1981European Journal of BiochemistryOpen access

Cell‐Free Synthesis and Glycosylatlon of the Major Human‐Red‐Cell Sialoglycoprotein, Glycophorin A

MIKKO JOKINEN, Ismo Ulmanen, Leif Christer Andersson, Leevi Kääriäinen, Carl Gustav Gahmberg

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Abstract

The human erythroid cell line, K562, synthesizes the major red cell sialoglycoprotein, glycophorin A. We have isolated an mRNA fraction which codes for glycophorin A from K562 cells and studied the synthesis of the sialoglycoprotein in a rabbit reticulocyte cell-free system. In the absence of membranes a precursor form of glycophorin A was synthesized. This was identified using specific anti-(glycophorin A) serum. The apparent molecular weight of the carbohydrate-free precursor of glycophorin A was 19 500. This exceeds the molecular weight of the glycophorin A apoprotein by approximately 5000. In the presence of membranes from dog pancreas, the synthesized glycophorin A precursor was N-glycosylated and probably also O-glycosylated. The oligosaccharide chains remained incomplete and the glycoprotein synthesized in vitro corresponded to the glycosylated precursor of glycophorin A obtained in intact cells.

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The human erythroid cell line, K562, synthesizes the major red cell sialoglycoprotein, glycophorin A. We have isolated an mRNA fraction which codes for glycophorin A from K562 cells and studied the synthesis of the sialoglycoprotein in a rabbit reticulocyte cell-free system. In the absence of membranes a precursor form of glycophorin A was synthesized. This was identified using specific anti-(glycophorin A) serum. The apparent molecular weight of the carbohydrate-free precursor of glycophorin A was 19 500. This exceeds the molecular weight of the glycophorin A apoprotein by approximately 5000. In the presence of membranes from dog pancreas, the synthesized glycophorin A precursor was N-glycosylated and probably also O-glycosylated. The oligosaccharide chains remained incomplete and the glycoprotein synthesized in vitro corresponded to the glycosylated precursor of glycophorin A obtained in intact cells.

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Available abstract

The human erythroid cell line, K562, synthesizes the major red cell sialoglycoprotein, glycophorin A. We have isolated an mRNA fraction which codes for glycophorin A from K562 cells and studied the synthesis of the sialoglycoprotein in a rabbit reticulocyte cell-free system. In the absence of membranes a precursor form of glycophorin A was synthesized. This was identified using specific anti-(glycophorin A) serum. The apparent molecular weight of the carbohydrate-free precursor of glycophorin A was 19 500. This exceeds the molecular weight of the glycophorin A apoprotein by approximately 5000. In the presence of membranes from dog pancreas, the synthesized glycophorin A precursor was N-glycosylated and probably also O-glycosylated. The oligosaccharide chains remained incomplete and the glycoprotein synthesized in vitro corresponded to the glycosylated precursor of glycophorin A obtained in intact cells.

Key concepts: Glycophorin, Sialoglycoprotein, Sialoglycoproteins, Biochemistry, Molecular biology, Reticulocyte, Glycoprotein, In vitro

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