λ-repressor oligomerization kinetics at high concentrations using fluorescence correlation spectroscopy in zero-mode waveguides

被引:88
作者
Samiee, KT
Foquet, M
Guo, L
Cox, EC
Craighead, HG
机构
[1] Cornell Univ, Sch Appl & Engn Phys, Ithaca, NY 14853 USA
[2] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
关键词
D O I
10.1529/biophysj.104.052795
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Fluorescence correlation spectroscopy (FCS) has demonstrated its utility for measuring transport properties and kinetics at low. uorophore concentrations. In this article, we demonstrate that simple optical nanostructures, known as zeromode waveguides, can be used to significantly reduce the FCS observation volume. This, in turn, allows FCS to be applied to solutions with significantly higher. uorophore concentrations. We derive an empirical FCS model accounting for one-dimensional diffusion in a finite tube with a simple exponential observation pro. le. This technique is used to measure the oligomerization of the bacteriophage l repressor protein at micromolar concentrations. The results agree with previous studies utilizing conventional techniques. Additionally, we demonstrate that the zero-mode waveguides can be used to assay biological activity by measuring changes in diffusion constant as a result of ligand binding.
引用
收藏
页码:2145 / 2153
页数:9
相关论文
共 25 条
[1]  
ARBER W, 1983, LAMBDA, V2, P433
[2]   SINGLE MOLECULES OBSERVED BY NEAR-FIELD SCANNING OPTICAL MICROSCOPY [J].
BETZIG, E ;
CHICHESTER, RJ .
SCIENCE, 1993, 262 (5138) :1422-1425
[3]   Cooperativity mutants of bacteriophage lambda cI repressor: Temperature dependence of self-assembly [J].
Burz, DS ;
Ackers, GK .
BIOCHEMISTRY, 1996, 35 (10) :3341-3350
[4]   An ultrasensitive bacterial motor revealed by monitoring signaling proteins in single cells [J].
Cluzel, P ;
Surette, M ;
Leibler, S .
SCIENCE, 2000, 287 (5458) :1652-1655
[5]  
de Lange F, 2001, J CELL SCI, V114, P4153
[6]   Octamerization of λ CI repressor is needed for effective repression of PRM and efficient switching from lysogeny [J].
Dodd, IB ;
Perkins, AJ ;
Tsemitsidis, D ;
Egan, JB .
GENES & DEVELOPMENT, 2001, 15 (22) :3013-3022
[7]   FLUORESCENCE CORRELATION SPECTROSCOPY .1. CONCEPTUAL BASIS AND THEORY [J].
ELSON, EL ;
MAGDE, D .
BIOPOLYMERS, 1974, 13 (01) :1-27
[8]   Focal volume confinement by submicrometer-sized fluidic channels [J].
Foquet, M ;
Korlach, J ;
Zipfel, WR ;
Webb, WW ;
Craighead, HG .
ANALYTICAL CHEMISTRY, 2004, 76 (06) :1618-1626
[9]   Fluorescence correlation spectroscopy in small cytosolic compartments depends critically on the diffusion model used [J].
Gennerich, A ;
Schild, D .
BIOPHYSICAL JOURNAL, 2000, 79 (06) :3294-3306
[10]   Focal volume optics and experimental artifacts in confocal fluorescence correlation spectroscopy [J].
Hess, ST ;
Webb, WW .
BIOPHYSICAL JOURNAL, 2002, 83 (04) :2300-2317