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Mass Cytometry: Protocol for Daily Tuning and Running Cell Samples on a CyTOF Mass Cytometer
Published on: November 2, 2012
Metal-Containing Polystyrene Beads as Standards for Mass Cytometry
Ahmed I Abdelrahman1, Olga Ornatsky, Dmitry Bandura
1Department of Chemistry, University of Toronto, 80 St George Street Toronto ON M5S3H6, Canada.
Journal of Analytical Atomic Spectrometry
|April 15, 2010
Summary
Metal-containing polymer beads are suitable for calibrating mass cytometers and serving as internal standards. Three-stage synthesis yielded beads with consistent lanthanide content, showing stability and no interference with cell analysis.
Area of Science:
- Analytical Chemistry
- Materials Science
- Biotechnology
Background:
- Mass cytometry is a powerful single-cell analysis technique.
- Accurate calibration and standardization are crucial for mass cytometry.
- Metal-containing polymer beads offer potential as calibration standards.
Purpose of the Study:
- To evaluate metal-containing polystyrene beads for mass cytometry calibration.
- To assess the suitability of these beads as internal standards.
- To investigate the synthesis and properties of these beads.
Main Methods:
- Dispersion polymerization was used to synthesize metal-containing polystyrene beads with acrylic acid.
- Mass cytometry was employed for bead-by-bead metal content measurement.
- Stability testing involved incubation in aqueous solutions of varying pH over six months.
Main Results:
- Three-stage dispersion polymerization resulted in beads with lower lanthanide content variation compared to two-stage synthesis.
- The beads demonstrated minimal lanthanide release across different pH levels for six months.
- The beads did not interfere with the mass cytometry analysis of element-tagged antibodies on cells.
Conclusions:
- Metal-containing polystyrene beads are effective for mass cytometry calibration and as internal standards.
- Optimized synthesis (three-stage polymerization) improves bead uniformity.
- These beads are stable and do not interfere with cellular analysis, enhancing mass cytometry reliability.

