Karl Deisseroth
A Stanford psychiatrist and bioengineer who helped turn light-sensitive microbial proteins into tools for controlling selected neurons. His contribution connects molecular discovery with experiments on living neural circuits.
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Nobel Prize in Physiology or Medicine 2026A Stanford psychiatrist and bioengineer who helped turn light-sensitive microbial proteins into tools for controlling selected neurons. His contribution connects molecular discovery with experiments on living neural circuits.
A researcher at Humboldt University in Berlin whose studies of light-sensing algae helped uncover channelrhodopsins. He investigated how these proteins respond to light, laying a molecular foundation for optogenetics.
A biophysicist associated with the University of Würzburg who helped show that channelrhodopsins act as light-gated ion channels. His electrophysiological experiments linked algal proteins to controllable electrical activity in other cells.
An endocrinology researcher whose work clarified the biological actions of GLP-1 and related gut hormones. His research helped connect basic hormone biology with medicines for metabolic disease.
A physiologist who studies how intestinal hormones regulate insulin secretion and metabolism. His experiments helped establish the activity of GLP-1 and its role in the gut–pancreas connection.
A peptide chemist whose work identified the biologically active form of GLP-1 and enabled its synthesis and measurement. This contribution helped researchers test how the hormone stimulates insulin secretion.
Optogenetics introduces light-sensitive proteins into selected cells so light can change their activity. This lets researchers test what a neural circuit does by perturbing it, rather than only observing it. A research tool’s success does not mean a treatment is ready for routine care.
GLP-1 is a gut hormone involved in glucose-dependent insulin secretion and other metabolic signals. Research on its active form and receptors helped enable medicines that mimic its action. The hormone, a drug and an individual treatment decision are different subjects.
Optical coherence tomography uses reflected light and interference to produce cross-sectional images of tissue. It can reveal structures such as retinal layers without cutting the tissue. Imaging structure is different from proving the cause of a disease.