Cosecretion of protease inhibitor stabilizes antibodies produced by plant roots

Plant Physiol. 2006 Aug;141(4):1185-93. doi: 10.1104/pp.105.074419.

Abstract

A plant-based system for continuous production of monoclonal antibodies based on the secretion of immunoglobulin complexes from plant roots into a hydroponic medium (rhizosecretion) was engineered to produce high levels of single-chain and full-size immunoglobulins. Replacing the original signal peptides of monoclonal antibodies with a plant-derived calreticulin signal increased the levels of antibody yield 2-fold. Cosecretion of Bowman-Birk Ser protease inhibitor reduced degradation of the immunoglobulin complexes in the default secretion pathway and further increased antibody production to 36.4 microg/g root dry weight per day for single-chain IgG1 and 21.8 microg/g root dry weight per day for full-size IgG4 antibodies. These results suggest that constitutive cosecretion of a protease inhibitor combined with the use of the plant signal peptide and the antibiotic marker-free transformation system offers a novel strategy to achieve high yields of complex therapeutic proteins secreted from plant roots.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / biosynthesis*
  • Antibodies, Monoclonal / genetics
  • Antibodies, Monoclonal / metabolism
  • Calreticulin / metabolism
  • Culture Media
  • Humans
  • Hydroponics
  • Immunoglobulin G / biosynthesis
  • Nicotiana / genetics
  • Plant Roots / metabolism*
  • Plants, Genetically Modified / metabolism
  • Protein Engineering / methods
  • Recombinant Proteins / biosynthesis
  • Serine Proteinase Inhibitors / genetics
  • Serine Proteinase Inhibitors / metabolism*
  • Trypsin Inhibitor, Bowman-Birk Soybean / genetics

Substances

  • Antibodies, Monoclonal
  • Calreticulin
  • Culture Media
  • Immunoglobulin G
  • Recombinant Proteins
  • Serine Proteinase Inhibitors
  • Trypsin Inhibitor, Bowman-Birk Soybean