Mitochondrial ATP Synthase and Mild Uncoupling by Butyl Ester of Rhodamine 19, C4R1.
Ljubava D ZorovaIrina B PevznerLjudmila S KhailovaGalina A KorshunovaMarina A KovalevaLeonid I KovalevMarina V SerebryakovaDenis N SilachevRoman V SudakovSavva D ZorovTatyana I RokitskayaVasily A PopkovEgor Yu PlotnikovYuriy N AntonenkoDmitry B ZorovPublished in: Antioxidants (Basel, Switzerland) (2023)
The homeostasis of the transmembrane potential of hydrogen ions in mitochondria is a prerequisite for the normal mitochondrial functioning. However, in different pathological conditions it is advisable to slightly reduce the membrane potential, while maintaining it at levels sufficient to produce ATP that will ensure the normal functioning of the cell. A number of chemical agents have been found to provide mild uncoupling; however, natural proteins residing in mitochondrial membrane can carry this mission, such as proteins from the UCP family, an adenine nucleotide translocator and a dicarboxylate carrier. In this study, we demonstrated that the butyl ester of rhodamine 19, C4R1, binds to the components of the mitochondrial ATP synthase complex due to electrostatic interaction and has a good uncoupling effect. The more hydrophobic derivative C12R1 binds poorly to mitochondria with less uncoupling activity. Mass spectrometry confirmed that C4R1 binds to the β-subunit of mitochondrial ATP synthase and based on molecular docking, a C4R1 binding model was constructed suggesting the binding site on the interface between the α- and β-subunits, close to the anionic amino acid residues of the β-subunit. The association of the uncoupling effect with binding suggests that the ATP synthase complex can provide induced uncoupling.
Keyphrases
- oxidative stress
- nitric oxide synthase
- molecular docking
- mass spectrometry
- nitric oxide
- amino acid
- diabetic rats
- cell death
- molecular dynamics simulations
- wastewater treatment
- single cell
- high glucose
- fluorescent probe
- quantum dots
- reactive oxygen species
- drug induced
- protein kinase
- endothelial cells
- risk assessment
- capillary electrophoresis
- dna binding
- transcription factor
- gas chromatography