Tandem Mass Spectrometry of Sphingolipids: Applications for Diagnosis of Sphingolipidoses
Language English Country United States Media print-electronic
Document type Journal Article, Review
PubMed
27717417
DOI
10.1016/bs.acc.2016.06.004
PII: S0065-2423(16)30038-5
Knihovny.cz E-resources
- Keywords
- Deacylated sphingolipids, Electrospray ionization, Enzymology, Lysosomal storage disorders, Sphingolipidoses, Sphingolipids, Tandem mass spectrometry,
- MeSH
- Humans MeSH
- Sphingolipidoses diagnosis MeSH
- Sphingolipids analysis chemistry physiology MeSH
- Tandem Mass Spectrometry methods MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Names of Substances
- Sphingolipids MeSH
In recent years, mass spectrometry (MS) has become the dominant technology in lipidomic analysis. It is widely used in diagnosis and research of lipid metabolism disorders including those characterized by impairment of lysosomal functions and storage of nondegraded-degraded substrates. These rare diseases, which include sphingolipidoses, have severe and often fatal clinical consequences. Modern MS methods have contributed significantly to achieve a definitive diagnosis, which is essential in clinical practice to begin properly targeted patient care. Here we summarize MS and tandem MS methods used for qualitative and quantitative analysis of sphingolipids (SL) relative to the diagnostic process for sphingolipidoses and studies focusing on alterations in cell functions due to these disorders. This review covers the following topics: Tandem MS is sensitive and robust in determining the composition of sphingolipid classes in various biological materials. Its ability to establish SL metabolomic profiles using MS bench-top analyzers, significantly benefits the first stages of a diagnosis as well as metabolic studies of these disorders. It can thus contribute to a better understanding of the biological significance of SL.
References provided by Crossref.org
Misprocessing of α -Galactosidase A, Endoplasmic Reticulum Stress, and the Unfolded Protein Response