dc.creatorPujals, Sílvia
dc.creatorFernández Carneado, Jimena
dc.creatorLópez Iglesias, Carmen
dc.creatorKogan Bocian, Marcelo
dc.creatorGiralt, Ernest
dc.date.accessioned2009-06-10T16:22:03Z
dc.date.available2009-06-10T16:22:03Z
dc.date.created2009-06-10T16:22:03Z
dc.date.issued2006-03
dc.identifierBIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES Volume: 1758 Issue: 3 Pages: 264-279 Published: MAR 2006
dc.identifier0005-2736
dc.identifierhttps://repositorio.uchile.cl/handle/2250/120665
dc.description.abstractIn recent years, cell-penetrating peptides have proven to be an efficient intracellular delivery system. The mechanism for CPP internalisation, which first involves interaction with the extracellular matrix, is followed in most cases by endocytosis and finally, depending on the type of endocytosis, an intracellular fate is reached. Delivery of cargo attached to a CPP requires endosomal release, for which different methods have recently been proposed. Positively charged amino acids, hydrophobicity and/or amphipathicity are common to CPPs. Moreover, some CPPs can self-assemble. Herein is discussed the role of self assembly in the cellular uptake of CPPs. Sweet Arrow Peptide (SAP) CPP has been shown to aggregate by CD and TEM (freeze-fixation/freeze-drying), although the internalised species have yet to be identified as either the monomer or an aggregate.
dc.languageen
dc.publisherELSEVIER
dc.subjectCELL-PENETRATING PEPTIDES
dc.titleMechanistic aspects of CPP-mediated intracellular drug delivery: Relevance of CPP self-assembly
dc.typeArtículo de revista


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