| Literature DB >> 27746032 |
Francyne Kubaski1, Harumi Osago2, Robert W Mason1, Seiji Yamaguchi3, Hironori Kobayashi3, Mikako Tsuchiya4, Tadao Orii5, Shunji Tomatsu6.
Abstract
Glycosaminoglycans (GAGs) are long blocks of negatively charged polysaccharides. They are one of the major components of the extracellular matrix and play multiple roles in different tissues and organs. The accumulation of undegraded GAGs causes mucopolysaccharidoses (MPS). GAGs are associated with other pathological conditions such as osteoarthritis, inflammation, diabetes mellitus, spinal cord injury, and cancer. The need for further understanding of GAG functions and mechanisms of action boosted the development of qualitative and quantitative (alcian blue, toluidine blue, paper and thin layer chromatography, gas chromatography, high pressure liquid chromatography, capillary electrophoresis, 1,9-dimethylmethylene blue, enzyme linked-immunosorbent assay, mass spectrometry) techniques. The availability of quantitative techniques has facilitated translational research on GAGs into the medical field for: 1) diagnosis, monitoring, and screening for MPS; 2) analysis of GAG synthetic and degradation pathways; and 3) determination of physiological and pathological roles of GAGs. This review provides a history of development of GAG assays and insights about the use of tandem mass spectrometry and its applications for GAG analysis.Entities:
Keywords: Alcian blue; Chromatography, mucopolysaccharidoses; ELISA; Glycosaminoglycans; Mass spectrometry
Mesh:
Substances:
Year: 2016 PMID: 27746032 PMCID: PMC5477676 DOI: 10.1016/j.ymgme.2016.09.005
Source DB: PubMed Journal: Mol Genet Metab ISSN: 1096-7192 Impact factor: 4.797