Literature DB >> 15924232

Fabry disease: correlation between structural changes in alpha-galactosidase, and clinical and biochemical phenotypes.

Fumiko Matsuzawa1, Sei-ichi Aikawa, Hirofumi Doi, Toshika Okumiya, Hitoshi Sakuraba.   

Abstract

Fabry disease comprises classic and variant phenotypes. The former needs early enzyme replacement therapy, and galactose infusion is effective for some variant cases. Attempts of early diagnosis before manifestations appear will begin in the near future. However, it is difficult to predict the phenotype, to determine the therapeutic approach, only from genetic information. Thus we attempted structural analysis from a novel viewpoint. We built structural models of mutant alpha-galactosidases resulting from 161 missense mutations (147 classic and 14 variant), and evaluated the influence of each replacement on the structure by calculating the numbers of atoms affected. Among them, 11 mutants, biochemically characterized, were further investigated by color imaging of the influenced atoms. In the variant group, the number of atoms influenced by amino-acid replacement was small, especially in the main chain. In 85% of the cases, less than three atoms in the main chain are influenced. In this group, small structural changes, located apart from the active site, result in destabilization of the mutant enzymes, but galactose can stabilize them. Structural changes caused by classic Fabry mutations are generally large or are located in functionally important regions. In 82% of the cases, three atoms or more in the main chain are affected. The classic group comprises dysfunctional and unstable types, and galactose is not expected to stabilize the mutant enzymes. This study demonstrated the correlation of structural changes, and clinical and biochemical phenotypes. Structural investigation is useful for elucidating the bases of Fabry disease and clinical treatment.

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Year:  2005        PMID: 15924232     DOI: 10.1007/s00439-005-1300-5

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  28 in total

1.  Improvement in cardiac function in the cardiac variant of Fabry's disease with galactose-infusion therapy.

Authors:  A Frustaci; C Chimenti; R Ricci; L Natale; M A Russo; M Pieroni; C M Eng; R J Desnick
Journal:  N Engl J Med       Date:  2001-07-05       Impact factor: 91.245

2.  Quantitative correlation between the residual activity of beta-hexosaminidase A and arylsulfatase A and the severity of the resulting lysosomal storage disease.

Authors:  P Leinekugel; S Michel; E Conzelmann; K Sandhoff
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

3.  Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease.

Authors:  C M Eng; N Guffon; W R Wilcox; D P Germain; P Lee; S Waldek; L Caplan; G E Linthorst; R J Desnick
Journal:  N Engl J Med       Date:  2001-07-05       Impact factor: 91.245

4.  A female heterozygous patient with Fabry's disease with renal accumulation of trihexosylceramide detected with a monoclonal antibody.

Authors:  M Fukushima; Y Tsuchiyama; T Nakato; T Yokoi; H Ikeda; S Yoshida; T Kusumoto; K Itoh; H Sakuraba
Journal:  Am J Kidney Dis       Date:  1995-12       Impact factor: 8.860

5.  Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry disease.

Authors:  G M Altarescu; L G Goldfarb; K Y Park; C Kaneski; N Jeffries; S Litvak; J W Nagle; R Schiffmann
Journal:  Clin Genet       Date:  2001-07       Impact factor: 4.438

6.  Molecular and structural studies of the GM2 gangliosidosis 0 variant.

Authors:  Hitoshi Sakuraba; Fumiko Matsuzawa; Sei-ichi Aikawa; Hirofumi Doi; Masaharu Kotani; Hou Lin; Kousaku Ohno; Akemi Tanaka; Hideo Yamada; Ei-ichiro Uyama
Journal:  J Hum Genet       Date:  2002       Impact factor: 3.172

7.  An atypical variant of Fabry's disease in men with left ventricular hypertrophy.

Authors:  S Nakao; T Takenaka; M Maeda; C Kodama; A Tanaka; M Tahara; A Yoshida; M Kuriyama; H Hayashibe; H Sakuraba
Journal:  N Engl J Med       Date:  1995-08-03       Impact factor: 91.245

8.  Galactose stabilizes various missense mutants of alpha-galactosidase in Fabry disease.

Authors:  T Okumiya; S Ishii; T Takenaka; R Kase; S Kamei; H Sakuraba; Y Suzuki
Journal:  Biochem Biophys Res Commun       Date:  1995-09-25       Impact factor: 3.575

9.  Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey.

Authors:  A Mehta; R Ricci; U Widmer; F Dehout; A Garcia de Lorenzo; C Kampmann; A Linhart; G Sunder-Plassmann; M Ries; M Beck
Journal:  Eur J Clin Invest       Date:  2004-03       Impact factor: 4.686

10.  Point mutation in the alpha-galactosidase A gene of atypical Fabry disease with only nephropathy.

Authors:  K Sawada; K Mizoguchi; A Hishida; E Kaneko; Y Koide; K Nishimura; M Kimura
Journal:  Clin Nephrol       Date:  1996-05       Impact factor: 0.975

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  18 in total

1.  α-Galactosidase aggregation is a determinant of pharmacological chaperone efficacy on Fabry disease mutants.

Authors:  Aleksandra Siekierska; Greet De Baets; Joke Reumers; Rodrigo Gallardo; Stanislav Rudyak; Kerensa Broersen; Jose Couceiro; Joost Van Durme; Joost Schymkowitz; Frederic Rousseau
Journal:  J Biol Chem       Date:  2012-07-06       Impact factor: 5.157

2.  Impact of cysteine variants on the structure, activity, and stability of recombinant human α-galactosidase A.

Authors:  Huawei Qiu; Denise M Honey; Jonathan S Kingsbury; Anna Park; Ekaterina Boudanova; Ronnie R Wei; Clark Q Pan; Tim Edmunds
Journal:  Protein Sci       Date:  2015-07-14       Impact factor: 6.725

3.  High incidence of later-onset fabry disease revealed by newborn screening.

Authors:  Marco Spada; Severo Pagliardini; Makiko Yasuda; Turgut Tukel; Geetha Thiagarajan; Hitoshi Sakuraba; Alberto Ponzone; Robert J Desnick
Journal:  Am J Hum Genet       Date:  2006-04-28       Impact factor: 11.025

4.  Functional analysis of variant lysosomal acid glycosidases of Anderson-Fabry and Pompe disease in a human embryonic kidney epithelial cell line (HEK 293 T).

Authors:  Hatim Y Ebrahim; Robert J Baker; Atul B Mehta; Derralynn A Hughes
Journal:  J Inherit Metab Dis       Date:  2011-10-05       Impact factor: 4.982

5.  ACE activity is modulated by the enzyme α-galactosidase A.

Authors:  Elice Carneiro Batista; Luiz Roberto Carvalho; Dulce Elena Casarini; Adriana Karaoglanovic Carmona; Edson Lucas dos Santos; Elton Dias da Silva; Robson Augusto dos Santos; Clovis Ryuichi Nakaie; Maria Verônica Munoz Rojas; Suzana Macedo de Oliveira; Michael Bader; Vânia D'Almeida; Ana Maria Martins; Kely de Picoly Souza; João Bosco Pesquero
Journal:  J Mol Med (Berl)       Date:  2010-10-13       Impact factor: 4.599

6.  Structural study on mutant alpha-L-iduronidases: insight into mucopolysaccharidosis type I.

Authors:  Kanako Sugawara; Seiji Saito; Kazuki Ohno; Torayuki Okuyama; Hitoshi Sakuraba
Journal:  J Hum Genet       Date:  2008-03-14       Impact factor: 3.172

7.  Effects of a chemical chaperone on genetic mutations in alpha-galactosidase A in Korean patients with Fabry disease.

Authors:  Jung Young Park; Gu Hwan Kim; Sung Su Kim; Jung Min Ko; Jin Joo Lee; Han Wook Yoo
Journal:  Exp Mol Med       Date:  2009-01-31       Impact factor: 8.718

8.  The pharmacological chaperone 1-deoxygalactonojirimycin increases alpha-galactosidase A levels in Fabry patient cell lines.

Authors:  E R Benjamin; J J Flanagan; A Schilling; H H Chang; L Agarwal; E Katz; X Wu; C Pine; B Wustman; R J Desnick; D J Lockhart; K J Valenzano
Journal:  J Inherit Metab Dis       Date:  2009-04-18       Impact factor: 4.982

9.  Structure-function relationships in alpha-galactosidase A.

Authors:  Scott C Garman
Journal:  Acta Paediatr       Date:  2007-04       Impact factor: 2.299

10.  Structural characterization of mutant alpha-galactosidases causing Fabry disease.

Authors:  Kanako Sugawara; Kazuki Ohno; Seiji Saito; Hitoshi Sakuraba
Journal:  J Hum Genet       Date:  2008-07-17       Impact factor: 3.172

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