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Glycan-based biomarkers for mucopolysaccharidoses.
Lawrence, Roger; Brown, Jillian R; Lorey, Fred; Dickson, Patricia I; Crawford, Brett E; Esko, Jeffrey D.
Affiliation
  • Lawrence R; Department of Cellular and Molecular Medicine, Glycobiology Research and Training Center, University of California San Diego, La Jolla, CA 92093, USA.
  • Brown JR; Zacharon Pharmaceuticals, Inc., San Diego, CA 92121, USA.
  • Lorey F; Genetic Disease Screening Program, California Department of Public Health, Richmond, CA 94804, USA.
  • Dickson PI; Department of Pediatrics, Los Angeles Biomedical Research Institute at Harbor-UCLA, Torrance, CA 90502, USA.
  • Crawford BE; Zacharon Pharmaceuticals, Inc., San Diego, CA 92121, USA. Electronic address: bcrawford@bmrn.com.
  • Esko JD; Department of Cellular and Molecular Medicine, Glycobiology Research and Training Center, University of California San Diego, La Jolla, CA 92093, USA. Electronic address: jesko@ucsd.edu.
Mol Genet Metab ; 111(2): 73-83, 2014 Feb.
Article in En | MEDLINE | ID: mdl-23958290
The mucopolysaccharidoses (MPS) result from attenuation or loss of enzyme activities required for lysosomal degradation of the glycosaminoglycans, hyaluronan, heparan sulfate, chondroitin/dermatan sulfate, and keratan sulfate. This review provides a summary of glycan biomarkers that have been used to characterize animal models of MPS, for diagnosis of patients, and for monitoring therapy based on hematopoietic stem cell transplantation and enzyme replacement therapy. Recent advances have focused on the non-reducing terminus of the glycosaminoglycans that accumulate as biomarkers, using a combination of enzymatic digestion with bacterial enzymes followed by quantitative liquid chromatography/mass spectrometry. These new methods provide a simple, rapid diagnostic strategy that can be applied to samples of urine, blood, cerebrospinal fluid, cultured cells and dried blood spots from newborn infants. Analysis of the non-reducing end glycans provides a method for monitoring enzyme replacement and substrate reduction therapies and serves as a discovery tool for uncovering novel biomarkers and new forms of mucopolysaccharidoses.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mucopolysaccharidoses / Glycosaminoglycans Type of study: Prognostic_studies Limits: Animals / Humans / Newborn Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2014 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mucopolysaccharidoses / Glycosaminoglycans Type of study: Prognostic_studies Limits: Animals / Humans / Newborn Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2014 Document type: Article Affiliation country: United States Country of publication: United States