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Updated: May 24, 2025

Simultaneous Measurement of Mitochondrial Calcium and Mitochondrial Membrane Potential in Live Cells by Fluorescent Microscopy
Published on: January 24, 2017
Self-Referenced Probe Enables Quantified Monitoring Mitochondrial Membrane Potential by Colocalization Coefficients
Qing Lyu1, Fangfang Meng2, Xingyu Lyu1
1State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, P. R. China.
Abstract:
Mitochondria are dynamic organelles that have a variety of physiological states. Mitochondrial membrane potential (MMP) maintains mitochondrial physiological activities and reflects cellular health and viability. Thus, it is essential to dynamically monitor changes in MMP for understanding mitochondria-related biological processes. However, in situ, synchronous and quantitative tracking of MMP dynamic processes remains a great challenge. In this work, we designed and synthesized a fluorescent probe CBTH that undergoes spirocyclization in response to pH and emits a two-color fluorescence. Relying on the electrostatic interaction with MMP, CBTH is able to dual-color target mitochondria in cells with normal MMP. During the reduction of MMP, the fluorescence signal of the red channel (λex = 543 nm) gradually migrated to the nucleus, while one from the green channel (λex = 405 nm) stayed in the mitochondria. Thus, taking the green channel as an internal reference, the probe can detect changes in MMP through the colocalization coefficient fluctuations between the two fluorescent channels. In cellular experiments, CLC exhibited reversibly detecting ability and a direct proportional relationship to MMP. Overall, this work provides a novel strategy to quantitatively detect MMP. Moreover, a detailed explanation of the design principle and response mechanism of CBTH has been provided for the creation of this kind of probe.

