ATP synthase F O F 1 structure, function, and structure-based drug design

ATP synthases are unique rotatory molecular machines that supply biochemical reactions with adenosine triphosphate (ATP)-the universal "currency", which cells use for synthesis of vital molecules and sustaining life. ATP synthases of F-type (F F ) are found embedded in bacterial cellular m...

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Veröffentlicht in:Cellular and molecular life sciences : CMLS 2022-03, Vol.79 (3), p.179
Hauptverfasser: Vlasov, Alexey V, Osipov, Stepan D, Bondarev, Nikolay A, Uversky, Vladimir N, Borshchevskiy, Valentin I, Yanyushin, Mikhail F, Manukhov, Ilya V, Rogachev, Andrey V, Vlasova, Anastasiia D, Ilyinsky, Nikolay S, Kuklin, Alexandr I, Dencher, Norbert A, Gordeliy, Valentin I
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container_issue 3
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container_title Cellular and molecular life sciences : CMLS
container_volume 79
creator Vlasov, Alexey V
Osipov, Stepan D
Bondarev, Nikolay A
Uversky, Vladimir N
Borshchevskiy, Valentin I
Yanyushin, Mikhail F
Manukhov, Ilya V
Rogachev, Andrey V
Vlasova, Anastasiia D
Ilyinsky, Nikolay S
Kuklin, Alexandr I
Dencher, Norbert A
Gordeliy, Valentin I
description ATP synthases are unique rotatory molecular machines that supply biochemical reactions with adenosine triphosphate (ATP)-the universal "currency", which cells use for synthesis of vital molecules and sustaining life. ATP synthases of F-type (F F ) are found embedded in bacterial cellular membrane, in thylakoid membranes of chloroplasts, and in mitochondrial inner membranes in eukaryotes. The main functions of ATP synthases are control of the ATP synthesis and transmembrane potential. Although the key subunits of the enzyme remain highly conserved, subunit composition and structural organization of ATP synthases and their assemblies are significantly different. In addition, there are hypotheses that the enzyme might be involved in the formation of the mitochondrial permeability transition pore and play a role in regulation of the cell death processes. Dysfunctions of this enzyme lead to numerous severe disorders with high fatality levels. In our review, we focus on F F -structure-based approach towards development of new therapies by using F F structural features inherited by the representatives of this enzyme family from different taxonomy groups. We analyzed and systematized the most relevant information about the structural organization of F F to discuss how this approach might help in the development of new therapies targeting ATP synthases and design tools for cellular bioenergetics control.
doi_str_mv 10.1007/s00018-022-04153-0
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ATP synthases of F-type (F F ) are found embedded in bacterial cellular membrane, in thylakoid membranes of chloroplasts, and in mitochondrial inner membranes in eukaryotes. The main functions of ATP synthases are control of the ATP synthesis and transmembrane potential. Although the key subunits of the enzyme remain highly conserved, subunit composition and structural organization of ATP synthases and their assemblies are significantly different. In addition, there are hypotheses that the enzyme might be involved in the formation of the mitochondrial permeability transition pore and play a role in regulation of the cell death processes. Dysfunctions of this enzyme lead to numerous severe disorders with high fatality levels. In our review, we focus on F F -structure-based approach towards development of new therapies by using F F structural features inherited by the representatives of this enzyme family from different taxonomy groups. 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subjects Adenosine Triphosphate - metabolism
Bacteria - metabolism
Bacterial Proteins - antagonists & inhibitors
Bacterial Proteins - classification
Bacterial Proteins - metabolism
Chloroplasts - metabolism
Drug Design
Eukaryota - metabolism
Phylogeny
Protein Subunits - metabolism
Proton-Translocating ATPases - antagonists & inhibitors
Proton-Translocating ATPases - classification
Proton-Translocating ATPases - metabolism
Small Molecule Libraries - chemistry
Small Molecule Libraries - metabolism
title ATP synthase F O F 1 structure, function, and structure-based drug design
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