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Analysis of Molecular Concentration and Brightness from Fluorescence Fluctuation Data with an Electron Multiplied CCD Camera

机译:电子倍增CCD相机从荧光涨落数据分析分子浓度和亮度

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摘要

We demonstrate the calculation of particle brightness and concentration from fluorescence-fluctuation photon-counting statistics using an electron-multiplied charge-coupled device (EMCCD) camera. This technique provides a concentration-independent measure of particle brightness in dynamic systems. The high sensitivity and highly parallel detection of EMCCD cameras allow for imaging of dynamic particle brightness, providing the capability to follow aggregation reactions in real time. A critical factor of the EMCCD camera is the presence of nonlinearity at high intensities. These nonlinearities arise due to limited capacity of the CCD well and to the analog-to-digital converter maximum range. However, we show that the specific camera we used (with a 16-bit analog-to-digital converter) has sufficient dynamic range for most microscopy applications. In addition, we explore the importance of camera timing behavior as it is affected by the vertical frame transfer speed of the camera. Although the camera has microsecond exposure time for illumination of a few pixels, the exposure time increased to milliseconds for full-field illumination. Finally, we demonstrate the ability of the technique to follow concentration changes and measure single-molecule brightness in real time in living cells.
机译:我们演示了使用电子倍增电荷耦合器件(EMCCD)相机从荧光波动光子计数统计数据计算粒子亮度和浓度。此技术提供了动态系统中粒子亮度的浓度独立度量。 EMCCD摄像机的高灵敏度和高度并行检测可对动态粒子亮度进行成像,从而能够实时跟踪聚集反应。 EMCCD摄像机的一个关键因素是在高强度下存在非线性。这些非线性是由于CCD井的容量有限以及模数转换器的最大范围而引起的。但是,我们表明,我们使用的特定相机(带有16位模数转换器)对于大多数显微镜应用而言具有足够的动态范围。此外,我们探讨了相机定时行为的重要性,因为它受相机垂直帧传输速度的影响。尽管相机的曝光时间为微秒,只有几个像素,但全场照明的曝光时间却增加到毫秒。最后,我们展示了该技术跟踪浓度变化并实时测量活细胞中单分子亮度的能力。

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