Assaying three-dimensional cellular architecture using X-ray tomographic and correlated imaging approaches

被引:11
作者
Bayguinov, Peter O. [1 ]
Fisher, Max R. [1 ]
Fitzpatrick, James A. J. [1 ,2 ,3 ,4 ]
机构
[1] Washington Univ, Sch Med, Ctr Cellular Imaging, St Louis, MO 63108 USA
[2] Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63108 USA
[3] Washington Univ, Sch Med, Dept Neurosci, St Louis, MO 63108 USA
[4] Washington Univ, Dept Biomed Engn, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
X-ray microscopy; tomography; subcellular organelle; yeast; S; cerevisiae; development; correlative microscopy; microscopy; Schizosaccharomyces pombe; hard and soft X-rays; water window; SCANNING-ELECTRON-MICROSCOPY; HIGH-RESOLUTION; COMPUTED-TOMOGRAPHY; CONTRAST AGENT; BIOLOGICAL APPLICATIONS; LIGHT-MICROSCOPY; FLUORESCENCE; RECONSTRUCTION; CELLS; TISSUE;
D O I
10.1074/jbc.REV120.009633
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Much of our understanding of the spatial organization of and interactions between cellular organelles and macromolecular complexes has been the result of imaging studies utilizing either light- or electron-based microscopic analyses. These classical approaches, while insightful, are nonetheless limited either by restrictions in resolution or by the sheer complexity of generating multidimensional data. Recent advances in the use and application of X-rays to acquire micro- and nanotomographic data sets offer an alternative methodology to visualize cellular architecture at the nanoscale. These new approaches allow for the subcellular analyses of unstained vitrified cells and three-dimensional localization of specific protein targets and have served as an essential tool in bridging light and electron correlative microscopy experiments. Here, we review the theory, instrumentation details, acquisition principles, and applications of both soft X-ray tomography and X-ray microscopy and how the use of these techniques offers a succinct means of analyzing three-dimensional cellular architecture. We discuss some of the recent work that has taken advantage of these approaches and detail how they have become integral in correlative microscopy workflows.
引用
收藏
页码:15782 / 15793
页数:12
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