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Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase.

Authors :
Dhamale OP
Lawrence R
Wiegmann EM
Shah BA
Al-Mafraji K
Lamanna WC
Lübke T
Dierks T
Boons GJ
Esko JD
Source :
ACS chemical biology [ACS Chem Biol] 2017 Feb 17; Vol. 12 (2), pp. 367-373. Date of Electronic Publication: 2017 Jan 17.
Publication Year :
2017

Abstract

The degradation of glycosaminoglycans (GAGs) involves a series of exolytic glycosidases and sulfatases that act sequentially on the nonreducing end of the polysaccharide chain. Enzymes have been cloned that catalyze all of the known linkages with the exception of the removal of the 2-O-sulfate group from 2-sulfoglucuronate, which is found in heparan sulfate and dermatan sulfate. Here, we show using synthetic disaccharide substrates that arylsulfatase K is the glucuronate-2-sulfatase. Arylsulfatase K acts selectively on 2-sulfoglucuronate and lacks activity against 2-sulfoiduronate, whereas iduronate-2-sulfatase (IDS) desulfates synthetic disaccharides containing 2-sulfoiduronate but not 2-sulfoglucuronate. As arylsulfatase K has all of the properties expected of a lysosomal enzyme, we conclude that arylsulfatase K is the long sought lysosomal glucuronate-2-sulfatase, which we designate GDS.

Details

Language :
English
ISSN :
1554-8937
Volume :
12
Issue :
2
Database :
MEDLINE
Journal :
ACS chemical biology
Publication Type :
Academic Journal
Accession number :
28055182
Full Text :
https://doi.org/10.1021/acschembio.6b01033