The quadrupole narrows the ion population by selecting precursor ions before analysis of their fragments. Selected precursors can undergo higher-energy collisional dissociation, producing fragment ions that retain structural information about the original molecule. Measuring these fragments in the Orbitrap adds precise mass information, strengthening identification of peptides, proteins, lipids, and other biomolecules in complex biological samples.
High resolution helps distinguish ions with closely related mass-to-charge ratios, while high mass accuracy improves confidence in assigning detected signals to specific biomolecules. Together, these properties make the resulting measurements more informative than signal intensity alone. In biological studies, they support clearer interpretation of complex molecular profiles and more reliable characterization of peptides, proteins, and small molecules.
Targeted ion selection focuses measurement on precursor ions of interest, whereas full-scan analysis captures a broader view of the ions present in a sample. Using both approaches connects detailed examination of selected molecules with comprehensive molecular profiling. This combination can reveal known biomolecules while also supporting discovery of changes in the wider composition of a biological sample.
The workflow begins by introducing ions from the biological sample into the instrument and selecting precursor ions with the quadrupole. Selected ions may then be fragmented by higher-energy collisional dissociation. The resulting precursor and fragment ions enter the Orbitrap for high-resolution measurement, generating mass and fragmentation information that can be used for molecular identification and quantification.
Q Exactive MS is applied across proteomics, metabolomics, and lipidomics. These fields use its measurements to investigate peptides and proteins, small molecules, and lipids within biological samples. Because the platform combines molecular mass information with fragmentation data, it can support studies that seek to characterize biomolecules and compare the molecular composition of different biological conditions.
Measurements from this platform can reveal changes in the molecular content of cells by identifying and quantifying biomolecules in complex samples. Fragmentation data adds evidence for molecular assignments, while full-scan measurements provide broader compositional coverage. Interpreting these changes helps connect altered profiles of peptides, proteins, lipids, or small molecules with cellular composition and function.