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The study, which enables the temporal and spatial control of HS in living cells, was published as the cover article in the January 2026 issue of Precision Chemistry

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Among the proteins with increased expression in ME/CFS were 3-hydroxybutyrate dehydrogenase type 1 (BDH1) and acetyl-CoA acetyltransferase 2 (ACAT2), both of which are integral to fatty acid metabolism and processing of ketone bodies

(1978) [1] reported that the alpha -aspartyl form of position 5 is biologically active in the delta-EEG rabbit assay, while the beta-aspartyl isomer showed substantially reduced activity