Structural Insights into Linkage-Specific Ubiquitin Chains Using Ion Mobility Mass Spectrometry

J Am Soc Mass Spectrom. 2024 May 1;35(5):982-991. doi: 10.1021/jasms.4c00019. Epub 2024 Apr 10.

Abstract

The structural characterization and differentiation of four types of oligoubiquitin conjugates [linear (Met1)-, Lys11-, Lys48-, Lys63-linked di-, tri-, and tetraubiquitin chains] using ion mobility mass spectrometry are reported. A comparison of collision cross sections for the same linkage of di-, tri-, and tetraubiquitin chains shows differences in conformational elongation for higher charge states due to the interplay of linkage-derived structure and Coulombic repulsion. For di- and triubiquitin chains, this elongation results in a single narrow feature representing an elongated conformation type for multiple higher charge state species. In contrast, higher charge state tetraubiquitin species do not form a single conformer type as readily. A comparison of different linkages in tetraubiquitin chains reveals greater similarity in conformation type at lower charge states; with increasing charge state, the four linkage types diverge in the relative proportions of elongated conformer types with Met1- ≥ Lys11- > Lys63- > Lys48-linkage. These differences in conformational trends could be discussed with respect to biological functions of linkage-specific polyubiquitinated proteins.

Keywords: (Met1-, Lys11-, Lys48-, and Lys63)-linked (di-, tri-, and tetra)ubiquitin chains; collision cross sections; ion mobility mass spectrometry; physiological roles of ubiquitin chains; ubiquitin chain structure.

MeSH terms

  • Ion Mobility Spectrometry* / methods
  • Lysine / chemistry
  • Mass Spectrometry / methods
  • Models, Molecular
  • Protein Conformation
  • Ubiquitin* / chemistry

Substances

  • Ubiquitin
  • Lysine