Structure of acid β-glucosidase with pharmacological chaperone provides insight into Gaucher disease-Reference-Cited by-同舟云学术

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Structure of acid β-glucosidase with pharmacological chaperone provides insight into Gaucher disease

Published:2006-12-24 Issue:2 Volume:3 Page:101-107
ISSN:1552-4450
Container-title:Nature Chemical Biology
language:en
Short-container-title:Nat Chem Biol

Author:

Lieberman Raquel L,Wustman Brandon A,Huertas Pedro,Powe Allan C,Pine Corey W,Khanna Richie,Schlossmacher Michael G,Ringe Dagmar,Petsko Gregory A

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology

Link

http://www.nature.com/articles/nchembio850.pdf

Reference30 articles.

1. Sawkar, A.R., D'Haeze, W. & Kelly, J.W. Therapeutic strategies to ameliorate lysosomal storage disorders–a focus on Gaucher disease. Cell. Mol. Life Sci. 63, 1179–1192 (2006).

2. Fan, J.Q. A contradictory treatment for lysosomal storage disorders: inhibitors enhance mutant enzyme activity. Trends Pharmacol. Sci. 24, 355–360 (2003).

3. Grace, M.E., Newman, K.M., Scheinker, V., Berg-Fussman, A. & Grabowski, G.A. Analysis of human acid beta-glucosidase by site-directed mutagenesis and heterologous expression. J. Biol. Chem. 269, 2283–2291 (1994).

4. Butters, T.D., Dwek, R.A. & Platt, F.M. Imino sugar inhibitors for treating the lysosomal glycosphingolipidoses. Glycobiology 15, 43R–52R (2005).

5. Beutler, E. & Gelbart, T. Glucocerebrosidase (Gaucher disease). Hum. Mutat. 8, 207–213 (1996).

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