Integrated fluorescence and transmission electron microscopy

被引:120
作者
Agronskaia, Alexandra V. [1 ]
Valentijn, Jack A. [2 ]
van Driel, Linda F. [2 ]
Schneijdenberg, Chris T. W. M. [3 ]
Humbel, Bruno M. [3 ]
Henegouwen, Paul M. P. van Bergen en [3 ]
Verkleij, Arie J. [3 ]
Koster, Abraham J. [2 ]
Gerritsen, Hans C. [1 ]
机构
[1] Univ Utrecht, Fac Sci, Dept Phys, NL-3584 CC Utrecht, Netherlands
[2] Leiden Univ, Med Ctr, NL-2333 ZA Leiden, Netherlands
[3] Univ Utrecht, Fac Sci, Dept Biol, NL-3584 CH Utrecht, Netherlands
关键词
Correlative microscopy; Fluorescence scanning microscope; Electron transmission microscope; Golgi apparatus; Peroxisomes;
D O I
10.1016/j.jsb.2008.07.003
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
Correlative microscopy is a powerful technique that combines the strengths of fluorescence microscopy and electron microscopy. The first enables rapid searching for regions of interest in large fields of view while the latter exhibits superior resolution over a narrow field of view. Routine use of correlative microscopy is seriously hampered by the cumbersome and elaborate experimental procedures. This is partly due to the use of two separate microscopes for fluorescence and electron microscopy. Here, an integrated approach to correlative microscopy is presented based on a laser scanning fluorescence microscope integrated in a transmission electron microscope. Using this approach the search for features in the specimen is greatly simplified and the time to carry out the experiment is strongly reduced. The potential of the integrated approach is demonstrated at room temperature on specimens of rat intestine cells labeled with AlexaFluor488 conjugated to wheat germ agglutinin and on rat liver peroxisomes immuno-labeled with anti-catalase antibodies and secondary AlexaFluor488 antibodies and 10 nm protein A-gold. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:183 / 189
页数:7
相关论文
共 27 条
[1]   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
[2]   CONFOCAL SCANNING LIGHT-MICROSCOPY WITH HIGH APERTURE IMMERSION LENSES [J].
BRAKENHOFF, GJ ;
BLOM, P ;
BARENDS, P .
JOURNAL OF MICROSCOPY-OXFORD, 1979, 117 (NOV) :219-232
[3]   RESIN DEVELOPMENT FOR ELECTRON-MICROSCOPY AND AN ANALYSIS OF EMBEDDING AT LOW-TEMPERATURE [J].
CARLEMALM, E ;
GARAVITO, RM ;
VILLIGER, W .
JOURNAL OF MICROSCOPY-OXFORD, 1982, 126 (MAY) :123-143
[4]   SUPERRESOLUTION 3-DIMENSIONAL IMAGES OF FLUORESCENCE IN CELLS WITH MINIMAL LIGHT EXPOSURE [J].
CARRINGTON, WA ;
LYNCH, RM ;
MOORE, EDW ;
ISENBERG, G ;
FOGARTY, KE ;
FREDRIC, FS .
SCIENCE, 1995, 268 (5216) :1483-1487
[5]  
DRIEL VLF, 2008, J STRUCT BIOL, V161, P372
[6]   True optical resolution beyond the Rayleigh limit achieved by standing wave illumination [J].
Frohn, JT ;
Knapp, HF ;
Stemmer, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (13) :7232-7236
[7]   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
[8]   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
[9]   Carbocyanine dyes as efficient reversible single-molecule optical switch [J].
Heilemann, M ;
Margeat, E ;
Kasper, R ;
Sauer, M ;
Tinnefeld, P .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (11) :3801-3806
[10]   Toward fluorescence nanoscopy [J].
Hell, SW .
NATURE BIOTECHNOLOGY, 2003, 21 (11) :1347-1355