Electron-microscopic and hydrodynamic characterization of recombinant apolipoprotein (a) and its association with LDL

Chem Phys Lipids. 1994 Jan:67-68:91-7. doi: 10.1016/0009-3084(94)90127-9.

Abstract

A recombinant apo(a) containing 17 kringle 4 domains as well as the kringle 5 and protease domains of apo(a) was characterized by hydrodynamic studies and electron microscopy. Recombinant apo(a) is a monomer in solution with a molecular weight of 325,000 by sedimentation equilibrium and 320,000 by sedimentation and diffusion, and it is a highly asymmetric molecule with a frictional ratio of 2.2. In the electron microscope recombinant apo(a) is visualized as a flexible chain of domains approximately 800 A long. Sedimentation velocity studies also demonstrate that when it is mixed with LDL, recombinant apo(a) reversibly forms an Lp(a)-like complex with a 1:1 stoichiometry; moreover, complex formation is inhibited by 6-amino hexanoic acid. Hydrodynamic modeling and electron microscopy suggest that only a small portion of the r-apo(a) molecule interacts with the LDL and the rest of the chain extends into solution. Preliminary studies indicate that recombinant apo(a) also binds mouse LDL.

MeSH terms

  • Animals
  • Apolipoproteins / chemistry
  • Apolipoproteins / metabolism*
  • Apolipoproteins / ultrastructure*
  • Apoprotein(a)
  • Humans
  • In Vitro Techniques
  • Kringles
  • Lipoprotein(a)*
  • Lipoproteins, LDL / metabolism*
  • Mice
  • Microscopy, Electron
  • Molecular Weight
  • Protein Binding
  • Protein Conformation
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • Recombinant Proteins / ultrastructure
  • Solutions
  • Ultracentrifugation

Substances

  • Apolipoproteins
  • Lipoprotein(a)
  • Lipoproteins, LDL
  • Recombinant Proteins
  • Solutions
  • Apoprotein(a)