Gauci M R, Vesey G, Narai J, Veal D, Williams K L, Piper J A
Centre for Lasers and Applications, Macquarie University, Sydney, Australia.
Cytometry. 1996 Dec 1;25(4):388-93. doi: 10.1002/(SICI)1097-0320(19961201)25:4<388::AID-CYTO11>3.0.CO;2-R.
We report the first demonstration of directly recording fluorescence spectra of single cells in flow cytometry. An intensified, 512-element photodiode array was used in conjunction with a dispersing prism to capture the fluorescence emission spectra of Coulter ImmunoCheck calibration beads and Dictyostelium discoideum spores stained with the indocarbocyanine derivative CY3, fluorescein isothiocyanate, or R-phycoerythrin. The demonstration was made feasible by enhancing the signal-to-noise ratio of the detection process by using a fast gating technique applied to the detector. Results show that the complete fluorescence spectra of individual stained cells contain information that is normally not captured by conventional flow cytometers. By using the spectrographic flow cytometer, all this information is recorded, allowing small features and shifts in the fluorescence spectra of labelled particles to be studied.
我们报告了在流式细胞术中直接记录单个细胞荧光光谱的首次演示。一个增强型的512元素光电二极管阵列与一个色散棱镜结合使用,以捕获用吲哚碳菁衍生物CY3、异硫氰酸荧光素或R-藻红蛋白染色的库尔特免疫检查校准珠和盘基网柄菌孢子的荧光发射光谱。通过对探测器应用快速门控技术提高检测过程的信噪比,使该演示成为可能。结果表明,单个染色细胞的完整荧光光谱包含传统流式细胞仪通常无法捕获的信息。通过使用光谱流式细胞仪,所有这些信息都被记录下来,从而能够研究标记颗粒荧光光谱中的微小特征和变化。