Toprak Erdal, Kural Comert, Selvin Paul R
Department of Biophysics, University of Illinois, Urbana, Illinois, USA.
Methods Enzymol. 2010;475:1-26. doi: 10.1016/S0076-6879(10)75001-1.
In many research areas such as biology, biochemistry, and biophysics, measuring distances or identifying and counting objects can be of great importance. To do this, researchers often need complicated and expensive tools in order to have accurate measurements. In addition, these measurements are often done under nonphysiological settings. X-ray diffraction, for example, gets Angstrom-level structures, but it requires crystallizing a biological specimen. Electron microscopy (EM) has about 10A resolution, but often requires frozen (liquid nitrogen) samples. Optical microscopy, while coming closest to physiologically relevant conditions, has been limited by the minimum distances to be measured, typically about the diffraction limit, or approximately 200 nm. However, most biological molecules are <5-10nm in diameter, and getting molecular details requires imaging at this scale. In this chapter, we will describe some of the experimental approaches, from our lab and others, that push the limits of localization accuracy and optical resolution in fluorescence microscopy.
在许多研究领域,如生物学、生物化学和生物物理学中,测量距离或识别及计数物体可能非常重要。为此,研究人员通常需要复杂且昂贵的工具才能进行精确测量。此外,这些测量往往是在非生理环境下进行的。例如,X射线衍射能够获得埃级别的结构,但它需要使生物样本结晶。电子显微镜(EM)具有约10埃的分辨率,但通常需要冷冻(液氮)样本。光学显微镜虽然最接近生理相关条件,但一直受到可测量的最小距离的限制,通常约为衍射极限,即约200纳米。然而,大多数生物分子的直径小于5 - 10纳米,要获得分子细节需要在此尺度下成像。在本章中,我们将描述一些来自我们实验室及其他实验室的实验方法,这些方法突破了荧光显微镜中定位精度和光学分辨率的极限。