Metal Carbonyls for the Biointerference-Free Ratiometric Surface-Enhanced Raman Spectroscopy-Based Assay for Cell-Free Circulating DNA of Epstein-Barr Virus in Blood.
Huijing LinTianxun GongZi-Yao HongSufang QiuJianji PanChinh-Yu TsengShangyuan FengRong ChenKien Voon KongPublished in: Analytical chemistry (2018)
By taking advantage of the spectral properties of metal carbonyls, we have designed a surface-enhanced Raman spectroscopy (SERS) ratiometric assay for measuring cell-free circulating DNA (cfDNA) from Epstein-Barr virus in blood for nasopharyngeal carcinoma (NPC). This assay consists of a rhenium carbonyl (Re-CO) to serve as a DNA probe, an osmium carbonyl (Os-CO) embedded within the SERS-active substrate as an internal reference, and a streptavidin layer on the surface of the substrate. Hybridization of cfDNA with biotinylated-capture sequence leads to immobilization of cfDNA on the substrate. The binding of Re-CO via daunorubicin (DNR) to cfDNA is accompanied by an appearance of a strong symmetry stretching vibrations peak at 2113 cm-1, which has spectral overlap with Os-CO (2025 cm-1). This results in an increase in the I2113/ I2025 ratio and quantitatively correlates with cfDNA. This SERS assay can be readily used to detect cfDNA in blood samples from patients due to the intensity ratio of I2113/ I2025 lying in a silent region (1780-2200 cm-1) in the SERS spectrum of the biomolecules.
Keyphrases
- raman spectroscopy
- cell free
- epstein barr virus
- circulating tumor
- high throughput
- diffuse large b cell lymphoma
- sensitive detection
- quantum dots
- living cells
- end stage renal disease
- optical coherence tomography
- fluorescent probe
- newly diagnosed
- chronic kidney disease
- amino acid
- single molecule
- hydrogen peroxide
- gold nanoparticles
- prognostic factors
- computed tomography
- magnetic resonance imaging
- magnetic resonance
- structural basis
- label free
- patient reported outcomes
- nucleic acid
- dna binding