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      Analysis of recombinant protein expression using localized surface plasmon resonance (LSPR).

      Biosensors & Bioelectronics
      Cloning, Molecular, Escherichia coli, Gold, Humans, Interleukin-6, analysis, biosynthesis, genetics, Recombinant Proteins, Surface Plasmon Resonance

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          Abstract

          The localized surface plasmon resonance (LSPR)-based optical biosensor using nano-structures of noble metals has been considered as a useful tool for label-free detection of DNA hybridization and protein-protein interactions. We fabricated LSPR-based optical biosensors using gold nano-islands (nominal thickness; 75 A) on glass substrates that were easily made using the conventional fabrication methods. The formation of gold nano-islands on glass substrates was realized by heat treatment of thin gold film deposited with a low deposition rate (approximately 0.05 A/s). The morphologies of sensor surfaces composed of gold nano-islands were observed using an atomic force microscope (AFM) with a non-contact mode. To investigate the sensing capacity of the gold nano-island sensor for the binding of proteins by affinity interactions, the streptavidin and biotin interaction was used as a model system. In addition, detection of recombinant glutathione-S-transferase (GST)-tagged human interleukin-6 (hIL6) expressed in Escherichia coli was carried out by LSPR. It is expected that the LSPR sensors composed of gold nano-islands can be an alternative to traditional methods such as SDS-polyacrylamide gel electrophoresis (SDS-PAGE) for fast analysis of protein expression.

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          Author and article information

          Journal
          17261365
          10.1016/j.bios.2006.12.028

          Chemistry
          Cloning, Molecular,Escherichia coli,Gold,Humans,Interleukin-6,analysis,biosynthesis,genetics,Recombinant Proteins,Surface Plasmon Resonance

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