1. Academic Validation
  2. A Novel Single-Molecule Fluorescence Lifetime Probe for Apoptosis Diagnosis Through Mitochondrial SO2 and DNA Co-Detection

A Novel Single-Molecule Fluorescence Lifetime Probe for Apoptosis Diagnosis Through Mitochondrial SO2 and DNA Co-Detection

  • Anal Chem. 2025 Aug 5;97(30):16439-16448. doi: 10.1021/acs.analchem.5c02360.
Hong Wang 1 2 Tong Zhu 2 Wanying Li 1 Zhangjun Hu 3 Xin Yang 2 Qiong Zhang 4 Peng Huang 1 Jiwen Hu 3 Zhihui Feng 1
Affiliations

Affiliations

  • 1 Anhui University of Chinese Medicine, Anhui Province Key Laboratory of Pharmaceutical Preparation Technology and Application, Hefei, Anhui 230012, P. R. China.
  • 2 South China Advanced Institute for Soft Matter Science and Technology, School of Emergent Soft Matter, Guangdong Provincial Key Laboratory of Functional and Intelligent Hybrid Materials and Devices, Guangdong Basic Research Center of Excellence for Energy and Information Polymer Materials, South China University of Technology, Guangzhou 510640, P. R. China.
  • 3 Department of Physics, Chemistry, and Biology (IFM) Linköping University, Linköping SE581 83, Sweden.
  • 4 College of Chemistry and Chemical Engineering, Key Laboratory of Functional Inorganic Materials Chemistry of Anhui Province, Anhui University, Hefei 230601, P. R. China.
Abstract

As a key signaling molecule, sulfur dioxide (SO2) plays a crucial role in maintaining physiological homeostasis. In this work, we designed a mitochondria-targeted fluorescent probe (MIC) for independently detect SO2 (short-wavelength) and DNA (long-wavelength) in real time. It is worth noting that our research reveals a dual role of that SO2 in regulating oxidative stress. At appropriate levels, it acts as a modulator, whereas excessive amounts induce Apoptosis by reducing mitochondrial membrane potential, upregulating p53/Bax, downregulating Bcl-2, and activating the Caspase-3 cascade. The apoptotic process induces mitochondrial membrane permeability changes, triggering the release and nuclear translocation of the probe MIC, which subsequently emits red fluorescence. Using time-resolved fluorescence imaging technology, we further observed a significant increase in the average fluorescence lifetime of the DNA channel. This finding demonstrates that the MIC probe not only enables dual-channel monitoring of mitochondrial SO2 and nuclear DNA but also precisely evaluates the apoptotic process through changes in fluorescence lifetime. This innovative tool provides an important means for in-depth study of the SO2-mediated apoptotic mechanism and opens up new strategies for the diagnosis of mitochondrial-related diseases.

Figures
Products