Modified Oligonucleotides for Guiding RNA Cleavage Using Bacterial RNase P
- Авторлар: 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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Мекемелер:
- 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
- Шығарылым: Том 52, № 6 (2018)
- Беттер: 905-912
- Бөлім: 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
Дәйексөз келтіру
Аннотация
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.
Авторлар туралы
D. Novopashina
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences; Novosibirsk State University
Хат алмасуға жауапты Автор.
Email: danov@niboch.nsc.ru
Ресей, 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
Ресей, 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
Ресей, Novosibirsk, 630090
M. Kuprushkin
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences
Email: danov@niboch.nsc.ru
Ресей, Novosibirsk, 630090
A. Davydova
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences
Email: danov@niboch.nsc.ru
Ресей, 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
Ресей, 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
Ресей, 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
АҚШ, 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
Ресей, Novosibirsk, 630090
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