Charge reversal by salt-induced aggregation in aqueous lactoferrin solutions.

We have observed salt-induced aggregation in lactoferrin solutions using dynamic light scattering (DLS). Aggregates start to form once the ionic strength exceeds 10 mM, and are of opposite charge to their monomer building blocks. The presence of aggregates was monitored by electrophoretic measurements, in which the change of isoelectric point in lactoferrin solutions was observed and found to depend on the concentration of background electrolyte. Complimentary atomic force microscopy (AFM) imaging of adsorbed lactoferrin films demonstrated that for negatively charged surfaces (mica, glass) the topography of the adsorbed film remains invariant to changes in ionic strength, whilst for positively charged surfaces (chitosan coated mica) we observed a salt-induced transition in deposited architecture, with approximately 100 nm aggregates being deposited together with monomers for ionic strengths in excess of 10 mM. The size of aggregates observed with AFM is consistent with those observed using DLS. These results suggest that negatively charged lactoferrin aggregates adsorb only onto positively charged surfaces, whereas isolated lactoferrin molecules are sufficiently amphiphilic and adsorb at surfaces of either charge, although without producing a charge inversion effect.

[1]  D. Choudhury,et al.  Tertiary structural changes associated with iron binding and release in hen serum transferrin: a crystallographic and spectroscopic study. , 2004, Biochemical and biophysical research communications.

[2]  T. Waigh,et al.  Molecular structure and rheological properties of short-side-chain heavily glycosylated porcine stomach mucin. , 2007, Biomacromolecules.

[3]  S. Provencher,et al.  Global Analysis of Dynamic Light Scattering Autocorrelation Functions , 1996 .

[4]  J. Ramsden Puzzles and paradoxes in protein adsorption , 1995 .

[5]  C. Groom,et al.  Three-dimensional structure of diferric bovine lactoferrin at 2.8 A resolution. , 1997, Journal of molecular biology.

[6]  Liang Hong,et al.  Clusters of amphiphilic colloidal spheres. , 2008, Langmuir : the ACS journal of surfaces and colloids.

[7]  J. Steijns,et al.  Occurrence, structure, biochemical properties and technological characteristics of lactoferrin , 2000, British Journal of Nutrition.

[8]  D. Mcclements Protein-stabilized emulsions , 2004 .

[9]  B. Lönnerdal,et al.  Lactoferrin: molecular structure and biological function. , 1995, Annual review of nutrition.

[10]  M. Britten,et al.  Heat-induced aggregation of bovine lactoferrin at neutral pH: Effect of iron saturation , 2007 .

[11]  M. Field,et al.  A computational study of the open and closed forms of the N-lobe human serum transferrin apoprotein. , 2003, Biophysical journal.

[12]  T. Ishii,et al.  Small-angle neutron scattering and dynamic light scattering studies of N- and C-terminal fragments of ovotransferrin. , 1998, Biochimica et biophysica acta.

[13]  O. Svensson,et al.  The salivary mucin MUC5B and lactoperoxidase can be used for layer-by-layer film formation. , 2007, Journal of colloid and interface science.

[14]  B. Ninham,et al.  pH-dependent interactions between adsorbed chitosan layers , 1992 .

[15]  Ariel Fernández,et al.  On adsorption-induced denaturation of folded proteins. , 2001 .

[16]  J. Mcghee,et al.  A bactericidal effect for human lactoferrin. , 1977, Science.

[17]  E. De Clercq,et al.  Antiviral effects of plasma and milk proteins: lactoferrin shows potent activity against both human immunodeficiency virus and human cytomegalovirus replication in vitro. , 1995, The Journal of infectious diseases.

[18]  J. Lu,et al.  Surface-induced unfolding of human lactoferrin. , 2005, Langmuir : the ACS journal of surfaces and colloids.

[19]  V. Martorana,et al.  Irreversible gelation of thermally unfolded proteins: structural and mechanical properties of lysozyme aggregates , 2010, European Biophysics Journal.

[20]  T. Waigh,et al.  Charge and interfacial behavior of short side-chain heavily glycosylated porcine stomach mucin. , 2007, Biomacromolecules.

[21]  T. Auletta,et al.  Mucin-chitosan complexes at the solid-liquid interface: multilayer formation and stability in surfactant solutions. , 2005, Langmuir : the ACS journal of surfaces and colloids.

[22]  V. Trusova,et al.  Electrostatically-controlled protein adsorption onto lipid bilayer: modeling adsorbate aggregation behavior. , 2008, Biophysical chemistry.

[23]  O. Svensson,et al.  Layer-by-layer assembly of mucin and chitosan--Influence of surface properties, concentration and type of mucin. , 2006, Journal of colloid and interface science.

[24]  M. Wahlgren,et al.  The Adsorption from Solutions of β-Lactoglobulin Mixed with Lactoferrin or Lysozyme onto Silica and Methylated Silica Surfaces , 1993 .

[25]  Richard C. Willson,et al.  Protein Adsorption Kinetics Drastically Altered by Repositioning a Single Charge , 1995 .

[26]  J. Ramsden,et al.  Effect of Ionic Strength on Protein Adsorption Kinetics , 1994 .

[27]  M. Viljoen,et al.  Lactoferrin: a general review. , 1995, Haematologica.

[28]  P. Pellegrino,et al.  Size dependence of refractive index of Si nanoclusters embedded in SiO2 , 2005 .

[29]  D. Mcclements,et al.  Formation, stability and properties of multilayer emulsions for application in the food industry. , 2006, Advances in colloid and interface science.