Expression of human interferon in transgenic chloroplasts
AssigneeUniversity of Central Florida
InventorHenry Daniell
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AssigneeUniversity of Central Florida
InventorHenry Daniell
Estimating the term…
A plastid transformation vector for a stably transforming a plastid genome is provided. The vector includes, as operably-linked components, a first flanking sequence, a DNA sequence coding for a therapeutic human IFN, which is capable of expression in the plastid and a second flanking sequence. The invention also provides isolated and purified IFN, wherein the IFN is configured in a monomeric or multimeric form and is a structural equivalent to orally administered human IFN. Also provided are methods for variable-expressing biopharmaceutical proteins in plants suitable for mammal consumption. The method includes integrating a plastid transformation vector into a plastid genome of a plant cell; growing the plant cell to express a biopharmaceutical protein, such as therapeutic human interferon IFN. Also disclosed are plants transformed with the aforementioned vectors, and the progeny thereof. Also, disclosed is the IFN, which is IFNα2b.
A plastid transformation vector for stably transforming a plastid, comprising, as operably-linked components, a first flanking sequence, a DNA sequence coding for a therapeutic human interferon (1N), which is capable of expression in a plastid, and a second flanking sequence.
An isolated and purified IFN, competent to produce and immunogenic response in a mammal.
An orally administerable therapeutic human interferon IFN, suitable for oral administration to a mammal.
A method of producing a biopharmaceutical protein of interest in a low-nicotine tobacco plant comprising:
A plastid transformation vector for a stably transforming a plastid genome, comprising, as operably-linked components, a first flanking sequence, a DNA sequence coding for a therapeutic human interferon IFN or a substantially homologous DNA sequence of therapeutic human interferon IFN, wherein the therapeutic human interferon IFN is operably linked to a polyhistidine purification tag and a thrombin cleavage site, and a second flanking sequence.
Dependencies are inferred from the claim text.