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  • lectin affinity chromatography  (1)
  • 1
    ISSN: 1573-4943
    Keywords: Apolipoprotein H ; β2-glycoprotein I ; lectin affinity chromatography ; glycosylation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The specific binding of digoxigenin-labeled lectins to carbohydrate moieties is used to characterize the carbohydrate chains bound to apolipoprotein H. Our results show that apolipoprotein H is rich in sialic acid linked α(2–6) to galactose or N-acetylgalactosamine. Sialic acid is not α(2–3)-linked to galactose. Galactose is β(1–4)-linked to N-acetylglucosamine and β(1–3)-linked to N-acetylgalactosamine. High-mannose N-glycan chains are barely detectable. After N-glycosidase F treatment the molecular weight is substantially reduced. The main band is 32,500 daltons. Carbohydrate O-linked chains, which are mainly represented by sialic acid, are α(2–6)-linked to galactose or N-acetylgalactosamine. Galactose is also organized in O-linked chains and it is β(1–4)-linked to N-acetylglucosamine and β(1–3)-linked to acetylgalactosamine. Biochemical analysis of carbohydrate structures reveals that no specific carbohydrate complex is bound to a single isoform.
    Type of Medium: Electronic Resource
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