Polyphenols have received a significant amount of attention in disease prevention because of their unique chemical and biological properties. However, the underlying molecular mechanism for their beneficial effects remains unclear. We have now identified a polyphenol as a source of innate epitopes detected in natural IgM and established a unique gain-of-function mechanism in the formation of innate epitopes by polyphenol via the polymerization of proteins. Upon incubation with bovine serum albumin (BSA) under physiological conditions, several polyphenols converted the protein into the innate epitopes recognized by the IgM Abs. Interestingly, piceatannol, a naturally occurring hydroxylated analogue of a red wine polyphenol, resveratrol, mediated the modification of BSA, whose polymerized form was specifically recognized by the IgMs. The piceatannol-mediated polymerization of the protein was associated with the formation of a lysine-derived cross-link, dehydrolysinonorleucine. In addition, an oxidatively deaminated product, α-aminoadipic semialdehyde, was detected as a potential precursor for the cross-link in the piceatannol-treated BSA, suggesting that the polymerization of the protein might be mediated by the oxidation of a lysine residue by piceatannol followed by a Schiff base reaction with the ε-amino group of an unoxidized lysine residue. The results of this study established a novel mechanism for the formation of innate epitopes by small dietary molecules and support the notion that many of the beneficial effects of polyphenols could be attributed, at least in part, to their lysyl oxidase-like activity. They also suggest that resveratrol may have beneficial effects on human health because of its conversion to piceatannol.
At J-PARC, the MuSEUM (Muonium Spectroscopy Experiment Using Microwave) collaboration aims to precisely measure the ground-state hyperfine splitting of muonium atoms arising from the muon and electron spins. The pulsed muon beam is stopped in a krypton gas cell to form muonium atoms. The transitions of spin states are induced with a microwave cavity, which are then measured by positron counters. After the previously performed successful measurements with a nearly-zero magnetic field, we are currently planning a measurement with the 2.9T magnetic field by measuring two Zeeman-split sub-levels, so that increased statistics will allow us to more precisely determine the transition frequency down to ∼1ppb. Moreover, a new microwave cavity with a unique geometry is being designed to perform the measurement at an even stronger field of 2.9T in the future.
Measurements of the muonic helium atom hyperfine structure (HFS) are a sensitive tool to test the theory of three-body atomic systems and bound-state quantum electrodynamics (QED) and to determine fundamental constants of the negative muon magnetic moment and mass. The world’s most intense pulsed negative muon beam at J-PARC MUSE brings an opportunity to improve previous measurements and test further CPT invariance by comparing the magnetic moments and masses of positive and negative muons. Test measurements at D-line are now in progress utilizing MuSEUM apparatus at zero field. The first results already have better accuracy than previous measurements in the 1980s. Also, the investigation of a new experimental approach to improve HFS measurements by repolarizing muonic helium atoms using a spin-exchange optical pumping (SEOP) technique was started. If successful, this would drastically improve the measurement accuracy.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.