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Time-of-flight secondary ion mass spectrometry imaging of subcellular lipid heterogeneity: Poisson counting and spatial resolution.

Piehowski, Paul D (author)
Davey, Angel M (author)
Kurczy, Michael, 1980 (author)
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Sheets, Erin D (author)
Winograd, Nicholas (author)
Ewing, Andrew G, 1957 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry,University of Gothenburg
Heien, Michael L (author)
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 (creator_code:org_t)
2009-06-16
2009
English.
In: Analytical chemistry. - : American Chemical Society (ACS). - 1520-6882 .- 0003-2700. ; 81:14, s. 5593-602
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Mass spectrometric imaging is a powerful tool to interrogate biological complexity. One such technique, time-of-flight secondary ion mass spectrometry (TOF-SIMS) imaging, has been successfully utilized for subcellular imaging of cell membrane components. In order for this technique to provide insight into biological processes, it is critical to characterize the figures of merit. Because a SIMS instrument counts individual events, the precision of the measurement is controlled by counting statistics. As the analysis area decreases, the number of molecules available for analysis diminishes. This becomes critical when imaging subcellular features; it limits the information obtainable, resulting in images with only a few counts of interest per pixel. Many features observed in low intensity images are artifacts of counting statistics, making validation of these features crucial to arriving at accurate conclusions. With TOF-SIMS imaging, the experimentally attainable spatial resolution is a function of the molecule of interest, sample matrix, concentration, primary ion, instrument transmission, and spot size of the primary ion beam. A model, based on Poisson statistics, has been developed to validate SIMS imaging data when signal is limited. This model can be used to estimate the effective spatial resolution and limits of detection prior to analysis, making it a powerful tool for tailoring future investigations. In addition, the model allows comparison of pixel-to-pixel intensity and can be used to validate the significance of observed image features. The implications and capabilities of the model are demonstrated by imaging the cell membrane of resting RBL-2H3 mast cells.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

Keyword

Animals
Cell Line
Cell Membrane
chemistry
metabolism
Cholesterol
metabolism
Intracellular Space
chemistry
metabolism
Lipid Metabolism
Lipids
chemistry
Mass Spectrometry
Mast Cells
chemistry
cytology
Poisson Distribution
Probability
Surface Properties
Poisson Distribution

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ref (subject category)
art (subject category)

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