Soft X-ray tomography and cryogenic light microscopy: the cool combination in cellular imaging

被引:128
作者
McDermott, Gerry [1 ]
Le Gros, Mark A. [2 ]
Knoechel, Christian G. [1 ]
Uchida, Maho [1 ]
Larabell, Carolyn A. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[2] Lawrence Berkeley Natl Lab, Phys Biosci Div, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
HIGH-SPATIAL-RESOLUTION; BIOLOGICAL SPECIMENS; PROTEIN LOCALIZATION; COMPUTED-TOMOGRAPHY; PHASE-CONTRAST; BESSY-II; CELLS; RECONSTRUCTIONS; MOLECULES; NM;
D O I
10.1016/j.tcb.2009.08.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Soft X-ray tomography (SXT) is ideally suited to imaging sub-cellular architecture and organization, particularly in eukaryotic cells. SXT is similar in concept to the well-established medical diagnostic technique computed axial tomography (CAT), except SXT is capable of imaging with a spatial resolution of 50 nm, or better. In SXT, cells are imaged using photons from a region of the spectrum known as the 'water window'. This results in quantitative, high-contrast images of intact, fully hydrated cells without the need to use contrast-enhancing agents. The cells that are visualized are in close-to-native, fully functional state. The utility of SXT has recently been enhanced by the development of high numerical aperture cryogenic light microscopy for correlated imaging. This multi-modal approach allows labelled molecules to be localized in the context of a high-resolution 3-D tomographic reconstruction of the cell.
引用
收藏
页码:587 / 595
页数:9
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