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Strong, specific, monodentate G-C base pair recognition by N7-inosine derivatives in the pyrimidine.purine-pyrimidine triple-helical binding motif.

机译:在嘧啶。嘌呤-嘧啶三螺旋结合基序中被N7-肌苷衍生物强烈,特异性,单齿G-C碱基对识别。

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摘要

The nucleoside analogs 7-(2'-deoxy-alpha-D-ribofuranosyl)hypoxanthine (alpha7H,1), 7-(2'-deoxy-beta-D-ribofuranosyl)hypoxanthine (beta7H,2) and 7-7-(2'-O-methyl-beta-D- ribofuranosyl)hypoxanthine (beta7HOMe,3) were prepared and incorporated into triplex forming oligodeoxynucleotides, designed to bind to DNA in the parallel (pyrimidine.purine-pyrimidine) motif. By DNase I footprinting techniques and UV-melting curve analysis it was found that, at pH 7. 0, the 15mer oligonucleotides d(TTTTTMeCTXTMeCTMeCTMeCT) (MeC = 5-methyl-deoxycytidine, X =beta7H,beta7HOMe) bind to a DNA target duplex forming a H.G-C base triple with equal to slightly increased (10-fold) stability compared to a control oligodeoxynucleotide in which the hypoxanthine residue is replaced by MeC. Remarkably, triple-helix formation is specific to G-C base pairs and up to 40 microM third strand concentration, no stable triplex exhibiting H.A-T, H.T-A or H.C-G base arrangements could be found (target duplex concentration approximately 0.1 nM). Multiply substituted sequences containing beta7H residues either in an isolated [d(TTTTTbeta7HTbeta7HTbeta7HTbeta7HTbeta7HT)] or in a contiguous [d(TTTbeta7Hbeta7Hbeta7Hbeta7HTTTTbeta7HTTT)] manner still form triplexes with their targets of comparable stability as the control (MeC-containing) sequences at pH 7.0 and high salt or spermine containing buffers. General considerations lead to a structural model in which the recognition of the G-C base pair by hypoxanthine takes place via only one H-bond of the N-H of hypoxanthine to N7 of guanine. This model is supported by a molecular dynamics simulation. A general comparison of the triplex forming properties of oligonucleotides containing beta7H with those containing MeC or N7-2'-deoxyguanosine (N7G) reveals that monodentate recognition in the former case can energetically compete with bidentate recognition in the latter two cases.
机译:核苷类似物7-(2'-脱氧-α-D-核呋喃核糖基)次黄嘌呤(alpha7H,1),7-(2'-脱氧-β-D-核糖呋喃糖基)次黄嘌呤(beta7H,2)和7-7-(制备2'-O-甲基-β-D-呋喃核糖基)次黄嘌呤(β7HOMe,3),并掺入形成三链体的寡脱氧核苷酸,设计为以平行(嘧啶。嘌呤-嘧啶)基序结合DNA。通过DNase I足迹技术和UV熔解曲线分析,发现在pH 7. 0下,15mer寡核苷酸d(TTTTTMeCTXTMeCTMeCTMeCT)(MeC = 5-甲基-脱氧胞苷,X = beta7H,beta7HOMe)与DNA靶双链体结合与其中次黄嘌呤残基被MeC取代的对照寡聚脱氧核苷酸相比,形成HG-C碱基三联体的稳定性略有提高(10倍)。值得注意的是,三螺旋的形成对G-C碱基对是特定的,并且高达40 microM的第三链浓度,未发现显示H.A-T,H.T-A或H.C-G碱基排列的稳定三链(目标双链体浓度约为0.1 nM)。在分离的[d(TTTTTbeta7HTbeta7HTbeta7HTbeta7HTbeta7HTbeta7HT)]或连续的[d(TTTbeta7Hbeta7Hbeta7Hbeta7HTTTTbeta7HTTT)]方式中包含beta7H残基的多取代序列仍形成三链体,其靶标在pH 7.0和高的条件下具有与对照(含MeC)序列相当的稳定性。含盐或精胺的缓冲液。一般的考虑导致了一种结构模型,其中次黄嘌呤仅通过次黄嘌呤的N-H的一个H键与鸟嘌呤的N7进行G-C碱基对的识别。该模型得到分子动力学仿真的支持。含有beta7H的寡核苷酸与含有MeC或N7-2'-脱氧鸟苷(N7G)的寡核苷酸的三链体形成特性的一般比较表明,在前一种情况下,单齿识别可以在后两种情况下与双齿识别强烈竞争。

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