Collision-Induced Affinity Selection Mass Spectrometry for Identification of Ligands.
Tin MakJamie RossjohnDene R LittlerMiaomiao LiuRonald J QuinnPublished in: ACS bio & med chem Au (2022)
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.
Keyphrases
- mass spectrometry
- liquid chromatography
- sars cov
- protein protein
- binding protein
- high resolution
- high resolution mass spectrometry
- multiple sclerosis
- high glucose
- amino acid
- high performance liquid chromatography
- drug induced
- machine learning
- electronic health record
- cell free
- gas chromatography
- coronavirus disease
- big data
- energy transfer
- dna binding