Improving parameter estimation for cell surface FRAP data

被引:10
作者
Dushek, Omer
Coombs, Daniel [1 ]
机构
[1] Univ British Columbia, Dept Math, Vancouver, BC V6T 1Z2, Canada
[2] Univ British Columbia, Inst Appl Math, Vancouver, BC V6T 1Z2, Canada
来源
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2008年 / 70卷 / 06期
基金
加拿大自然科学与工程研究理事会;
关键词
fluorescence recovery after photobleaching; membrane diffusion; confocal microscopy; mathematical modeling;
D O I
10.1016/j.jbbm.2007.07.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fluorescence Recovery After Photobleaching (FRAP) using the confocal laser scanning microscope has become a standard method used to determine the diffusion coefficient and mobile fraction of cell surface proteins. A common experimental approach is to bleach a stripe on the cell surface and fit the ensuing FRAP curve to a I D diffusion model. This model is derived from the time course of recovery to an infinitely long stripe bleached on an infinite flat plane. This choice of model dictates the use of a long bleach stripe. We demonstrate that, in the case of a long bleach stripe, the finite extent of the cell leads to significant errors in parameter estimation. We further show that these errors are reduced when a relatively small stripe is bleached. Unfortunately, diffusion to such a region is fundamentally two dimensional and therefore applying the I D model of diffusion leads to significant errors. We derive an equation suitable for fitting to FRAP data acquired from small bleach regions and analyze its accuracy using simulated data. We propose that the use of a small bleach region along with a two dimensional diffusion model is the ideal protocol for cell surface FRAP. (c) 2007 Elsevier B.V. All fights reserved.
引用
收藏
页码:1224 / 1231
页数:8
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