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嘧啶-嘌呤-嘧啶三螺旋结合基序中N7-肌苷衍生物对G-C碱基对的强特异性单齿识别。

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

作者信息

Marfurt J, Parel S P, Leumann C J

机构信息

Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, CH-3012 Bern, Switzerland.

出版信息

Nucleic Acids Res. 1997 May 15;25(10):1875-82. doi: 10.1093/nar/25.10.1875.

Abstract

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.

摘要

制备了核苷类似物7-(2'-脱氧-α-D-呋喃核糖基)次黄嘌呤(α7H,1)、7-(2'-脱氧-β-D-呋喃核糖基)次黄嘌呤(β7H,2)和7-(2'-O-甲基-β-D-呋喃核糖基)次黄嘌呤(β7HOMe,3),并将其掺入到三链形成寡脱氧核苷酸中,这些寡脱氧核苷酸设计用于以平行(嘧啶·嘌呤-嘧啶)基序与DNA结合。通过DNase I足迹技术和紫外熔解曲线分析发现,在pH 7.0时,15聚体寡核苷酸d(TTTTTMeCTXTMeCTMeCTMeCT) (MeC = 5-甲基-脱氧胞苷,X =β7H,β7HOMe)与DNA靶双链体结合,形成H.G-C碱基三联体,与次黄嘌呤残基被MeC取代的对照寡脱氧核苷酸相比,稳定性相等或略有增加(10倍)。值得注意的是,三链体形成对G-C碱基对具有特异性,在高达40 μM的第三链浓度下,未发现具有H.A-T、H.T-A或H.C-G碱基排列的稳定三链体(靶双链体浓度约为0.1 nM)。在pH 7.0以及高盐或含精胺的缓冲液中,含有β7H残基的多重取代序列,无论是以孤立的方式[d(TTTTTβ7HTβ7HTβ7HTβ7HTβ7HT)]还是连续的方式[d(TTTβ7Hβ7Hβ7Hβ7HTTTTβ7HTTT)],仍然与它们的靶标形成稳定性与对照(含MeC)序列相当的三链体。综合考虑得出一个结构模型,其中次黄嘌呤对G-C碱基对的识别仅通过次黄嘌呤的N-H与鸟嘌呤的N7之间的一个氢键发生。分子动力学模拟支持了该模型

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Ribosyl derivatives of hypoxanthine.次黄嘌呤的核糖基衍生物。
J Org Chem. 1969 Sep;34(9):2646-50. doi: 10.1021/jo01261a034.

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