TY - JOUR
T1 - Development of an Azoreductase-based Reporter System with Synthetic Fluorogenic Substrates
AU - Shin, Narae
AU - Hanaoka, Kenjiro
AU - Piao, Wen
AU - Miyakawa, Takuya
AU - Fujisawa, Tomotsumi
AU - Takeuchi, Satoshi
AU - Takahashi, Shodai
AU - Komatsu, Toru
AU - Ueno, Tasuku
AU - Terai, Takuya
AU - Tahara, Tahei
AU - Tanokura, Masaru
AU - Nagano, Tetsuo
AU - Urano, Yasuteru
N1 - Funding Information:
This work was supported in part by JSPS KAKENHI Grant Numbers JP22000006 to T.N., 26104509, 16H00823 and 16H05099 to K.H., JP24655147 to T.K., JP25104005 to T.Tahara, JP16H04102 to S.T., JP16K17859 to T.F., and SENTAN, JST, to K.H. K.H. was also supported by grants from Mochida Memorial Foundation for Medical and Pharmaceutical Research, and The Asahi Glass Foundation.
Publisher Copyright:
© 2016 American Chemical Society.
PY - 2017/2/17
Y1 - 2017/2/17
N2 - 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.
AB - 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.
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U2 - 10.1021/acschembio.6b00852
DO - 10.1021/acschembio.6b00852
M3 - Article
C2 - 28036168
AN - SCOPUS:85013499838
SN - 1554-8929
VL - 12
SP - 558
EP - 563
JO - ACS chemical biology
JF - ACS chemical biology
IS - 2
ER -