Zhang Wenchang, Lou Xiaoping, Meng Xiaochen, Zhu Lianqing
School of Instrumentation Science & Opto-Electronics Engineering, Hefei University of Technology, Hefei 230009, China.
Beijing Key Laboratory for Optoelectronic Measurement Technology, Beijing Information Science & Technology University, Beijing 100101, China.
Sensors (Basel). 2016 Nov 23;16(11):1978. doi: 10.3390/s16111978.
Flow cytometry is being applied more extensively because of the outstanding advantages of multicolor fluorescence analysis. However, the intensity measurement is susceptible to the nonlinearity of the detection method. Moreover, in multicolor analysis, it is impossible to discriminate between fluorophores that spectrally overlap; this influences the accuracy of the fluorescence pulse signal representation. Here, we focus on spectral overlap in two-color analysis, and assume that the fluorescence follows the single exponential decay model. We overcome these problems by analyzing the influence of the spectral overlap quantitatively, which enables us to propose a method of fluorescence pulse signal representation based on time-delay estimation (between fluorescence and scattered pulse signals). First, the time delays are estimated using a modified chirp Z-transform (MCZT) algorithm and a fine interpolation of the correlation peak (FICP) algorithm. Second, the influence of hardware is removed via calibration, in order to acquire the original fluorescence lifetimes. Finally, modulated signals containing phase shifts associated with these lifetimes are created artificially, using a digital signal processing method, and reference signals are introduced in order to eliminate the influence of spectral overlap. Time-delay estimation simulation and fluorescence signal representation experiments are conducted on fluorescently labeled cells. With taking the potentially overlap of autofluorescence as part of the observed fluorescence spectrum, rather than distinguishing the individual influence, the results show that the calculated lifetimes with spectral overlap can be rectified from 8.28 and 4.86 ns to 8.51 and 4.63 ns, respectively, using the comprehensive approach presented in this work. These values agree well with the lifetimes (8.48 and 4.67 ns) acquired for cells stained with single-color fluorochrome. Further, these results indicate that the influence of spectral overlap can be eliminated effectively. Moreover, modulation, mixing with reference signals, and low-pass filtering are performed with a digital signal processing method, thereby obviating the need for a high-speed analog device and complex circuit system. Finally, the flexibility of the comprehensive method presented in this work is significantly higher than that of existing methods.
由于多色荧光分析具有突出优势,流式细胞术的应用越来越广泛。然而,强度测量易受检测方法非线性的影响。此外,在多色分析中,无法区分光谱重叠的荧光团;这影响了荧光脉冲信号表示的准确性。在此,我们聚焦于双色分析中的光谱重叠,并假设荧光遵循单指数衰减模型。我们通过定量分析光谱重叠的影响来克服这些问题,这使我们能够提出一种基于时延估计(荧光与散射脉冲信号之间)的荧光脉冲信号表示方法。首先,使用改进的线性调频Z变换(MCZT)算法和相关峰精细插值(FICP)算法估计时延。其次,通过校准消除硬件的影响,以获取原始荧光寿命。最后,使用数字信号处理方法人工创建包含与这些寿命相关的相移的调制信号,并引入参考信号以消除光谱重叠的影响。对荧光标记细胞进行了时延估计模拟和荧光信号表示实验。将自发荧光的潜在重叠视为观察到的荧光光谱的一部分,而不是区分其个体影响,结果表明,使用本工作提出的综合方法,光谱重叠情况下计算出的寿命可分别从8.28纳秒和4.86纳秒校正为8.51纳秒和4.63纳秒。这些值与用单色荧光染料染色的细胞获得的寿命(8.48纳秒和4.67纳秒)非常吻合。此外,这些结果表明光谱重叠的影响可以有效消除。而且,调制、与参考信号混合以及低通滤波均采用数字信号处理方法进行,从而无需高速模拟设备和复杂的电路系统。最后,本工作提出的综合方法的灵活性明显高于现有方法。