Depth-of-Focus Correction in Single-Molecule Data Allows Analysis of 3D Diffusion of the Glucocorticoid Receptor in the Nucleus

被引:2
|
作者
Harkes, Rolf [1 ]
Keizer, Veer I. P. [2 ]
Schaaf, Marcel J. M. [2 ]
Schmidt, Thomas [1 ]
机构
[1] Leiden Univ, Phys Life Proc, Huygens Kamerlingh Onnes Lab, Leiden, Netherlands
[2] Leiden Univ, IBL, Leiden, Netherlands
来源
PLOS ONE | 2015年 / 10卷 / 11期
关键词
TRANSCRIPTION FACTOR-BINDING; LIVING CELLS; PARTICLE TRACKING; PLASMA-MEMBRANE; HIGH-DENSITY; LIVE CELLS; MICROSCOPY; MICRODOMAINS; PROTEIN; DNA;
D O I
10.1371/journal.pone.0141080
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Single-molecule imaging of proteins in a 2D environment like membranes has been frequently used to extract diffusive properties of multiple fractions of receptors. In a 3D environment the apparent fractions however change with observation time due to the movements of molecules out of the depth-of-field of the microscope. Here we developed a mathematical framework that allowed us to correct for the change in fraction size due to the limited detection volume in 3D single-molecule imaging. We applied our findings on the mobility of activated glucocorticoid receptors in the cell nucleus, and found a freely diffusing fraction of 0.49 +/- 0.02. Our analysis further showed that interchange between this mobile fraction and an immobile fraction does not occur on time scales shorter than 150 ms.
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页数:13
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