A molecular scaffold for concurrent targeting of plasma and mitochondrial membranes

Abstract

The ability to specifically sense and image plasma membranes and mitochondrial membranes with fluorescent probes is paramount for the visualization and mechanistic understanding of these fundamental, dynamic cellular compartments. However, dual-targeting membrane probes combining a fluorophore and two distinct targeting ligands face synthetic challenges and potential functional group interference. Therefore, we designed a molecular scaffold (dual-targeting ligand) that combines both a mitochondrial anchor and a plasma membrane protein ligand to simultaneously localize at both membranes. Using this molecular scaffold, we engineered a series of fluorescent probes, T-1 to T-5. Furthermore, we demonstrate the functional applications of two probes from this series, T-1 and T-4. Owing to the distinct physicochemical properties of the targeted plasma and mitochondria membrane, T-1 can differentiate multiple cell states, including live, dead, and early apoptotic cells. Additionally, T-4, designed as a dual-targeting photosensitizer, induces cancer cell necrosis by simultaneously rupturing the plasma membrane and inducing mitochondrial swelling, leading to enhanced photosensitizing efficiency. Significantly, this research advances the development of fluorescent probe based labeling strategies and provides effective tools for biochemical and biomedical applications.

Graphical abstract: A molecular scaffold for concurrent targeting of plasma and mitochondrial membranes

Supplementary files

Article information

Article type
Edge Article
Submitted
17 Aug 2025
Accepted
29 Dec 2025
First published
16 Jan 2026
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2026, Advance Article

A molecular scaffold for concurrent targeting of plasma and mitochondrial membranes

Y. Lai, Y. Yang, Y. Zhao, T. D. James and W. Lin, Chem. Sci., 2026, Advance Article , DOI: 10.1039/D5SC06276D

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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