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Updated: Jan 27, 2026

Optical Trapping of Plasmonic Nanoparticles for In Situ Surface-Enhanced Raman Spectroscopy Characterizations
Published on: June 23, 2022
New strategy for the gene mutation identification using surface enhanced Raman spectroscopy (SERS).
Agata Kowalczyk1, Jan Krajczewski1, Artur Kowalik2
1Faculty of Chemistry, University of Warsaw, Pasteura 1 Str., PL 02-093 Warsaw, Poland.
This study introduces a novel DNA biosensor for rapid and accurate identification of the BRAF V600E gene mutation. The sensor utilizes surface-enhanced Raman scattering (SERS) for precise detection in clinical samples.
Area of Science:
- Nanotechnology
- Molecular Biology
- Spectroscopy
Background:
- Early and accurate diagnosis of specific DNA mutations is crucial for effective cancer treatment.
- Rapid confirmation of clinical findings is vital for immediate treatment decisions.
- The BRAF c.1799T>A; p. V600E mutation is a key target in several cancers.
Purpose of the Study:
- To develop a new strategy for identifying the BRAF V600E gene mutation.
- To create a highly sensitive and reproducible DNA biosensor.
- To demonstrate the utility of the biosensor in analyzing clinical samples.
Main Methods:
- Utilized a novel SERS substrate: photo-etched Gallium Nitride (GaN) covered with gold.
- Employed surface-enhanced Raman scattering (SERS) spectroscopy for detection.
- Detection based on conformation change of alkanethiol linker during DNA hybridization.
Main Results:
- Achieved a low detection limit at the picogram per microliter (pg/μL) level.
- Demonstrated a wide analytical range from 6.75 pg/μL to 67.5 ng/μL.
- The intensity ratio of specific Raman bands indicated mutation presence with high selectivity.
Conclusions:
- The developed DNA SERS biosensor enables rapid and precise identification of the BRAF V600E mutation.
- The nanostructured GaN-based platform offers high sensitivity, selectivity, and reproducibility.
- This bioactive platform shows potential for clinical sample analysis and personalized medicine.
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