Abstract
Heterogeneities in the density of hepatitis C virus (HCV)-RNA-carrying material from human sera (1.03-1.20 g/ml) are partially due to the binding of lipoproteins [low density (LDL), very low density (VLDL), high density (HDL) lipoproteins] and immunoglobulins. In this study we demonstrate the binding of recombinant HCV envelope protein (El/E2) to human LDL, VLDL and HDL on a molecular basis. The binding of lipoproteins was restricted to the middle part of the El gene product (amino acids 222-336) and the C-terminal part of the E2 protein (amino acids 523-809). Lipoproteins did not bind to recombinant HCV core protein.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Baculoviridae
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Genetic Vectors
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Hepacivirus / genetics
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Hepacivirus / metabolism*
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Humans
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Lipoproteins, HDL / metabolism*
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Lipoproteins, LDL / metabolism*
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Lipoproteins, VLDL / metabolism*
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Protein Binding
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Rabbits
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Recombinant Fusion Proteins / genetics
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Recombinant Fusion Proteins / metabolism
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Reticulocytes / metabolism
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Viral Envelope Proteins / genetics
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Viral Envelope Proteins / metabolism*
Substances
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E1 protein, Hepatitis C virus
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Lipoproteins, HDL
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Lipoproteins, LDL
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Lipoproteins, VLDL
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Recombinant Fusion Proteins
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Viral Envelope Proteins
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glycoprotein E2, Hepatitis C virus