Journal
CHEMICAL COMMUNICATIONS
Volume 46, Issue 39, Pages 7403-7405Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c0cc02432e
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Funding
- Japan Society for the Promotion of Science (JSPS)
- Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan
- Ministry of Health, Labour and Welfare (MHLW) of Japan
- New Energy and Industrial Technology Development Organization (NEDO) of Japan
- Takeda Science Foundation
- Osaka University
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The targeted protein of interest is fused with genetically modified beta-lactamase enzyme, which reacts with the probe in physiological conditions to break the aggregated interaction between the fluorophore and quencher. This alliance-separation technique is new for protein labeling and is probed in vitro and in live cell imaging studies.
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