苯并咪唑:小凹槽结合配体诱导的三螺旋稳定。

Akash K Jain, Sharad K Gupta, Urmila Tawar, Sneh K Dogra, Vibha Tandon
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引用次数: 3

摘要

据报道,非插层的次要凹槽结合配体netropsin、Hoechst 33258和DAPI会破坏三联体的稳定性。考察了双苯并咪唑和特苯并咪唑的苯基环上不同取代配体对C+稳定性的影响。GC三房和Hoogsteen双房。我们发现新合成的苯并咪唑稳定了三联体,如荧光和熔融研究所示。模型研究表明,这些分子结合在三联体的沃森-克里克小凹槽中,这可以对宿主三联体的性质产生深远的影响。环二色性结合研究表明5.77碱基三联体/配体是双-和8.66特苯并咪唑的明显结合位点。在pH值为5.2的条件下,苯并咪唑的氮和胺的质子化补偿了磷酸主链的负电荷,从而减少了链间的排斥力,从而使三络合物稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Benzimidazoles: a minor groove-binding ligand-induced stabilization of triple helix.

Nonintercalating minor groove-binding ligands netropsin, Hoechst 33258, and DAPI are reported to destabilize the triplex. Ligands with different substitutions on the phenyl ring of bis- and terbenzimidazoles were evaluated for their effect on the stability of C+.GC triplex and Hoogsteen duplex. We found that newly synthesized benzimidazoles stabilize the triplex as shown by fluorescence and melting studies. Modeling studies showed that these molecules bind in the Watson-Crick minor groove of triplex, which can exert a profound impact on the properties of the host triplex. Circular dichroism-binding studies indicate 5.77 base triplets/ligand as an apparent binding site for bis- and 8.66 for terbenzimidazoles. The stabilization of triplex can be attributed to the protonation of nitrogens and amines of benzimidazoles at pH 5.2 that compensate the negative charge of phosphate backbone to reduce the repulsion between the strands resulting in the stabilization.

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来源期刊
Oligonucleotides
Oligonucleotides 生物-生化与分子生物学
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