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Mass spectrometry in the detection and diagnosis of congenital disorders of
glycosylation Yoshinao Wada Osaka Medical Center and Research Institute for Maternal and Child Health, Department of Molecular Medicine. 840 Murodo-
cho, Izumi, Osaka 594-1101, Japan
ABSTRACT:
Mass spectrometry (MS) of large molecules such as proteins and oligosaccharides has not been employed in clinical practices, while
that of small metabolites is widely used for the screening and diagnosis of various congenital diseases. Congenital disorders of glycosylation (CDG) is a newly recognized group
of diseases derived from defects in the biosynthetic pathway of protein glycosylation and the patients are never decisively diagnosed unless the glycoprotein molecules are
analyzed. We have constructed a diagnostic system where MS of glycoproteins and glycopeptides identifies abnormalities in their glycan moieties. This program is anticipated to
reveal the prevalence of CDG and to demonstrate the essential role of MS in the emerging field of medicine, disease glycomics and glycoproteomics.
Keywords:
glycoproteins, congenital
disorders of glycosylation, glycomics, proteome
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