Protein-bound polyphenols create "ghost" band artifacts during chemiluminescence-based antigen detection.
Nathalie PlundrichMary Ann LilaEdward FoegedingPublished in: F1000Research (2017)
Antigen detection during Western blotting commonly utilizes a horseradish peroxidase-coupled secondary antibody and enhanced chemiluminescent substrate. We utilized this technique to examine the impact of green tea-derived polyphenols on the binding of egg white protein-specific IgE antibodies from allergic human plasma to their cognate antigens. Our experiments unexpectedly showed that green tea-derived polyphenols, when stably complexed with egg white proteins, caused "ghost" band formation in the presence of horseradish peroxide. This study suggests that caution should be taken when evaluating polyphenol-bound proteins by enhanced chemiluminescence Western blotting using horseradish peroxidase and demonstrates that protein-bound polyphenols can be a source of "ghost" band artifacts on Western blots.
Keyphrases
- south africa
- protein protein
- binding protein
- amino acid
- loop mediated isothermal amplification
- label free
- computed tomography
- real time pcr
- magnetic resonance
- small molecule
- mass spectrometry
- oxidative stress
- nitric oxide
- transcription factor
- high resolution
- heat shock
- atopic dermatitis
- cone beam
- contrast enhanced
- allergic rhinitis