| Literature DB >> 28036168 |
Narae Shin1, Kenjiro Hanaoka1, Wen Piao1, Takuya Miyakawa2, Tomotsumi Fujisawa3, Satoshi Takeuchi3,4, Shodai Takahashi1, Toru Komatsu1,5, Tasuku Ueno1, Takuya Terai1, Tahei Tahara3,4, Masaru Tanokura2, Tetsuo Nagano6, Yasuteru Urano1,7,8.
Abstract
Enzyme/substrate pairs, such as β-galactosidase with chromogenic x-gal substrate, are widely used as reporters to monitor biological events, but there is still a requirement for new reporter systems, which may be orthogonal to existing systems. Here, we focused on azoreductase (AzoR). We designed and synthesized a library of azo-rhodamine derivatives as candidate fluorogenic substrates. These derivatives were nonfluorescent, probably due to ultrafast conformational change around the N═N bond after photoexcitation. We found that AzoR-mediated reduction of the azo bond of derivatives bearing an electron-donating group on the azobenzene moiety was followed by nonenzymatic cleavage to afford highly fluorescent 2-methyl-rhodamine green (2-Me RG), which was well retained in cells. We show that the AzoR/compound 9 reporter system can detect azoreductase-expressing live cells at the single cell level.Entities:
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Year: 2017 PMID: 28036168 DOI: 10.1021/acschembio.6b00852
Source DB: PubMed Journal: ACS Chem Biol ISSN: 1554-8929 Impact factor: 5.100