Dynamic light scattering microscopy. A novel optical technique to image submicroscopic motions. II: Experimental applications

被引:23
作者
Dzakpasu, R [1 ]
Axelrod, D
机构
[1] Univ Michigan, Dept Phys, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Div Biophys Res, Ann Arbor, MI 48109 USA
关键词
D O I
10.1529/biophysj.104.041400
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
An experimental veri. cation of an optical microscope technique to create spatial map images of dynamically scattered light fluctuation decay rates is presented. The dynamic light scattering microscopy technique is demonstrated on polystyrene beads and living macrophage cells. With a slow progressive scan charge-coupled device camera employed in a streak-like mode, rapid intensity fluctuations with timescales the order of milliseconds can be recorded from these samples. From such streak images, the autocorrelation function of these fluctuations can be computed at each location in the sample. The characteristic decay times of the autocorrelation functions report the rates of motion of scattering centers. These rates show reasonable agreement to theoretically expected values for known samples with good signal/noise ratio. The rates can be used to construct an image-like spatial map of the rapidity of submicroscopic motions of scattering centers.
引用
收藏
页码:1288 / 1297
页数:10
相关论文
共 11 条
[1]  
Axelrod D, 2003, METHOD ENZYMOL, V361, P1
[2]   Three-dimensional high-resolution second-harmonic generation imaging of endogenous structural proteins in biological tissues [J].
Campagnola, PJ ;
Millard, AC ;
Terasaki, M ;
Hoppe, PE ;
Malone, CJ ;
Mohler, WA .
BIOPHYSICAL JOURNAL, 2002, 82 (01) :493-508
[3]   Second-harmonic imaging microscopy of living cells [J].
Campagnola, PJ ;
Clark, HA ;
Mohler, WA ;
Lewis, A ;
Loew, LM .
JOURNAL OF BIOMEDICAL OPTICS, 2001, 6 (03) :277-286
[4]  
CANNON GJ, 1992, J CELL SCI, V101, P907
[5]  
Davenport W.B., 1958, An Introduction to the Theory of Random Signals and Noise, V159
[6]   Dynamic light scattering microscopy. A novel optical technique to image submicroscopic motions. I: Theory [J].
Dzakpasu, R ;
Axelrod, D .
BIOPHYSICAL JOURNAL, 2004, 87 (02) :1279-1287
[8]   Cell membrane orientation visualized by polarized total internal reflection fluorescence [J].
Sund, SE ;
Swanson, JA ;
Axelrod, D .
BIOPHYSICAL JOURNAL, 1999, 77 (04) :2266-2283
[9]  
SWANSON JA, 1992, J CELL SCI, V103, P201
[10]   Light-scattering submicroscopic particles as highly fluorescent analogs and their use as tracer labels in clinical and biological applications - I. Theory [J].
Yguerabide, J ;
Yguerabide, EE .
ANALYTICAL BIOCHEMISTRY, 1998, 262 (02) :137-156