Cysteine-Activatable Near-Infrared Fluorescent Probe for Dual-Channel Tracking Lipid Droplets and Mitochondria in Epilepsy.
Songjiao LiPeipei WangMiantai YeKe YangDan ChengZhiqiang MaoLongwei HeZhihong LiuPublished in: Analytical chemistry (2023)
Dual-channel fluorescent probes could respond to a specific target and emit different wavelengths of fluorescence before and after the response. Such probes could alleviate the influence caused by the variation of the probe concentration, excitation intensity, and so on. However, for most dual-channel fluorescent probes, the probe and fluorophore faced spectral overlap, which reduced sensitivity and accuracy. Herein, we introduced a cysteine (Cys)-responsive and near-infrared (NIR) emissive AIEgen (named TSQC ) with good biocompatibility to dual-channel monitor Cys in mitochondria and lipid droplets (LDs) during cell apoptosis through wash-free fluorescence bio-imaging. TSQC can label mitochondria with bright fluorescence around 750 nm, and after reacting with Cys, the reaction product TSQ could spontaneously target LDs with emissions around 650 nm. Such spatially separated dual-channel fluorescence responses could significantly improve detection sensitivity and accuracy. Furthermore, the Cys-triggered dual-channel fluorescence imaging in LDs and mitochondria during apoptosis induced by UV light exposure, H 2 O 2 , or LPS treatment is clearly observed for the first time. Besides, we also report here that TSQC can be used to image subcellular Cys in different cell lines by measuring the fluorescence intensities of different emission channels. In particular, TSQC shows superior utility for the in vivo imaging of apoptosis in acute and chronic epilepsy mice. In brief, the newly designed NIR AIEgen TSQC can respond to Cys and separate two fluorescence signals to mitochondria and LDs, respectively, to study Cys-related apoptosis.
Keyphrases
- living cells
- fluorescent probe
- single molecule
- fluorescence imaging
- cell death
- photodynamic therapy
- energy transfer
- oxidative stress
- reactive oxygen species
- cell cycle arrest
- endoplasmic reticulum stress
- high resolution
- endoplasmic reticulum
- metabolic syndrome
- risk assessment
- small molecule
- inflammatory response
- drug induced
- cell proliferation
- liver failure
- deep learning
- magnetic resonance
- hepatitis b virus
- fatty acid
- type diabetes
- high fat diet induced
- signaling pathway
- dual energy
- combination therapy
- machine learning
- drug release
- solid state
- temporal lobe epilepsy