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Collision-Induced Affinity Selection Mass Spectrometry for Identification of Ligands

Tin Mak, Jamie Rossjohn, Dene R. Littler, Miaomiao Liu, Ronald J. Quinn

2022ACS Bio & Med Chem Au21 citationsDOIOpen Access PDF

Abstract

Hyphenated mass spectrometry has been used to identify ligands binding to proteins. It involves mixing protein and compounds, separation of protein-ligand complexes from unbound compounds, dissociation of the protein-ligand complex, separation to remove protein, and injection of the supernatant into a mass spectrometer to observe the ligand. Here we report collision-induced affinity selection mass spectrometry (CIAS-MS), which allows separation and dissociation inside the instrument. The quadrupole was used to select the ligand-protein complex and allow unbound molecules to be exhausted to vacuum. Collision-induced dissociation (CID) dissociated the protein-ligand complex, and the ion guide and resonance frequency were used to selectively detect the ligand. A known SARS-CoV-2 Nsp9 ligand, oridonin, was successfully detected when it was mixed with Nsp9. We provide proof-of-concept data that the CIAS-MS method can be used to identify binding ligands for any purified protein.

Topics & Concepts

ChemistryMass spectrometryDissociation (chemistry)Ligand (biochemistry)Collision-induced dissociationProtein ligandTarget proteinChromatographyTandem mass spectrometryMoleculeAnalytical Chemistry (journal)BiochemistryPhysical chemistryOrganic chemistryReceptorGeneMass Spectrometry Techniques and ApplicationsAnalytical chemistry methods developmentIon-surface interactions and analysis
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