核酸外切酶
寡核苷酸
组合化学
核苷酸
化学
基因
体外
生物化学
生物
DNA聚合酶
作者
D. Pandolfi,Francesca Rauzi,Massimo L. Capobianco
标识
DOI:10.1080/07328319908044864
摘要
Abstract Synthetic oligonucleotides are increasingly used because of their potential activity as regulators of gene expression. One of their major drawbacks is instability toward nucleases, in particular exonucleases. In this article, we studied some terminal modifications that can enhance exonuclease resistance, such as end-capping with alkylic chains (1,3-propanediol and 1,6-hexanediol), and with a modified nucleotide (2′,3′ -secouridine). These compounds were compared with the parent (natural) oligodeoxynucleotide and with different analogs containing a progressive number of phosphorothioate linkages. The resistance toward SVPDE and CSPDE (a 3′ - and a 5′ -exonuclease) was assessed, in vitro, by two independent techniques, UV and HPLC. Our results showed that the stability of all the modified oligonucleotides was at least 12 times that of the parent compound.
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