Modified Oligonucleotides for Guiding RNA Cleavage Using Bacterial RNase P
- 作者: Novopashina D.S.1,2, Nazarov A.S.1,2, Vorobjeva M.A.1, Kuprushkin M.S.1, Davydova A.S.1, Lomzov A.A.1,2, Pyshnyi D.V.1,2, Altman S.3,4, Venyaminova A.G.1
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隶属关系:
- Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences
- Novosibirsk State University
- Department of Molecular, Cellular and Developmental Biology, Yale University
- Division of Life Sciences, Arizona State University
- 期: 卷 52, 编号 6 (2018)
- 页面: 905-912
- 栏目: Structural-Functional Analysis of Biopolymers and Their Complexes
- URL: https://journal-vniispk.ru/0026-8933/article/view/163752
- DOI: https://doi.org/10.1134/S0026893318060134
- ID: 163752
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详细
The ability of a series of novel modified external guide sequences (EGS oligonucleotides) to induce the hydrolysis of target RNA with bacterial ribonuclease P has been studied; the most efficient modification variants have been selected. We have found patterns of the oligonucleotide sugar-phosphate backbone modi-fications that enhance oligonucleotide stability in the biological environment and do not violate the ability to interact with the enzyme and induce the RNA hydrolysis. It has been shown that analogues of EGS oligonucleotides selectively modified at 2'-position (2'-O-methyl and 2'-fluoro) or at internucleotide phosphates (phosphoryl guanidines) can be used for the addressed cleavage of a model RNA target by bacterial RNase P. The ability of new phosphoryl guanidine analogues of oligodeoxyribonucleotides that are stable in biological media to induce the hydrolysis of target RNA with bacterial ribonuclease P has been shown for the first time. The modified EGS oligonucleotides with an optimal balance between functional activity and stability in biological media can be considered as potential antibacterial agents.
作者简介
D. Novopashina
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences; Novosibirsk State University
编辑信件的主要联系方式.
Email: danov@niboch.nsc.ru
俄罗斯联邦, Novosibirsk, 630090; Novosibirsk, 630090
A. Nazarov
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences; Novosibirsk State University
Email: danov@niboch.nsc.ru
俄罗斯联邦, Novosibirsk, 630090; Novosibirsk, 630090
M. Vorobjeva
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences
Email: danov@niboch.nsc.ru
俄罗斯联邦, Novosibirsk, 630090
M. Kuprushkin
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences
Email: danov@niboch.nsc.ru
俄罗斯联邦, Novosibirsk, 630090
A. Davydova
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences
Email: danov@niboch.nsc.ru
俄罗斯联邦, Novosibirsk, 630090
A. Lomzov
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences; Novosibirsk State University
Email: danov@niboch.nsc.ru
俄罗斯联邦, Novosibirsk, 630090; Novosibirsk, 630090
D. Pyshnyi
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences; Novosibirsk State University
Email: danov@niboch.nsc.ru
俄罗斯联邦, Novosibirsk, 630090; Novosibirsk, 630090
S. Altman
Department of Molecular, Cellular and Developmental Biology, Yale University; Division of Life Sciences, Arizona State University
Email: danov@niboch.nsc.ru
美国, New Haven,, CT 06520; Tempe, AZ,
A. Venyaminova
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences
Email: danov@niboch.nsc.ru
俄罗斯联邦, Novosibirsk, 630090
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