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首页> 外文期刊>Biopolymers: Original Research on Biomolecules and Biomolecular Assemblies >NOVEL HOOGSTEEN-LIKE BASES FOR CONFIGURATIONAL RECOGNITION OF THE T-A BASE PAIR BY DNA TRIPLEX FORMATION
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NOVEL HOOGSTEEN-LIKE BASES FOR CONFIGURATIONAL RECOGNITION OF THE T-A BASE PAIR BY DNA TRIPLEX FORMATION

机译:通过DNA TRIPLEX形成构象识别T-A碱基对的新型HOOGSTEEN-like碱基

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摘要

Effective sequence-specific recognition of duplex DNA is possible by triplex formation with natural oligonucleotides via Hoogsteen H-bonding. However, triplex formation is in practice limited to pyrimidine oligonucleotides binding duplex A-T or G-C base-pair DNA sequences specifically at homopurine sites in the major groove as T . A-T and C+. G-C triplets. Here we report the successful modeling of novel unnatural nucleosides that recognize the T-A DNA base pair by Hoogsteen interaction. Since the DNA triplex can be considered to assume an A-type or B-type conformation, these novel Hoogsteen nucleotides are tested within model A-type and B-type conformation triplex structures. A triplex consisting of the T-A base pair and one of the one novel Hoogsteen nucleotides replaces the central T . A-T triplet in the triplex using the same deoxyribose-phosphodiester and base-deoxyribose dihedral angle configuration. The entire triplex is energy minimized and the presence of any structural or energetic perturbations due to the central triplet is assessed with respect to the unmodified energy-minimized (T . A-T)(11) proposed starting structures. Incorporation of these novel triplets into both A-type and B-type natural triplex structures provokes minimal charge in the configuration of the central and adjacent triplets. The plan is to produce a series of Hoogsteen-like bases that preferentially bind the T-A major groove in either an A-type or B-type conformation. Selective recognition of the T-A major groove with respect to the G-C major groove, which presents similar keto and amine placement, is also assessed with configurational preference. Evaluation of the triplex solution structure by using these unnatural bases as binding conformational probes is a prerequisite to the further design of triplet forming bases. (C) 1996 John Wiley & Sons, Inc. [References: 45]
机译:通过天然寡核苷酸通过Hoogsteen H键形成三链体,可以有效地识别双链DNA。但是,实际上,三链体的形成仅限于结合双链A-T或G-C碱基对DNA序列的嘧啶寡核苷酸,该双特异性A-T或G-C碱基对DNA序列特别是在大沟中的高嘌呤位点作为T。 A-T和C +。 G-C三胞胎。在这里,我们报告成功的新型非天然核苷建模,通过Hoogsteen相互作用识别T-A DNA碱基对。由于可以将DNA三链体假定为A型或B型构象,因此需要在模型A型和B型构象三链体结构中测试这些新颖的Hoogsteen核苷酸。由T-A碱基对和一个新的Hoogsteen核苷酸之一组成的三链体取代了中心T。三元组中的A-T三元组使用相同的脱氧核糖-磷酸二酯和碱基-脱氧核糖二面角构型。相对于未修改的能量最小化(T.A-T)(11)提出的起始结构,将整个三元组的能量最小化,并评估由于中央三元组而引起的任何结构或能量扰动的存在。将这些新颖的三联体结合到A型和B型天然三链体结构中,在中心和相邻三联体的构型中产生的电荷最小。该计划是要生产一系列类似Hoogsteen的碱基,这些碱基优先结合A型或B型构型的T-A主沟。相对于G-C主槽的T-A主槽的选择性识别,其表现出相似的酮和胺位置,也通过构型偏爱进行评估。通过使用这些非天然碱基作为结合构象探针来评估三链体溶液结构是进一步设计三链体形成碱基的先决条件。 (C)1996 John Wiley&Sons,Inc. [参考:45]

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