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dc.contributor.author
Dellafiore, María Andrea
dc.contributor.author
Aviñó, Anna
dc.contributor.author
Alagia, Adele
dc.contributor.author
Montserrat, Javier Marcelo
dc.contributor.author
Iribarren, Adolfo Marcelo
dc.contributor.author
Eritja, Ramon
dc.date.available
2020-03-03T19:38:35Z
dc.date.issued
2018-03
dc.identifier.citation
Dellafiore, María Andrea; Aviñó, Anna; Alagia, Adele; Montserrat, Javier Marcelo; Iribarren, Adolfo Marcelo; et al.; siRNA modified with 2′-deoxy-2′-c-methylpyrimidine nucleosides; Wiley VCH Verlag; Chembiochem; 19; 13; 3-2018; 1409-1413
dc.identifier.issn
1439-4227
dc.identifier.uri
http://hdl.handle.net/11336/98721
dc.description.abstract
(2′S)-2′-Deoxy-2′-C-methyluridine and (2′R)-2′-deoxy-2′-C-meth-yluridine were incorporated in the 3’-overhang region of the sense and antisense strands and in positions 2 and 5 of the seed region of siRNA duplexes directed against Renilla luciferase, whereas (2′S)-2′-deoxy-2′-C-methylcytidine was incorporated in the 6-position of the seed region of the same constructions. A dual luciferase reporter assay in transfected HeLa cells was used as a model system to measure the IC50 values of 24 different modified duplexes. The best results were obtained by the substitution of one thymidine unit in the antisense 3’-overhang region by (2′S)-or (2′R)-2′-deoxy-2′-C-methyluridine, reducing IC50 to half of the value observed for the natural control. The selectivity of the modified siRNA was measured, it being found that modifications in positions 5 and 6 of the seed region had a positive effect on the ON/OFF activity.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Wiley VCH Verlag
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
ACTIVITY RELATIONSHIPS
dc.subject
DEOXYMETHYLPYRIMIDINE BASES
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NUCLEOSIDES
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SIRNA
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STABILITY
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STRUCTURE
dc.subject.classification
Otras Ciencias Químicas
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Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
siRNA modified with 2′-deoxy-2′-c-methylpyrimidine nucleosides
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2020-02-26T15:01:14Z
dc.journal.volume
19
dc.journal.number
13
dc.journal.pagination
1409-1413
dc.journal.pais
Alemania
dc.journal.ciudad
Weinheim
dc.description.fil
Fil: Dellafiore, María Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
dc.description.fil
Fil: Aviñó, Anna. Consejo Superior de Investigaciones Científicas. Instituto de Química Avanzada de Catalunya; España. Ciber Bioingenieria, Biomateriales y Nanomedicina; España
dc.description.fil
Fil: Alagia, Adele. Consejo Superior de Investigaciones Científicas. Instituto de Química Avanzada de Catalunya; España. Ciber Bioingenieria, Biomateriales y Nanomedicina; España
dc.description.fil
Fil: Montserrat, Javier Marcelo. Universidad Nacional de General Sarmiento. Instituto de Ciencias; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
dc.description.fil
Fil: Iribarren, Adolfo Marcelo. Universidad Nacional de Quilmes. Departamento de Ciencia y Tecnología. Área Química. Laboratorio de Biotransformaciones; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
dc.description.fil
Fil: Eritja, Ramon. Consejo Superior de Investigaciones Científicas. Instituto de Química Avanzada de Catalunya; España. Ciber Bioingenieria, Biomateriales y Nanomedicina; España
dc.journal.title
Chembiochem
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/cbic.201800077
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/pdf/10.1002/cbic.201800077
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