Department of Chemistry, New York University, New York, NY 10003, USA.
Physiology, Biophysics, and Systems Biology Graduate Program and Department of Biochemistry, Weill Cornell Medicine, New York, NY 10065, USA.
Angew Chem Int Ed Engl. 2022 Apr 25;61(18):e202117094. doi: 10.1002/anie.202117094. Epub 2022 Mar 7.
Serotonin receptors play central roles in neuromodulation and are critical drug targets for psychiatric disorders. Optical control of serotonin receptor subtypes has the potential to greatly enhance our understanding of the spatiotemporal dynamics of receptor function. While other neuromodulatory receptors have been successfully rendered photoswitchable, reversible photocontrol of serotonin receptors has not been achieved, representing a major gap in GPCR photopharmacology. Herein, we develop the first tools that allow for such control. Azo5HT-2 shows light-dependent 5-HT R agonism, with greater activity in the cis-form. Based on docking and test compound analysis, we also develop photoswitchable orthogonal, remotely-tethered ligands (PORTLs). These BG-Azo5HTs provide rapid, reversible, and repeatable optical control following conjugation to SNAP-tagged 5-HT R. Overall, this study provides a foundation for the broad extension of photopharmacology to the serotonin receptor family.
血清素受体在神经调节中发挥核心作用,是精神疾病的关键药物靶点。血清素受体亚型的光学控制有可能极大地增强我们对受体功能时空动态的理解。虽然已经成功地将其他神经调质受体转化为光可切换的,但血清素受体的可逆光控尚未实现,这代表着 GPCR 光药理学中的一个主要空白。在此,我们开发了第一批允许进行此类控制的工具。Azo5HT-2 表现出依赖于光的 5-HT R 激动作用,顺式构象的活性更高。基于对接和测试化合物分析,我们还开发了光可切换的正交、远程连接配体 (PORTL)。这些 BG-Azo5HTs 在与 SNAP 标记的 5-HT R 缀合后,可提供快速、可逆和可重复的光学控制。总的来说,这项研究为将光药理学广泛扩展到血清素受体家族提供了基础。