An experimental comparison of the maximum likelihood estimation and nonlinear least squares fluorescence lifetime analysis of single molecules

被引:198
作者
Maus, M
Cotlet, M
Hofkens, J
Gensch, T
De Schryver, FC
Schaffer, J
Seidel, CAM
机构
[1] Katholieke Univ Leuven, Dept Chem, Div Photochem & Spect, B-3001 Heverlee, Belgium
[2] Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
关键词
D O I
10.1021/ac000877g
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Two procedures based on the weighted least-squares (LS) and the maximum likelihood estimation (MLE) method to confidently analyze single-molecule (SM! fluorescence decays with a total number (N) of 2500-60 000 counts have been elucidated and experimentally compared by analyzing measured bulk and SM decays. The key observation of this comparison is that the LS systematically underestimates the fluorescence lifetimes by similar to5%, for the range of 1000-20 000 events, whereas the MLE method gives stable results over the whole intensity range, even at counts N less than 1000, where the by analysis delivers unreasonable values. This difference can be attributed to the different statistics approaches and results from improper weighting of the LS method. As expected from theory, the results of both methods became equivalent above a certain threshold of N detected photons per decay, which is here experimentally determined to be similar to 20 000. In contrast to the hulk lifetime distributions, the SM fluorescence lifetime distributions exhibit standard deviations that are sizably larger than the statistically-expected values. This comparison proves the strong influence of the inhomogenuous microenvironment on the photophysical behavior of single molecules embedded in a 10-30-nm thin polymer layer.
引用
收藏
页码:2078 / 2086
页数:9
相关论文
共 49 条
[1]   MAXIMUM-LIKELIHOOD METHOD FOR THE ANALYSIS OF TIME-RESOLVED FLUORESCENCE DECAY CURVES [J].
BAJZER, Z ;
THERNEAU, TM ;
SHARP, JC ;
PRENDERGAST, FG .
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 1991, 20 (05) :247-262
[3]   DETECTION OF SINGLE RHODAMINE-6G MOLECULES IN LEVITATED MICRODROPLETS [J].
BARNES, MD ;
NG, KC ;
WHITTEN, WB ;
RAMSEY, JM .
ANALYTICAL CHEMISTRY, 1993, 65 (17) :2360-2365
[4]  
BOENS N, 1991, LUMINESCENCE TECHNIQ, P21
[5]   Fluorescence and photobleaching dynamics of single light-harvesting complexes [J].
Bopp, MA ;
Jia, YW ;
Li, LQ ;
Cogdell, RJ ;
Hochstrasser, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (20) :10630-10635
[6]   Single-molecule identification of Coumarin-120 by time-resolved fluorescence detection: Comparison of one- and two-photon excitation in solution [J].
Brand, L ;
Eggeling, C ;
Zander, C ;
Drexhage, KH ;
Seidel, CAM .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (24) :4313-4321
[7]   Single-molecule detection in capillary electrophoresis: Molecular shot noise as a fundamental limit to chemical analysis [J].
Chen, DY ;
Dovichi, NJ .
ANALYTICAL CHEMISTRY, 1996, 68 (04) :690-696
[8]  
Draaijer A., 1995, P491
[9]   Monitoring conformational dynamics of a single molecule by selective fluorescence spectroscopy [J].
Eggeling, C ;
Fries, JR ;
Brand, L ;
Günther, R ;
Seidel, CAM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) :1556-1561
[10]  
ENDERLEIN J, 1997, J PHYS CHEM-US, V270, P4464