Ion mobility-mass spectrometry and orthogonal gas-phase techniques to study amyloid formation and inhibition

Curr Opin Struct Biol. 2017 Oct:46:7-15. doi: 10.1016/j.sbi.2017.03.002. Epub 2017 Mar 23.

Abstract

Amyloidogenic peptide oligomers are responsible for a variety of neurodegenerative disorders such as Alzheimer's and Parkinson's disease. Due to their dynamic, polydisperse, and polymorphic nature, these oligomers are very challenging to characterize using traditional condensed-phase methods. In the last decade, ion mobility-mass spectrometry (IM-MS) and related gas-phase techniques have emerged as a powerful alternative to disentangle the structure and assembly characteristics of amyloid forming systems. This review highlights recent advances in which IM-MS was used to characterize amyloid oligomers and their underlying assembly pathway. In addition, we summarize recent studies in which IM-MS was used to size- and mass-select species for a further spectroscopic investigation and outline the potential of IM-MS as a tool for the screening of amyloid inhibitors.

Publication types

  • Review

MeSH terms

  • Amyloid / chemistry*
  • Drug Discovery
  • Gases / chemistry*
  • Humans
  • Mass Spectrometry / methods*
  • Protein Aggregates / drug effects
  • Protein Multimerization / drug effects

Substances

  • Amyloid
  • Gases
  • Protein Aggregates