Moving EM: the Rapid Transfer System as a new tool for correlative light and electron microscopy and high throughput for high-pressure freezing

被引:120
作者
Verkade, P. [1 ]
机构
[1] Univ Walk, Sch Med Sci, Bristol BS8 1TD, Avon, England
关键词
biopsy; correlative light and electron microscopy; CLEM; endocytosis; high-pressure freezing;
D O I
10.1111/j.1365-2818.2008.01989.x
中图分类号
TH742 [显微镜];
学科分类号
摘要
In this paper, the Rapid Transfer System (RTS), an attachment to the Leica EMPACT2 high-pressure freezer, is described as a new tool for special applications within the cryofixation field. The RTS is an automated system that allows for fast processing of samples (< 5 s) that make it possible for the first time to use high-pressure freezing in combination with high time resolution correlative light and electron microscopy. In addition, with a working cycle of 30 s this rapid turn over time allows one to acquire more samples of biopsy material before it deteriorates than with other HPF machines with longer cycle times. With the use of the RTS it was possible to obtain three samples each of four different tissues in 6 min. Together with the finding that 90% of samples of cells grown on sapphire discs were well frozen, the RTS was both fast and reliable. Most important, together with other newly developed accessories, the RTS made it possible to capture specific events occurring live in the cell as observed by light microscopy, to cryofix that sample/event within 4 s, and then to analyze that event at high resolution in the electron microscope with excellent preservation of ultra-structure. These developments should give us the tools to unravel intracellular processes that can be observed by live cell imaging but are too rare or fast to be picked up by routine EM methods or where the history of a structure is necessary to be able to discern its nature.
引用
收藏
页码:317 / 328
页数:12
相关论文
共 34 条
[1]   Cryo-electron microscopy of vitreous sections [J].
Al-Amoudi, A ;
Chang, JJ ;
Leforestier, A ;
McDowall, A ;
Salamin, LM ;
Norlén, LPO ;
Richter, K ;
Blanc, NS ;
Studer, D ;
Dubochet, J .
EMBO JOURNAL, 2004, 23 (18) :3583-3588
[2]   From tissue to cellular ultrastructure: closing the gap between micro- and nanostructural imaging [J].
Biel, SS ;
Kawaschinski, K ;
Wittern, KP ;
Hintze, U ;
Wepf, R .
JOURNAL OF MICROSCOPY, 2003, 212 :91-99
[3]   HIGH-PRESSURE FREEZING FOR THE PRESERVATION OF BIOLOGICAL STRUCTURE - THEORY AND PRACTICE [J].
DAHL, R ;
STAEHELIN, LA .
JOURNAL OF ELECTRON MICROSCOPY TECHNIQUE, 1989, 13 (03) :165-174
[4]   KINASE-ACTIVITY CONTROLS THE SORTING OF THE EPIDERMAL GROWTH-FACTOR RECEPTOR WITHIN THE MULTIVESICULAR BODY [J].
FELDER, S ;
MILLER, K ;
MOEHREN, G ;
ULLRICH, A ;
SCHLESSINGER, J ;
HOPKINS, CR .
CELL, 1990, 61 (04) :623-634
[5]   Multicolor and electron microscopic imaging of connexin trafficking [J].
Gaietta, G ;
Deerinck, TJ ;
Adams, SR ;
Bouwer, J ;
Tour, O ;
Laird, DW ;
Sosinsky, GE ;
Tsien, RY ;
Ellisman, MH .
SCIENCE, 2002, 296 (5567) :503-507
[6]   Freeze-substitution protocols for improved visualization of membranes in high-pressure frozen samples [J].
Giddings, TH .
JOURNAL OF MICROSCOPY, 2003, 212 :53-61
[7]   Correlated light and electron microscopic imaging of multiple endogenous proteins using Quantum dots [J].
Giepmans, BNG ;
Deerinck, TJ ;
Smarr, BL ;
Jones, YZ ;
Ellisman, MH .
NATURE METHODS, 2005, 2 (10) :743-749
[8]   Correlative microscopy and electron tomography of GFP through photooxidation [J].
Grabenbauer, M ;
Geerts, WJC ;
Fernadez-Rodriguez, J ;
Hoenger, A ;
Koster, AJ ;
Nilsson, T .
NATURE METHODS, 2005, 2 (11) :857-862
[9]   Rapid freeze-substitution preserves membranes in high-pressure frozen tissue culture cells [J].
Hawes, P. ;
Netherton, C. L. ;
Mueller, M. ;
Wileman, T. ;
Monaghan, P. .
JOURNAL OF MICROSCOPY, 2007, 226 (02) :182-189
[10]  
Hayat M. A., 1987, CORRELATIVE MICROSCO