Department of Physiology, University of California, San Francisco, California, USA; email:
Current affiliation: Structural Biology Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Annu Rev Biochem. 2022 Jun 21;91:629-649. doi: 10.1146/annurev-biochem-032620-105738. Epub 2022 Mar 14.
Transient receptor potential (TRP) ion channels are sophisticated signaling machines that detect a wide variety of environmental and physiological signals. Every cell in the body expresses one or more members of the extended TRP channel family, which consists of over 30 subtypes, each likely possessing distinct pharmacological, biophysical, and/or structural attributes. While the function of some TRP subtypes remains enigmatic, those involved in sensory signaling are perhaps best characterized and have served as models for understanding how these excitatory ion channels serve as polymodal signal integrators. With the recent resolution revolution in cryo-electron microscopy, these and other TRP channel subtypes are now yielding their secrets to detailed atomic analysis, which is beginning to reveal structural underpinnings of stimulus detection and gating, ion permeation, and allosteric mechanisms governing signal integration. These insights are providing a framework for designing and evaluating modality-specific pharmacological agents for treating sensory and other TRP channel-associated disorders.
瞬时受体电位 (TRP) 离子通道是复杂的信号转导机器,可检测多种环境和生理信号。体内的每个细胞都表达扩展的 TRP 通道家族的一个或多个成员,该家族由超过 30 种亚型组成,每种亚型可能具有独特的药理学、生物物理学和/或结构特性。虽然一些 TRP 亚型的功能仍然神秘,但那些参与感觉信号转导的 TRP 亚型可能是特征最明显的,它们被用作理解这些兴奋性离子通道如何作为多模式信号整合器的模型。随着冷冻电子显微镜分辨率革命的到来,这些和其他 TRP 通道亚型现在正在向详细的原子分析揭示其秘密,这开始揭示刺激检测和门控、离子渗透以及控制信号整合的变构机制的结构基础。这些见解为设计和评估用于治疗感觉和其他与 TRP 通道相关的疾病的特定模式的药理学药物提供了一个框架。