The construction and expression of deletion mutant of human pro-urokinase cDNA

Chin J Biotechnol. 1997;13(2):71-7.

Abstract

The human pro-urokinase mutant deleting 150-156 amino acids was constructed by overlap-extension PCR and other molecular cloning techniques. The mutant was expressed transiently in COS-7 cells and constitutively in CHO cells; the expression level is 450-500 IU/10(6) cells/24 h. SDS-PAGE and Western blotting analysis showed that the molecular weight of the expression product is 54 kDa, which is similar to that of the mature pro-UK and recombinant pro-UK (rPro-UK) expressed by full-length cDNA. Most of the products exist in the form of single chain; the percentage of single chain is much higher than that of rPro-UK. In addition, the mutant product is more resistant to proteinases and its affinity to fibrin is also improved slightly.

MeSH terms

  • Animals
  • CHO Cells
  • COS Cells
  • Cloning, Molecular
  • Cricetinae
  • DNA, Complementary
  • Gene Expression*
  • Humans
  • Plasmids
  • Protein Precursors / analysis
  • Protein Precursors / genetics*
  • Recombinant Fusion Proteins / analysis
  • Recombinant Fusion Proteins / genetics
  • Sequence Deletion
  • Urokinase-Type Plasminogen Activator / analysis
  • Urokinase-Type Plasminogen Activator / genetics*

Substances

  • DNA, Complementary
  • Protein Precursors
  • Recombinant Fusion Proteins
  • Urokinase-Type Plasminogen Activator