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通过结合二氨基荧光素和二氨基罗丹明实现一氧化氮和脱氢抗坏血酸的同步成像。

Simultaneous nitric oxide and dehydroascorbic acid imaging by combining diaminofluoresceins and diaminorhodamines.

作者信息

Ye Xiaoying, Rubakhin Stanislav S, Sweedler Jonathan V

机构信息

Department of Chemistry and the Beckman Institute, University of Illinois, 600 South Mathews Avenue 63-5, Urbana, IL 61801, USA.

出版信息

J Neurosci Methods. 2008 Mar 15;168(2):373-82. doi: 10.1016/j.jneumeth.2007.10.026. Epub 2007 Nov 13.

Abstract

Spatial measurements of nitric oxide (NO) production are important to understand the function and metabolism of this molecule. The reagent, 4,5-diaminofluorescein (DAF-2) and several structurally similar probes are widely used for detection and imaging of NO. However, DAF-2 also reacts with dehydroascorbic acid (DHA) in biological samples, with both products having nearly indistinguishable fluorescence spectra. Measurements using fluorimetry and fluorescence microscopy cannot easily differentiate NO-related fluorescent signals from DHA-related signals. While DAFs and the structurally related diaminorhodamines (DARs) both react with NO and DHA, they do so to different extents. We report a multiderivatization method to image NO and DHA simultaneously by using both DAF and DAR. Specifically, DAF-2 and DAR-4M are used to image NO and DHA concentrations; after reaction, the solutions are excited, at 495 nm to measure fluorescence emission from DAF-2, and at 560 nm to measure fluorescence emission from DAR-4M. Using the appropriate calibrations, images are created that depend either on the relative NO or the relative DHA concentration, even though each probe reacts to both compounds. The method has been validated by imaging NO production in both undifferentiated and differentiated pheochromocytoma (PC12) cells.

摘要

一氧化氮(NO)生成的空间测量对于理解该分子的功能和代谢非常重要。试剂4,5-二氨基荧光素(DAF-2)和几种结构相似的探针被广泛用于NO的检测和成像。然而,DAF-2也会与生物样品中的脱氢抗坏血酸(DHA)发生反应,两种产物的荧光光谱几乎无法区分。使用荧光测定法和荧光显微镜进行测量时,很难将与NO相关的荧光信号与与DHA相关的信号区分开来。虽然DAF和结构相关的二氨基罗丹明(DAR)都能与NO和DHA发生反应,但反应程度不同。我们报告了一种多衍生化方法,通过同时使用DAF和DAR对NO和DHA进行成像。具体来说,DAF-2和DAR-4M用于对NO和DHA浓度进行成像;反应后,溶液在495nm激发以测量DAF-2的荧光发射,在560nm激发以测量DAR-4M的荧光发射。通过适当的校准,即使每个探针都能与两种化合物发生反应,也可以创建依赖于相对NO或相对DHA浓度的图像。该方法已通过对未分化和分化的嗜铬细胞瘤(PC12)细胞中NO生成的成像得到验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/2291520/9758c2af8e27/nihms-41170-f0001.jpg

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