The selected reaction monitoring/multiple reaction monitoring-based mass spectrometry approach for the accurate quantitation of proteins: clinical applications in the cardiovascular diseases
Selected reaction monitoring, also known as multiple reaction monitoring, is a powerful targeted mass spectrometry approach for a confident quantitation of proteins/peptides in complex biological samples. In recent years, its optimization and application have become pivotal and of great interest in clinical research to derive useful outcomes for patient care. Thus, selected reaction monitoring/multiple reaction monitoring is now used as a highly sensitive and selective method for the evaluation of protein abundances and biomarker verification with potential applications in medical screening. This review describes technical aspects for the development of a robust multiplex assay and discussing its recent applications in cardiovascular proteomics: verification of promising disease candidates to select only the highest quality peptides/proteins for a preclinical validation, as well as quantitation of protein isoforms and post-translational modifications.
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Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, CanadaUniv Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
Kuzyk, Michael A.
Smith, Derek
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Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, CanadaUniv Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
Smith, Derek
Yang, Juncong
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Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, CanadaUniv Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
Yang, Juncong
Cross, Tyra J.
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Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, CanadaUniv Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
Cross, Tyra J.
Jackson, Angela M.
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Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, CanadaUniv Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
Jackson, Angela M.
Hardie, Darryl B.
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Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, CanadaUniv Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
Hardie, Darryl B.
Anderson, N. Leigh
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Plasma Proteome Inst, Washington, DC 20009 USAUniv Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
Anderson, N. Leigh
Borchers, Christoph H.
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Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
Univ Victoria, Dept Biochem & Microbiol, Victoria, BC V8W 3P6, CanadaUniv Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
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Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, CanadaUniv Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
Chambers, Andrew G.
Percy, Andrew J.
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Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, CanadaUniv Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
Percy, Andrew J.
Yang, Juncong
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Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, CanadaUniv Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
Yang, Juncong
Camenzind, Alexander G.
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Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, CanadaUniv Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
Camenzind, Alexander G.
Borchers, Christoph H.
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Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
Univ Victoria, Dept Biochem & Microbiol, Victoria, BC V8P 5C2, CanadaUniv Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada