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首页> 外文期刊>Journal of Medicinal Chemistry >DNA Loop Sequence as the Determinant for Chiral Supramolecular Compound G-QuadruplexSelectivity
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DNA Loop Sequence as the Determinant for Chiral Supramolecular Compound G-QuadruplexSelectivity

机译:DNA环序列作为手性超分子化合物G四联体选择性的决定因素。

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摘要

It is important to develop G-quadruplex binding agents that can discriminate between different quadruplexes. Recently we reported the first example that a chiral supramolecular complex can selectively stabilize human telomeric G-quadruplex among different G-quadruplex and duplex DNA, and the two enantiomers showdifferent inhibition effect on telomerase activity.Here, we report thatDNAloop sequence can be determinant for this chiral complex G-quadruplex selectivity. Adenine in the diagonal loop plays an important role in G-quadruplex hybrid structural transition, thus, it strongly influences the chiral complex induced DNA structural transition. The complex’s preference for human telomeric DNA and its chiral selectivity prompted us to investigate whether the two enantiomers,Mand P, can show different effects on cancer cells. The P enantiomer’s chiral selectivity has been demonstrated in cancer cells by telomere shortening, β-galactosidase activity, and up-regulation of cyclin-dependent kinase inhibitors p16 and p21.
机译:重要的是开发能够区分不同四链体的G-四链体结合剂。最近,我们报道了第一个例子,一个手性超分子复合物可以选择性地稳定不同G-四链体和双链体DNA之间的人类端粒G-四链体,并且两种对映体对端粒酶活性的抑制作用不同。在这里,我们报道DNAloop序列可以决定这一点。手性络合物G-四链体选择性。对角环中的腺嘌呤在G-四链体杂交结构转变中起重要作用,因此,它强烈影响手性复合物诱导的DNA结构转变。该复合物对人类端粒DNA的偏爱及其手性选择性促使我们研究这两种对映异构体Mand P是否对癌细胞具有不同的作用。端粒缩短,β-半乳糖苷酶活性以及细胞周期蛋白依赖性激酶抑制剂p16和p21的上调证明了P对映体的手性选择性。

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