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Quantitative Counting of Single Fluorescent Molecules by Combined Electrochemical Adsorption Accumulation and Total Internal Reflection Fluorescence Microscopy

机译:电化学吸附累积与全内反射荧光显微镜相结合的单分子荧光定量计数

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We developed an ultrasensitive quantitative single-molecule imaging method for fluorescent molecules using a combination of electrochemical adsorption accumulation and total internal reflection fluorescence microscopy(ITRFM).We chose rhodamine 6G(R6G,fluorescence dye)or goat anti-rat IgG(H+L)(IgG(H+L)-488),a protein labeled by Alexa Fluor 488 or DNA labeled by 6-CR6G(DNA-R6G)as the model molecules.The fluorescent molecules were accumulated on a light transparent indium tin oxide(ITO)conductive microscope coverslip using electrochemical adsorption in a stirred solution.Then,images of the fluorescent molecules accumulated on the ITO coverslip sized 40X40 mu m were acquired using an objective-type TIRFM instrument coupled with a high-sensitivity electron multiplying charge-coupled device.One hundred images of the fluorescent molecules accumulated on the coverslip were taken consecutively,one by one,by moving the coverslip with the aid of a three-dimensional positioner.Finally,we counted the number of fluorescent spots corresponding to single fluorescent molecules on the images.The linear relationships between the number of fluorescent molecules and the concentration were obtained in the range of 5X10~(-15)to 5X10~(-12)mol/Lfor R6G,3X10~(-15)to 2X10~(-12)mol/L for IgG(H+L)-488,and 3X10~(-15)to 2X10~(-12)mol/Lfor DNA-R6G.
机译:我们结合电化学吸附积累和全内反射荧光显微镜(ITRFM)开发了一种用于荧光分子的超灵敏定量单分子成像方法。我们选择了若丹明6G(R6G,荧光染料)或山羊抗大鼠IgG(H + L) )(IgG(H + L)-488),以Alexa Fluor 488标记的蛋白质或以6-CR6G(DNA-R6G)标记的DNA作为模型分子。荧光分子聚集在透光的氧化铟锡(ITO)上电镜显微镜盖玻片,在搅拌的溶液中进行电化学吸附,然后使用物镜TIRFM仪器与高灵敏度电子倍增电荷耦合装置相结合,获得ITO盖玻片上累积的荧光分子的图像(尺寸为40X40μm)。通过在三维定位器的帮助下移动盖玻片,连续一张一张地采集盖玻片上累积的荧光分子的一百张图像。最后,我们计算了t对于R6G,在5X10〜(-15)〜5X10〜(-12)mol / L的范围内得到了荧光分子数量与浓度的线性关系。 IgG(H + L)-488为3X10〜(-15)至2X10〜(-12)mol / L,DNA-R6G为3X10〜(-15)至2X10〜(-12)mol / L。

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