Abstract |
Type III galactosemia is an inherited disease caused by mutations which affect the activity of UDP-galactose 4'-epimerase (GALE). We evaluated the impact of four disease-associated variants (p.N34S, p.G90E, p.V94M and p.K161N) on the conformational stability and dynamics of GALE. Thermal denaturation studies showed that wild-type GALE denatures at temperatures close to physiological, and disease-associated mutations often reduce GALE's thermal stability. This denaturation is under kinetic control and results partly from dimer dissociation. The natural ligands, NAD(+) and UDP-glucose, stabilize GALE. Proteolysis studies showed that the natural ligands and disease-associated variations affect local dynamics in the N-terminal region of GALE. Proteolysis kinetics followed a two-step irreversible model in which the intact protein is cleaved at Ala38 forming a long-lived intermediate in the first step. NAD(+) reduces the rate of the first step, increasing the amount of undigested protein whereas UDP-glucose reduces the rate of the second step, increasing accumulation of the intermediate. Disease-associated variants affect these rates and the amounts of protein in each state. Our results also suggest communication between domains in GALE. We hypothesize that, in vivo, concentrations of natural ligands modulate GALE stability and that it should be possible to discover compounds which mimic the stabilising effects of the natural ligands overcoming mutation-induced destabilization.
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Authors | Angel L Pey, Esperanza Padín-Gonzalez, Noel Mesa-Torres, David J Timson |
Journal | Archives of biochemistry and biophysics
(Arch Biochem Biophys)
Vol. 562
Pg. 103-14
(Nov 15 2014)
ISSN: 1096-0384 [Electronic] United States |
PMID | 25150110
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2014 Elsevier Inc. All rights reserved. |
Chemical References |
- Ligands
- Thermolysin
- UDPglucose 4-Epimerase
- Uridine Diphosphate Glucose
- Galactose
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Topics |
- Bacillus
(metabolism)
- Calorimetry
- Crystallography, X-Ray
- DNA Mutational Analysis
- Escherichia coli
(metabolism)
- Galactose
(chemistry)
- Galactosemias
(enzymology, genetics)
- Genetic Variation
- Humans
- Ligands
- Mutation
- Protein Binding
- Protein Structure, Tertiary
- Proteolysis
- Spectrophotometry
- Substrate Specificity
- Temperature
- Thermolysin
(chemistry)
- UDPglucose 4-Epimerase
(chemistry)
- Uridine Diphosphate Glucose
(chemistry)
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