在有偏见的G蛋白结合受体上,符合性选择指导β-arrestin的招募
Andrew B Kleist1,2, Shawn Jenjak1, Andrija Sente3
1Department of Biochemistry, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
与G蛋白结合的受体 (GPCRs) 与非典型的化学因子受体 (ACKRs) 一样,会招募β-arrestin. 这项研究揭示了ACKR3的结构动态是β-arrestin结合的关键,为偏差的GPCR信号提供了洞察力.
科学领域:
- 生物化学
- 结构生物学
- 药理学
背景情况:
- G蛋白结合受体 (GPCR) 是细胞信号的关键蛋白质.
- 在GPCR下游,β-arrestins调解多种细胞功能.
- 非典型的化学因子受体 (ACKRs) 是偏向的GPCRs,可以招募β-arrestin,但不能招募G蛋白.
研究的目的:
- 调查β-arrestin被ACKR3招募的结构动态.
- 阐明ACKR3中偏差信号的机制.
主要方法:
- 核磁共振 (NMR) 光谱在标有13CH3-ε-methionine的ACKR3上
- 在β-arrestin招募中缺陷的ACKR3突变的分析.
主要成果:
- 对ACKR3的β-arrestin招募与联体结合口袋和β-arrestin合区域的形态交换有关.
- 接收器核心中的异质枢纽调节着形态状态.
- 在β-arrestin招募过程中,受体动态在细胞内和细胞外区域进行调整.
结论:
- 符合性选择是指导β-arrestin向ACKR3的关键机制.
- 了解ACKR3动态可以了解偏差的GPCR信号通路.
更多相关视频
09:03Parallel Interrogation of β-Arrestin2 Recruitment for Ligand Screening on a GPCR-Wide Scale using PRESTO-Tango Assay
Published on: March 10, 2020
09:12G Protein-selective GPCR Conformations Measured Using FRET Sensors in a Live Cell Suspension Fluorometer Assay
Published on: September 10, 2016
相关概念视频
GPCR Desensitization
Activation and Inactivation of G Proteins
Assembly of Signaling Complexes
Interaction domains in cell signaling
Interaction domains recognize exposed features of their binding partners containing post-translationally modified sequences,...
Transducer Mechanism: G Protein–Coupled Receptors
GPCRs are also called heptahelical,...
G Protein-coupled Receptors
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
G-protein Coupled Receptors
