首页> 美国卫生研究院文献>Nucleic Acids Research >Alpha-DNA. IV: Alpha-anomeric and beta-anomeric tetrathymidylates covalently linked to intercalating oxazolopyridocarbazole. Synthesis physicochemical properties and poly (rA) binding.
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Alpha-DNA. IV: Alpha-anomeric and beta-anomeric tetrathymidylates covalently linked to intercalating oxazolopyridocarbazole. Synthesis physicochemical properties and poly (rA) binding.

机译:α-DNA。 IV:与插入的恶唑并吡咯并咔唑共价连接的α-异头和β-异头四甲基。合成理化性质和聚(rA)结合。

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摘要

A new set of molecules made of an intercalating agent (oxazolopyridocarbazole, OPC) covalently linked through a polymethylene chain of various length to the 3' end of alpha-anomeric or beta-anomeric tetradeoxynucleotides (alpha- or beta-T4) have been synthesized. The beta-thymidylate modified compound (beta-T4C5OPC) is able to interact with the complementary sequence, beta-poly (rA); this interaction is strongly stabilized compared to the parent compound, beta-oligo(dT)4 and is specific for poly (rA). The molecule synthesized from the unnatural alpha-anomer, alpha-T4C5OPC, is also able to interact with poly (rA) leading to the formation of an alpha-beta hybrid stabilized by the energy provided by the OPC moiety. The stoechiometry of the binding reaction shows that an A-T pairing occurs in the alpha-beta heterohybrids. Tm studies reveal that the alpha-beta heterohybrids are more stable than their beta-beta counterparts.
机译:已经合成了一组新的分子,该分子由嵌入剂(恶唑并吡啶并咔唑,OPC)通过各种长度的多亚甲基链共价连接至α-异头或β-异头四脱氧核苷酸(α-或β-T4)的3'端。 β-胸苷酸修饰的化合物(β-T4C5OPC)能够与互补序列β-poly(rA)相互作用;与母体化合物β-oligo(dT)4相比,这种相互作用非常稳定,并且对聚(rA)具有特异性。由非天然α-异头物α-T4C5OPC合成的分子也能够与聚(rA)相互作用,导致形成由OPC部分提供的能量稳定的α-β杂化物。结合反应的化学计量表明,A-T配对发生在alpha-beta杂种中。 Tm研究表明,α-β杂种比其β-β杂种更稳定。

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