Abstract
The cancer-testis antigen, NY-ESO-1, has been engineered into a bacterial expression plasmid which incorporates a His6-tag. The plasmid was transfected into E. coli strain BL21 and Master and Working cell banks generated from this expression system. Three 15-litre fermentations were performed under cGMP (code of Good Manufacturing Practice) conditions and the crude NY-ESO-1 tagged protein isolated as solubilised inclusion bodies. A three-step cGMP chromatography process (immobilised metal affinity, anion exchange, and hydrophobic interaction) was utilised to purify the protein. The purified NY-ESO-1 is being used in early stage human cancer vaccine trials in Australia and the U.S.A.
MeSH terms
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Antigens, Neoplasm / biosynthesis*
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Antigens, Neoplasm / genetics
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Antigens, Neoplasm / isolation & purification*
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Antigens, Neoplasm / therapeutic use
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Australia
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Cancer Vaccines / biosynthesis*
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Cancer Vaccines / genetics
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Cancer Vaccines / isolation & purification*
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Drug Industry / standards
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Guidelines as Topic
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Humans
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Membrane Proteins / biosynthesis*
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Membrane Proteins / genetics
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Membrane Proteins / isolation & purification*
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Membrane Proteins / therapeutic use
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Protein Engineering / methods*
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Protein Engineering / standards
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Quality Assurance, Health Care / standards
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Recombinant Proteins / biosynthesis
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Recombinant Proteins / isolation & purification
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Reference Standards
Substances
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Antigens, Neoplasm
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CTAG1B protein, human
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Cancer Vaccines
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Membrane Proteins
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Recombinant Proteins