Expression in Escherichia coli of synthetic human interleukin-1 alpha genes encoding the processed active protein, mutant proteins, and beta-galactosidase fusion proteins

Gene. 1986;49(1):61-8. doi: 10.1016/0378-1119(86)90385-9.

Abstract

We have synthesized, cloned, and expressed the coding region for the C-terminal 159 amino acids (aa) of the human active interleukin polypeptide hormone IL-1 alpha. The sequence was assembled in stages and includes preferred Escherichia coli codons and unique restriction sites. The coding region was cloned on a multicopy plasmid vector adjacent to signals for transcription and translation that directed synthesis of 6% of total E. coli protein as IL-1 alpha. Active IL-1 alpha mutants that have a C-terminal additional eleven aa and that have N-terminal deletions of six and fourteen aa are described. Plasmids expressing beta-galactosidase fusion proteins with various parts of IL-1 alpha at their N-termini were constructed.

MeSH terms

  • Base Sequence
  • Escherichia coli / enzymology
  • Escherichia coli / genetics*
  • Galactosidases / genetics*
  • Genes*
  • Genes, Bacterial
  • Genes, Synthetic*
  • Humans
  • Interleukin-1 / genetics*
  • Mutation*
  • Protein Biosynthesis
  • Transcription, Genetic
  • beta-Galactosidase / genetics*

Substances

  • Interleukin-1
  • Galactosidases
  • beta-Galactosidase

Associated data

  • GENBANK/M15419