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聚合酶导向的 C5-乙炔基锁核酸合成。

Polymerase-directed synthesis of C5-ethynyl locked nucleic acids.

机构信息

Nucleic Acid Center, Department of Physics & Chemistry, University of Southern Denmark, Campusvej 55, Odense M 5230, Denmark.

出版信息

Bioorg Med Chem Lett. 2010 Nov 15;20(22):6565-8. doi: 10.1016/j.bmcl.2010.09.044. Epub 2010 Sep 21.

Abstract

Modified nucleic acids have considerable potential in nanobiotechnology for the development of nanomedicines and new materials. Locked nucleic acid (LNA) is one of the most prominent nucleic acid analogues reported so far and we herein for the first time report the enzymatic incorporation of LNA-U and C5-ethynyl LNA-U nucleotides into oligonucleotides. Phusion High Fidelity and KOD DNA polymerases efficiently incorporated LNA-U and C5-ethynyl LNA-U nucleotides into a DNA strand and T7 RNA polymerase successfully accepted the LNA-U nucleoside 5'-triphosphate as substrate for RNA transcripts.

摘要

修饰后的核酸在纳米生物技术中有很大的潜力,可用于开发纳米药物和新材料。锁核酸 (LNA) 是迄今为止报道的最突出的核酸类似物之一,本文首次报道了 LNA-U 和 C5-乙炔基 LNA-U 核苷酸在寡核苷酸中的酶促掺入。Phusion High Fidelity 和 KOD DNA 聚合酶能有效地将 LNA-U 和 C5-乙炔基 LNA-U 核苷酸掺入 DNA 链中,T7 RNA 聚合酶成功地接受 LNA-U 核苷 5'-三磷酸作为 RNA 转录物的底物。

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