Lattice micropatterning for cryo-electron tomography studies of cell-cell contacts

被引:8
|
作者
Engel, Leeya [1 ]
Vasquez, Claudia G. [1 ]
Montabana, Elizabeth A. [2 ]
Sow, Belle M. [1 ]
Walkiewicz, Marcin P. [3 ]
Weis, William, I [4 ,5 ]
Dunn, Alexander R. [1 ]
机构
[1] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[2] Stanford SLAG CryoEM Initiat, Stanford, CA 94305 USA
[3] Stanford Univ, Cell Sci Imaging Facil, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Struct Biol, Stanford, CA 94305 USA
[5] Stanford Univ, Sch Med, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
cryo-ET; cryo-EM; micropatterning; bioengineering; EUKARYOTIC CELLS; ARCHITECTURE; IMAGE;
D O I
10.1016/j.jsb.2021.107791
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
ABSTR A C T Cryo-electron tomography is the highest resolution tool available for structural analysis of macromolecular complexes within their native cellular environments. At present, data acquisition suffers from low throughput, in part due to the low probability of positioning a cell such that the subcellular structure of interest is on a region of the electron microscopy (EM) grid that is suitable for imaging. Here, we photo-micropatterned EM grids to optimally position endothelial cells so as to enable high-throughput imaging of cell-cell contacts. Lattice micropatterned grids increased the average distance between intercellular contacts and thicker cell nuclei such that the regions of interest were sufficiently thin for direct imaging. We observed a diverse array of membranous and cytoskeletal structures at intercellular contacts, demonstrating the utility of this technique in enhancing the rate of data acquisition for cellular cryo-electron tomography studies.
引用
收藏
页数:6
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