An all solid-state near-infrared time-correlated single photon counting instrument for dynamic lifetime measurements in DNA sequencing applications

被引:27
作者
Legendre, BL [1 ]
Williams, DC [1 ]
Soper, SA [1 ]
Erdmann, R [1 ]
Ortmann, U [1 ]
Enderlein, J [1 ]
机构
[1] PICOQUANT GMBH,D-12489 BERLIN,GERMANY
关键词
D O I
10.1063/1.1147302
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
We have constructed a simple, all solid-state, time-correlated single photon counting device for collecting decay profiles of chromophores attached to DNA fragments moving through a capillary tube filled with a sieving gel under the influence of an applied electric field (capillary electrophoresis). The major components of the instrument consist of an actively pulsed GaAlAs diode laser (lambda(excitation)=780 nm; tau(p)<200 ps; repetition rate=80 MHz; average power=5.0 mW), single photon avalanche diode (dark count rate <50 cps: quantum efficiency=65% at 800 nm) and a PC board containing a constant fraction discriminator, time-to-amplitude converter, and an analog-to-digital converter (maximum processing count rate=3x10(6) cps). The instrument possessed a response function of approximately 275 ps (full width at half-maximum), adequate for measuring fluorescence lifetimes in the subnanosecond regime. To demonstrate the utility and the sensitivity of the instrument, dynamic measurements of fluorescence lifetimes for near-IR dye-labeled DNA fragments were measured during capillary electrophoresis for the identification of the dye-labeled nucleotide bases via temporal discrimination. The results indicated that in a two-dye experiment, in which only two of the four constituent bases which comprise DNA were labeled with unique fluorescent probes, the characteristic lifetime of the probe could be used to readily identify the terminal nucleotide base. Decay profiles were constructed from roughly 17 500 photoelectrons accumulated over a 2 s counting interval at a loading level of approximately 6.2x10(-21) mol (3900 molecules) of DNA per electrophoretic band. The lifetimes of the two labeling dyes were determined to be 669 ps (+/-42 ps) and 528 ps (+/-68 ps). (C) 1996 American Institute of Physics.
引用
收藏
页码:3984 / 3989
页数:6
相关论文
共 18 条
[1]   2-LABEL PEAK-HEIGHT ENCODED DNA SEQUENCING BY CAPILLARY GEL-ELECTROPHORESIS - 3 EXAMPLES [J].
CHEN, DY ;
HARKE, HR ;
DOVICHI, NJ .
NUCLEIC ACIDS RESEARCH, 1992, 20 (18) :4873-4880
[2]   High speed electronics for the detection of time-resolved fluorescence in a continuous flow system [J].
Erdmann, R ;
Ortmann, U ;
Enderlein, J ;
Becker, W ;
Wahl, M ;
Klose, E .
ULTRASENSITIVE BIOCHEMICAL DIAGNOSTICS, PROCEEDINGS OF, 1996, 2680 :176-181
[3]  
ERDMANN R, 1995, P SOC PHOTO-OPT INS, V2388, P330, DOI 10.1117/12.208493
[4]   SUBNANOSECOND SINGLE PHOTON TIMING MEASUREMENTS USING A PULSED DIODE-LASER [J].
FARRENS, DL ;
SONG, PS .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1991, 54 (02) :313-317
[5]  
FLANAGAN JH, UNPUB ANAL CHEM
[6]  
HALL P, 1985, J PHYS CHEM-US, V85, P2941
[7]  
IMASAKI T, 1985, ANAL CHEM, V67, P947
[8]   High repetition rate picosecond diode lasers for potential use in single molecule detection [J].
Ortmann, U ;
Krahl, R ;
Kell, G ;
Erdmann, R ;
Enderlein, J ;
Klose, E .
ULTRASENSITIVE BIOCHEMICAL DIAGNOSTICS, PROCEEDINGS OF, 1996, 2680 :182-186
[9]   A SYSTEM FOR RAPID DNA SEQUENCING WITH FLUORESCENT CHAIN-TERMINATING DIDEOXYNUCLEOTIDES [J].
PROBER, JM ;
TRAINOR, GL ;
DAM, RJ ;
HOBBS, FW ;
ROBERTSON, CW ;
ZAGURSKY, RJ ;
COCUZZA, AJ ;
JENSEN, MA ;
BAUMEISTER, K .
SCIENCE, 1987, 238 (4825) :336-341
[10]   DNA SEQUENCING WITH CHAIN-TERMINATING INHIBITORS [J].
SANGER, F ;
NICKLEN, S ;
COULSON, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5463-5467