Siegel Micah S, Isacoff Ehud Y
Cold Spring Harb Protoc. 2010 Apr;2010(4):pdb.top76. doi: 10.1101/pdb.top76.
Measuring signal transduction in large numbers of cells, with high spatial and temporal resolution, is a fundamental problem for studying information processing in the nervous system. To address this problem, a family of detectors that are chimeras between signal transduction proteins and fluorescent proteins has been designed. The prototype sensor is a genetically encoded probe that can be used to measure transmembrane voltage in single cells. This article describes a modified green fluorescent protein (GFP), fused to a voltage-sensitive K(+) channel, so that voltage-dependent rearrangements in the K(+) channel induce changes in the fluorescence of GFP. The probe has a maximal fractional fluorescence change of 5.1%, making it comparable to some of the best organic voltage-sensitive dyes. Moreover, the fluorescent signal is expanded in time in a manner that makes the signal 30-fold easier to detect than a traditional linear dye. DNA-encoded sensors have the advantage that they may be introduced into an organism noninvasively and targeted to specific brain regions, cell types, and subcellular compartments.
以高空间和时间分辨率测量大量细胞中的信号转导,是研究神经系统信息处理的一个基本问题。为了解决这个问题,人们设计了一类探测器,它们是信号转导蛋白和荧光蛋白的嵌合体。原型传感器是一种基因编码探针,可用于测量单细胞中的跨膜电压。本文描述了一种与电压敏感钾通道融合的改良绿色荧光蛋白(GFP),使得钾通道中依赖电压的重排会引起GFP荧光的变化。该探针的最大荧光分数变化为5.1%,与一些最好的有机电压敏感染料相当。此外,荧光信号在时间上被放大,使得该信号比传统线性染料的信号易于检测30倍。DNA编码传感器的优点是可以无创地引入生物体,并靶向特定的脑区、细胞类型和亚细胞区室。