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Protein determination by the method based on bicinchoninic acid use in liquids from cultures of filamentous fungi

100%

Czakaj J., Wiacek-Zychlinska A., Sawicka-Zukowska R.

Polish Journal of Food and Nutrition Sciences

1992

tom 01

nr 4

The 35 kDa acid metallophosphatase of the frog Rana esculenta liver: studies on its cellular localization and protein phosphatase activity

100%

Szalewicz A., Strzelczyk B., Sopel M., Kubicz A.

Acta Biochimica Polonica

2003

tom 50

nr 2

The cellular localization of the 35 kDa, low molecular mass acid metallophosphatase (LMW AcPase) from the frog (Rana esculenta) liver and its activity towards P-Ser and P-Tyr phosphorylated peptides were studied. This enzyme was localized to the cytoplasm of hepatocytes but did not appear in other cells of liver tissue (endothelium, macrophages, blood cells). This LMW AcPase does not display activity towards 32P-phosphorylase a under conditions standard for the enzymes of PPP family. Proteins containing P-Ser: rabbit 32P-phosphorylase a and phosvitin are hydrolysed only at acidic pH and are poor substrates for this enzyme. The frog AcPase is not inhibited by okadaic acid and F- ions, the Ser/Thr protein phosphatase inhibitors. Moreover, the frog enzyme does not cross-react with specific antisera directed against N-terminal fragment of human PP2A and C-terminal conserved fragment of the eukaryotic PP2A catalytic subunits. These results exclude LMW AcPase from belonging to Ser/Thr protein phosphatases: PP1c or PP2Ac. In addition to P-Tyr, this enzyme hydrolyses efficiently at acidic pH P-Tyr phosphorylated peptides (hirudin and gastrin fragments). Km value for the hirudin fragment (7.55 ± 1.59 10–6M) is 2–3 orders of magnitude lower in comparison with other substrates tested. The enzyme is inhibited competitively by typical inhibitors of protein tyrosine phosphatases (PTPases): sodium orthovanadate, molybdate and tungstate. These results may suggest that the LMW AcPase of frog liver can act as PTPase in vivo. A different cellular localization and different response to inhibition by tetrahedral oxyanions (molybdate, vanadate and tungstate) provide further evidence that LMW AcPase of frog liver is distinct from the mammalian tartrate-resistant acid phosphatases.

Ograniczanie wyników

1 Acta Biochimica Polonica

1 Polish Journal of Food and Nutrition Sciences

1 Czakaj J.

1 Kubicz A.

1 Sawicka-Zukowska R.

1 Sopel M.

1 Strzelczyk B.

1 Szalewicz A.

1 Wiacek-Zychlinska A.

1 2003

1 1992

Wyniki wyszukiwania

Protein determination by the method based on bicinchoninic acid use in liquids from cultures of filamentous fungi

The 35 kDa acid metallophosphatase of the frog Rana esculenta liver: studies on its cellular localization and protein phosphatase activity