Kinetic analysis of IgM monoclonal antibodies for determination of dengue sample concentration using SPR technique

Bioengineered. 2017 May 4;8(3):239-247. doi: 10.1080/21655979.2016.1223413. Epub 2016 Aug 17.

Abstract

Surface plasmon resonance (SPR) sensing is recently emerging as a valuable technique for measuring the binding constants, association and dissociation rate constants, and stoichimetry for a binding interaction kinetics in a number of emerging biological areas. This technique can be applied to the study of immune system diseases in order to contribute to improved understanding and evaluation of binding parameters for a variety of interactions between antigens and antibodies biochemically and clinically. Since the binding constants determination of an anti-protein dengue antibody (Ab) to a protein dengue antigen (Ag) is mostly complicated, the SPR technique aids a determination of binding parameters directly for a variety of particular dengue Ag_Ab interactions in the real-time. The study highlights the doctrine of real-time dengue Ag_Ab interaction kinetics as well as to determine the binding parameters that is performed with SPR technique. In addition, this article presents a precise prediction as a reference curve for determination of dengue sample concentration.

Keywords: biosensor; dengue virus; kinetic analysis; surface plasmon resonance.

MeSH terms

  • Antibodies, Monoclonal / analysis
  • Antibodies, Monoclonal / immunology*
  • Antigen-Antibody Reactions / immunology
  • Biosensing Techniques / instrumentation*
  • Biosensing Techniques / methods
  • Dengue Virus / immunology*
  • Equipment Design
  • Equipment Failure Analysis
  • Immunoassay / instrumentation*
  • Immunoassay / methods
  • Immunoglobulin M / analysis
  • Immunoglobulin M / immunology*
  • Kinetics
  • Protein Binding
  • Protein Interaction Mapping / instrumentation
  • Protein Interaction Mapping / methods
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Surface Plasmon Resonance / methods*

Substances

  • Antibodies, Monoclonal
  • Immunoglobulin M

Grants and funding

This work has been supported by National Science Foundation of China (No. 51435009), University of Malaya High Impact Research Grant UM.0000005/HIR.C1, and MOHE UM.C/625/1/HIR/H-20001-00-E000053.