| Literature DB >> 36180703 |
Jean A Boutin1,2, Johann Stojko3, Gilles Ferry3, Sarah Cianferani4,5.
Abstract
Melatonin exerts its effects through a series of target proteins/receptors and enzymes. Its antioxidant capacity might be due to its capacity to inhibit a quinone reductase (NQO2) at high concentration (50 μM). Demonstrating the existence of a complex between a compound and a protein is often not easy. It requires either that the compound is an inhibitor-and the complex translates by an inhibition of the catalytic activity-or the compound is radiolabeled-and the complex translates in standard binding approaches, such as in receptology. Outside these two cases, the detection of the protein:small molecule complexes by mass spectrometry has recently been made possible, thanks to the development of so-called native mass spectrometry. Using this approach, one can measure masses corresponding to an intact noncovalent complex between a compound and its target, usually after titration or competition experiments. In the present chapter, we detail the characterization of NQO2:melatonin interaction using native mass spectrometry.Entities:
Keywords: Co-substrate; Complex; Melatonin; NQO2; Native mass spectrometry
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Year: 2022 PMID: 36180703 DOI: 10.1007/978-1-0716-2593-4_34
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745