TY - JOUR
T1 - Analyte Regeneration Fluorescent Probes for Formaldehyde Enabled by Regiospecific Formaldehyde-Induced Intramolecularity
AU - Xu, Hang
AU - Xu, Huan
AU - Ma, Shengnan
AU - Chen, Xiani
AU - Huang, Lixian
AU - Chen, Junwei
AU - Gao, Feng
AU - Wang, Rui
AU - Lou, Kaiyan
AU - Wang, Wei
N1 - Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/12/5
Y1 - 2018/12/5
N2 - An important challenge for reaction-based fluorescent probes is that they generally require analyte consumption for fluorescence signal generation, thus creating potential perturbation of native analyte homeostasis or change of local concentrations. Herein, we reported two formaldehyde (FA) regeneration fluorescent probes, NAP-FAP-1 and NAP-FAP-2. An unprecedented regiospecific FA-induced intramolecularity strategy is implemented in the probe design, which adopts 3-(benzylamino)-succinimide as the FA-selective reaction group. The probes are able to capture the analyte molecule, induce regiospecific imide bond cleavage, and then release the captured FA molecule with simultaneous fluorescence turn-on response via a unique dual PeT/ICT quenching mechanism. The probes have shown potentials in detection, comparison, and imaging of FA levels intracellularly and inside lysosomes. These features make them useful for the study of FA homeostasis and functions in biological systems with minimal perturbation.
AB - An important challenge for reaction-based fluorescent probes is that they generally require analyte consumption for fluorescence signal generation, thus creating potential perturbation of native analyte homeostasis or change of local concentrations. Herein, we reported two formaldehyde (FA) regeneration fluorescent probes, NAP-FAP-1 and NAP-FAP-2. An unprecedented regiospecific FA-induced intramolecularity strategy is implemented in the probe design, which adopts 3-(benzylamino)-succinimide as the FA-selective reaction group. The probes are able to capture the analyte molecule, induce regiospecific imide bond cleavage, and then release the captured FA molecule with simultaneous fluorescence turn-on response via a unique dual PeT/ICT quenching mechanism. The probes have shown potentials in detection, comparison, and imaging of FA levels intracellularly and inside lysosomes. These features make them useful for the study of FA homeostasis and functions in biological systems with minimal perturbation.
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U2 - 10.1021/jacs.8b09794
DO - 10.1021/jacs.8b09794
M3 - Article
C2 - 30457848
AN - SCOPUS:85057891839
SN - 0002-7863
VL - 140
SP - 16408
EP - 16412
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 48
ER -