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Título

Activity of core-modified 10-23 DNAzymes against HCV

Autor Robaldo, L; Berzal-Herranz, Alfredo; Montserrat, J.M; Iribarren, A.M
Fecha de publicación 2014
EditorJohn Wiley & Sons
Citación ChemMedChem 9: 2172- 2177 (2014)
ResumenThe highly conserved untranslated regions of the hepatitis C virus (HCV) play a fundamental role in viral translation and replication and are therefore attractive targets for drug development. A set of modified DNAzymes carrying (2¿R)-, (2¿S)-2¿-deoxy-2¿-C-methyl- and -2¿-O-methylnucleosides at various positions of the catalytic core were assayed against the 5¿-internal ribosome entry site element (5¿-IRES) region of HCV. Intracellular stability studies showed that the highest stabilization effects were obtained when the DNAzymes¿ cores were jointly modified with 2¿-C-methyl- and 2¿-O-methylnucleosides, yielding an increase by up to fivefold in the total DNAzyme accumulation within the cell milieu within 48 h of transfection. Different regions of the HCV IRES were explored with unmodified 10¿23 DNAzymes for accessibility. A subset of these positions was tested for DNAzyme activity using an HCV IRES-firefly luciferase translation-dependent RNA (IRES-FLuc) transcript, in the rabbit reticulocyte lysate system and in the Huh-7 human hepatocarcinoma cell line. Inhibition of IRES-dependent translation by up to 65% was observed for DNAzymes targeting its 285 position, and it was also shown that the modified DNAzymes are as active as the unmodified one.
URI http://hdl.handle.net/10261/113033
DOI10.1002/cmdc.201402222
Identificadoresdoi: 10.1002/cmdc.201402222
issn: 1860-7179
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