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第12章:纳米级生物荧光成像:突破衍射极限

Chapter 12: Nanoscale biological fluorescence imaging: breaking the diffraction barrier.

作者信息

Gould Travis J, Hess Samuel T

机构信息

Department of Physics and Astronomy and Institute for Molecular Biophysics, University of Maine, Orono, Maine 04469, USA.

出版信息

Methods Cell Biol. 2008;89:329-58. doi: 10.1016/S0091-679X(08)00612-2.

Abstract

Biological imaging has been limited by the finite resolution of light microscopy. Recent developments in ultra-high-resolution microscopy methods, many of which are based on fluorescence, are breaking the diffraction barrier; it is becoming possible to image intracellular protein distributions with resolution of tens of nanometers or better. Fluorescence photoactivation localization microscopy (FPALM) is an example of such an ultra-high-resolution method which can image living or fixed cells with demonstrated lateral resolution of better than 20 nm. A detailed description of the methods involved in FPALM imaging of biological samples is presented here, accompanied by comparison with existing methods from the literature.

摘要

生物成像一直受到光学显微镜有限分辨率的限制。超高分辨率显微镜方法的最新进展,其中许多基于荧光,正在突破衍射极限;现在有可能以几十纳米或更高的分辨率对细胞内蛋白质分布进行成像。荧光光激活定位显微镜(FPALM)就是这样一种超高分辨率方法的例子,它可以对活细胞或固定细胞进行成像,其横向分辨率已证明优于20纳米。本文详细介绍了生物样品FPALM成像所涉及的方法,并与文献中的现有方法进行了比较。

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