G蛋白偶联受体
计算生物学
生物
受体
化学
纳米技术
生物化学
材料科学
作者
Anastasiia Gusach,Javier García‐Nafría,Christopher G. Tate
标识
DOI:10.1016/j.sbi.2023.102574
摘要
Over the past three years (2020-2022) more structures of GPCRs have been determined than in the previous twenty years (2000-2019), primarily of GPCR complexes that are large enough for structure determination by single-particle cryo-EM. This review will present some structural highlights that have advanced our molecular understanding of promiscuous G protein coupling, how a G protein receptor kinase and β-arrestins couple to GPCRs, and GPCR dimerisation. We will also discuss advances in the use of gene fusions, nanobodies, and F
科研通智能强力驱动
Strongly Powered by AbleSci AI