Ecto-F0/F1 ATPase as a novel candidate of prothymosin α receptor. (31st May 2018)

• Record Type: Journal Article
• Authors: Ueda, Hiroshi; Matsunaga, Hayato; Matsushita, Yosuke; Maeda, Shiori; Iwamoto, Ryusei; Yokoyama, Shigeyuki; Shirouzu, Mikako
• Is Part Of: Expert opinion on biological therapy. Volume 18(2018)Supplement 1
• Page Start: 89
• Page End: 94
• Publication Date: 2018-05-31
• Subjects: Prothymosin α -- ecto-F0/F1 ATPase -- N18-RE-105 cells -- HUVEC -- protein-protein interaction; Gene therapy -- Periodicals; Protein drugs -- Periodicals; Peptide drugs -- Periodicals; Immunotherapy -- Periodicals; Drug delivery systems -- Periodicals; 615.5
• DOI: 10.1080/14712598.2018.1454427
• Languages: English
• ISSNs: 1471-2598

Abstract

ABSTRACT: Objectives : Prothymosin α (ProTα) was reported to inhibit the neuronal necrosis by facilitating the plasma membrane localization of endocytosed glucose transporter 1/4 through an activation of putative Gi -coupled receptor. The present study aims to identify a novel ProTα target, which may lead to an activation of Gi -coupled receptor. Methods : We used Gi -rich lipid rafts fraction of retinal cell line N18-RE-105 cells for affinity cross-linking. The biological confirmation that F0 /F1 ATPase is a target protein complex was performed by cell-free experiments using ELISA-based binding assay, surface plasmon resonance assay and quartz crystal microbalance assay, and cell-based experiments to measure extracellular ATP level in the HUVECs culture. Results : From the cross-linking study and above-mentioned protein-protein interaction assays, ATP5A1 and ATP5B, F1 ATPase subunits were found to ProTα binding target proteins. In the culture of HUVEC cells, furthermore, ProTα increased the extracellular ATP levels in a reversible manner by anti-ATP5A1- and ATP5B-antibodies. Conclusion : The present study suggests that ProTα may activate ecto-F0 /F1 ATPase and produced ATP. This study leads to next subjects whether produced ATP and its metabolites, ADP or adenosine may activate corresponding Gi -coupled receptors.