Electron microscopy of whole cells in liquid with nanometer resolution

被引:394
作者
de Jonge, N. [1 ,2 ]
Peckys, D. B. [2 ,3 ]
Kremers, G. J. [1 ]
Piston, D. W. [1 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
[2] Oak Ridge Natl Lab, Div Mat Sci & Technol, Oak Ridge, TN 37831 USA
[3] Univ Tennessee, Knoxville, TN 37996 USA
基金
美国国家卫生研究院;
关键词
cellular imaging; molecular labels; IN-SITU; SPECIMENS; GROWTH; STEM; NM;
D O I
10.1073/pnas.0809567106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Single gold-tagged epidermal growth factor (EGF) molecules bound to cellular EGF receptors of fixed fibroblast cells were imaged in liquid with a scanning transmission electron microscope (STEM). The cells were placed in buffer solution in a microfluidic device with electron transparent windows inside the vacuum of the electron microscope. A spatial resolution of 4 nm and a pixel dwell time of 20 mu s were obtained. The liquid layer was sufficiently thick to contain the cells with a thickness of 7 +/- 1 mu m. The experimental findings are consistent with a theoretical calculation. Liquid STEM is a unique approach for imaging single molecules in whole cells with significantly improved resolution and imaging speed over existing methods.
引用
收藏
页码:2159 / 2164
页数:6
相关论文
共 35 条
[1]
Multicolor super-resolution imaging with photo-switchable fluorescent probes [J].
Bates, Mark ;
Huang, Bo ;
Dempsey, Graham T. ;
Zhuang, Xiaowei .
SCIENCE, 2007, 317 (5845) :1749-1753
[2]
Imaging intracellular fluorescent proteins at nanometer resolution [J].
Betzig, Eric ;
Patterson, George H. ;
Sougrat, Rachid ;
Lindwasser, O. Wolf ;
Olenych, Scott ;
Bonifacino, Juan S. ;
Davidson, Michael W. ;
Lippincott-Schwartz, Jennifer ;
Hess, Harald F. .
SCIENCE, 2006, 313 (5793) :1642-1645
[3]
Wet STEM: A new development in environmental SEM for imaging nano-objects included in a liquid phase [J].
Bogner, A ;
Thollet, G ;
Basset, D ;
Jouneau, PH ;
Gauthier, C .
ULTRAMICROSCOPY, 2005, 104 (3-4) :290-301
[4]
Nano-scale dynamic recognition imaging on vascular endothelial cells [J].
Chtcheglova, Lilia A. ;
Waschke, Jens ;
Wildling, Linda ;
Drenckhahn, Detlev ;
Hinterdorfer, Peter .
BIOPHYSICAL JOURNAL, 2007, 93 (02) :L11-L13
[5]
UNCONVENTIONAL MODES FOR STEM IMAGING OF BIOLOGICAL STRUCTURES [J].
COLLIEX, C ;
JEANGUILLAUME, C ;
MORY, C .
JOURNAL OF ULTRASTRUCTURE RESEARCH, 1984, 88 (02) :177-206
[6]
VISIBILITY OF SINGLE ATOMS [J].
CREWE, AV ;
WALL, J ;
LANGMORE, J .
SCIENCE, 1970, 168 (3937) :1338-&
[7]
Daulton TL, 2001, MICROSC MICROANAL, V7, P470
[8]
de Jonge N, 2007, NANOTECHNOLOGY IN BIOLOGY AND MEDICINE: METHODS, DEVICES, AND APPLICATIONS
[9]
Dynein is required for receptor sorting and the morphogenesis of early endosomes [J].
Driskell, Owen J. ;
Mironov, Aleksandr ;
Allan, Victoria J. ;
Woodman, Philip G. .
NATURE CELL BIOLOGY, 2007, 9 (01) :113-U152
[10]
Gai PL, 2002, MICROSC MICROANAL, V8, P21, DOI 10.1017/S1431927601010054