Internal ribosome-binding site directs expression of parathyroid hormone analogue (8–84) in Escherichia coli

Expression of the human parathyroid hormone (PTH) gene in E. coli yielded intact PTH and PTH-(8–84). To determine if PTH-(8–84) is the result of a competing translation initiated from methionine codon-8 or degradation of the intact PTH, twelve new gene constructs with or without an internal ribosome...

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Veröffentlicht in:Biochemical and biophysical research communications 1991-11, Vol.181 (1), p.481-485
Hauptverfasser: Sung, Wing L., Luk, Cathy K., Zahab, Diana M., Barbier, Jean R., Lafontaine, Marc, Willick, Gordon E.
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Sprache:eng
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Zusammenfassung:Expression of the human parathyroid hormone (PTH) gene in E. coli yielded intact PTH and PTH-(8–84). To determine if PTH-(8–84) is the result of a competing translation initiated from methionine codon-8 or degradation of the intact PTH, twelve new gene constructs with or without an internal ribosome-binding site (iRBS) in the PTH-(1–5) region were prepared via substitution with degenerate codons. Expression of constructs without iRBS produced only intact PTH. Constructs with weak iRBS, including one that resembles the cDNA sequence, yielded PTH-(8–84) as a minor product. In contrast, constructs with strong iRBS produced predominantly or exclusively this shorter analogue.
ISSN:0006-291X
1090-2104
DOI:10.1016/S0006-291X(05)81444-5