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Poppe, M.

Publications and source records attributed to Poppe, M..

2 recordsLinked to original sources

EEG biomarkers of reinforcement learning and motivation: A multi-task battery

Serotonin and dopamine make dissociable contributions to reinforcement learning (RL) sub-components, yet we lack neural biomarkers capable of detecting their differential effects. Here, we report the development of a five-task EEG battery designed to probe these dissociable RL mechanisms. Using a model-free analytical approach in healthy volunteers, we identify distinct neural markers across probabilistic instrumental learning, motivational vigour, Pavlovian-instrumental transfer, reversal learning, and a working memory-RL task. A centroparietal P300 tracked incremental learning across three paradigms and showed cross-task convergent validity. Readiness potentials and beta suppression indexed value-based motor preparation, while frontal theta captured Pavlovian-instrumental conflict. The largely independent pattern across markers supports the batterys capacity to detect selective pharmacological effects on distinct neural systems.

neuroscience↗

PERK inhibition rewires translational and CMGC protein kinase networks into an antiviral state

Protein kinases (PKs) are central regulators of cellular signaling, yet only a small fraction of the human kinome is targeted therapeutically, and kinase-substrate relationships remain incompletely defined. Here, we systematically characterize kinome regulation during human coronavirus 229E (HCoV-229E) infection across transcriptomic, translational, proteomic, and phospho-proteomic layers. We reveal that pharmacological inhibition of the ER stress sensor kinase PERK reprograms host protein biosynthesis and phospho-proteomic landscapes, simultaneously blocking viral nucleocapsid phosphorylation and modulating multiple host kinases. This rewiring antagonizes virus-induced translational shutdown, along with pronounced regulation of the CMGC kinase family, a pattern conserved in SARS-CoV and SARS-CoV-2 infected cells. Comparative analyses with PERK depletion distinguish on-target from off-target effects of PERK inhibition. Our findings uncover the kinome-scale consequences of PERK perturbation in coronavirus infection and demonstrate how the polypharmacology of PERK inhibitors can be harnessed to establish a potent antiviral state, revealing new avenues for host-directed antiviral strategies.

systems biology↗