| Literature DB >> 30872534 |
Christopher J Magnus1, Peter H Lee1, Jordi Bonaventura2, Roland Zemla3,4, Juan L Gomez2, Melissa H Ramirez1, Xing Hu5, Adriana Galvan5, Jayeeta Basu3,6, Michael Michaelides2,7, Scott M Sternson8.
Abstract
Chemogenetics enables noninvasive chemical control over cell populations in behaving animals. However, existing small-molecule agonists show insufficient potency or selectivity. There is also a need for chemogenetic systems compatible with both research and human therapeutic applications. We developed a new ion channel-based platform for cell activation and silencing that is controlled by low doses of the smoking cessation drug varenicline. We then synthesized subnanomolar-potency agonists, called uPSEMs, with high selectivity for the chemogenetic receptors. uPSEMs and their receptors were characterized in brains of mice and a rhesus monkey by in vivo electrophysiology, calcium imaging, positron emission tomography, behavioral efficacy testing, and receptor counterscreening. This platform of receptors and selective ultrapotent agonists enables potential research and clinical applications of chemogenetics.Entities:
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Year: 2019 PMID: 30872534 PMCID: PMC7252514 DOI: 10.1126/science.aav5282
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728