Real-time monitoring of RNA helicase activity using fluorescence resonance energy transfer in vitro

Hidenori Tani, Osamu Fujita, Atsushi Furuta, Yasuyoshi Matsuda, Ryo Miyata, Nobuyoshi Akimitsu, Junichi Tanaka, Satoshi Tsuneda, Yuji Sekiguchi, Naohiro Noda*

*この研究の対応する著者

研究成果: Article査読

25 被引用数 (Scopus)

抄録

We have developed a continuous fluorescence assay based on fluorescence resonance energy transfer (FRET) for the monitoring of RNA helicase activity in vitro. The assay is tested using the hepatitis C virus (HCV) NS3 helicase as a model. We prepared a double-stranded RNA (dsRNA) substrate with a 5′ fluorophore-labeled strand hybridized to a 3′ quencher-labeled strand. When the dsRNA is unwound by helicase, the fluorescence of the fluorophore is emitted following the separation of the strands. Unlike in conventional gel-based assays, this new assay eliminates the complex and time-consuming steps, and can be used to simply measure the real-time kinetics in a single helicase reaction. Our results demonstrate that Alexa Fluor 488 and BHQ1 are an effective fluorophore-quencher pair, and this assay is suitable for the quantitative measurement of the RNA helicase activity of HCV NS3. Moreover, we found that several extracts of marine organisms exhibited different inhibitory effects on the RNA and DNA helicase activities of HCV NS3. We propose that this assay will be useful for monitoring the detailed kinetics of RNA unwinding mechanisms and screening RNA helicase inhibitors at high throughput.

本文言語English
ページ(範囲)131-136
ページ数6
ジャーナルBiochemical and Biophysical Research Communications
393
1
DOI
出版ステータスPublished - 2010 2月 26

ASJC Scopus subject areas

  • 生物理学
  • 生化学
  • 分子生物学
  • 細胞生物学

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