Gold nanoparticle-based localized surface plasmon immunosensor for staphylococcal enterotoxin A (SEA) detection

被引:0
作者
Maroua Ben Haddada
David Hu
Michèle Salmain
Lu Zhang
Chen Peng
Yi Wang
Bo Liedberg
Souhir Boujday
机构
[1] Sorbonne Universités,UPMC Univ Paris 6, CNRS, Laboratoire de Réactivité de Surface (LRS)
[2] Sorbonne Universités,UPMC Univ Paris 06, CNRS, Institut Parisien de Chimie Moléculaire (IPCM)
[3] Nanyang Technological University,Centre for Biomimetic Sensor Science, School of Material Science and Engineering
[4] MajuLab,undefined
[5] UMI 3654,undefined
[6] CNRS-UNS-NUS-NTU International Joint Research Unit,undefined
来源
Analytical and Bioanalytical Chemistry | 2017年 / 409卷
关键词
Immunosensor; Localized surface plasmon resonance; Staphylococcal enterotoxin A; Gold nanoparticles;
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中图分类号
学科分类号
摘要
We describe the engineering of stable gold nanoparticle (AuNP) bioconjugates for the detection of staphylococcal enterotoxin A (SEA) using localized surface plasmon resonance (LSPR). Two types of AuNP bioconjugates were prepared by covalently attaching anti-SEA antibody (Ab) or SEA to AuNPs. This was achieved by reacting Traut’s reagent with lysine residues of both proteins to generate thiol groups that bind to gold atoms on the AuNP surface. These bioconjugates were characterized in-depth by absorption spectroscopy, cryo-transmission electron microscopy, dynamic light scattering, and zeta potential measurements. Their stability over time was assessed after 1 year storage in the refrigerator at 4 °C. Two formats of homogeneous binding assays were set up on the basis of monitoring of LSPR peak shifts resulting from the immunological reaction between the (i) immobilized antibody and free SEA, the direct assay, or (ii) immobilized SEA and free antibody, the competitive assay. In both formats, a correlation between the LSPR band shift and SEA concentration could be established. Though the competitive format did not meet the expected analytical performance, the direct format, the implementation of which was very simple, afforded a specific and sensitive response within a broad dynamic range—nanogram per milliliter to microgram per milliliter. The limit of detection (LOD) of SEA was estimated to equal 5 ng/mL, which was substantially lower than the LOD obtained using a quartz crystal microbalance. Moreover, the analytical performance of AuNP-Ab bioconjugate was preserved after 1 year of storage at 4 °C. Finally, the LSPR biosensor was successfully applied to the detection of SEA in milk samples. The homogeneous nanoplasmonic immunosensor described herein provides an attractive alternative for stable and reliable detection of SEA in the nanogram per milliliter range and offers a promising avenue for rapid, easy to implement, and sensitive biotoxin detection.
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页码:6227 / 6234
页数:7
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