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Application of a proteolysis/mass spectrometry method for investigating the effects of inhibitors on hydroxylase structure.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2009 May 14; Vol. 52 (9), pp. 2799-805. - Publication Year :
- 2009
-
Abstract
- Limited proteolysis coupled to matrix-assisted laser desorption/ionization (MALDI) mass spectrometric analyses can be used to screen for compounds that alter protein structure by monitoring stabilizing/destabilizing effects with respect to the rate and nature of proteolysis. When applied to prolyl hydroxylase 2, a key enzyme involved in human oxygen sensing, the method efficiently revealed differential effects on proteolytic stability for structurally similar compounds and for different substrates.
- Subjects :
- Animals
Catalytic Domain drug effects
Enzyme Inhibitors metabolism
Humans
Hypoxia-Inducible Factor 1, alpha Subunit chemistry
Hypoxia-Inducible Factor 1, alpha Subunit metabolism
Inhibitory Concentration 50
Mixed Function Oxygenases antagonists & inhibitors
Models, Molecular
Peptide Fragments metabolism
Protein Stability drug effects
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Enzyme Inhibitors pharmacology
Mixed Function Oxygenases chemistry
Mixed Function Oxygenases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 52
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 19364117
- Full Text :
- https://doi.org/10.1021/jm900285r