Baker B J, Lee H, Pieribone V A, Cohen L B, Isacoff E Y, Knopfel T, Kosmidis E K
Department of Cellular and Molecular Physiology, Yale University School of Medicine, 333 Cedar St., New Haven, CT 06520, USA.
J Neurosci Methods. 2007 Mar 30;161(1):32-8. doi: 10.1016/j.jneumeth.2006.10.005. Epub 2006 Nov 28.
Three first-generation fluorescent protein voltage sensitive probes (FP-voltage sensors) were characterized in mammalian cells. Flare, a Kv1.4 variant of FlaSh [Siegel MS, Isacoff EY. Neuron 1997;19(October (4)):735-41], SPARC [Ataka K, Pieribone VA. Biophys J 2002;82(January (1 Pt 1)):509-16], and VSFP-1 [Sakai R, Repunte-Canonigo V, Raj CD, Knopfel T. Eur J Neurosci 2001;13(June (12)):2314-18] were expressed, imaged and voltage clamped in HEK 293 cells and in dissociated hippocampal neurons. We were unable to detect a signal in response to changes in membrane potential after averaging16 trials with any of the three constructs. Using the hydrophobic voltage sensitive dye, di8-ANEPPS, as a surface marker, confocal analyses demonstrated poor plasma membrane expression for Flare, SPARC and VSFP-1 in both HEK 293 cells and dissociated hippocampal neurons. Almost all of the expressed FP-voltage sensors reside in internal membranes in both cell types. This internal expression generates a background fluorescence that increases the noise in the optical measurement.
在哺乳动物细胞中对三种第一代荧光蛋白电压敏感探针(FP - 电压传感器)进行了特性研究。FlaSh的Kv1.4变体Flare [Siegel MS, Isacoff EY.《神经元》1997年;19(10月(4)):735 - 41]、SPARC [Ataka K, Pieribone VA.《生物物理杂志》2002年;82(1月(1 Pt 1)):509 - 16]以及VSFP - 1 [Sakai R, Repunte - Canonigo V, Raj CD, Knopfel T.《欧洲神经科学杂志》2001年;13(6月(12)):2314 - 18]在HEK 293细胞和离体海马神经元中进行表达、成像及电压钳制。对这三种构建体中的任何一种进行16次试验平均后,我们未能检测到响应膜电位变化的信号。使用疏水性电压敏感染料di8 - ANEPPS作为表面标记,共聚焦分析表明,在HEK 293细胞和离体海马神经元中,Flare、SPARC和VSFP - 1在质膜上的表达均较差。在这两种细胞类型中,几乎所有表达的FP - 电压传感器都位于内膜中。这种内膜表达产生背景荧光,增加了光学测量中的噪声。