Development of sandwich enzyme-linked immunosorbent assay systems for plasma β-galactoside α2,6-sialyltransferase, a possible hepatic disease biomarker
Autor: | Yasuhiro Hashimoto, Kazuko Ogawa, Satoshi Futakawa, Yoshiaki Hagiwara, Ritsuko Oka, Akinori Kinoshita, Shinobu Kitazume, Kazuya Miyashita |
---|---|
Rok vydání: | 2009 |
Předmět: |
Male
Sialyltransferase Molecular Sequence Data Enzyme-Linked Immunosorbent Assay CCL4 Sensitivity and Specificity Biochemistry Antibodies Analytical Chemistry Mice chemistry.chemical_compound medicine Animals Humans Environmental Chemistry Amino Acid Sequence beta-D-Galactoside alpha 2-6-Sialyltransferase Spectroscopy Alanine Liver injury chemistry.chemical_classification biology Chemistry Liver Diseases medicine.disease Galactoside Molecular biology Sialyltransferases Rats Enzyme Solubility biology.protein Carbon tetrachloride Biomarker (medicine) Biomarkers Blood Chemical Analysis |
Zdroj: | Analytica Chimica Acta. 631:116-120 |
ISSN: | 0003-2670 |
Popis: | Previous reports, including our work, have shown that plasma beta-galactoside alpha2,6-sialyltransferase (ST6Gal I) activity is significantly increased in particular hepatopathological situations, suggesting that it may represent a sensitive biomarker for diagnosing hepatic diseases. So far, activity of ST6Gal I have been measured by using radioactive tracer method in place of measuring amount of ST6Gal I. However, this method is tangled and cannot exclude other sialyltransferase activities. Thus, simple and specific methods for measuring plasma ST6Gal I had been unavailable. Here, we developed two kinds of sandwich enzyme-linked immunosorbent assay (ELISA) systems that specifically detect the soluble cleaved form of ST6Gal I in plasma. In one sandwich ELISA, we detected rat specific sequence, EFQMPK, which is N-terminus of soluble ST6Gal I. In the other sandwich ELISA, we detected internal common sequence among rat, mouse and human ST6Gal I in plasma (M2 ELISA). Using the M2 ELISA, we observed that elevation of plasma ST6Gal I was much faster than elevation of plasma aspartate aminotransferase (AST) and alanine aminotransferase (ALT) in a carbon tetrachloride (CCl(4))-induced mouse liver injury model. Our data suggest that these ELISA systems are very useful tools for measuring plasma ST6Gal I, which represents a potential biomarker for diagnosing hepatic diseases. |
Databáze: | OpenAIRE |
Externí odkaz: |