Yonsei University · 生化学・遺伝学・分子生物学
Professor Yong Shin's research lab specializes in the development of innovative microfluidic and nanomaterial-based platforms for point-of-care molecular diagnostics and liquid biopsy applications. The lab focuses on advancing sensitive, rapid, and label-free detection of genetic and epigenetic biomarkers—such as single-point mutations, cell-free nucleic acids, and extracellular vesicles—using cutting-edge technologies like silicon microring sensors, SERS substrates, and magnetic nanoparticle composites. A central theme in the lab’s work is the design of non-chaotropic, high-efficiency nucleic acid capture systems and isothermal amplification techniques to improve clinical translation of molecular diagnostics.
Figures are computed from collected data and may differ slightly.
Here, we first present an isothermal solid-phase amplification/detection (ISAD) technique for the detection of single-point mutations that can be performed without labelling in real-time by utilizing both silicon microring-based solid-phase amplification and isothermal recombinase polymerase amplification (RPA). The ISAD technique was performed on a silicon microring device with a plastic chamber containing 10 μL of the reaction mixture, and characterized with an assay for the detection of the H
Cell-free nucleic acids (cfNAs) are emerging diagnostic biomarkers for monitoring the treatment and recurrence of cancers. In particular, the biological role and clinical usefulness of cfNAs obtained from the plasma of patients with various cancers are popular and still intensely explored, yet most studies are limited by technical problems during cfNA isolation. A dimethyl dithiobispropionimidate (DTBP)-based microchannel platform that enables spontaneous cfNA capture in 15 min with minimal cell
Surface-enhanced Raman scattering (SERS) has evolved into a robust analytical technique capable of detecting a variety of biomolecules despite challenges in securing a reliable Raman signal. Conventional SERS-based nucleic acid detection relies on hybridization assays, but reproducibility and signal strength issues have hindered research on directly amplifying nucleic acids on SERS surfaces. This study introduces a deep learning assisted ZnO-Au-SERS-based direct amplification (ZADA) system for r
Miniaturized lab-on-a-chip (LOC) systems have been developed for genetic and epigenetic analyses in clinical applications because of advantages such as reduced sample size and reagent consumption, rapid processing speed, simplicity, and enhanced sensitivity. Despite tremendous efforts made towards developing LOC systems for use in the clinical setting, the development of LOC systems to analyze DNA methylation, which is an emerging epigenetic marker causing the abnormal silencing of genes includi
Cancer cell-derived extracellular vesicles (EVs) are promising biomarkers for cancer diagnosis and prognosis. However, the lack of rapid and sensitive isolation techniques to obtain EVs from clinical samples at a sufficiently high yield limits their practicability. Chimeric nanocomposites of lactoferrin conjugated 2,2-bis(methylol)propionic acid dendrimer-modified magnetic nanoparticles (LF-bis-MPA-MNPs) are fabricated and used for simple and sensitive EV isolation from various biological sample
Diagnosis of Q fever is difficult due to the lack of distinct clinical features that distinguish it from other febrile diseases. Serologic testing is the gold standard method for diagnosing Q fever, but antibody formation may not be detectable for 2 to 3 weeks from symptom onset, limiting early diagnosis. We thus evaluated the diagnostic utility of polymerase chain reaction (PCR) to detect Coxellia burnetii DNA in serum from patients with suspected acute Q fever.All adult patients with suspected
Here, we present a silicon microfluidic system for the purification and extraction of nucleic acids from human body fluid samples utilizing a dimethyl adipimidate (DMA)-based solid-phase extraction method. We propose DMA, which has been used as an amino-reactive cross-linking agent within cells and proteins, as a non-chaotropic reagent for the capture of nucleic acids to overcome the limitations of existing chaotropic and non-chaotropic techniques such as low binding efficiency, PCR inhibition a
The tensor polarization ${t}_{20}$ in ${\ensuremath{\pi}}^{+}d$ elastic scattering has been measured as a function of energy at 15\ifmmode^\circ\else\textdegree\fi{} (laboratory) over the energy range ${T}_{\ensuremath{\pi}}=118 \mathrm{to} 148$ MeV. The angular distributions at 135 and 142 MeV between 15\ifmmode^\circ\else\textdegree\fi{} and 35\ifmmode^\circ\else\textdegree\fi{} were also measured. The ${t}_{20}$ values are negative for all energies and angles investigated and are consistent w
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