Huckabay Heath A, Armendariz Kevin P, Newhart William H, Wildgen Sarah M, Dunn Robert C
Ralph N. Adams Institute for Bioanalytical Chemistry, University of Kansas, Lawrence, KS, USA.
Methods Mol Biol. 2013;950:373-94. doi: 10.1007/978-1-62703-137-0_21.
The desire to directly probe biological structures on the length scales that they exist has driven the steady development of various high-resolution microscopy techniques. Among these, optical microscopy and, in particular, fluorescence-based approaches continue to occupy dominant roles in biological studies given their favorable attributes. Fluorescence microscopy is both sensitive and specific, is generally noninvasive toward biological samples, has excellent temporal resolution for dynamic studies, and is relatively inexpensive. Light-based microscopies can also exploit a myriad of contrast mechanisms based on spectroscopic signatures, energy transfer, polarization, and lifetimes to further enhance the specificity or information content of a measurement. Historically, however, spatial resolution has been limited to approximately half the wavelength due to the diffraction of light. Near-field scanning optical microscopy (NSOM) is one of several optical approaches currently being developed that combines the favorable attributes of fluorescence microscopy with superior spatial resolution. NSOM is particularly well suited for studies of both model and biological membranes and application to these systems is discussed.
直接探测生物结构在其实际存在的长度尺度上的需求推动了各种高分辨率显微镜技术的稳步发展。其中,光学显微镜,特别是基于荧光的方法,由于其有利特性,在生物学研究中继续占据主导地位。荧光显微镜既灵敏又特异,对生物样品通常是非侵入性的,对于动态研究具有出色的时间分辨率,并且相对便宜。基于光的显微镜还可以利用基于光谱特征、能量转移、偏振和寿命的多种对比机制,进一步提高测量的特异性或信息含量。然而,从历史上看,由于光的衍射,空间分辨率一直限制在大约半个波长左右。近场扫描光学显微镜(NSOM)是目前正在开发的几种光学方法之一,它将荧光显微镜的有利特性与卓越的空间分辨率结合在一起。NSOM特别适合于对模型膜和生物膜的研究,并将讨论其在这些系统中的应用。