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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/23119
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DC FieldValueLanguage
dc.contributor.advisorGraham, F. L.-
dc.contributor.authorWaye, John-
dc.date.accessioned2018-06-21T14:19:01Z-
dc.date.available2018-06-21T14:19:01Z-
dc.date.issued1983-12-
dc.identifier.urihttp://hdl.handle.net/11375/23119-
dc.description.abstractThe Ad5 E1B antigens of MW 58000 and 19000 are known to be involved in oncogenic transformation of mammalian cells. To obtain sufficient quantities of these proteins for biochemical studies on their mechanism of action, I have attempted to express the Ad5 E1B genes in Escherichia coli. Using the strategy developed by Guarente et al. (1980), I have constructed plasmids which have the trancriptional and translational controls of the E. coli lac operon linked 5' of the 19k and 58k coding sequences. One plasmid was shown to synthesize high levels of a stable, immunoreactive 19k analogue consisting of 19k with 29 adenovirus-coded ribosome-binding sequence is functional in directing translation of this protein. Synthesis of 58k was not demonstrated, perhaps the result of [protein instability in E. coli. However, immunoreactive proteins which may correspond to the amino terminal region of 58k were demonstrated.en_US
dc.language.isoenen_US
dc.subjecte. colien_US
dc.subjecttumoren_US
dc.subjectantigensen_US
dc.subjectadenovirusen_US
dc.titleExpression of Adenovirus Type-5 E1B Tumor Antigens in Escherichia Colien_US
dc.title.alternativeExpression of Adenovirus Tumor Antigens in E. Colien_US
dc.typeThesisen_US
dc.contributor.departmentBiologyen_US
dc.description.degreetypeThesisen_US
dc.description.degreeMaster of Science (MS)en_US
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