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Authordc.contributor.authorFlores, Karen A. 
Authordc.contributor.authorSalgado, J. Cristian 
Authordc.contributor.authorZapata Torres, Gerald 
Authordc.contributor.authorGerdtzen Hakim, Ziomara 
Authordc.contributor.authorGonzalez, María Julieta 
Authordc.contributor.authorHermoso Ramello, Marcela 
Admission datedc.date.accessioned2018-12-20T14:13:20Z
Available datedc.date.available2018-12-20T14:13:20Z
Publication datedc.date.issued2012
Cita de ítemdc.identifier.citationBiotechnology and Bioprocess Engineering, Volumen 17, Issue 3, 2018, Pages 485-499
Identifierdc.identifier.issn12268372
Identifierdc.identifier.issn19763816
Identifierdc.identifier.other10.1007/s12257-011-0482-z
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/154965
Abstractdc.description.abstractIn order to develop future therapeutic applications for cell penetrating peptides (CPPs), it is essential to characterize their internalization mechanisms, as they might affect the stability and the accessibility of the carried drug. Several internalization mechanisms have been described in literature, such as endocytosis and transduction. In this work we study the internalization mechanism in HeLa cells of two TIRAP derived peptides: pepTIRAP and pepTIRAPALA, where some of the cationic amino acids were replaced with alanines. Detailed analysis of inter-nalization and the peptides electrostatic potential was carried out, to shed light on the internalization mechanism involved. Molecular modeling studies showed that the main difference identified between pepTIRAP and pepTIRAPALA is the distribution of their electrostatic potential field. The structure of pepTIRAP displays a predominantly positive potential when compared to pepTIRAPALA, which has a more balanced potential distribution. I
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceBiotechnology and Bioprocess Engineering
Keywordsdc.subjectCell penetrating peptide
Keywordsdc.subjectElectrostatic potential
Keywordsdc.subjectInternalization mechanism
Keywordsdc.subjectTIRAP
Keywordsdc.subjectTransduction
Títulodc.titleEffect of the electrostatic potential on the internalization mechanism of cell penetrating peptides derived from TIRAP
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile