Immunological heterogeneity of hepatic alanine:glyoxylate aminotransferase in primary hyperoxaluria type 1

FEBS Lett. 1987 Sep 28;222(1):17-20. doi: 10.1016/0014-5793(87)80183-7.

Abstract

Immunoblotting of human liver sonicates, after SDS-polyacrylamide gel electrophoresis, demonstrated the presence of a 40 kDa protein, corresponding to the subunit of alanine:glyoxylate aminotransferase, in six controls and three patients with primary hyperoxaluria type 1 (peroxisomal alanine:glyoxylate aminotransferase deficiency). This immunoreactive 40 kDa protein was absent in a further nine patients. Subcellular fractionation of patients' livers showed that the 40 kDa protein, when present, was located mainly in the peroxisomes. In a heterozygote liver, the 40 kDa protein was also mainly peroxisomal and paralleled the distribution of alanine:glyoxylate aminotransferase activity.

MeSH terms

  • Alanine Transaminase / genetics*
  • Alanine Transaminase / immunology
  • Epitopes / analysis
  • Genetic Carrier Screening
  • Homozygote
  • Humans
  • Hyperoxaluria / enzymology*
  • Hyperoxaluria, Primary / enzymology*
  • Hyperoxaluria, Primary / genetics
  • Liver / enzymology*
  • Macromolecular Substances
  • Subcellular Fractions / enzymology
  • Transaminases*

Substances

  • Epitopes
  • Macromolecular Substances
  • Transaminases
  • Alanine Transaminase
  • Alanine-glyoxylate transaminase