摘要
Cysteine is well-known to be an important biothiol and related to many diseases. However, the in vivo detection of endogenous cysteine still suffers from lacking small-molecule fluorophores with both excitation and emission in the near-infrared(650-900 nm)/shortwave-infrared region. Herein, we report a molecular engineering strategy for shortwave infrared(SWIR, 900-1700 nm) sensing of cysteine, which integrated an excited-state intermolecular proton transfer(ESIPT) building block into the intramolecular charge transfer(ICT) scaffold. The obtained novel fluorophore SH-OH displays a maximum absorption at the NIR region, and emission at the SWIR region. We introduce the cysteine-recognition moiety to SH-OH structure, and demonstrate sensing of endogenous cysteine in living animals, using the SWIR emission as a reliable off-on fluorescence signal. This fluorophore design strategy of cooperation of ICT and ESIPT processes expands the in vivo sensing toolbox for accurate analysis in clinical applications.
基金
supported by the National Natural Science Foundation of China (Nos.21878087,21908060)
the Innovation Program of Shanghai Municipal Education Commission,Shuguang Program (No.18SG27)
the NIH guidelines for the care and use of laboratory animals (NIH Publication No.85-23,Rev.1985)
approved by the Institutional Animal Care and Use Committee of National Tissue Engineering Center (Shanghai,China)。
