The long-term goal of this project is to develop advanced flow cytometric methods to measure phase-resolved florescence emissions and excited-state lifetimes of fluorescent probes bound to macromolecules in cells and chromosomes by phase-sensitive detection. In addition, we propose to apply the technology to biological systems that take advantage of these unique measurement capabilities and thus demonstrate the efficacy of the technology for applications in biomedical research. A first-generation, phase-sensitive cytometer has been developed which combines flow cytometry and frequency-domain fluorescence lifetime spectroscopy principles to provide unique capabilities for making lifetime-based sensing measurements on cells labeled with fluorescent probes, while maintaining the capability to make conventional flow cytometric measurements.
The specific aims of this proposal are to: 1) advance the data acquisition technology for making excited-state lifetime and phase- resolved fluorescence emission measurements by implementing a digital signal processing-based (DSP) system; 2) utilize the phase-sensitive detection technology to reduce or eliminate background interferences in flow cytometric measurements caused by cellular autofluorescence, by unbound (non-specific) fluorophore labeling, by fluorescence spectral emission signal-crosstalk between measurement channels, by light scatter in fluorescence detection channels of multi-laser excitation measurements, and by laser-excitation of the acceptor fluorophore in donor/acceptor fluorescence resonance energy transfer measurements; and 3) apply the technology to biological systems that can take advantage of these unique measurement capabilities to demonstrate the efficacy of the technology for application to biomedical research. We propose to take advantage of progress made during the previous grant period and the technical expertise in our laboratory for design/construction of complex digital/analog electronics, cell-cycle analyses, radiation damage and repair biology, chromosomes and chromatin structure, cell-surface receptor architecture, cellular damage mechanisms (e.g., oxygen free radicals), and DNA, RNA, and protein cytochemistry to test the efficacy of the technology for application to biological and biomedical research problems that will contribute to improving diagnoses, treatment, and to understanding the mechanisms of human diseases.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Research Project (R01)
Project #
2R01RR007855-07
Application #
2703180
Study Section
Special Emphasis Panel (ZRG4-SSS-5 (02))
Project Start
1992-09-30
Project End
2001-08-31
Budget Start
1998-09-30
Budget End
1999-08-31
Support Year
7
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Los Alamos National Lab
Department
Type
Schools of Arts and Sciences
DUNS #
City
Los Alamos
State
NM
Country
United States
Zip Code
87545
Cui, H Helen; Valdez, Joseph G; Steinkamp, John A et al. (2003) Fluorescence lifetime-based discrimination and quantification of cellular DNA and RNA with phase-sensitive flow cytometry. Cytometry A 52:46-55
Crissman, H A; Steinkamp, J A (2001) Flow cytometric fluorescence lifetime measurements. Methods Cell Biol 63:131-48
Steinkamp, J A (2001) Time-resolved fluorescence measurements. Curr Protoc Cytom Chapter 1:Unit 1.15
Steinkamp, J A; Valdez, Y E; Lehnert, B E (2000) Flow cytometric, phase-resolved fluorescence measurement of propidium iodide uptake in macrophages containing phagocytized fluorescent microspheres. Cytometry 39:45-55
Keij, J F; Bell-Prince, C; Steinkamp, J A (2000) Staining of mitochondrial membranes with 10-nonyl acridine orange, MitoFluor Green, and MitoTracker Green is affected by mitochondrial membrane potential altering drugs. Cytometry 39:203-10
Keij, J F; Bell-Prince, C; Steinkamp, J A (1999) Simultaneous analysis of relative DNA and glutathione content in viable cells by phase-resolved flow cytometry. Cytometry 35:48-54
Steinkamp, J A; Lehnert, B E; Lehnert, N M (1999) Discrimination of damaged/dead cells by propidium iodide uptake in immunofluorescently labeled populations analyzed by phase-sensitive flow cytometry. J Immunol Methods 226:59-70
Steinkamp, J A; Lehnert, N M; Keij, J F et al. (1999) Enhanced immunofluorescence measurement resolution of surface antigens on highly autofluorescent, glutaraldehyde-fixed cells analyzed by phase-sensitive flow cytometry. Cytometry 37:275-83
Sailer, B L; Valdez, J G; Steinkamp, J A et al. (1998) Apoptosis induced with different cycle-perturbing agents produces differential changes in the fluorescence lifetime of DNA-bound ethidium bromide. Cytometry 31:208-16
Cobo, J M; Garcia-Canero, R; Valdez, J G et al. (1998) Attenuation of apoptotic DNA fragmentation by amiloride. J Cell Physiol 175:59-67

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