Taktakishvili M O, Tabdzhun A
Bioorg Khim. 1991 Jun;17(6):806-8.
A series of self-complementary decadeoxynucleotides containing a native or modified HaeIII site GGCC (with one or both guanine residues 6-O-cetylated) have been synthesized by the phosphotriester approach. The nonmodified decanucleotide is normally digested with snake venom phosphodiesterase as well as with HaeIII and BspI restriction endonucleases, whereas the bulky 6-O-alkyl substituent strongly inhibits the VPDE hydrolysis and completely prevents digestion with the endonucleases.
通过磷酸三酯法合成了一系列含有天然或修饰的HaeIII位点GGCC(一个或两个鸟嘌呤残基被6-O-乙酰化)的自互补十聚脱氧核苷酸。未修饰的十聚核苷酸通常会被蛇毒磷酸二酯酶以及HaeIII和BspI限制性内切酶消化,而庞大的6-O-烷基取代基会强烈抑制蛇毒磷酸二酯酶的水解作用,并完全阻止内切酶的消化。