Kang Hye Jin, Krumm Brian E, Tassou Adrien, Geron Matan, DiBerto Jeffrey F, Kapolka Nicholas J, Gumpper Ryan H, Sakamoto Kensuke, Dewran Kocak D, Olsen Reid H J, Huang Xi-Ping, Zhang Shicheng, Huang Karen L, Zaidi Saheem A, Nguyen MyV T, Jo Min Jeong, Katritch Vsevolod, Fay Jonathan F, Scherrer Grégory, Roth Bryan L
Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Department of Pharmacology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Cell. 2024 Dec 26;187(26):7433-7449.e20. doi: 10.1016/j.cell.2024.11.001. Epub 2024 Dec 3.
Designer receptors exclusively activated by designer drugs (DREADDs) are chemogenetic tools for remotely controlling cellular signaling, neural activity, behavior, and physiology. Using a structure-guided approach, we provide a peripherally restricted Gi-DREADD, hydroxycarboxylic acid receptor DREADD (HCAD), whose native receptor is minimally expressed in the brain, and a chemical actuator that does not cross the blood-brain barrier (BBB). This was accomplished by combined mutagenesis, analoging via an ultra-large make-on-demand library, structural determination of the designed DREADD receptor via cryoelectron microscopy (cryo-EM), and validation of HCAD function. Expression and activation of HCAD in dorsal root ganglion (DRG) neurons inhibit action potential (AP) firing and reduce both acute and tissue-injury-induced inflammatory pain. The HCAD chemogenetic system expands the possibilities for studying numerous peripheral systems with little adverse effects on the central nervous system (CNS). The structure-guided approach used to generate HCAD also has the potential to accelerate the development of emerging chemogenetic tools for basic and translational sciences.
仅由设计药物激活的设计受体(DREADDs)是用于远程控制细胞信号传导、神经活动、行为和生理功能的化学遗传工具。我们采用结构导向方法,提供了一种外周限制型Gi-DREADD,即羟基羧酸受体DREADD(HCAD),其天然受体在大脑中表达极少,还提供了一种不会穿过血脑屏障(BBB)的化学激活剂。这是通过组合诱变、借助超大型按需合成文库进行类似物合成、通过冷冻电子显微镜(cryo-EM)确定设计的DREADD受体的结构以及验证HCAD功能来实现的。HCAD在背根神经节(DRG)神经元中的表达和激活可抑制动作电位(AP)发放,并减轻急性和组织损伤诱导的炎性疼痛。HCAD化学遗传系统扩展了研究众多外周系统的可能性,且对中枢神经系统(CNS)几乎没有不良影响。用于生成HCAD的结构导向方法也有可能加速基础科学和转化科学中新兴化学遗传工具的开发。