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单分子显微镜的定量分析

Quantitative Aspects of Single Molecule Microscopy.

作者信息

Ober Raimund J, Tahmasbi Amir, Ram Sripad, Lin Zhiping, Ward E Sally

出版信息

IEEE Signal Process Mag. 2015 Jan;32(1):58-69. doi: 10.1109/MSP.2014.2353664.

Abstract

Single molecule microscopy is a relatively new optical microscopy technique that allows the detection of individual molecules such as proteins in a cellular context. This technique has generated significant interest among biologists, biophysicists and biochemists, as it holds the promise to provide novel insights into subcellular processes and structures that otherwise cannot be gained through traditional experimental approaches. Single molecule experiments place stringent demands on experimental and algorithmic tools due to the low signal levels and the presence of significant extraneous noise sources. Consequently, this has necessitated the use of advanced statistical signal and image processing techniques for the design and analysis of single molecule experiments. In this tutorial paper, we provide an overview of single molecule microscopy from early works to current applications and challenges. Specific emphasis will be on the quantitative aspects of this imaging modality, in particular single molecule localization and resolvability, which will be discussed from an information theoretic perspective. We review the stochastic framework for image formation, different types of estimation techniques and expressions for the Fisher information matrix. We also discuss several open problems in the field that demand highly non-trivial signal processing algorithms.

摘要

单分子显微镜是一种相对较新的光学显微镜技术,它能够在细胞环境中检测诸如蛋白质等单个分子。这项技术在生物学家、生物物理学家和生物化学家当中引起了极大的兴趣,因为它有望为亚细胞过程和结构提供全新的见解,而这些是通过传统实验方法无法获得的。由于信号水平较低且存在大量外部噪声源,单分子实验对实验工具和算法工具提出了严格的要求。因此,这就需要使用先进的统计信号和图像处理技术来设计和分析单分子实验。在这篇教程论文中,我们将概述单分子显微镜从早期工作到当前应用及挑战的发展历程。特别强调的将是这种成像方式的定量方面,尤其是单分子定位和可分辨性,我们将从信息论的角度对其进行讨论。我们回顾图像形成的随机框架、不同类型的估计技术以及费希尔信息矩阵的表达式。我们还将讨论该领域中一些需要高度复杂信号处理算法的开放问题。

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