Elucidating the molecular logic of a metabotropic glutamate receptor heterodimer

Xin Lin, Davide Provasi, Colleen M. Niswender, Wesley B. Asher () and Jonathan A. Javitch ()
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Xin Lin: Columbia University
Davide Provasi: Icahn School of Medicine at Mount Sinai
Colleen M. Niswender: Vanderbilt University
Wesley B. Asher: Columbia University
Jonathan A. Javitch: Columbia University

Nature Communications, 2024, vol. 15, issue 1, 1-15

Abstract: Abstract Metabotropic glutamate (mGlu) receptor protomers can heterodimerize, leading to different pharmacology compared to their homodimeric counterparts. Here, we use complemented donor-acceptor resonance energy transfer (CODA-RET) technology that distinguishes signaling from defined mGlu heterodimers or homodimers, together with targeted mutagenesis of receptor protomers and computational docking, to elucidate the mechanism of activation and differential pharmacology in mGlu2/4 heteromers. We demonstrate that positive allosteric modulators (PAMs) that bind an upper allosteric pocket in the mGlu4 transmembrane domain are active at both mGlu4/4 homomers and mGlu2/4 heteromers, while those that bind a lower allosteric pocket within the same domain are efficacious in homomers but not heteromers. We further demonstrate that both protomers of mGlu2/4 heteromers are cis-activated by their orthosteric agonists, signaling independently with no trans-activation detected. Intriguingly, however, upper pocket mGlu4 PAMs enable trans-activation in mGlu2/4 heteromers from mGlu4 to the mGlu2 protomer and also enhance cis-activation of the mGlu2 protomer. While mGlu2 PAMs enhanced mGlu2 cis-activation in the heterodimer, we were unable to detect trans-activation in the opposite direction from mGlu2 to the mGlu4 protomer, suggesting an asymmetry of signaling. These insights into the molecular logic of this receptor heteromer are critical to building toward precision targeted therapies for multiple neuropsychiatric disorders.

Date: 2024
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DOI: 10.1038/s41467-024-52822-4

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