4.8 Article

A virus-based nanoplasmonic structure as a surface-enhanced Raman biosensor

Journal

BIOSENSORS & BIOELECTRONICS
Volume 77, Issue -, Pages 306-314

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2015.09.032

Keywords

Virus-like particles; Cowpea mosaic virus; Raman; SERS; Gold nanoparticles; Self-assembly

Funding

  1. US Office of Naval Research
  2. UK Biotechnology and Biological Sciences Research Council (BBSRC) [BB/I002294/1, BB/J004561/1]
  3. John Innes Foundation
  4. Biotechnology and Biological Sciences Research Council [BB/L014130/1, BB/I002294/1, BBS/E/J/00000166, BB/L020955/1] Funding Source: researchfish
  5. BBSRC [BB/I002294/1, BB/L020955/1, BB/L014130/1] Funding Source: UKRI

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Fabrication of nanoscale structures with localized surface plasmons allows for substantial increase in sensitivity of chem/bio sensors. The main challenge for realizing complex nanoplasmonic structures in solution is the high level of precision required at the nanoscale to position metal nanoparticles in 3D. In this study, we report a virus-like particle (VLP) for building a 3D plasmonic nanostructure in solution in which gold nanoparticles are precisely positioned on the VLP by directed self-assembly techniques. These structures allow for concentration of electromagnetic fields in the desired locations between the gold nanoparticles or hot spots. We measure the efficiency of the optical field spatial concentration for the first time, which results in a ten-fold enhancement of the capsid Raman peaks. Our experimental results agree with our 3D finite element simulations. Furthermore, we demonstrate as a proof-of-principle that the plasmonic nanostructures can be utilized in DNA detection down to 0.25 ng/mu l (lowest concentration tested), while the protein peaks from the interior of the nanoplasmonic structures, potentially, can serve as an internal tracer for the biosensors. Published by Elsevier B.V.

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