A new dynamic in mass spectral imaging of single biological cells

Research output: Contribution to journalArticle

  • External authors:
  • John S. Fletcher
  • Sadia Rabbani
  • Paul Blenkinsopp
  • Steve P. Thompson
  • John C. Vickerman

Abstract

Time-of-flight secondary ion mass spectrometry (TOF-SIMS) has unique capabilities in the area of high-resolution mass spectrometric imaging of biological samples. The technique offers parallel detection of native and non-native molecules at physiological concentrations with potentially submicrometer spatial resolution. Recent advances in SIMS technology have been focused on generating new ion sources that can in turn be used to eject more intact molecular and biological characteristic species from a sample. The introduction of polyatomic ion beams, particularly C60, for TOF-SIMS analysis has created a whole new application of molecular depth profiling and 3D molecular imaging. However, such analyses, particularly at high lateral resolution, are severely hampered by the accompanying mass spectrometry associated with current TOF-SIMS instruments. Hence, we have developed an instrument that overcomes many of the drawbacks of current TOF-SIMS spectrometers by removing the need to pulse the primary ion beam. The instrument samples the secondary ions using a buncher that feeds into a specially designed time-of-flight analyzer. We have validated this new instrumental concept by analyzing a number of biological samples generating 2D and 3D images showing molecular localization on a subcellular scale, over a practical time frame, while maintaining high mass resolution. We also demonstrate large area mapping and the MS/MS capability of the instrument. © 2008 American Chemical Society.

Bibliographical metadata

Original languageEnglish
Pages (from-to)9058-9064
Number of pages6
JournalAnalytical Chemistry
Volume80
Issue number23
Early online date24 Oct 2008
DOIs
Publication statusPublished - 1 Dec 2008

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