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An overview of ATP synthase, inhibitors, and their toxicity.

作者信息

Althaher Arwa R, Alwahsh Mohammad

机构信息

Department of Pharmacy, Al-Zaytoonah University of Jordan, Amman 11733, Jordan.

出版信息

Heliyon. 2023 Nov 20;9(11):e22459. doi: 10.1016/j.heliyon.2023.e22459. eCollection 2023 Nov.


DOI:10.1016/j.heliyon.2023.e22459
PMID:38106656
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10722325/
Abstract

Mitochondrial complex V (ATP synthase) is a remarkable molecular motor crucial in generating ATP and sustaining mitochondrial function. Its importance in cellular metabolism cannot be overstated, as malfunction of ATP synthase has been linked to various pathological conditions. Both natural and synthetic ATP synthase inhibitors have been extensively studied, revealing their inhibitory sites and modes of action. These findings have opened exciting avenues for developing new therapeutics and discovering new pesticides and herbicides to safeguard global food supplies. However, it is essential to remember that these compounds can also adversely affect human and animal health, impacting vital organs such as the nervous system, heart, and kidneys. This review aims to provide a comprehensive overview of mitochondrial ATP synthase, its structural and functional features, and the most common inhibitors and their potential toxicities.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/3f645416c129/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/cbe0491da441/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/1cce2c014353/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/0a8a168ec60c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/c5c3ef68455f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/9e0cabc22dca/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/ae8a502fd605/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/be25a5911e06/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/3f645416c129/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/cbe0491da441/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/1cce2c014353/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/0a8a168ec60c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/c5c3ef68455f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/9e0cabc22dca/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/ae8a502fd605/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/be25a5911e06/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7a3/10722325/3f645416c129/gr8.jpg

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An overview of ATP synthase, inhibitors, and their toxicity.

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本文引用的文献

[1]
Structure of the human ATP synthase.

Mol Cell. 2023-6-15

[2]
Inhibitors of ATP Synthase as New Antibacterial Candidates.

Antibiotics (Basel). 2023-3-24

[3]
Molecular mechanism on forcible ejection of ATPase inhibitory factor 1 from mitochondrial ATP synthase.

Nat Commun. 2023-3-31

[4]
The Mechanism of Bacterial Resistance and Potential Bacteriostatic Strategies.

Antibiotics (Basel). 2022-9-8

[5]
ATP synthase: a moonlighting enzyme with unprecedented functions.

Chem Commun (Camb). 2022-2-22

[6]
Antibiotics and the Nervous System-Which Face of Antibiotic Therapy Is Real, Dr. Jekyll (Neurotoxicity) or Mr. Hyde (Neuroprotection)?

Molecules. 2021-12-9

[7]
Apoptolidin family glycomacrolides target leukemia through inhibition of ATP synthase.

Nat Chem Biol. 2022-4

[8]
Curcumin-tannic acid-poloxamer nanoassemblies enhance curcumin's uptake and bioactivity against cancer cells in vitro.

Int J Pharm. 2021-12-15

[9]
The mitochondrial permeability transition: Recent progress and open questions.

FEBS J. 2022-11

[10]
The ATP Synthase Deficiency in Human Diseases.

Life (Basel). 2021-4-8

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