Highly multiparametric analysis by mass cytometry
This review paper describes a new technology, mass cytometry, that addresses applications typically run by flow cytometer analyzers, but extends the capability to highly multiparametric analysis. The detection technology is based on atomic mass spectrometry. It offers quantitation, specificity and d...
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| Published in | Journal of immunological methods Vol. 361; no. 1-2; pp. 1 - 20 |
|---|---|
| Main Authors | , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Amsterdam
Elsevier B.V
30.09.2010
Elsevier |
| Subjects | |
| Online Access | Get full text |
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| Abstract | This review paper describes a new technology, mass cytometry, that addresses applications typically run by flow cytometer analyzers, but extends the capability to highly multiparametric analysis. The detection technology is based on atomic mass spectrometry. It offers quantitation, specificity and dynamic range of mass spectrometry in a format that is familiar to flow cytometry practitioners. The mass cytometer does not require compensation, allowing the application of statistical techniques; this has been impossible given the constraints of fluorescence noise with traditional cytometry instruments. Instead of “colors” the mass cytometer “reads” the stable isotope tags attached to antibodies using metal-chelating labeling reagents. Because there are many available stable isotopes, and the mass spectrometer provides exquisite resolution between detection channels, many parameters can be measured as easily as one. For example, in a single tube the technique allows for the ready detection and characterization of the major cell subsets in blood or bone marrow. Here we describe mass cytometric immunophenotyping of human leukemia cell lines and leukemia patient samples, differential cell analysis of normal peripheral and umbilical cord blood; intracellular protein identification and metal-encoded bead arrays. |
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| AbstractList | This review paper describes a new technology, mass cytometry, that addresses applications typically run by flow cytometer analyzers, but extends the capability to highly multiparametric analysis. The detection technology is based on atomic mass spectrometry. It offers quantitation, specificity and dynamic range of mass spectrometry in a format that is familiar to flow cytometry practitioners. The mass cytometer does not require compensation, allowing the application of statistical techniques; this has been impossible given the constraints of fluorescence noise with traditional cytometry instruments. Instead of "colors" the mass cytometer "reads" the stable isotope tags attached to antibodies using metal-chelating labeling reagents. Because there are many available stable isotopes, and the mass spectrometer provides exquisite resolution between detection channels, many parameters can be measured as easily as one. For example, in a single tube the technique allows for the ready detection and characterization of the major cell subsets in blood or bone marrow. Here we describe mass cytometric immunophenotyping of human leukemia cell lines and leukemia patient samples, differential cell analysis of normal peripheral and umbilical cord blood; intracellular protein identification and metal-encoded bead arrays. |
| Author | Baranov, Vladimir Bandura, Dmitry Winnik, Mitchell A. Tanner, Scott Nitz, Mark Ornatsky, Olga |
| Author_xml | – sequence: 1 givenname: Olga surname: Ornatsky fullname: Ornatsky, Olga email: olga.ornatsky@utoronto.ca organization: Department of Chemistry, University of Toronto, 80 St. George St., Toronto ON, Canada M5S 3H6 – sequence: 2 givenname: Dmitry surname: Bandura fullname: Bandura, Dmitry organization: Department of Chemistry, University of Toronto, 80 St. George St., Toronto ON, Canada M5S 3H6 – sequence: 3 givenname: Vladimir surname: Baranov fullname: Baranov, Vladimir organization: Department of Chemistry, University of Toronto, 80 St. George St., Toronto ON, Canada M5S 3H6 – sequence: 4 givenname: Mark surname: Nitz fullname: Nitz, Mark organization: Department of Chemistry, University of Toronto, 80 St. George St., Toronto ON, Canada M5S 3H6 – sequence: 5 givenname: Mitchell A. surname: Winnik fullname: Winnik, Mitchell A. organization: Department of Chemistry, University of Toronto, 80 St. George St., Toronto ON, Canada M5S 3H6 – sequence: 6 givenname: Scott surname: Tanner fullname: Tanner, Scott organization: Department of Chemistry, University of Toronto, 80 St. George St., Toronto ON, Canada M5S 3H6 |
| BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23307465$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/20655312$$D View this record in MEDLINE/PubMed |
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| Keywords | Bead array Flow cytometry Mass cytometry Metal-tagged antibodies Metal-encoded beads Multiparametric single cell assay Antibody Isolated cell Immunological method |
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| SubjectTerms | Bead array Biological and medical sciences Bone Marrow Cells - immunology Chelating Agents - chemistry Fetal Blood - immunology Flow cytometry Fundamental and applied biological sciences. Psychology Fundamental immunology HL-60 Cells Humans Immunophenotyping - instrumentation Immunophenotyping - methods Jurkat Cells Lanthanoid Series Elements - chemistry Leukemia - immunology Mass cytometry Mass Spectrometry - instrumentation Mass Spectrometry - methods Metal-encoded beads Metal-tagged antibodies Microspheres Molecular immunology Multiparametric single cell assay Techniques |
| Title | Highly multiparametric analysis by mass cytometry |
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