VOPROSY MEDITSINSKOI KHIMII (ISSN 0042-8809)

Analysis of molecular microheterogeneity of the glycoproteins from plasma of a patient with syalidosis

   
Zakharova E.T., Puchkova L.V., Shavlovsky M.M., Neuimina M.V., Rujdi E.P., Gaitskhoki V.S.
PubMed Id: 9575619
Year: 1998  Volume: 44  Issue: 1  Pages: 98-105
Using specific polyclonal monovalent antibodies, the molecular microheterogeneity of acute phase proteins: orosomucoid, alpha1-antitrypsin and ceruloplasmin, circulating in peripheral blood of a healthy donor and a patient with a hereditary deficiency of lysosomal neuraminidase (syalidosis I or the cherry stone syndrome), was analyzed by use of 2D electrophoresis. The specific distinctions due to a deficiency [caused by a deficiency] of lysosomal neuraminidase were revealed in the population of ceruloplasmin molecules, but not in the molecules of alpha1-antitrypsin and orosomucoid (alpha 1-acid glycoprotein). The molecular genetic bases of molecular microheterogeneity of some plasma glycoproteins and the possible use of natural models in studies of GP's functional role and the pathways of its transfer after internalization into non-hepatocytic (?) cells are discussed.
Download PDF:  
Keywords: glycoproteins, sialidosis 1, ceruloplasmin, acid alpha 1-glycoprotein, alpha1-antitrypsin
Citation:

Zakharova, E. T., Puchkova, L. V., Shavlovsky, M. M., Neuimina, M. V., Rujdi, E. P., Gaitskhoki, V. S. (1998). Analysis of molecular microheterogeneity of the glycoproteins from plasma of a patient with syalidosis. Voprosy Meditsinskoi Khimii, 44(1), 98-105.
References  
 2002 (vol 48)
 2001 (vol 47)
 2000 (vol 46)
 1999 (vol 45)
 1998 (vol 44)
 1997 (vol 43)
 1996 (vol 42)
 1995 (vol 41)
 1994 (vol 40)
 1993 (vol 39)
 1992 (vol 38)
 1991 (vol 37)
 1990 (vol 36)
 1989 (vol 35)
 1988 (vol 34)
 1987 (vol 33)
 1986 (vol 32)
 1985 (vol 31)