变构调节
门控
烟碱乙酰胆碱受体
化学
跨膜结构域
兴奋剂
生物物理学
乙酰胆碱受体
离子通道
神经递质受体
神经递质
受体
烟碱激动剂
G蛋白偶联受体
神经科学
细胞生物学
生物化学
生物
标识
DOI:10.1016/j.bpj.2024.01.003
摘要
How do agonists turn on receptors? The model system we have used to address this question is the adult-type skeletal muscle nicotinic acetylcholine receptor. This ligand-gated ion channel has two orthosteric sites (for neurotransmitters) in the extracellular domain linked to an allosteric site (a gate) in the transmembrane domain. The goal of this perspective is to summarize how measurements of agonist binding energy reveal the dynamics of the neurotransmitter sites and the fundamental link between binding and gating.
科研通智能强力驱动
Strongly Powered by AbleSci AI