Isofagomine induced stabilization of glucocerebrosidase
| Autor: | Steven J. Tuske, Yoshitomo Hamuro, G. Kornhaber, Don J. Mahuran, Gustavo Maegawa, Stephen J. Coales, Michael B. Tropak |
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| Rok vydání: | 2008 |
| Předmět: |
endocrine system diseases
Stereochemistry Mutant Molecular Sequence Data Iminosugar medicine.disease_cause Biochemistry Mass Spectrometry Article Cell Line Protein structure Catalytic Domain Enzyme Stability medicine Humans Fluorometry Amino Acid Sequence Molecular Biology Mutation biology Chemistry Organic Chemistry Active site nutritional and metabolic diseases Deuterium Exchange Measurement Fibroblasts Pharmacological chaperone biology.protein Molecular Medicine Glucosylceramidase Hydrogen–deuterium exchange Lysosomes Glucocerebrosidase medicine.drug Imino Pyranoses |
| Zdroj: | Chembiochem : a European journal of chemical biology. 9(16) |
| ISSN: | 1439-7633 |
| Popis: | Structurally destabilizing mutations in acid beta-glucosidase (GCase) can result in Gaucher disease (GD). The iminosugar isofagomine (IFG), a competitive inhibitor and a potential pharmacological chaperone of GCase, is currently undergoing clinical evaluation for the treatment of GD. An X-ray crystallographic study of the GCase-IFG complex revealed a hydrogen bonding network between IFG and certain active site residues. It was suggested that this network may translate into greater global stability. Here it is demonstrated that IFG does increase the global stability of wild-type GCase, shifting its melting curve by approximately 15 degrees C and that it enhances mutant GCase activity in pre-treated N370S/N370S and F213I/L444P patient fibroblasts. Additionally, amide hydrogen/deuterium exchange mass spectroscopy (H/D-Ex) was employed to identify regions within GCase that undergo stabilization upon IFG-binding. H/D-Ex data indicate that the binding of IFG not only restricts the local protein dynamics of the active site, but also propagates this effect into surrounding regions. |
| Databáze: | OpenAIRE |
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