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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

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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-1ynyl) uridine] recognizes AT base pairs with high affinity, P-Me (3-methyl-2 aminopyridine) binds to GC at higher pHs than cytosine, while (PP)-P-A (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, P-Me and (PP)-P-A 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:我们已经通过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,P-Me(3-甲基-2氨基吡啶)在比pH更高的pH值下与GC结合,而(PP) -PA(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-酰基-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。该配合物是pH依赖性的,但是在pH 7.0下仍然稳定。 BAU,P-Me和(PP)-P-A保留了相当大的选择性,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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