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Rupture force changes between the third strand and the double strand within an oligonucleotide-directed triplex in the presence of intercalative molecules

机译:在插入分子存在下,寡核苷酸定向三链体中第三链和双链之间的断裂力变化

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The rupture force changes to separate the third strand from the duplex within an oligonucleotide-directed triplex (triplex DNA) were measured in the presence of small DNA binding molecules by means of atomic force spectroscopy. Rupture force histograms revealed a rupture force of 44.3 ±0.4 pN to separate the third strand from duplex DNA in pure buffer solution at a rupture velocity of 400 nm/s. In 30 μM of Ru(bipy)_2(dppz)~(2+) buffer solution an increase of rupture force to 57±2.2 pN was observed. For 30 μM Ru(phen)_2(dppz)~(2+) a rupture force of 65.1±3.9 pN was determined. These results show that both intercalative molecules increase the stability of triplex DNA significantly.
机译:在存在小的DNA结合分子的情况下,通过原子力光谱法测量了在寡核苷酸定向的三链体(三链体DNA)内将第三链与双链体分开的断裂力变化。破裂力直方图显示破裂力为44.3±0.4 pN,以纯缓冲液在400 nm / s的破裂速度下将第三链与双链体DNA分离。在30μM的Ru(bipy)_2(dppz)〜(2+)缓冲溶液中,断裂力增加到57±2.2 pN。对于30μMRu(phen)_2(dppz)〜(2+),确定的断裂力为65.1±3.9 pN。这些结果表明,两种插入分子均显着增加了三链DNA的稳定性。

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