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arXiv 0801.0691q-bio.SCphysics.bio-phq-bio.BMq-bio.QM
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有界区域内蛋白质反应扩散的FRAP模型:一种理论方法

A FRAP model to investigate reaction-diffusion of proteins within a bounded domain: a theoretical approach

George D. Tsibidis

摘要:

细胞内蛋白质转运的时间和空间分辨测量为生物系统的功能结构和动力学提供了重要线索。光漂白后荧光恢复(FRAP)技术在过去的三十年中被用于测量大分子的迁移率和蛋白质的运输以及与细胞核内固定结构的相互作用。提出了一个理论模型,其目的是描述蛋白质运输的细胞核内,这是一个过程的存在下的边界(即膜)的影响。采用一组反应扩散方程来模拟蛋白质的扩散及其与固定结合位点的相互作用。所提出的模型已被设计为应用于生物样品的共聚焦激光扫描显微镜(CLSM)配备的功能,以漂白的扫描光束,具有径向高斯分布的轮廓特征的区域。所提出的模型导致FRAP曲线,依赖于上和关闭率。半解析表达式被用来定义的开(关)率参数空间的边界在简化的情况下,当分子在一个有界域内移动。该理论模型可与CLSM获得的实验数据结合使用,以研究活细胞中蛋白质的生物物理性质。

英文摘要:

Temporally and spatially resolved measurements of protein transport inside cells provide important clues to the functional architecture and dynamics of biological systems. Fluorescence Recovery After Photobleaching (FRAP) technique has been used over the past three decades to measure the mobility of macromolecules and protein transport and interaction with immobile structures inside the cell nucleus. A theoretical model is presented that aims to describe protein transport inside the nucleus, a process which is influenced by the presence of a boundary (i.e. membrane). A set of reaction-diffusion equations is employed to model both the diffusion of proteins and their interaction with immobile binding sites. The proposed model has been designed to be applied to biological samples with a Confocal Laser Scanning Microscope (CLSM) equipped with the feature to bleach regions characterised by a scanning beam that has a radially Gaussian distributed profile. The proposed model leads to FRAP curves that depend on the on- and off-rates. Semi-analytical expressions are used to define the boundaries of on- (off-) rate parameter space in simplified cases when molecules move within a bounded domain. The theoretical model can be used in conjunction to experimental data acquired by CLSM to investigate the biophysical properties of proteins in living cells.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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