Abstract
A plasmid vector was used to express the HIV-1 pol open reading frame under the regulation of the bacterial trp promoter in Escherichia coli. This expression system has been used as a source of recombinant viral protease. The self-processed active enzyme was recovered from a soluble fraction of a bacterial cell lysate and purified by a procedure involving four steps of chromatography. The protocol yielded 0.3 mg of protease for each liter of bacterial culture. The protease formed tetragonal bipyramidal crystals which have been used in high-resolution X-ray diffraction studies.
MeSH terms
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Acquired Immunodeficiency Syndrome / immunology
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Amino Acid Sequence
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Base Sequence
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Blotting, Western
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Chromatography
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Crystallization
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Electrophoresis, Polyacrylamide Gel
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Endopeptidases / genetics*
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Endopeptidases / isolation & purification
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Escherichia coli / genetics*
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Gene Expression*
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Genes, Viral / genetics*
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HIV Protease
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HIV-1 / enzymology*
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HIV-1 / genetics
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Humans
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Molecular Sequence Data
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Plasmids
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Promoter Regions, Genetic / genetics
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Recombinant Proteins / genetics
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Recombinant Proteins / isolation & purification
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Transformation, Bacterial
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X-Ray Diffraction
Substances
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Recombinant Proteins
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Endopeptidases
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HIV Protease