LAUSR

Abstract Mitochondrial autophagy (mitophagy) is critical to the quality and quantity control of mitochondria. Real-time monitoring of the occurrence of mitophagy is necessary for understanding mitochondrial metabolism and screening mitophagy-related therapeutic drugs. Here, we report a new type of fluorescence resonance energy transfer (FRET) switch constructed by the mixed assembly of two cyanine dyes. The FRET switch exhibits a highly selective fluorescence response to the G-quadruplex structure, and its fluorescence intensity decreases or increases correspondingly with the binding and separation of G-quadruplexes. This property enables the switch to track the progression and termination of mitophagy by identifying the G-quadruplex structures that enter the lysosome during autophagy. This work not only provides a new strategy for constructing non-covalent FRET probes, but also offers a reliable tool for tracking mitophagy.