Proteomics

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Determination of highly accurate small molecule:protein affinity constants at amino acid resolution using Hydrogen Deuterium Exchange Mass Spectrometry (HDX-MS)


ABSTRACT: Hydrogen Deuterium Exchange Mass Spectrometry (HDX-MS) has been widely adopted as part of the drug development pipeline, frequently used in both the development of biopharmaceuticals and small molecule compound development to assess target engagement spatially. Frequently, HDX-MS analyses are conducted at saturating compound concentrations to produce a compound binding “footprint” where typically the reductions in solvent exchange associated with compound engagement can be interpreted as evidence of a localized hydrogen bond network disruption caused by a binding event. Here we present a workflow of compound titration in both HDX-MS and HDX-MS/MS workflows using ECD to determine compound dissociation constants at a global, peptide and single amino acid resolution. The ability to determine affinity constants in a spatially resolved manner using the automation available to HDX-MS sample production and data analysis is likely to have applications in drug discovery and medicinal chemistry.

INSTRUMENT(S):

ORGANISM(S): Plasmodium Falciparum 58.1

SUBMITTER: Glenn Masson  

LAB HEAD: Glenn Masson

PROVIDER: PXD070051 | Pride | 2026-04-01

REPOSITORIES: Pride

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Publications

Residue-Level Determination of Small-Molecule-Protein Affinities by Hydrogen-Deuterium Exchange Mass Spectrometry.

Lin De   Magalhaes Luma Godoy LG   McMillan Joel J   Eadsforth Thomas C TC   Stewart Greg G   Cartmill Kieran R KR   Postis Vincent L G VLG   Masson Glenn R GR  

Journal of the American Society for Mass Spectrometry 20260331


Hydrogen-Deuterium Exchange Mass Spectrometry (HDX-MS) is an established tool in drug discovery, used to characterize target engagement and conformational dynamics, and frequently used in both biopharmaceutical and small molecule drug discovery. Conventional HDX-MS experiments are performed at saturating ligand concentrations to generate a binding "footprint", where decreased solvent exchange reflects a local structural stabilization or reduced solvent accessibility upon binding. Here, we presen  ...[more]

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