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Four base recognition by triplex-forming oligonucleotides at physiological pH

机译:在生理pH下通过三链体形成寡核苷酸识别四碱基

摘要

We have achieved recognition of all 4 bp by triple helix formation at physiological pH, using triplex-forming oligonucleotides that contain four different synthetic nucleotides. BAU [2′-aminoethoxy-5-(3-aminoprop-1-ynyl)uridine] recognizes AT base pairs with high affinity, MeP (3-methyl-2 aminopyridine) binds to GC at higher pHs than cytosine, while APP (6-(3-aminopropyl)-7-methyl-3H-pyrrolo[2,3-d]pyrimidin-2(7H)-one) and S [N-(4-(3-acetamidophenyl)thiazol-2-yl-acetamide)] bind to CG and TA base pairs, respectively. Fluorescence melting and DNase I footprinting demonstrate successful triplex formation at a 19mer oligopurine sequence that contains two CG and two TA interruptions. The complexes are pH dependent, but are still stable at pH 7.0. BAU, MeP and APP retain considerable selectivity, and single base pair changes opposite these residues cause a large reduction in affinity. In contrast, S is less selective and tolerates CG pairs as well as TA.
机译:我们已使用包含四个不同合成核苷酸的三链体形成寡核苷酸,在生理pH值下通过三链螺旋形成实现了对所有4 bp的识别。 BAU [2'-氨基乙氧基-5-(3-氨基丙-1-炔基)尿苷]能够以高亲和力识别AT碱基对,MeP(3-甲基-2氨基吡啶)在比pH更高的pH下与GC结合,而APP(6 -(3-氨基丙基)-7-甲基-3H-吡咯并[2,3-d]嘧啶-2(7H)-one)和S [N-(4-(3-乙酰氨基苯基)噻唑-2-基-乙酰胺)]分别与CG和TA碱基对结合。荧光熔解和DNase I足迹证明在包含两个CG和两个TA中断的19mer寡嘌呤序列上成功形成三链体。配合物是pH依赖性的,但是在pH 7.0下仍然稳定。 BAU,MeP和APP保留了相当高的选择性,并且与这些残基相反的单个碱基对变化导致亲和力大大降低。相反,S具有较低的选择性,并且可以耐受CG对和TA。

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