Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of RAS, Lavrentiev Ave. 8, 630090 Novosibirsk, Russia.
Int J Mol Sci. 2023 Sep 27;24(19):14637. doi: 10.3390/ijms241914637.
Lipophilic oligonucleotide conjugates represent a powerful tool for nucleic acid cellular delivery, and many methods for their synthesis have been developed over the past few decades. In the present study, a number of chemical approaches for the synthesis of different fork- and comb-like dodecyl-containing oligonucleotide structures were performed, including use of non-nucleotide units and different types of phosphate modifications such as alkyl phosphoramidate, phosphoryl guanidine, and triazinyl phosphoramidate. The influence of the number of introduced lipophilic residues, their mutual arrangement, and the type of formed modification backbone on cell penetration was evaluated. The results obtained indicate great potential in the developed chemical approaches, not only for the synthesis of complex oligonucleotide structures but also for the fine-tuning of their properties.
亲脂性寡核苷酸缀合物是一种用于核酸细胞递送的强大工具,在过去几十年中已经开发出许多用于其合成的方法。在本研究中,进行了多种化学方法来合成不同的叉形和梳形含十二烷基的寡核苷酸结构,包括使用非核苷酸单元和不同类型的磷酸酯修饰,如烷基磷酰胺、磷酸胍和三嗪基磷酰胺。评估了引入的亲脂性残基的数量、它们的相互排列以及形成的修饰主链的类型对细胞穿透的影响。所获得的结果表明,所开发的化学方法具有很大的潜力,不仅可用于合成复杂的寡核苷酸结构,还可用于精细调整它们的性质。