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具有二酮哌嗪骨架的双面肽核酸的合成。

Synthesis of Bifacial Peptide Nucleic Acids with Diketopiperazine Backbones.

作者信息

Devari Shekaraiah, Bhunia Debmalya, Bong Dennis

机构信息

Department of Chemistry and Biochemistry, The Ohio State University, 100 W. 18th Avenue, Columbus, Ohio 43210, USA.

出版信息

Synlett. 2022 Jun;33(10):965-968. doi: 10.1055/a-1802-6873. Epub 2022 Apr 28.

Abstract

We report a synthesis of bifacial peptide nucleic acids (bPNAs) with novel diketopiperazine (DKP) backbones that display unnatural melamine (M) bases, as well as native bases. To examine the structure-function scope of DKP bPNAs, we synthesized a set of bPNAs by using diaminopropionic acid, diaminobutyric acid, ornithine, and lysine derivatives to display the base-tripling motifs, which result in one, two, three, or four carbons linking the alpha carbon to the side-chain amine. Thermal denaturation of DNA hybrids with these bPNAs revealed that the optimal side-chain linkage was four carbons, corresponding to the lysine derivative. Accordingly, monomers displaying two bases per side-chain were prepared through double reductive alkylation of the ε-amine of Fmoc-lysine with acetaldehyde derivatives of adenine, cytidine, uridine, and melamine. With these building blocks in hand, DKP bPNAs were prepared to display a combination of native and synthetic (melamine) bases. Preliminary melting studies indicate binding signatures of cytidine- and melamine-displaying bPNAs to T-rich DNAs of noncanonical structure, though full characterization of this behavior is ongoing. The convenient and potentially scalable method described enables rapid access to DNA-binding scaffolds of low (<1 kD) molecular weight and previously established cell permeability. We expect that this straightforward and efficient approach to nucleic acid binders will enable studies on noncanonical nucleic acid hybridization.

摘要

我们报道了一种具有新型二酮哌嗪(DKP)骨架的双功能肽核酸(bPNA)的合成方法,该骨架展示了非天然的三聚氰胺(M)碱基以及天然碱基。为了研究DKP bPNA的结构-功能范围,我们使用二氨基丙酸、二氨基丁酸、鸟氨酸和赖氨酸衍生物合成了一组bPNA,以展示碱基三联基序,这导致α-碳与侧链胺之间连接一、二、三或四个碳。与这些bPNA的DNA杂交体的热变性表明,最佳侧链连接是四个碳,对应于赖氨酸衍生物。因此,通过将Fmoc-赖氨酸的ε-胺与腺嘌呤、胞嘧啶、尿嘧啶和三聚氰胺的乙醛衍生物进行双重还原烷基化,制备了每条侧链展示两个碱基的单体。有了这些构建模块,就可以制备展示天然和合成(三聚氰胺)碱基组合的DKP bPNA。初步的解链研究表明,展示胞嘧啶和三聚氰胺的bPNA与非经典结构的富含T的DNA具有结合特征,不过这种行为的全面表征仍在进行中。所描述的方便且可能可扩展的方法能够快速获得低分子量(<1 kD)且先前已确定具有细胞通透性的DNA结合支架。我们预计,这种直接且高效的核酸结合剂制备方法将有助于非经典核酸杂交的研究。

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本文引用的文献

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