Abstract
Crosslinking mass spectrometry (XL-MS) has emerged as a powerful tool in its own right for the investigation of protein structures and interactions. Utilizing standard shotgun MS mass spectrometry equipment and specialized database search software, crosslinked peptide-pairs can be identified and directly translated into distance constraints for protein structure and protein-protein interaction investigations. Whereas the gas-phase dissociation behavior of linear peptides is well understood, less is however known about the gas-phase dissociation behavior of crosslinked peptides. In this work, we set out to expose the behavior of commonly used non-cleavable and gas-phase cleavable crosslinking reagents using synthetic peptides to establish mechanistic insights. We describe that crosslinked peptide pairs generate specific fragmentation patterns and diagnostic ions under HCD and CID fragmentation conditions, distinct from mono-linked peptide and non-modified peptides. We discuss in detail the resulting diagnostic ions that can help distinguishing linear peptides from mono-linked and crosslinked peptide pairs and how that may be used to further increase the efficiency of XL-MS analysis.
Original language | English |
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Article number | 116184 |
Pages (from-to) | 1-10 |
Journal | International Journal of Mass Spectrometry |
Volume | 444 |
DOIs | |
Publication status | Published - 1 Oct 2019 |
Funding
We thank all members of the Heck-group for their helpful contributions and congratulate Albert J.R. Heck for recieving the Thomson Medal. We acknowledge financial support by the large-scale proteomics facility Proteins@Work (Project 184.032.201 ) embedded in the Netherlands Proteomics Centre and supported by the Netherlands Organization for Scientific Research (NWO) . Additional support came through a seed grant kindly provided by the Utrecht Institute for Pharmaceutical Sciences (UIPS) . And finally, this work was supported by many evenings with guitar and trumpet in front of the mass spectrometer. Appendix A
Keywords
- Crosslinking mass spectrometry
- Fragmentation behavior
- Protein-protein interactions
- Structural biology
- XL-MS
- XlinkX