Mitochondrial ATP synthase as a direct molecular target of chromium(III) to ameliorate hyperglycaemia stress

• Published in: Nature communications Vol. 14; no. 1; p. 1738
• Main Authors: Wang, Haibo, Hu, Ligang, Li, Hongyan, Lai, Yau-Tsz, Wei, Xueying, Xu, Xiaohan, Cao, Zhenkun, Cao, Huiming, Wan, Qianya, Chang, Yuen-Yan, Xu, Aimin, Zhou, Qunfang, Jiang, Guibin, He, Ming-Liang, Sun, Hongzhe
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 28.03.2023; Nature Publishing Group UK; Nature Portfolio
• Subjects: Adenosine Triphosphate; Animals; ATP; ATP synthase; Binding; Chromium; Diabetes; Diabetes Mellitus; Fluorescence; Glucose metabolism; Hyperglycemia; Hyperglycemia - drug therapy; Male; Mice; Mitochondria; Mitochondrial Proton-Translocating ATPases; Mode of action; Nucleotides; Pharmacology; Physiological effects; Proteomes; Proteomics; Stress; Trivalent chromium
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-023-37351-w

Chromium(III) is extensively used as a supplement for muscle development and the treatment of diabetes mellitus. However, its mode of action, essentiality, and physiological/pharmacological effects have been a subject of scientific debate for over half a century owing to the failure in identifying the molecular targets of Cr(III). Herein, by integrating fluorescence imaging with a proteomic approach, we visualized the Cr(III) proteome being mainly localized in the mitochondria, and subsequently identified and validated eight Cr(III)-binding proteins, which are predominately associated with ATP synthesis. We show that Cr(III) binds to ATP synthase at its beta subunit via the catalytic residues of Thr213/Glu242 and the nucleotide in the active site. Such a binding suppresses ATP synthase activity, leading to the activation of AMPK, improving glucose metabolism, and rescuing mitochondria from hyperglycaemia-induced fragmentation. The mode of action of Cr(III) in cells also holds true in type II diabetic male mice. Through this study, we resolve the long-standing question of how Cr(III) ameliorates hyperglycaemia stress at the molecular level, opening a new horizon for further exploration of the pharmacological effects of Cr(III).