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两面派肽核酸:同胸腺嘧啶-同胞嘧啶双模态 Cα-PNA(-Cα-PNA)形成 -PNA:DNA 三聚体的双链体。

Peptide Nucleic Acid with Double Face: Homothymine-Homocytosine Bimodal Cα-PNA (-Cα-PNA) Forms a Double Duplex of the -PNA:DNA Triplex.

机构信息

Department of Chemistry, Indian Institute of Science Education and Research (IISER) Pune, Dr Homi Bhabha Road, Pune 411008, India.

Department of Chemistry, Indian Institute of Science Education and Research (IISER) Tirupati, Karkambadi Road, Tirupati 517507, India.

出版信息

J Org Chem. 2021 Jan 1;86(1):414-428. doi: 10.1021/acs.joc.0c02158. Epub 2020 Nov 30.

DOI:10.1021/acs.joc.0c02158
PMID:33256406
Abstract

Cα-bimodal peptide nucleic acids (-Cα-PNA) are PNAs with two faces and are designed homologues of PNAs in which each aminoethylglycine () repeating unit in the standard PNA backbone hosts a second nucleobase at Cα through a spacer chain with a triazole linker. Such -Cα-PNA with mixed sequences can form double duplexes by simultaneous binding to two complementary DNAs, one to the base sequence on t-amide side and the other to the bases on the Cα side chain. The synthesis of -Cα-PNA with homothymine (T) on the t-amide face and homocytosine (C) on the Cα side chain through the triazole linker was achieved by solid phase synthesis with the global click reaction. In the presence of complementary DNAs dA and dG at neutral pH, -Cα-PNA forms a higher order pentameric double duplex of a triplex composed of two -Cα-PNA-C:dG duplexes built on a core (-Cα-PNA-T):dA triplex. Circular dichroism studies showed that assembly can be achieved by either triplex first and duplex later or vice versa. Isothermal titration calorimetry data indicated that the assembly is driven by favorable enthalpy. These results validate concurrent multiple complex formation by bimodal PNAs with additional nucleobases at Cα or Cγ on the -PNA backbone and open up ways to design programmed supramolecular assemblies.

摘要

α-双模态肽核酸(-Cα-PNA)是两面性的 PNA,是标准 PNA 骨架中每个氨基乙基甘氨酸()重复单元通过三唑连接子的间隔链在 Cα 位上承载第二个碱基的 PNA 类似物。这种具有混合序列的-Cα-PNA 可以通过同时与两个互补 DNA 结合形成双链体,一个结合到酰胺侧的碱基序列上,另一个结合到 Cα 侧链上的碱基上。通过固相合成和全局点击反应,实现了通过三唑键连接在酰胺侧的胸腺嘧啶(T)和在 Cα 侧链上的胞嘧啶(C)的 -Cα-PNA 的同系物合成。在中性 pH 下存在互补 DNA dA 和 dG 时,-Cα-PNA 形成了一个由两个 -Cα-PNA-C:dG 双链体构建在核心 (-Cα-PNA-T):dA 三链体上的三聚体五聚体双链体。圆二色性研究表明,组装可以通过三链体首先形成双链体,或者反之亦然。等温滴定量热法数据表明,组装是由有利的焓驱动的。这些结果验证了在-PNA 骨架的 Cα 或 Cγ 上具有额外碱基的双模态 PNA 可以同时形成多个复合物,并为设计可编程超分子组装开辟了道路。

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