Halpern Aaron R, Howard Marco D, Vaughan Joshua C
Department of Chemistry, University of Washington, Seattle, Washington.
Department of Physiology and Biophysics, University of Washington, Seattle, Washington.
Curr Protoc Chem Biol. 2015 Jun 1;7(2):103-20. doi: 10.1002/9780470559277.ch140241.
Single-molecule, localization-based, super resolution microscopy is able to reveal detailed subcellular structures and protein distributions below the classical ∼250-nm diffraction limit of light, but utilizing this technique effectively requires a combination of careful sample preparation, data acquisition, and data analysis, which can be daunting to novice researchers. In this protocol, detailed instructions on preparation of robust reference samples for super-resolution microscopy, including the cytoskeleton (microtubules), membrane-bound organelles (peroxisomes), and scaffold proteins (clathrin), are provided. These samples also constitute a representative subset of imaging targets of interest to biological researchers and highlight the differences and similarities in sample preparation.
基于单分子定位的超分辨率显微镜能够揭示低于经典的约250纳米光衍射极限的详细亚细胞结构和蛋白质分布,但有效利用该技术需要精心的样品制备、数据采集和数据分析相结合,这对新手研究人员来说可能令人生畏。在本方案中,提供了关于为超分辨率显微镜制备稳健参考样品的详细说明,包括细胞骨架(微管)、膜结合细胞器(过氧化物酶体)和支架蛋白(网格蛋白)。这些样品也构成了生物研究人员感兴趣的成像目标的代表性子集,并突出了样品制备中的差异和相似之处。