215301660
dc.identifier.urihttps://hdl.handle.net/20.500.14352/24382
dc.journal.titleVirus Research
dc.language.isoeng
dc.publisherElsevier
dc.relation.projectIDBFU 2010-22014
dc.rights.accessRightsopen access
dc.subject.cdu577.1
dc.subject.keywordhepatitis C virus
dc.subject.keywordviral envelope proteins
dc.subject.keywordlipid-protein interaction
dc.subject.keywordmembrane fusion
dc.subject.keywordprotein spectroscopic properties.
dc.subject.ucmBiología molecular (Biología)
dc.subject.ucmBioquímica (Biología)
dc.subject.unesco2415 Biología Molecular
dc.subject.unesco2302 Bioquímica
dc.titleThe deletion of residues 268-292 of E1 impairs the ability of HCV envelope proteins to induce pore formation
dc.typejournal article
dspace.entity.typePublication
relation.isAuthorOfPublication9a5864e1-4f64-4204-bb1d-0d2c95e67a3a
relation.isAuthorOfPublication.latestForDiscovery9a5864e1-4f64-4204-bb1d-0d2c95e67a3a

Download

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Virus Research 2016 (Gavilanes).pdf
Size:
420.02 KB
Format:
Adobe Portable Document Format

Collections