Disruption of interkringle disulfide bond of plasminogen kringle 1-3 changes the lysine binding capability of kringle 2, but not its antiangiogenic activity

Arch Biochem Biophys. 2000 Mar 15;375(2):359-63. doi: 10.1006/abbi.1999.1675.

Abstract

Kringle 1-3 of human plasminogen is a potent inhibitor of endothelial cell proliferation. To understand a possible role for the unique cystine bridge between kringle 2 and kringle 3, we disrupted the interkringle disulfide bond by mutating Cys(169) and Cys(297) to serine residues. The yield of the mutant during the refolding process was decreased significantly. Anti-endothelial cell proliferative activity of the mutant was similar to that of the wild type. There was no significant difference in in vivo antiangiogenic activity between the wild type and the mutant in chorioallantoic membrane assay. However, in the mutant, the weak lysine binding capability of kringle 2 was not detected and its mobility in nonreducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis is different from that of the wild type. These results support the notion that the overall antiangiogenic function of angiostatin is mediated by individual kringles, and suggest that the lysine binding capability of kringle 2 is likely not important for the antiangiogenic activity of kringle 1-3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution / genetics
  • Angiogenesis Inhibitors / chemistry
  • Angiogenesis Inhibitors / genetics
  • Angiogenesis Inhibitors / metabolism
  • Angiogenesis Inhibitors / pharmacology
  • Animals
  • Cattle
  • Cell Division / drug effects
  • Chick Embryo
  • Chorion / cytology
  • Chorion / drug effects
  • Chorion / physiology
  • Cysteine / genetics
  • Cysteine / metabolism
  • Disulfides / metabolism*
  • Electrophoresis, Polyacrylamide Gel
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / physiology
  • Humans
  • Kringles / genetics
  • Kringles / physiology*
  • Ligands
  • Lysine / metabolism*
  • Mutation / genetics
  • Neovascularization, Physiologic* / drug effects
  • Plasminogen / chemistry*
  • Plasminogen / genetics
  • Plasminogen / metabolism*
  • Plasminogen / pharmacology
  • Protein Binding
  • Protein Folding
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Recombinant Proteins / pharmacology
  • Thermodynamics

Substances

  • Angiogenesis Inhibitors
  • Disulfides
  • Ligands
  • Recombinant Proteins
  • Plasminogen
  • Lysine
  • Cysteine