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Hallucinogen chemistry guides antidepressant drug discovery

Bethany Halford

C&EN Global Enterprise February 7, 2022 DOI: 10.1021/cen-10005-leadcon (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Structural biology study Peer reviewed
Keywords Hallucinogen Antidepressant Drug discovery Pharmacology
Key points Crystal structures of the 5-HT 2A receptor bound to different ligands reveal binding differences that can guide the design of nonhallucinogenic mood-altering compounds.

Abstract

Scientists have long sought the secrets of the 5-HT 2A serotonin receptor—a central nervous system receptor that binds hallucinogenic compounds, including LSD and psilocybin. Many hope to discover why these molecules cause hallucinations when they bind to 5-HT 2A while other compounds that bind to the receptor, including serotonin, do not. LSD and psilocybin have been shown to treat mood disorders such as depression, and scientists wonder if they can design molecules that maintain that mood-altering ability without causing hallucinations. Researchers now report a structural biology–guided strategy for making such molecules. A team led by Sheng Wang of the Chinese Academy of Sciences and Jianjun Cheng of ShanghaiTech University determined the crystal structures of the 5-HT 2A receptor bound to LSD, psilocin (the active form of psilocybin), serotonin, or lisuride, a nonhallucinogenic treatment for Parkinson's disease . After visualizing the differences in how those molecules bind, the researchers then designed

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