Mass Spectrometry Techniques: Principles and Practices for Quantitative Proteomics

In the current omics-age of research, major developments have been made in technologies that attempt to survey the entire repertoire of genes, transcripts, proteins, and metabolites present within a cell. While genomics has led to a dramatic increase in our understanding of such things as disease morphology and how organisms respond to medications, it is critical to obtain information at the proteome level since proteins carry out most of the functions within the cell. The primary tool for obtaining proteome-wide information on proteins within the cell is mass spectrometry (MS). While it has historically been associated with the protein identification, developments over the past couple of decades have made MS a robust technology for protein quantitation as well. Identifying quantitative changes in proteomes is complicated by its dynamic nature and the inability of any technique to guarantee complete coverage of every protein within a proteome sample. Fortunately, the combined development of sample preparation and MS methods have made it capable of quantitatively comparing many thousands of proteins obtained from cells and organisms.

Automated summary

In the era of genomics research, mass spectrometry has become a vital tool for quantitatively comparing proteins within cells and organisms, despite the complexity of identifying quantitative changes in proteomes due to their dynamic nature and limitations in technology coverage. The combined development of sample preparation and MS methods has enabled the quantitation of thousands of proteins obtained from cells and organisms.