Universidad de Granada Digibug

Repositorio Institucional de la Universidad de Granada >
1.-Investigación >
Departamentos, Grupos de Investigación e Institutos >
Departamento de Química Física >
DQF - Artículos >

Please use this identifier to cite or link to this item: http://hdl.handle.net/10481/42968

Title: Experimental and computational evidence on conformational fluctuations as a source of catalytic defects in genetic diseases
Authors: Fuchs, Julian E.
Muñoz, Inés G.
Timson, David J.
Pey, Ángel L.
Issue Date: 2016
Abstract: Theoretical and experimental evidence has shown that protein function, regulation and degradation are intrinsically linked to the dynamic and fluctuating nature of protein ensembles. However, the effect of missense mutations on catalytic performance are often interpreted from conformational analyses derived from X-ray crystallography, molecular dynamics and modeling, while effects on conformational fluctuations at the active site as the source of catalytic defects are rarely investigated. Here, we explore the role of conformational fluctuations in the catalytic efficiency of WT and three missense mutations in the UDP-galactose 4′-epimerase (GALE) protein causing type III galactosemia. Using comprehensive molecular dynamics simulations and small angle X-ray scattering we correlate low NAD+ binding affinity in some mutants with an increased population of non-competent conformations for NAD+ binding. Proteolysis studies combined with thermodynamic calculations reveal that mutations affecting GALE catalytic performance favor larger conformational fluctuations at the N-terminal domain and NAD+ binding site, shifting the equilibrium towards non-binding competent states in the native ensemble. Therefore, we provide a novel ensemble-based thermodynamic mechanism to explain catalytic defects caused by missense mutations that links large and transient conformational fluctuations and loss of catalytic efficiency and substrate/coenzyme affinity. In the context of this mechanism, we propose that allosteric ligands aimed at modulating these transient conformational fluctuations might correct catalytic defects in inherited metabolic diseases, representing a different approach to current small ligand therapies which target the low stability, but not catalytic defects, of mutations.
Sponsorship: This work was supported by grants from MINECO (BIO2015-66426-R, CSD2009-00088) and Junta de Andaluc´ıa (P11-CTS-07187). A. L. P. was supported by a Ram´on y Cajal research contract from MINECO/University of Granada (RYC-2009-04147).
Publisher: Royal Society of Chemistry
Keywords: Genetic diseases
Conformational fluctuations
Inherited metabolic diseases
URI: http://hdl.handle.net/10481/42968
ISSN: 2046-2069
Rights : Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License
Citation: Fuchs, J.E.; Muñoz, I.G.; Timson, D.J.; Pey, A.L. Experimental and computational evidence on conformational fluctuations as a source of catalytic defects in genetic diseases. RSC Advances, 6: 58604-58612 (2016). [http://hdl.handle.net/10481/42968]
Appears in Collections:DQF - Artículos

Files in This Item:

File Description SizeFormat
Fuchs_CatalyticDefects.pdf1.43 MBAdobe PDFView/Open
Recommend this item

This item is licensed under a Creative Commons License
Creative Commons

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.


Valid XHTML 1.0! OpenAire compliant DSpace Software Copyright © 2002-2007 MIT and Hewlett-Packard - Feedback

© Universidad de Granada