Publicidad

Publicidad

becas.universia.netBiblioteca.Net

Buscar recursos:

Buscador Google

Polyamine derivatives as selective RNaseA mimics

Descargar SCORM

Este recurso ha sido solicitado 1 veces (0 veces en los últimos 31 días).

Para poder solicitar este recurso debe identificarse como usuario de la biblioteca

 
Ver

Detalles del recurso

Marcadores Sociales
Polyamine derivatives as selective RNaseA mimics
Id. 17940275
Idioma inglés
Titulo Polyamine derivatives as selective RNaseA mimics
Autor(es) Fouace, Sandra
Gaudin, Cyril
Picard, Sylvie
Corvaisier, Sophie
Renault, Jacques
Carboni, Bertrand
Felden, Brice
Localización http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=373269
Versión 1.0
Estado Final
Descripción Site-selective scission of ribonucleic acids (RNAs) has attracted considerable interest, since RNA is an intermediate in gene expression and the genetic material of many pathogenic viruses. Polyamine-imidazole conjugates for site-selective RNA scission, without free imidazole, were synthesized and tested on yeast phenylalanine transfer RNA. These molecules catalyze RNA hydrolysis non-randomly. Within the polyamine chain, the location of the imidazole residue, the numbers of nitrogen atoms and their relative distances have notable influence on cleavage selectivity. A norspermine derivative reduces the cleavage sites to a unique location, in the anticodon loop of the tRNA, in the absence of complementary sequence. Experimental results are consistent with a cooperative participation of an ammonium group of the polyamine moiety, in addition to itâ??s binding to the negatively charged ribose-phosphate backbone, as proton source, and the imidazole moiety as a base. There is correlation between the location of the magnesium binding sites and the RNA cleavage sites, suggesting that the protonated nitrogens of the polycationic chain compete with some of the magnesium ions for RNA binding. Therefore, the cleavage pattern is specific of the RNA structure. These compounds cleave at physiological pH, representing novel reactive groups for antisense oligonucleotide derivatives or to enhance ribozyme activity.
Palabras clave Articles
Tipo de recurso Text
Tipo de Interactividad Expositivo
Nivel de Interactividad muy bajo
Audiencia Estudiante
Profesor
Autor
Estructura Atomic
Coste no
Copyright
Copyright © 2004 Oxford University Press
Requerimientos técnicos Browser: Any
Fecha de contribución 11-feb-2008
Contacto

Valoración de los usuarios

No hay ninguna valoración para este recurso. Sea el primero en valorar este recurso.