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一种DNA编码的电压敏感荧光蛋白的设计与表征

Design and characterization of a DNA-encoded, voltage-sensitive fluorescent protein.

作者信息

Sakai R, Repunte-Canonigo V, Raj C D, Knöpfel T

机构信息

Laboratory for Neuronal Circuit Dynamics, Brain Science Institute, RIKEN, 2-1 Hirosawa, Wako-Shi, Saitama 351-0198, Japan.

出版信息

Eur J Neurosci. 2001 Jun;13(12):2314-8. doi: 10.1046/j.0953-816x.2001.01617.x.

Abstract

Optical imaging of electrical activity has been suggested as a promising approach to investigate the multineuronal representation of information processing in brain tissue. While considerable progress has been made in the development of instrumentation suitable for high-speed imaging, intrinsic or extrinsic dye-mediated optical signals are often of limited use due to their slow response dynamics, low effective sensitivity, toxicity or undefined cellular origin. Protein-based and DNA-encoded voltage sensors could overcome these limitations. Here we report the design and generation of a voltage-sensitive fluorescent protein (VSFP) consisting of a voltage sensing domain of a potassium channel and a pair of cyan and yellow emitting mutants of green fluorescent protein (GFP). In response to a change in transmembrane voltage, the voltage sensor alters the amount of fluorescence resonance energy transfer (FRET) between the pair of GFP mutants. The optical signals respond in the millisecond time-scale of fast electrical signalling and are large enough to allow monitoring of voltage changes at the single cell level.

摘要

电活动的光学成像已被认为是一种很有前景的方法,用于研究脑组织中信息处理的多神经元表征。虽然在开发适用于高速成像的仪器方面已经取得了相当大的进展,但由于其响应动力学缓慢、有效灵敏度低、毒性或细胞起源不明确,内在或外在染料介导的光学信号的用途往往有限。基于蛋白质和DNA编码的电压传感器可以克服这些限制。在这里,我们报告了一种电压敏感荧光蛋白(VSFP)的设计和生成,它由钾通道的电压传感结构域和一对绿色荧光蛋白(GFP)的青色和黄色发射突变体组成。响应跨膜电压的变化,电压传感器会改变这对GFP突变体之间的荧光共振能量转移(FRET)量。光学信号在快速电信号的毫秒时间尺度内响应,并且足够大,能够在单细胞水平上监测电压变化。

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