Pilch D S, Breslauer K J
Department of Chemistry, Rutgers-The State University of New Jersey, New Brunswick 08903.
Proc Natl Acad Sci U S A. 1994 Sep 27;91(20):9332-6. doi: 10.1073/pnas.91.20.9332.
We demonstrate that ligand binding can be used to induce the formation of triplex structures that would not otherwise form. Specifically, we show that binding of berenil or 4',6-diamidino-2-phenylindole DAPI) induces formation of the poly(rA).poly(rA).poly(dT) triplex, providing an example of an RNA(purine).RNA(purine).DNA(pyrimidine) triplex. We also show that binding of berenil, DAPI, ethidium, or netropsin can induce formation of the poly(dT).poly(rA).poly(dT) triplex, thereby overcoming a practical limitation to the formation of DNA.RNA.DNA triplexes with a purine RNA strand. Based on the enhanced thermal stabilities of the drug-bound poly(dT).poly(rA).poly(dT) complexes at 18 mM Na+, we define the relative triplex-inducing efficiencies of these four ligands to be: berenil > DAPI > ethidium > netropsin. Our results demonstrate that ligand binding can be used to induce the formation of triplex structures that do not form in the absence of the ligand. This triplex-inducing capacity has potentially important implications in the design of novel antisense, antigene, and diagnostic strategies.
我们证明配体结合可用于诱导原本不会形成的三链体结构的形成。具体而言,我们表明贝尼尔或4',6-二脒基-2-苯基吲哚(DAPI)的结合可诱导聚(rA)·聚(rA)·聚(dT)三链体的形成,提供了一种RNA(嘌呤)·RNA(嘌呤)·DNA(嘧啶)三链体的示例。我们还表明贝尼尔、DAPI、溴化乙锭或纺锤菌素的结合可诱导聚(dT)·聚(rA)·聚(dT)三链体的形成,从而克服了形成具有嘌呤RNA链的DNA·RNA·DNA三链体的实际限制。基于在18 mM Na+条件下药物结合的聚(dT)·聚(rA)·聚(dT)复合物增强的热稳定性,我们确定这四种配体的相对三链体诱导效率为:贝尼尔>DAPI>溴化乙锭>纺锤菌素。我们的结果表明配体结合可用于诱导在没有配体时不会形成的三链体结构的形成。这种三链体诱导能力在新型反义、反基因和诊断策略的设计中可能具有重要意义。