谷氨酸受体
运输机
兴奋性氨基酸转运体
谷氨酸-天冬氨酸转运体
生物化学
兴奋性突触后电位
抑制性突触后电位
化学
氨基酸
神经递质
生物
细胞生物学
神经科学
受体
基因
作者
Tosio Kato,Tsukasa Kusakizako,Chunhuan Jin,Xinyu Zhou,Ryuichi Ohgaki,Lili Quan,Minhui Xu,Suguru Okuda,Kan Kobayashi,Keitaro Yamashita,Takashi Nishizawa,Yoshikatsu Kanai,Osamu Nureki
标识
DOI:10.1038/s41467-022-32442-6
摘要
Glutamate is a pivotal excitatory neurotransmitter in mammalian brains, but excessive glutamate causes numerous neural disorders. Almost all extracellular glutamate is retrieved by the glial transporter, Excitatory Amino Acid Transporter 2 (EAAT2), belonging to the SLC1A family. However, in some cancers, EAAT2 expression is enhanced and causes resistance to therapies by metabolic disturbance. Despite its crucial roles, the detailed structural information about EAAT2 has not been available. Here, we report cryo-EM structures of human EAAT2 in substrate-free and selective inhibitor WAY213613-bound states at 3.2 Å and 2.8 Å, respectively. EAAT2 forms a trimer, with each protomer consisting of transport and scaffold domains. Along with a glutamate-binding site, the transport domain possesses a cavity that could be disrupted during the transport cycle. WAY213613 occupies both the glutamate-binding site and cavity of EAAT2 to interfere with its alternating access, where the sensitivity is defined by the inner environment of the cavity. We provide the characterization of the molecular features of EAAT2 and its selective inhibition mechanism that may facilitate structure-based drug design for EAAT2.
科研通智能强力驱动
Strongly Powered by AbleSci AI