研究目的
To develop a reliable and easily obtainable co-localization coefficient (CLC) of a fluorescent probe as a new indicator for mitochondrial membrane potential (MMP) and to design a target-switchable fluorescent probe (Mito-Lyso) for this purpose.
研究成果
The study successfully developed a target-switchable fluorescent probe (Mito-Lyso) that can reversibly transfer between mitochondria and lysosomes with changes in MMP. The co-localization coefficient (CLC) between Mito-Lyso and a commercial lysosomal probe (NIR-Lyso) was found to be a reliable and easily obtainable parameter for indicating MMP changes. This new method provides a practical tool for monitoring MMP in living cells, with potential applications in biological and biomedical research.
研究不足
The study focuses on the development and initial testing of the Mito-Lyso probe and its application as an MMP indicator. Further studies may be needed to explore its applicability in more complex biological systems and its potential limitations in different cell types or under various physiological conditions.
1:Experimental Design and Method Selection:
The study involved the design of a target-switchable fluorescent probe (Mito-Lyso) that can reversibly transfer between mitochondria and lysosomes upon triggering of MMP change. The probe's selectivity to mitochondria with normal MMP and its ability to target lysosomes when MMP decreases were tested.
2:Sample Selection and Data Sources:
SiHa, HeLa, and Fibroblast cells were used to test the probe's selectivity and the change in CLCs with MMP.
3:List of Experimental Equipment and Materials:
A Hitachi U-2910 spectrophotometer and a Hitachi F-2700 spectrofluorimeter were used for UV absorption and fluorescent spectrum measurements. Confocal fluorescent photos were obtained from Olympus FV 1200 confocal fluorescent microscope.
4:Experimental Procedures and Operational Workflow:
Cells were incubated with Mito-Lyso and commercial probes (MTDR or Lyso-NIR) under different conditions to observe the change in CLCs with MMP.
5:Data Analysis Methods:
The co-localization coefficients of the probes were determined by the software of the Olympus FV 1200 confocal fluorescent microscope.
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