Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
Graduate School of Nanoscience and Technology, KAIST, Daejeon, Republic of Korea.
Nat Chem Biol. 2016 Jun;12(6):431-6. doi: 10.1038/nchembio.2064. Epub 2016 Apr 11.
Intracellular membrane trafficking, which is involved in diverse cellular processes, is dynamic and difficult to study in a spatiotemporal manner. Here we report an optogenetic strategy, termed light-activated reversible inhibition by assembled trap of intracellular membranes (IM-LARIAT), that uses various Rab GTPases combined with blue-light-induced hetero-interaction between cryptochrome 2 and CIB1. In this system, illumination induces a rapid and reversible intracellular membrane aggregation that disrupts the dynamics and functions of the targeted membrane. We applied IM-LARIAT to specifically perturb several Rab-mediated trafficking processes, including receptor transport, protein sorting and secretion, and signaling initiated from endosomes. We finally used this tool to reveal different functions of local Rab5-mediated and Rab11-mediated membrane trafficking in growth cones and soma of young hippocampal neurons. Our results show that IM-LARIAT is a versatile tool that can be used to dissect spatiotemporal functions of intracellular membranes in diverse systems.
细胞内膜运输涉及多种细胞过程,其时空动态难以研究。在这里,我们报告了一种光遗传学策略,称为通过组装的细胞内膜捕获物进行光激活的可逆抑制(light-activated reversible inhibition by assembled trap of intracellular membranes,IM-LARIAT),该策略使用各种 Rab GTPases 结合蓝光诱导的隐色体 2 和 CIB1 之间的异相互作用。在该系统中,光照会诱导快速且可逆的细胞内膜聚集,从而破坏靶向膜的动力学和功能。我们将 IM-LARIAT 应用于特异性干扰几种 Rab 介导的运输过程,包括受体运输、蛋白质分拣和分泌,以及从内体起始的信号转导。我们最终使用该工具揭示了局部 Rab5 介导和 Rab11 介导的质膜运输在年轻海马神经元的生长锥和胞体中的不同功能。我们的结果表明,IM-LARIAT 是一种多功能工具,可用于在不同系统中剖析细胞内膜的时空功能。