A Fluorogenic Chemogenetic pH Sensor for Imaging Protein Exocytosis.
Justine CoïsMarie-Laure NieponManon WittwerHessam Sepasi TehraniPhilippe BunJean-Maurice MalletVincent VialouBlaise DumatPublished in: ACS sensors (2024)
Fluorescent protein-based pH biosensors enable the tracking of pH changes during protein trafficking and, in particular, exocytosis. The recent development of chemogenetic reporters combining synthetic fluorophores with self-labeling protein tags offers a versatile alternative to fluorescent proteins that combines the diversity of chemical probes and indicators with the selectivity of the genetic encoding. However, this hybrid protein labeling strategy does not avoid common drawbacks of organic fluorophores such as the risk of off-target signal due to unbound molecules. Here, we describe a novel fluorogenic and chemogenetic pH sensor based on a cell-permeable molecular pH indicator called pHluo-Halo-1 , whose fluorescence can be locally activated in cells by reaction with HaloTag, ensuring excellent signal selectivity in wash-free imaging experiments. pHluo-Halo-1 was selected out of a series of four fluorogenic molecular rotor structures based on protein chromophore analogues. It displays good pH sensitivity with a p K a of 6.3 well-suited to monitor pH variations during exocytosis and an excellent labeling selectivity in cells. It was applied to follow the secretion of CD63-HaloTag fusion proteins using TIRF microscopy. We anticipate that this strategy based on the combination of a tunable and chemically accessible fluorogenic probe with a well-established protein tag will open new possibilities for the development of versatile alternatives to fluorescent proteins for elucidating the dynamics and regulatory mechanisms of proteins in living cells.
Keyphrases
- living cells
- single molecule
- protein protein
- high resolution
- binding protein
- amino acid
- quantum dots
- induced apoptosis
- fluorescent probe
- mesenchymal stem cells
- signaling pathway
- endoplasmic reticulum stress
- molecular docking
- transcription factor
- mass spectrometry
- copy number
- fluorescence imaging
- high speed
- structure activity relationship