In silico and in vivo models for Qatari-Specific classical homocystinuria as basis for development of novel therapies.
Author | Ismail, Hesham M |
Author | Krishnamoorthy, Navaneethakrishnan |
Author | Al-Dewik, Nader |
Author | Zayed, Hatem |
Author | Mohamed, Nura A |
Author | Giacomo, Valeria Di |
Author | Gupta, Sapna |
Author | Häberle, Johannes |
Author | Thöny, Beat |
Author | Blom, Henk J |
Author | Kruger, Waren D |
Author | Ben-Omran, Tawfeg |
Author | Nasrallah, Gheyath K |
Available date | 2018-11-14T11:38:12Z |
Publication Date | 2018-11-01 |
Publication Name | Human Mutation |
Identifier | http://dx.doi.org/10.1002/humu.23682 |
Citation | Ismail, H. M., Krishnamoorthy, N. , Al‐Dewik, N. , Zayed, H. , Mohamed, N. A., Giacomo, V. D., Gupta, S. , Häberle, J. , Thöny, B. , Blom, H. J., Kruger, W. D., Ben‐Omran, T. and Nasrallah, G. K. (2018), In silico and in vivo models for Qatari‐Specific classical homocystinuria as basis for development of novel therapies. Human Mutation. Accepted Author Manuscript. . doi:10.1002/humu.23682 |
ISSN | 1059-7794 |
Abstract | Homocystinuria is a rare inborn error of methionine metabolism caused by cystathionine β-synthase (CBS) deficiency. The prevalence of homocystinuria in Qatar is 1:1,800 births, mainly due to a founder Qatari missense mutation, c.1006C>T; p.R336C (p.Arg336Cys). We characterized the structure-function relationship of the p.R336C mutant protein, and investigated the effect of different chemical chaperones to restore p.R336C-CBS activity using three models: In silico, ΔCBS yeast, and CRISPR/Cas9 p.R336C knock-in HEK293T and HepG2 cell lines. Protein modeling suggested that the p.R336C induces severe conformational and structural changes, perhaps influencing CBS activity. Wildtype CBS, but not the p.R336C mutant, was able to restore the yeast growth in ΔCBS deficient yeast in a complementation assay. The p.R336C knock-in HEK293T and HepG2 cells decreased the level of CBS expression and reduce its structural stability; however, treatment of the p.R336C knock-in HEK293T cells with betaine, a chemical chaperone, restored the stability and tetrameric conformation of CBS, but not its activity. Collectively, these results indicate that the p.R336C mutation has a deleterious effect on CBS structure, stability, and activity, and using the chemical chaperones approach for treatment could be ineffective in restoring p.R336C CBS activity. This article is protected by copyright. All rights reserved. |
Sponsor | QNRF |
Language | en |
Publisher | Wiley |
Subject | CBS Homocystinuria Qatar chemical chaperones in silico in vivo models p.R336C mutation |
Type | Article |
ESSN | 1098-1004 |
Files in this item
Files | Size | Format | View |
---|---|---|---|
There are no files associated with this item. |
This item appears in the following Collection(s)
-
Biomedical Sciences [692 items ]