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PMID: 7638490 Published · ppublish English Journal Article

Biological electron energy loss spectroscopy in the field-emission scanning transmission electron microscope.

Scanning microscopy. Supplement ·Vol. 8 ·1994-00-00 ·Pages 245-58; discussion 258-9

Leapman RD, Sun SQ, Hunt JA, Andrews SB

Abstract

The dedicated scanning transmission electron microscope (STEM) combined with parallel electron energy loss spectroscopy (EELS) provides a very sensitive means of detecting specific elements in small structures. EELS is more sensitive than optimized energy-dispersive X-ray spectroscopy by a factor of about three for calcium. Measurement of such low concentrations requires special processing methods such as difference-acquisition techniques and multiple least squares procedures for fitting reference spectra. By analyzing data recorded at each pixel in a spectrum-image it is possible to map quantitatively the elemental distributions in a specimen. It is possible to prepare cryosections that are sufficiently thin to avoid excessive plural inelastic scattering so analysis can be performed at 100 keV beam energy. Under optimal conditions, a resolution of 10 nm and detection limits of a few atoms are achievable for elements such as calcium, phosphorus and iron. In the field emission STEM certain types of chemical information can be extracted from biological specimens. Valence EELS has been exploited to measure water distributions in frozen hydrated cryosections.

MeSH Terms
Animals Calcium/analysis Cerebellar Cortex/ultrastructure Dendrites/ultrastructure Endoplasmic Reticulum/ultrastructure Freezing Mathematics Mice Microscopy, Electron, Scanning Transmission/instrumentation,methods Mitochondria/ultrastructure Neurons/ultrastructure Purkinje Cells/ultrastructure Sensitivity and Specificity Spectrum Analysis
Chemicals
Calcium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Leapman R D
Biomedical Engineering & Instrumentation Program, NCRR, National Institutes of Health, Bethesda, MD 20892, USA.
Sun S Q
Hunt J A
Andrews S B
Article Info
Journal
Scanning microscopy. Supplement
Abbr.
Scanning Microsc Suppl
ISSN
0892-953X
Published
1994-00-00
Pages
245-58; discussion 258-9
Language
English
Region
United States
NLM ID
8710881
Subset
IM
External Links
PubMed source
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