Digital Analysis and Sorting of Fluorescence Lifetime by Flow Cytometry

被引:46
|
作者
Houston, Jessica P. [1 ]
Naivar, Mark A. [1 ]
Freyer, James P. [1 ]
机构
[1] Los Alamos Natl Lab, Biosci Div, Los Alamos, NM 87545 USA
基金
美国国家卫生研究院;
关键词
fluorescence lifetime; digital flow cytometry; phase-sensitive flow cytometry; FLUOROCHROME-LABELED CELLS; DEUTERIUM-OXIDE; DNA; PARTICLES; BINDING; SIGNALS;
D O I
10.1002/cyto.a.20930
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Frequency-domain flow cytometry techniques are combined with modifications to the digital signal-processing capabilities of the open reconfigurable cytometric acquisition system (ORCAS) to analyze fluorescence decay lifetimes and control sorting. Real-time fluorescence lifetime analysis is accomplished by rapidly digitizing correlated, radiofrequency (RF)-modulated detector signals, implementing Fourier analysis programming with ORCAS' digital signal processor (DSP) and converting the processed data into standard cytometric list mode data. To systematically test the capabilities of the ORCAS 50 MS/sec analog-to-digital converter (ADC) and our DSP programming, an error analysis was performed using simulated light scatter and fluorescence waveforms (0.5-25 ns simulated lifetime), pulse widths ranging from 2 to 15 mu s, and modulation frequencies from 2.5 to 16.667 MHz. The standard deviations of digitally acquired lifetime values ranged from 0.112 to >2 ns, corresponding to errors in actual phase shifts from 0.0142 degrees to 1.6 degrees. The lowest coefficients of variation (<1%) were found for 10-MHz modulated waveforms having pulse widths of 6 is and simulated lifetimes of 4 ns. Direct comparison of the digital analysis system to a previous analog phase-sensitive flow cytometer demonstrated similar precision and accuracy on measurements of a range of fluorescent microspheres, unstained cells, and cells stained with three common fluorophores. Sorting based on fluorescence lifetime was accomplished by adding analog outputs to ORCAS and interfacing with a commercial cell sorter with a RF-modulated solid-state laser. Two populations of fluorescent microspheres with overlapping fluorescence intensities but different lifetimes (2 and 7 ns) were separated to similar to 98% purity. Overall, the digital signal acquisition and processing methods we introduce present a simple yet robust approach to phase-sensitive measurements in flow cytometry. The ability to simply and inexpensively implement this system on a commercial flow sorter will allow both better dissemination of this technology and better exploitation of the traditionally underutilized parameter of fluorescence lifetime. Published 2010 Wiley-Liss, Inc.(dagger)
引用
收藏
页码:861 / 872
页数:12
相关论文
共 50 条
  • [1] Fluorescence lifetime measurements in flow cytometry
    Beisker, W
    Klocke, A
    OPTICAL DIAGNOSTICS OF BIOLOGICAL FLUIDS AND ADVANCED TECHNIQUES IN ANALYTICAL CYTOLOGY, PROCEEDINGS OF, 1997, 2982 : 436 - 446
  • [2] Fluorescence lifetime-dependent flow cytometry: a new parameter for high-throughput single-cell sorting and analysis
    Houston, J. P.
    Houston, K. D.
    Cao, R.
    Gohar, A. Vaziri
    MOLECULAR BIOLOGY OF THE CELL, 2013, 24
  • [3] Endogenous fluorescence lifetime of viable cells by flow cytometry
    Houston, Jessica P.
    Naivar, Mark
    Martin, John C.
    Goddard, Greg
    Carpenter, Susan
    Mourant, Judith R.
    Freyer, James P.
    IMAGING, MANIPULATION, AND ANALYSIS OF BIOMOLECULES, CELLS, AND TISSUES VI, 2008, 6859
  • [4] PLANT CHROMOSOME ANALYSIS AND SORTING BY FLOW CYTOMETRY
    DOLEZEL, J
    LUCRETTI, S
    SCHUBERT, I
    CRITICAL REVIEWS IN PLANT SCIENCES, 1994, 13 (03) : 275 - 309
  • [5] Mammalian Chromosome Analysis and Sorting by Flow Cytometry
    Mukhopadhyay, Risani
    Varshitha, Dv
    Telford, William G.
    Sanders, Claire K.
    Chakraborty, Uttara
    CURRENT PROTOCOLS, 2023, 3 (05):
  • [6] High-throughput fluorescence lifetime imaging flow cytometry
    Kanno, Hiroshi
    Hiramatsu, Kotaro
    Mikami, Hideharu
    Nakayashiki, Atsushi
    Yamashita, Shota
    Nagai, Arata
    Okabe, Kohki
    Li, Fan
    Yin, Fei
    Tominaga, Keita
    Bicer, Omer Faruk
    Noma, Ryohei
    Kiani, Bahareh
    Efa, Olga
    Buescher, Martin
    Wazawa, Tetsuichi
    Sonoshita, Masahiro
    Shintaku, Hirofumi
    Nagai, Takeharu
    Braun, Sigurd
    Houston, Jessica P.
    Rashad, Sherif
    Niizuma, Kuniyasu
    Goda, Keisuke
    NATURE COMMUNICATIONS, 2024, 15 (01)
  • [7] Effect of Viscosity on Fluorescence Lifetime Measured Using Flow Cytometry
    Alturkistany, Faisal H.
    Nichani, Kapil
    Li, Wenyan
    Houston, Jessica P.
    2018 CONFERENCE ON LASERS AND ELECTRO-OPTICS (CLEO), 2018,
  • [8] Analysis of bacterial function by multi-colour fluorescence flow cytometry and single cell sorting
    Nebe-von-Caron, G
    Stephens, PJ
    Hewitt, CJ
    Powell, JR
    Badley, RA
    JOURNAL OF MICROBIOLOGICAL METHODS, 2000, 42 (01) : 97 - 114
  • [9] Digital flow cytometry: An improved scheme for pulse capture and cell sorting
    Galbraith, D
    Murthi, S
    Sankaranarayanan, S
    Rodriguez, J
    CYTOMETRY, 2002, : 47 - 47
  • [10] ANALYSIS AND SORTING OF MAMMALIAN MICROCOLONIES BY FLOW-CYTOMETRY
    NIR, R
    ALROY, Y
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1994, 207 : 36 - BIOT