Structure and mass analysis by scanning transmission electron microscopy

被引:48
作者
Müller, SA [1 ]
Engel, A [1 ]
机构
[1] Univ Basel, Maurice E Muller Inst Struct Biol, Biozentrum, CH-4056 Basel, Switzerland
关键词
scanning transmission electron microscope; mass measurement; electron beam sensitivity;
D O I
10.1016/S0968-4328(00)00022-6
中图分类号
TH742 [显微镜];
学科分类号
摘要
In the scanning transmission electron microscope (STEM) an electron beam of a few angstroms diameter is raster scanned over a thin sample and the scattered electrons are sequentially measured for each sample element irradiated. The mass, the elemental composition and the structure of a protein can be simultaneously assessed if all detector systems of the STEM are used. Aspects affecting the accuracy of the mass measurement technique and the demands placed on the instrument's dark-field detector system are outlined. In addition, the influences of some sample preparation techniques are noted and the mass-loss induced at ambient temperatures by the incidence of 80 kV electrons on various biological samples is reported. Finally, the importance of the STEM for the structural analysis of proteins is documented by examples. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:21 / 31
页数:11
相关论文
共 79 条
[31]   DNA-PROTEIN COMPLEXES SPREAD ON N-2-DISCHARGED CARBON-FILM AND CHARACTERIZED BY MOLECULAR-WEIGHT AND ITS PROJECTED DISTRIBUTION - NUCLEOSOME FORMATION BY AN INVITRO TRANSCRIPTION SYSTEM [J].
HOUGH, PVC ;
MASTRANGELO, IA ;
WALL, JS ;
HAINFELD, JF ;
SIMON, MN ;
MANLEY, JL .
JOURNAL OF MOLECULAR BIOLOGY, 1982, 160 (02) :375-386
[32]   IDENTIFICATION AND ELECTRON-MICROSCOPIC ANALYSIS OF A CHAPERONIN OLIGOMER FROM NEUROSPORA-CRASSA MITOCHONDRIA [J].
HUTCHINSON, EG ;
TICHELAAR, W ;
HOFHAUS, G ;
WEISS, H ;
LEONARD, KR .
EMBO JOURNAL, 1989, 8 (05) :1485-1490
[33]  
JOHNSON KA, 1983, J SUBMICR CYTOL PATH, V15, P181
[34]   Z-CONTRAST IN BIOLOGY - A COMPARISON WITH OTHER IMAGING MODES [J].
KELLENBERGER, E ;
CARLEMALM, E ;
VILLIGER, W ;
WURTZ, M ;
MORY, C ;
COLLIEX, C .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1986, 483 :202-228
[35]   THE INFLUENCE OF THE SURFACE RELIEF OF THIN-SECTIONS OF EMBEDDED, UNSTAINED BIOLOGICAL-MATERIAL ON IMAGE QUALITY [J].
KELLENBERGER, E ;
VILLIGER, W ;
CARLEMALM, E .
MICRON AND MICROSCOPICA ACTA, 1986, 17 (04) :331-348
[36]  
Kramer A., 1995, PREMRNA PROCESSING, P35
[37]   CHAPERONIN-MEDIATED PROTEIN FOLDING - GROES BINDS TO ONE END OF THE GROEL CYLINDER, WHICH ACCOMMODATES THE PROTEIN SUBSTRATE WITHIN ITS CENTRAL CAVITY [J].
LANGER, T ;
PFEIFER, G ;
MARTIN, J ;
BAUMEISTER, W ;
HARTL, FU .
EMBO JOURNAL, 1992, 11 (13) :4757-4765
[38]   CHARACTERIZATION OF BIOLOGICAL MACROMOLECULES BY COMBINED MASS MAPPING AND ELECTRON ENERGY-LOSS SPECTROSCOPY [J].
LEAPMAN, RD ;
ANDREWS, SB .
JOURNAL OF MICROSCOPY, 1992, 165 :225-238
[39]   Phosphorylation and subunit organization of axonal neurofilaments determined by scanning transmission electron microscopy [J].
Leapman, RD ;
Gallant, PE ;
Reese, TS ;
Andrews, SB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (15) :7820-7824
[40]  
LEAPMAN RD, 1995, J MICROSC SOC AM, V1, P93