期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 143, 期 37, 页码 14951-14955出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c05530
关键词
-
资金
- NIH [R35 CA197622, R01 DK073368]
Super-resolution activity imaging currently does not consider the locations of collaborating regulators/effectors in living cells. The DrFLINC technique, based on the FLINC principle, utilizes nonfluorescent Dronpa to enhance fluorescence fluctuations, leading to the development of a superior red label and a next-generation activity sensor for context-rich super-resolution biosensing.
Super-resolution activity imaging maps the biochemical architecture of living cells yet currently overlooks the locations of collaborating regulators/effectors. Building on the fluorescence fluctuation increase by contact (FLINC) principle, here we devise Dronpa-chromophore-removed FLINC (DrFLINC), where the nonfluorescent Dronpa can nevertheless enhance TagRFP-T fluorescence fluctuations. Exploiting DrFLINC, we develop a superior red label and a next-generation activity sensor for context-rich super-resolution biosensing.
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