Differential effects of sodium on agonist-induced conformational transitions and signaling at μ and κ opioid receptors

Roth, B. L.; Kuijer, B.; Fulton, C. J.; Albert, T. L.; Knobloch, P. M.; Wang, J.; Krumm, B. E.; Che, T.; Varga, B. R.; Majumdar, S.; Katritch, V.; Gumpper, R. H.; Kenakin, T.; Huang, X.-P.

doi:10.1101/2025.08.28.672897

bioRxiv · 10.1101/2025.08.28.672897

Differential effects of sodium on agonist-induced conformational transitions and signaling at μ and κ opioid receptors

Roth, B. L.·Kuijer, B.·Fulton, C. J.·Albert, T. L.·Knobloch, P. M.·Wang, J.·Krumm, B. E.·Che, T.·Varga, B. R.·Majumdar, S.·Katritch, V.·Gumpper, R. H.·Kenakin, T.·Huang, X.-P.

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Abstract

Sodium ions are classically conceptualized as negative allosteric modulators for G protein coupled receptors (GPCRs), although there have been reports of either positive allosteric modulation or no effect of sodium on GPCR function. Here we identified opposing actions of sodium on the and {kappa} opioid receptors. We utilized a variety of methods including radioligand binding, real-time conformational monitoring of transitions using bioluminescence resonance energy transfer and signaling assays using the TRUPATH resource. At the receptors, sodium behaved as a negative allosteric modulator of binding, conformational transitions and signaling. Intriguingly, bitopic agonists were unaffected by sodium concentrations. By contrast, at the {kappa} opioid receptor sodium negatively modulated agonist binding and positively modulated conformational transitions and signaling. Taken together, these findings support the notion that the differential sensitivities to sodium concentrations will result in opposing effects on cell surface and intracellular signaling.

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Roth, B. L., Kuijer, B., Fulton, C. J., Albert, T. L., Knobloch, P. M., Wang, J., Krumm, B. E., Che, T., Varga, B. R., Majumdar, S., Katritch, V., Gumpper, R. H., Kenakin, T., Huang, X.-P.. 2025-09-02. Differential effects of sodium on agonist-induced conformational transitions and signaling at μ and κ opioid receptors. https://doi.org/10.1101/2025.08.28.672897

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