Mitochondrial functions are heavily influenced by acid–base
homeostasis. Hence, elucidation of the mitochondrial pH is essential
in living cells, and its alterations during pathologies is an interesting
question to be addressed. Small molecular fluorescent probes are progressively
applied to quantify the mitochondrial pH by fluorescence imaging.
Herein, we designed a unique small molecular fluorescent probe, PM-Mor-OH, based on the lipophilic morpholine ligand-conjugated
pyridinium derivative of “IndiFluors”. The morpholine-conjugated
fluorescent probe usually localized the lysosome. However, herein,
we observed unusual phenomena of morpholine-tagged PM-Mor-OH that localized mitochondria explicitly. The morpholine ligand also
plays a pivotal role in tuning optical properties via photoinduced
electron transfer (PET) during internal pH alteration (ΔpHi).
In the mitophagy process, lysosomes engulf damaged mitochondria, leading
to ΔpHi, which can be monitored using our probe. It exhibited
“ratiometric” emission at single wavelength excitation
(ex. 488) and is suitable for monitoring and quantifying the ΔpHi
using confocal microscope high-resolution image analysis during mitophagy.
The bathochromic emission shifts due to intramolecular charge transfer
(ICT) in basic pH were well explained by the time-dependent density
functional theory (TD-DFT/PCM). Similarly, the change in the emission
ratio (green/red) with pH variations was also validated by the PET
process. In addition, PM-Mor-OH can quantify the pH change
during oxidative stress induced by rapamycin, mutant A53T α-synuclein-mediated
protein misfolding stress in mitochondria, and during starvation.
Rapamycin-induced mitophagy was further elucidated by the translocation
of mCherry Parkin to damaged mitochondria, which well correlates with
our probe. Thus, PM-Mito-OH is a valuable probe for visualizing
mitophagy and can act as a suitable tool for the diagnosis of mitochondrial
diseases.
A unique highly water-soluble ICT-based fluorescent probe is developed for efficient detection and discrimination of reactive monocarbonyl formaldehyde (FA) from dicarbonyl methylglyoxal (MGO)/glyoxal (GO) by modulating the ICT process that...
Intracellular pH (pHi) in organelles, including mitochondria, endoplasmic reticulum, lysosome, and nuclei, differ from cytoplasmic pH, and maintaining the pH of those organelles is crucial for cellular homeostasis. Alteration of...
Mitochondria are the powerhouse of the cell and function at pH ~8.0. Dysfunctions of mitochondria, includes mitochondrial damage, leading to pH alteration. Hence, researchers aim to develop efficient pH probes for tracking mitochondrial pH dynamics. Herein, we developed a PETbased fluorescent probe for pH monitoring during mitochondrial dysfunctions. Three derivatives were synthesized with a variable spacer's length in pentacyclic pyridinium fluorophores (PM-C2, PM-C3, and PM-C6). An efficient electron transfers from the receptor (tertiary amine) was observed in the case of PM-C2 compared to the other two derivatives. This PET process was inhibited when tertiary amine was protonated in acidic pH. However, PM-C3 showed minimal fluorescence intensity at similar conditions and almost negligible change in case of PM-C6, suggesting poor PET process for both the derivatives. Furthermore, DFT/TD-DFT quantum chemical calculation well supported this optical phenomena and PET process. Biocompatible, photostable, and mitochondria-specific PM-C2 could monitor pH dynamics during mitochondrial damage which were engulfed by lysosome, also known as mitophagy. This mitophagy process were induced by rapamycin and starvation, which can be monitored by turn-on fluorescence enhancement. This process was further validated by tracking Parkin-protein translocation from cytoplasm to damaged mitochondria using our developed probe.
We report design, synthesis and biological evaluation of a unique molecular framework, annulated indolizines as a fluorescent probe. The compounds were generated through an eco-friendly, blue LED induced domino reaction...
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