APPLICATIONS OF MEDIUM-VOLTAGE STEM FOR THE 3-D STUDY OF ORGANELLES WITHIN VERY THICK SECTIONS

被引:23
作者
BEORCHIA, A [1 ]
HELIOT, L [1 ]
MENAGER, M [1 ]
KAPLAN, H [1 ]
PLOTON, D [1 ]
机构
[1] LME, F-51100 REIMS, FRANCE
关键词
STEM; 3-DIMENSIONAL STUDY OF ORGANELLES; THICK SECTION; NUCLEOLUS; AG-NOR PROTEINS;
D O I
10.1111/j.1365-2818.1993.tb03348.x
中图分类号
TH742 [显微镜];
学科分类号
摘要
Scanning transmission electron microscopy at 300 kV enables the visualization of nucleolar silver-stained structures within thick sections (3-8 mum) of Epon-embedded cells at high tilt angles (-50-degrees; +50-degrees). Thick sections coated with gold particles were used to determine the best conditions for obtaining images with high contrast and good resolution. For a 6-mum-thick section the values of thinning and shrinkage under the beam are 35 to 10%, respectively. At the electron density used in these experiments (100 e-/angstrom2/s) it is estimated that these modifications of the section stabilized in less than 10 min. The broadening of the beam through the section was measured and calculations indicated that the subsequent resolution reached 100 nm for objects localized near the lower side of 4-mum-thick sections with a spot-size of 5.6 nm. Comparing the same biological samples, viewed alternately in CTEM and STEM, demonstrated that images obtained in STEM have a better resolution and contrast for sections thicker than 3 mum. Therefore, the visualization of densely stained structures, observed through very thick sections in the STEM mode, will be very useful in the near future for microtomographic reconstruction of cellular organelles.
引用
收藏
页码:247 / 258
页数:12
相关论文
共 29 条
  • [1] ARIL T, 1987, J ELECTRON MICROSC, V36, P177
  • [2] BAHR GF, 1965, LAB INVEST, V14, P377
  • [3] DIGITAL 3-DIMENSIONAL VISUALIZATION OF CELLULAR ORGANELLES STUDIED BY MEDIUM-VOLTAGE AND HIGH-VOLTAGE ELECTRON-MICROSCOPY
    BEORCHIA, A
    PLOTON, D
    MENAGER, M
    LEBONVALLET, S
    THIRY, M
    BONNET, N
    [J]. JOURNAL OF MICROSCOPY, 1991, 163 : 221 - 231
  • [4] METHODS FOR SPECIMEN THICKNESS DETERMINATION IN ELECTRON-MICROSCOPY .2. CHANGES IN THICKNESS WITH DOSE
    BERRIMAN, J
    LEONARD, KR
    [J]. ULTRAMICROSCOPY, 1986, 19 (04) : 349 - 366
  • [5] BRAKENHOFF GJ, 1990, OPTICAL MICROSCOPY FOR BIOLOGY, P19
  • [6] ENERGY FILTERED STEM IMAGING OF THICK BIOLOGICAL SECTIONS
    COLLIEX, C
    MORY, C
    OLINS, AL
    OLINS, DE
    TENCE, M
    [J]. JOURNAL OF MICROSCOPY, 1989, 153 : 1 - 21
  • [7] THICK SPECIMENS IN CEM AND STEM .1. CONTRAST
    CREWE, AV
    GROVES, T
    [J]. JOURNAL OF APPLIED PHYSICS, 1974, 45 (08) : 3662 - 3672
  • [8] 3-DIMENSIONAL IMMUNOGOLD LABELING OF NUCLEAR MATRIX PROTEINS IN PERMEABILIZED CELLS
    DEGRAAF, A
    HUMBEL, BM
    STUURMAN, N
    ENHENEGOUWEN, PMPV
    VERKLEIJ, AJ
    [J]. CELL BIOLOGY INTERNATIONAL REPORTS, 1992, 16 (08) : 827 - 836
  • [9] CONTROLLED NUCLEATION FOR REGULATION OF PARTICLE-SIZE IN MONODISPERSE GOLD SUSPENSIONS
    FRENS, G
    [J]. NATURE-PHYSICAL SCIENCE, 1973, 241 (105): : 20 - 22
  • [10] MEASUREMENT OF TOP BOTTOM EFFECT IN SCANNING-TRANSMISSION ELECTRON-MICROSCOPY OF THICK AMORPHOUS SPECIMENS
    GENTSCH, P
    GILDE, H
    REIMER, L
    [J]. JOURNAL OF MICROSCOPY-OXFORD, 1974, 100 (JAN): : 81 - 92