Optimal terminal sequences for continuous or serial isothermal amplification of dsRNA with norovirus RNA replicase
Author:
Affiliation:
1. Graduate School of Science and Engineering, Saitama University
2. Innovative Research Organization, Saitama University
Publisher
Biophysical Society of Japan
Subject
Biophysics
Link
https://www.jstage.jst.go.jp/article/biophysics/10/0/10_15/_pdf
Reference16 articles.
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2. 2. Bansho, Y., Ichihashi, N., Kazuta, Y., Matsuura, T., Suzuki, H. & Yomo, T. Importance of parasite RNA species repression for prolonged translation-coupled RNA self-replication. Chem. Biol. 19, 478-487 (2012).
3. 3. Usui, K., Ichihashi, N., Kazuta, Y., Matsuura, T. & Yomo, T. Kinetic model of double-stranded RNA formation during long RNA replication by Qβ replicase. FEBS Lett. 587, 2565-2571 (2013).
4. 4. Blumenthal, T. & Carmichael, G. G. RNA replication: Function and structure of Qβ-replicase. Annu. Rev. Biochem. 48, 525-548 (1979).
5. 5. Brown, D. & Gold, L. RNA replication by Qβ replicase: A working model. Proc. Natl. Acad. Sci. USA 93, 11558-11562 (1996).
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1. What can we learn from the construction of in vitro replication systems?;Annals of the New York Academy of Sciences;2019-04-08
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