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Updated: Jan 21, 2026

Assessing Protein Interactions in Live-Cells with FRET-Sensitized Emission
Published on: April 22, 2021
An effective FRET-based two-photon ratiometric fluorescent probe with double well-resolved emission bands for
Gangqiang Yuan1, Haiyuan Ding1, Liyi Zhou1
1Hunan Key Laboratory of Processed Food for Special Medical Purpose, National Engineering Laboratory for Deep Process of Rice and Byproducts, Hunan Key Laboratory of Grain-oil Deep Process and Quality Control, College of Food Science and Engineering, Central South University of Forestry and Technology, Changsha, Hunan 41004, China.
Abstract:
In cells, lysosome is an acidic organelle (approximately pH 4.5-5.5), whose pH changes plays a key role in mediating various biological processes. To address this issue, a lot of fluorescent probes have been developed and prepared for tracking lysosomal pH changes. However, few of these probes can realize the imaging of lysosomal pH changes in biosystems. Herein, a new two-photon (TP) ratiometric fluorescent probe (NpRhLys-pH) by adopting the fluorescence resonance energy transfer (FRET) strategy has been developed for imaging of lysosomal pH changes in living cells and zebrafish. In this probe NpRhLys-pH, constructed by conjugating a TP fluorophore (D-Π-A-structured naphthalimide derivative) with a rhodamine B fluorophore via a non-conjugated flexible linker, the morpholine moiety serves as a targeting unit for anchoring lysosomes, and the xanthane derivative shows a pH-modulated open/close form of the spirocycle. Such a scaffold affords the NpRhLys-pH is a reliable and specific probe for anchoring lysosomes in living cells and zebrafish with dual-channel emission peaks separated by 85 nm, and responds to lysosomal pH rapidly and reversibly with high selectivity and sensitivity, demonstrating it can be used as a powerful tool for the biological research of the relationship between physiology and pathology and lysosomal pH changes in biological systems.
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