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Label-free C-reactive protein SERS detection with silver nanoparticle aggregates
In this work, we report a qualitative approach for detecting the adsorption of C-reactive protein on phosphocholine-terminated self-assembled monolayers without the use of any labels. An amplified plasmon of concentration-induced silver nanoparticle aggregates located ∼4.0 nm away from the C-reactiv...
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Published in: | RSC advances 2015-01, Vol.5 (44), p.34720-34729 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | In this work, we report a qualitative approach for detecting the adsorption of C-reactive protein on phosphocholine-terminated self-assembled monolayers without the use of any labels. An amplified plasmon of concentration-induced silver nanoparticle aggregates located ∼4.0 nm away from the C-reactive protein
via
the phosphocholine-terminated self-assembled monolayer linker is considered to be the source of the robust electromagnetic enhancement. The high level (10
9
to 10
10
M
−1
) of apparent binding constant (
K
A
) of C-reactive protein suggests that the immobilized surface was well-oriented without extreme random stacking. A Raman sensitivity toward the C-reactive protein around 2800–3000 cm
−1
was noted, which gradually increased upon the addition of successive layers up to approximately 6–7 layers of phosphocholine-coated silver nanoparticle aggregates, with minimum detection amounts of ∼0.01 ng mL
−1
in buffer and ∼0.1 ng mL
−1
in 1% serum. A cross-reactivity test confirmed the excellent selectivity and specificity of the measured signals. A computational study based on the finite-difference-time-domain method successfully demonstrated the enhanced (∼1.1 × 10
6
) electromagnetic field of the 2-D silver nanoparticle aggregates as compared with that of isolated particles, and was congruent with the analytical enhancement factor (1.7 × 10
5
). |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/C5RA00040H |