4.7 Article

Mechanism of immunoglobulin G adsorption on polystyrene microspheres

Journal

COLLOIDS AND SURFACES B-BIOINTERFACES
Volume 137, Issue -, Pages 183-190

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.colsurfb.2015.07.037

Keywords

AFM measurements of IgG adsorption; IgG adsorption on polystyrene particles; Electrophoretic mobility of IgG covered polystyrene particles; Monolayers of IgG on polystyrene particles; Stability of IgG monolayers on polystyrene particles; Zeta potential of IgG covered polystyrene particles

Funding

  1. project Interdisciplinary PhD Studies Molecular sciences for medicine (European Social Fund within Human Capital Operational Programme)
  2. NCN GRANT [UMO-2012/07/B/ST4/00559]

Ask authors/readers for more resources

The adsorption of polyclonal immunoglobulin G (IgG) on negatively charged polystyrene microparticle suspension (latex) was studied by using the Laser Doppler Velocimetry (LDV) measurements. Using this technique, the dependence of the electrophoretic mobility of particles on the IgG concentration in the suspension was measured for various ionic strengths and pH 3.5. The increase in the electrophoretic mobility was quantitatively interpreted in terms of the 3D electrokinetic model. On the other hand, the maximum coverage of IgG on latex was determined using the depletion method based on AFM imaging. It was shown that IgG adsorption was irreversible and that its maximum coverage on the microspheres increased from 1.4 mg m(-2) for 0.001 M NaCl to 2.0 mg m(-2) for 0.15 M NaCl. This was interpreted in terms of reduced electrostatic repulsion among adsorbed molecules. The stability of IgG monolayers on the particles was confirmed in separate experiments where changes in its electrophoretic mobility were monitored over prolonged time periods. Additionally, the acid-base properties of the IgG monolayers on latex were determined in pH cycling experiments. The isoelectric point of the IgG monolayers on the microspheres was 4.8. The results obtained in this work indicate that basic physicochemical characteristics of IgG can be acquired via electrophoretic mobility measurements using microgram quantities of the protein. (C) 2015 Elsevier B.V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available