ArticleThe journal of physical chemistry. C, Nanomaterials and interfaces2007
Metal-Enhanced Fluorescence of Phycobiliproteins from Heterogeneous Plasmonic Nanostructures.
Article in The journal of physical chemistry. C, Nanomaterials and interfaces, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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The trial behind it
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Who cites it
9 citing papers in PubMed, 50 citations in OpenAlex.
- Silver Nanoparticles Improve Fluorophore Photostability: Application to a Hypericin Study.International journal of molecular sciences · 2024Article
- Review: Applications of surface-enhanced fluorescence (SEF) spectroscopy in bio-detection and biosensing.Sensing and Bio-Sensing Research · 2020Review
- Silver Island Film for Enhancing Light Harvesting in Natural Photosynthetic Proteins.International journal of molecular sciences · 2020Review
- Strong antenna-enhanced fluorescence of a single light-harvesting complex shows photon antibunching.Nature communications · 2014Article
- Engineering of bacterial phytochromes for near-infrared imaging, sensing, and light-control in mammals.Chemical Society reviews · 2013Review
- Absorption Enhancement in Peridinin-Chlorophyll-Protein Light-Harvesting Complexes Coupled to Semicontinuous Silver Film.Plasmonics (Norwell, Mass.) · 2012Article
- Plasmon-controlled fluorescence towards high-sensitivity optical sensing.Advances in biochemical engineering/biotechnology · 2009Review
- Review
- Single-molecule spectroscopic study of enhanced intrinsic phycoerythrin fluorescence on silver nanostructured surfaces.Analytical chemistry · 2008Article
Corrections and comments
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Authors and funding
5 authors at 3 institutions in 1 country.
Funding
Abstract
We report here the use of plasmonic metal nanostructures in the form of silver island films (SiFs) to enhance the fluorescence emission of five different phycobiliproteins. Our findings clearly show that the phycobiliproteins display up to a 9-fold increase in fluorescence emission intensity, with a maximum 7-fold decrease in lifetime when they are assembled as a monolayer above SiFs, as compared to a monolayer assembled on the surface of amine-terminated glass slides of the control sample. The study was also repeated with a thin liquid layer of the phycobiliproteins sandwiched between two glass substrates (and a SiFs and a glass substrate) clamped together. Similarly, the results show a maximum 10-fold increase in fluorescence emission intensity coupled with a 2-fold decrease in lifetime of the phycobiliproteins in the SiF-glass setup as compared to the glass control sample, implying that near-field enhancement of phycobiliprotein emission can be attained both with and without chemical linkage of the proteins to the SiFs. Hence, our results clearly show that metal-enhanced fluorescence (MEF) can potentially be employed to increase the sensitivity and detection limit of the plethora of bioassays that employ phycobiliproteins as fluorescence labels, such as in fluoro-immunoassays where the assay can be tethered on the surface of SiFs, and also in flow cytometry where analytes in the liquid phase could potentially flow through channels coated with SiFs without actually being attached to the silver.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.