RIKEN Brain Science Institute, Laboratory for Neuronal Circuit Dynamics, 2-1 Hirosawa, Wako-shi, Saitama, 351-0198, Japan.
Exp Physiol. 2011 Jan;96(1):13-8. doi: 10.1113/expphysiol.2010.053942. Epub 2010 Sep 17.
Over the last decade, researchers in our laboratory have engineered and developed several series of genetically encoded voltage-sensitive fluorescent proteins (VSFPs) by molecular fusion of a voltage-sensing domain operand with different fluorescent reporter proteins. These genetically encoded VSFPs have been shown to provide a reliable optical report of membrane potential from targeted neurons and muscle cells in culture or in living animals. However, these various reporters also exhibit discrepancies in both their voltage-sensing and targeting properties that are essentially related to the intrinsic characteristics of the fluorescent reporter proteins. It is therefore important carefully to select the sensor that is most appropriate for the particular question being investigated experimentally. Here we examine the current state of this subfield of optogenetics, address current limitations and challenges, and discuss what is likely to be feasible in the near future.
在过去的十年中,我们实验室的研究人员通过将电压敏感受体结构域与不同的荧光报告蛋白进行分子融合,设计和开发了几系列遗传编码的电压敏感荧光蛋白(VSFP)。这些遗传编码的 VSFPs 已被证明可提供来自培养的靶神经元和肌肉细胞或活体动物中膜电位的可靠光学报告。然而,这些不同的报告器在电压感应和靶向特性方面也存在差异,这些差异主要与荧光报告蛋白的固有特性有关。因此,仔细选择最适合正在进行的实验的传感器非常重要。在这里,我们检查了光遗传学这一分支领域的现状,讨论了当前的局限性和挑战,并探讨了在不久的将来可能实现的目标。