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Hybrid Mass Spectrometers
Instruments that contain multiple mass spectrometry units for proteomics and metabolomics.
Precursor Ion Scan
A method where the first quadrupole (Q1) selects a wide mass range of ions for detection without fragmentation.
Fragment Ion Scan
Also known as tandem MS/MS or MS2, where Q1 selects a subset of masses and Q2 induces fragmentation before detection.
Data Dependent Acquisition (DDA)
A method where the MS scan sequence depends on the data collected, leading to variability in scans across runs.
Data Independent Acquisition (DIA)
A method where the scan sequence is independent of the data, resulting in consistent scans across analyses.
Targeted Methods
Approaches used for hypothesis testing, focusing on specific proteins or peptides of interest.
Untargeted Methods
Approaches used for hypothesis generation, allowing for the discovery of unknown proteins or changes in biological conditions.
Targeted DDA
A method that uses an inclusion list to monitor specific peptides during data collection.
Untargeted DDA
A method that collects data based on the most abundant precursor ions detected at any moment, also known as the top strategy.
Selected Reaction Monitoring (SRM)
A targeted DIA method performed on a triple quadrupole mass spectrometer.
Parallel Reaction Monitoring (PRM)
A targeted DIA method performed on high-resolution instruments like Orbitrap or Q-Exactive.
SWATH
An untargeted DIA method that selects and fragments larger predefined mass ranges throughout the elution gradient.
Precursor MS Spectra
The initial mass spectra produced by allowing all peptides through Q1 unfragmented.
Fragment Ion Spectra
The mass spectra produced from the fragments of selected precursor ions after fragmentation in Q2.
Stochasticity of DDA
The variability in protein identification across repeated analyses of the same sample, leading to diminishing returns in unique identifications.