Maximizing Tandem MS Acquisition Rates for Shotgun Proteomics

Advances in tandem mass spectrometry (MS/MS) acquisition rate have steadily led to increased performance in shotgun proteomics experiments. To that end, contemporary mass spectrometers are outfitted with multiple analyzers allowing for the simultaneous collection of survey (MS1) and MS/MS spectra. In the latest generation Orbitrap hybrid, MS/MS scans can be acquired at a high rate using the dual cell linear ion trap analyzer, all while the next precursor is being dissociated in a collision cell and a MS1 scan is occurring in the Orbitrap. Often overlooked in these experiments is that the ion trap scan duration is highly variable and dependent upon precursor mass. Here, we examine the use of various static m/z scan ranges for ion trap MS/MS acquisition and determine performance relative to conventional dynamic m/z range scanning. We demonstrate that a fixed m/z scan range generate 12% more MS/MS scans and more unique peptide identifications as compared to the standard dynamic approach, respectively.