Optimal terminal sequences for continuous or serial isothermal amplification of dsRNA with norovirus RNA replicase
スポンサーリンク
概要
- 論文の詳細を見る
The norovirus RNA replicase (NV3Dpol, 56 kDa, single chain monomeric protein) can amplify double-stranded (ds) RNA isothermally. It will play an alternative role in the in vitro evolution against traditional Qβ RNA replicase, which cannot amplify dsRNA and consists of four subunits, three of which are borrowed from host E.coli. In order to identify the optimal 3′-terminal sequence of the RNA template for NV3Dpol, an in vitro selection using the serial transfer was performed for a random library having the 3′-terminal sequence of ---UUUUUUNNNN-3′. The population landscape on the 4-dimensional sequence space of the 17th round of transfer gave a main peak around ---CAAC-3′. In the preceding studies on the batch amplification reaction starting from a single-stranded RNA, a template with 3′-terminal C-stretch was amplified effectively. It was confirmed that in the batch amplification the ---CCC-3′ was much more effective than the ---CAAC-3′, but in the serial transfer condition in which the ----CAAC-3′ was sustained stably, the ---CCC-3′ was washed out. Based on these results we proposed the existence of the "shuttle mode" replication of dsRNA. We also proposed the optimal terminal sequences of RNA for in vitro evolution with NV3Dpol.
- 日本生物物理学会の論文
日本生物物理学会 | 論文
- 2SD3 トランスジェニック発現系を用いたマウス嗅覚受容体遺伝子の解析
- 分子生物学のためのバイオインフォマティクス入門 : 生物情報解析の理論とアルゴリズム, 共立出版, J. C. Setubal and J. Meidanis(著), 五條堀孝(監訳), 遠藤俊徳(代表訳), B5判, 286ページ, 本体5,300円, 2001年12月
- 3P079 分子動力学シミュレーションによるPhoB DNA結合タンパクのダイナミクス解析(蛋白質(物性(安定性、折れ畳みなど)),ポスター発表,第45回日本生物物理学会年会)
- S12A3 転写関連因子の動的構造と天然変性状態(蛋白質の再発見によるゲノムから細胞に至る生物の統一的理解,シンポジウム,第45回日本生物物理学会年会)
- 1P026 水溶液環境下でのディスタンスジオメトリ法によるタンパク質の構造決定 : simulated annealingによる構造精密化(蛋白質 A) 構造))