4.8 Article

Oligopeptides functionalized surface plasmon resonance biosensors for detecting thiacloprid and imidacloprid

Journal

BIOSENSORS & BIOELECTRONICS
Volume 35, Issue 1, Pages 271-276

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2012.02.060

Keywords

SPR; Biosensor; Phage display; Peptide receptor; Neonicotinoid

Funding

  1. National University of Singapore

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By using phage display library, we identified two highly specific oligopeptide sequences RKRIRRMMPRPS and RNRHTHLRTRPR for binding neonicotinoids such as thiacloprid and imidacloprid. The former shows high affinity for thiacloprid whereas the latter shows high affinity for imidacloprid. Surprisingly, cross binding is minimal despite the similarity of the two molecules. To develop a neonicotinoid biosensor, these two oligopeptides are synthesized and immobilized on the surface of a surface plasmon resonance (SPR) chip with a bare-gold surface. This oligopeptide functionalized SPR biosensor can rapidly detect thiacloprid and imidacloprid in buffer solutions in a real-time manner. The limit of detection (LOD) for thiacloprid and imidacloprid is 1.2 mu M and 0.9 mu M. respectively. (C) 2012 Elsevier B.V. All rights reserved.

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