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Article Dans Une Revue Chemical Monthly = Monatshefte für Chemie Année : 2013

Boronic acid-based autoligation of nucleic acids: influence of the nature of the 30-end ribonucleotidic strand

Résumé

The development of synthetic systems displaying dynamic and adaptive characteristics is a formidable challenge with wide applications from biotechnology to therapeutics. Recently, we described a dynamic and programmable nucleic acid-based system relying on the formation of reversible boronate internucleosidic linkages. The DNA- or RNA-templated system comprises a 50 -ended boronic acid probe connecting a 30 -ended ribonucleosidic oligonucleotide partner. To explore the dominant factors that control the reversible linkage, we synthesized a series of 30 -end modified ribonucleotidic strands. Evidence suggests that geometric and steric factors are key features for controlling the equilibria.

Domaines

Chimie organique

Dates et versions

hal-00821002 , version 1 (07-05-2013)

Identifiants

Citer

Renaud Barbeyron, Jesper Wengel, Jean-Jacques Vasseur, Michaël Smietana. Boronic acid-based autoligation of nucleic acids: influence of the nature of the 30-end ribonucleotidic strand. Chemical Monthly = Monatshefte für Chemie, 2013, 144, pp.495-500. ⟨10.1007/s00706-012-0881-7⟩. ⟨hal-00821002⟩
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