As researchers press further into the understanding of life sciences, quantification provides greater insight into proteomic mysteries.
PEAKS Q is the optional module of PEAKS for protein quantification analysis based on mass spectrometry
data. PEAKS Q has both labeling and label-free methods, including:
- Label Free Quantification
- SILAC (Stable Isotope Labeling with Amino Acids in Cell Culture)
- ICAT (Isotope Coded Affinity Tags)
- iTRAQ (Isobaric Tag for Relative and Absolute Quantification)
- TMT (Tandem Mass Tags)
- ICPL (Isotope Coded Protein Labels)
- N-Terminal Labeling (e.g. methylation)
- O18
- User Defined Labeling
PEAKS Q uses well-accepted methods for feature detection and calculates the peptide ratios
based on either peak intensity (for labeling method) or peak areas (for label free method).
The protein ratios are calculated based on the total intensities or peak areas of
the top-3 unique peptides identified for the protein. The use of the unique peptides
ensures that the protein ratio is not adversely affected by peptides shared by multiple
proteins. Ratios and absolute intensities of the detected features and identified
peptides can be easily exported to text files (.csv) for customized analyses by
the users, such as ratio calculation using a different algorithm (e.g. spectrum count).
PEAKS Q provides a very user-friendly graphical interface to easily visualize
the quantification results and the detected features used for the ratio calculation.
For the table view of peptide/protein ratios, users can choose to display absolute
intensities or ratios to a reference sample or the sum of the samples.
Further, the summary view clusters the proteins according to their ratios
and provides a bird's eye view of all protein changes.
Users can easily examine the supporting evidences of each peptide's ratio calculation. There are several ways that PEAKS Q provides to examine a peptide feature.