A molecular beacon strategy for real-time monitoring of triplex DNA formation kinetics.

T. Antony, V. Subramaniam
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引用次数: 17

Abstract

We used a molecular beacon (MB) containing a 15-mer triplex-forming oligonucleotide (TFO) to probe in real-time the kinetics of triplex DNA formation in the left side of the TCl tract (502-516) of the c-src proto-oncogene in vitro. The metal ions Na+, K+, and Mg2+ stabilized triplex DNA at this site. The pseudo-first-order rate constant (kpsi) and the second-order association rate constant (k1) for the binding of the MB to the target duplex in 10 mM sodium phosphate buffer, pH 7.3, increased from 3.2 +/- 0.9 to 15 +/- 2.8 x 10(-3) s(-1) and 6.4 +/- 1.8 to 30 +/- 5.6 x 102 M(-1) s(-1), respectively, on increasing the MgCl2 concentration from 1 to 2.5 mM. Similar values were obtained for the triplex DNA stabilized by NaCl (100-250 mM). Surprisingly, the values were around 2 times higher in the presence of KCl. The AG of triplex formation in the presence of 1 mM MgCl2, 150 mM NaCl, and 150 mM KCl were -7.8 +/- 0.3, -8.2 +/- 0.3 and -8.7 +/- 0.7 kcal/mol respectively, despite significant differences in the values of deltaH and deltaS, suggesting enthalpy-entropy compensation in the stabilization of the triplex DNA by these metal ions. These results show the utility of MBs ih probing triplex DNA formation and in evaluating kinetic and thermodynamic parameters important for the design and development of TFOs as triplex DNA-based therapeutic agents.
实时监测三重DNA形成动力学的分子信标策略。
我们使用含有15-mer三联体形成寡核苷酸(TFO)的分子信标(MB)在体外实时探测c-src原癌基因TCl束左侧(502-516)三联体DNA形成的动力学。金属离子Na+、K+和Mg2+稳定了这一位点的三联体DNA。在10 mM磷酸钠缓冲液(pH 7.3)中,当MgCl2浓度从1增加到2.5 mM时,MB与目标双链结合的准一级速率常数(kpsi)和二级结合速率常数(k1)分别从3.2 +/- 0.9增加到15 +/- 2.8 × 10(-3) s(-1)和6.4 +/- 1.8增加到30 +/- 5.6 × 102 M(-1) s(-1)。NaCl (100-250 mM)稳定的三链DNA也获得了类似的值。令人惊讶的是,在氯化钾存在的情况下,这些值大约高出2倍。在1 mM MgCl2、150 mM NaCl和150 mM KCl存在下,三聚体形成的AG分别为-7.8 +/- 0.3、-8.2 +/- 0.3和-8.7 +/- 0.7 kcal/mol,尽管δ tah和δ tas的值存在显著差异,这表明这些金属离子对三聚体DNA的稳定起到了焓熵补偿作用。这些结果表明,MBs在探测三重DNA形成和评估动力学和热力学参数方面的效用,对于设计和开发tfo作为三重DNA为基础的治疗剂至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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