Structural O-Glycoform Heterogeneity of the SARS-CoV-2 Spike Protein Receptor-Binding Domain Revealed by Native Top-Down Mass Spectrometry.
David S RobertsMorgan W MannJake A MelbyEli J LarsonYanlong ZhuAllan R BrasierSong JinYing GePublished in: bioRxiv : the preprint server for biology (2021)
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) utilizes an extensively glycosylated surface spike (S) protein to mediate host cell entry and the S protein glycosylation is strongly implicated in altering viral binding/function and infectivity. However, the structures and relative abundance of the new O-glycans found on the S protein regional-binding domain (S-RBD) remain cryptic because of the challenges in intact glycoform analysis. Here, we report the complete structural characterization of intact O-glycan proteoforms using native top-down mass spectrometry (MS). By combining trapped ion mobility spectrometry (TIMS), which can separate the protein conformers of S-RBD and analyze their gas phase structural variants, with ultrahigh-resolution Fourier transform ion cyclotron resonance (FTICR) MS analysis, the O-glycoforms of the S-RBD are comprehensively characterized, so that seven O-glycoforms and their relative molecular abundance are structurally elucidated for the first time. These findings demonstrate that native top-down MS can provide a high-resolution proteoform-resolved mapping of diverse O-glycoforms of the S glycoprotein, which lays a strong molecular foundation to uncover the functional roles of their O-glycans. This proteoform-resolved approach can be applied to reveal the structural O-glycoform heterogeneity of emergent SARS-CoV-2 S-RBD variants, as well as other O-glycoproteins in general.
Keyphrases
- sars cov
- mass spectrometry
- high resolution
- respiratory syndrome coronavirus
- binding protein
- single cell
- liquid chromatography
- multiple sclerosis
- amino acid
- ms ms
- gas chromatography
- coronavirus disease
- single molecule
- capillary electrophoresis
- multidrug resistant
- gene expression
- dna methylation
- mesenchymal stem cells
- transcription factor
- microbial community
- bone marrow
- simultaneous determination
- quantum dots