Literature DB >> 27112153

Substrate and Substrate-Mimetic Chaperone Binding Sites in Human α-Galactosidase A Revealed by Affinity-Mass Spectrometry.

Adrian Moise1,2, Stefan Maeser1, Stephan Rawer3, Frederike Eggers2, Mary Murphy4, Jeff Bornheim4, Michael Przybylski5,6.   

Abstract

Fabry disease (FD) is a rare metabolic disorder of a group of lysosomal storage diseases, caused by deficiency or reduced activity of the enzyme α-galactosidase. Human α-galactosidase A (hαGAL) hydrolyses the terminal α-galactosyl moiety from glycosphingolipids, predominantly globotriaosylceramide (Gb3). Enzyme deficiency leads to incomplete or blocked breakdown and progressive accumulation of Gb3, with detrimental effects on normal organ functions. FD is successfully treated by enzyme replacement therapy (ERT) with purified recombinant hαGAL. An emerging treatment strategy, pharmacologic chaperone therapy (PCT), employs small molecules that can increase and/or reconstitute the activity of lysosomal enzyme trafficking by stabilizing misfolded isoforms. One such chaperone, 1-deoxygalactonojirimycin (DGJ), is a structural galactose analogue currently validated in clinical trials. DGJ is an active-site-chaperone that binds at the same or similar location as galactose; however, the molecular determination of chaperone binding sites in lysosomal enzymes represents a considerable challenge. Here we report the identification of the galactose and DGJ binding sites in recombinant α-galactosidase through a new affinity-mass spectrometry-based approach that employs selective proteolytic digestion of the enzyme-galactose or -inhibitor complex. Binding site peptides identified by mass spectrometry, [39-49], [83-100], and [141-168], contain the essential ligand-contacting amino acids, in agreement with the known X-ray crystal structures. The inhibitory effect of DGJ on galactose recognition was directly characterized through competitive binding experiments and mass spectrometry. The methods successfully employed in this study should have high potential for the characterization of (mutated) enzyme-substrate and -chaperone interactions, and for identifying chaperones without inhibitory effects. Graphical Abstract ᅟ.

Entities:  

Keywords:  Affinity-mass spectrometry; Binding sites; Chaperones; Fabry disease; Human α-galactosidase; Proteolytic extraction

Mesh:

Substances:

Year:  2016        PMID: 27112153     DOI: 10.1007/s13361-016-1386-0

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  24 in total

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Journal:  Arch Pediatr       Date:  2011-08-27       Impact factor: 1.180

Review 2.  Agalsidase alfa--a preparation for enzyme replacement therapy in Anderson-Fabry disease.

Authors:  Michael Beck
Journal:  Expert Opin Investig Drugs       Date:  2002-06       Impact factor: 6.206

Review 3.  Fabry disease: recent advances in enzyme replacement therapy.

Authors:  Dominique P Germain
Journal:  Expert Opin Investig Drugs       Date:  2002-10       Impact factor: 6.206

4.  Epitope structure of the carbohydrate recognition domain of asialoglycoprotein receptor to a monoclonal antibody revealed by high-resolution proteolytic excision mass spectrometry.

Authors:  Raluca Stefanescu; Rita Born; Adrian Moise; Beat Ernst; Michael Przybylski
Journal:  J Am Soc Mass Spectrom       Date:  2011-01-20       Impact factor: 3.109

Review 5.  Treatment of lysosomal storage diseases: recent patents and future strategies.

Authors:  Saida Ortolano; Irene Viéitez; Carmen Navarro; Carlos Spuch
Journal:  Recent Pat Endocr Metab Immune Drug Discov       Date:  2014-01

6.  The pharmacological chaperone 1-deoxygalactonojirimycin reduces tissue globotriaosylceramide levels in a mouse model of Fabry disease.

Authors:  Richie Khanna; Rebecca Soska; Yi Lun; Jessie Feng; Michelle Frascella; Brandy Young; Nastry Brignol; Lee Pellegrino; Sheela A Sitaraman; Robert J Desnick; Elfrida R Benjamin; David J Lockhart; Kenneth J Valenzano
Journal:  Mol Ther       Date:  2009-09-22       Impact factor: 11.454

7.  Human alpha-galactosidase A: glycosylation site 3 is essential for enzyme solubility.

Authors:  Y A Ioannou; K M Zeidner; M E Grace; R J Desnick
Journal:  Biochem J       Date:  1998-06-15       Impact factor: 3.857

Review 8.  Enzyme replacement and enhancement therapies for lysosomal diseases.

Authors:  R J Desnick
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

Review 9.  Treating lysosomal storage diseases with pharmacological chaperones: from concept to clinics.

Authors:  Giancarlo Parenti
Journal:  EMBO Mol Med       Date:  2009-08       Impact factor: 12.137

10.  Ambroxol as a pharmacological chaperone for mutant glucocerebrosidase.

Authors:  Inna Bendikov-Bar; Gali Maor; Mirella Filocamo; Mia Horowitz
Journal:  Blood Cells Mol Dis       Date:  2012-11-14       Impact factor: 3.039

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  2 in total

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Authors:  Nithya Selvan; Nickita Mehta; Suresh Venkateswaran; Nastry Brignol; Matthew Graziano; M Osman Sheikh; Yuliya McAnany; Finn Hung; Matthew Madrid; Renee Krampetz; Nicholas Siano; Anuj Mehta; Jon Brudvig; Russell Gotschall; Jill M Weimer; Hung V Do
Journal:  J Biol Chem       Date:  2021-05-07       Impact factor: 5.157

Review 2.  Identification and Affinity Determination of Protein-Antibody and Protein-Aptamer Epitopes by Biosensor-Mass Spectrometry Combination.

Authors:  Loredana-Mirela Lupu; Pascal Wiegand; Daria Holdschick; Delia Mihoc; Stefan Maeser; Stephan Rawer; Friedemann Völklein; Ebrahim Malek; Frederik Barka; Sascha Knauer; Christina Uth; Julia Hennermann; Wolfgang Kleinekofort; Andreas Hahn; Günes Barka; Michael Przybylski
Journal:  Int J Mol Sci       Date:  2021-11-27       Impact factor: 5.923

  2 in total

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