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• W4380730596 abstract "The Acinetobacter baumannii F1FO-ATP synthase (α3:β3:γ:δ:ε:a:b2:c10), which is essential for this strictly respiratory opportunistic human pathogen, is incapable of ATP-driven proton translocation due to its latent ATPase activity. Here, we generated and purified the first recombinant A. baumannii F1-ATPase (AbF1–ATPase) composed of subunits α3:β3:γ:ε, showing latent ATP hydrolysis. A 3.0 Å cryo-electron microscopy structure visualizes the architecture and regulatory element of this enzyme, in which the C-terminal domain of subunit ε (Abε) is present in an extended position. An ε-free AbF1-ɑβγ complex generated showed a 21.5-fold ATP hydrolysis increase, demonstrating that Abε is the major regulator of AbF1-ATPase's latent ATP hydrolysis. The recombinant system enabled mutational studies of single amino acid substitutions within Abε or its interacting subunits β and γ, respectively, as well as C-terminal truncated mutants of Abε, providing a detailed picture of Abε's main element for the self-inhibition mechanism of ATP hydrolysis. Using a heterologous expression system, the importance of Abε's C-terminus in ATP synthesis of inverted membrane vesicles, including AbF1FO-ATP synthases, has been explored. In addition, we are presenting the first NMR solution structure of the compact form of Abε, revealing interaction of its N-terminal β-barrel and C-terminal ɑ-hairpin domain. A double mutant of Abε highlights critical residues for Abε's domain–domain formation which is important also for AbF1–ATPase's stability. Abε does not bind MgATP, which is described to regulate the up and down movements in other bacterial counterparts. The data are compared to regulatory elements of F1-ATPases in bacteria, chloroplasts, and mitochondria to prevent wasting of ATP." @default.
• W4380730596 created "2023-06-16" @default.
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• W4380730596 date "2023-06-15" @default.
• W4380730596 modified "2023-09-25" @default.
• W4380730596 title "Atomic insights of an up and down conformation of the <i>Acinetobacter baumannii</i><scp>F₁‐ATPase</scp> subunit ε and deciphering the residues critical for <scp>ATP</scp> hydrolysis inhibition and <scp>ATP</scp> synthesis" @default.
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• W4380730596 doi "https://doi.org/10.1096/fj.202300175rr" @default.
• W4380730596 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/37318822" @default.
• W4380730596 hasPublicationYear "2023" @default.
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