Kinetic and thermodynamic parameters for heat denaturation of human recombinant lactoferrin from rice

Biochem Cell Biol. 2012 Jun;90(3):389-96. doi: 10.1139/o11-073. Epub 2012 Feb 14.

Abstract

Heat denaturation of recombinant human lactoferrin (rhLf) from rice with 3 different iron-saturation degrees, holo rhLf (iron-saturated), AsIs rhLf (60% iron saturation), and apo rhLf (iron-depleted), was studied. The 3 forms of rhLf were subjected to heat treatment, and the kinetic and thermodynamic parameters of the denaturation process were determined. Thermal denaturation of rhLf was assessed by measuring the loss of reactivity against specific antibodies. D(t) values (time to reduce 90% of immunoreactivity) decreased with increasing temperature of treatment for apo and holo rhLf, those values being higher for the iron-saturated form, which indicates that iron confers thermal stability to rhLf. However, AsIs rhLf showed a different behaviour with an increase in resistance to heat between 79 °C and 84 °C, so that the kinetic parameters could not be calculated. The heat denaturation process for apo and holo rhLf was best described assuming a reaction order of 1.5. The activation energy of the denaturation process was 648.20 kJ/mol for holo rhLf and 406.94 kJ/mol for apo rhLf, confirming that iron-depleted rhLf is more sensitive to heat treatment than iron-saturated rhLf.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies / chemistry
  • Hot Temperature
  • Humans
  • Iron / chemistry
  • Kinetics
  • Lactoferrin / biosynthesis
  • Lactoferrin / chemistry*
  • Oryza / genetics
  • Oryza / metabolism
  • Plants, Genetically Modified
  • Protein Binding
  • Protein Denaturation*
  • Protein Stability
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / chemistry
  • Thermodynamics

Substances

  • Antibodies
  • Recombinant Proteins
  • Iron
  • Lactoferrin