靳国瑞  (教授)

博士生导师 硕士生导师

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所在单位:生命科学与技术学院

职务:教授

学历:博士研究生毕业

性别:男

学位:博士

主要任职:仿生工程与生物力学研究所

毕业院校:新加坡国立大学

   

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祝贺硕士生冯鲲鹏关于线粒体温度探针论文被Dyes and Pigments 接收~!

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发布时间:2026-07-07

发布时间:2026-07-07

文章标题:祝贺硕士生冯鲲鹏关于线粒体温度探针论文被Dyes and Pigments 接收~!

摘要:Mitochondria are essential organelles for cellular energy production and also serve as key sources of heat, linking cellular metabolism to temperature homeostasis. However, measuring mitochondrial temperature dynamics with high fidelity remains challenging, as traditional single-dye thermometers often lack sensitivity and quantitative accuracy. Here we show that integrating two thermoresponsive fluorophores into a single Forster ¨ resonance energy transfer (FRET)-coupled probe dramatically amplifies temperature-induced fluorescence changes, enabling more sensitive and quantitative mitocho

内容:

Mitochondria are essential organelles for cellular energy production and also serve as key sources of heat, linking  cellular metabolism to temperature homeostasis. However, measuring mitochondrial temperature dynamics with  high fidelity remains challenging, as traditional single-dye thermometers often lack sensitivity and quantitative  accuracy. Here we show that integrating two thermoresponsive fluorophores into a single Forster ¨ resonance  energy transfer (FRET)-coupled probe dramatically amplifies temperature-induced fluorescence changes,  enabling more sensitive and quantitative mitochondrial thermometry. The new probe, Mito-TPE, covalently  links a flexible aggregation-induced emission donor to a rhodamine B acceptor, so that minor temperaturedependent molecular motions produce a large fluorescence response under single-wavelength excitation. MitoTPE exhibits a linear fluorescence decrease with rising temperature, with a relative sensitivity (Sr) of 13.82%/ C at 37 C, which is much higher than that of conventional mitochondrial probes. It localizes specifically to  mitochondria and allows estimation of organelle temperatures in living cells. Using Mito-TPE, we quantitatively  detect subtle mitochondrial temperature differences induced by chemical uncouplers and inhibitors, as well as  higher basal mitochondrial temperatures in aggressively metastatic cancer cells compared to less invasive or  normal cells. These findings suggest a general strategy to boost the performance of molecular thermometers by  dual-unit FRET coupling. By enabling more precise imaging of intracellular heat, this approach may open new  opportunities to investigate fundamental bioenergetics and to identify thermal signatures of disease.

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