| 摘要 |
Specific polypeptides are prepared by expression of a heterologous gene coding for them in a recombinant microbial cloning vehicle. The gene is arraged to be in reading phase with a DNA sequence coding for another polypeptide so that when the DNA is expressed a precursor protein is produced comprising both the desired polypeptide and the additional polypeptide, there being a cleavage site between them where the precursor protein may subsequently be cleaved. Plasmids or cloning vehicles containing this type of DNA sequence may be used to transform bacterial cultures in particular to enable the bacteria to produce an immunogenic substance comprising a polyeptide hapten, the DNA sequence coding for the hapten and an additional protein sufficient in size to confer immunogenicity on the product of expression and enable antibodies to be raised to it. Alternatively, the bacteria may be enabled to produce a desired polypeptide product e.g. somatostatin linked to additional protein from which the desired product may be cleaved. |
