Biomedical subjects

Min Gon Kim

Publications and source records attributed to Min Gon Kim.

4 recordsLinked to original sources

PubMed2005

Micropatterning proteins on polyhydroxyalkanoate substrates by using the substrate binding domain as a fusion partner.

A novel strategy for micropatterning proteins on the surface of polyhydroxyalkanoate (PHA) biopolymer by microcontact printing (microCP) is described. The substrate binding domain (SBD) of the Pseudomonas stutzeri PHA depolymerase was used as a fusion partner for specifically immobilizing proteins on PHA substrate. Enhanced green fluorescent protein (EGFP) and red fluorescent protein (RFP) fused to the SBD could be specifically immobilized on the micropatterns of poly(3-hydroxybutyrate) and poly(3-hydroxybutyrate-co-3-hydroxyhexanoate). Laser scanning confocal microscopic studies suggested that two fusion proteins were micropatterned in their functionally active forms. Also, antibody binding assay by surface plasmon resonance suggested that protein-protein interaction studies could be carried out using this system.

Adsorption↗

PubMed2005

Non-contact sound speed measurement by optical probing of beam deflection due to sound wave.

We report a non-contact and non-invasive method of sound speed measurement by optical probing of deflected laser beam due to normally incident degenerated shock wave. In this study the shock wave from an exploding wire was degenerated to an ordinary sound wave at the distance exceeding 0.23 m. Temporal resolution of the deflected beam signal was improved by passing through an adequate electronic high-pass filter, as a result we obtained a better temporal resolution than that of the acoustic pressure detection by PZT transducer in terms of rising time. The spatial resolution was improved by passing the refracted beam signal into the edge of focusing lens to make a larger deflection angle. Sound speed was calculated by monitoring the time of flight of transient deflected signal at the predetermined position. Sound speed has been measured in air, distilled water and acryl, agreed well with the published values. The sound speed measured in the solution of glycerin, magnesium sulfate (MgSO4), and dimethylformamide with various mole fractions also agrees within 3% of relative error with those measured in the present work by ultrasonic pulse echo method. The results suggest that the method proposed is to be reliable and reproducible.

Journal Article↗

PubMed2005

Surface plasmon resonance imaging-based protein arrays for high-throughput screening of protein-protein interaction inhibitors.

The E7 protein produced by high-risk human papillomavirus (HPV) induces a degradation of the retinoblastoma tumor suppressor RB through direct interaction, which suggests that an inhibitor for the interaction can be a potential anticancer drug. A surface plasmon resonance (SPR) imaging-based protein array chip was developed for the high-throughput screening of inhibitor molecules targeting RB-E7 interaction. The glutathione S-transferase-fused E7 protein (GST-E7) was first layered onto a glutathionylated gold chip surface that had been designed to specifically bind to GST-fused proteins. Subsequently, a microarrayer was used to spot the hexa-histidine-tagged RB proteins (His(6)-RB) onto the GST-E7-layered gold chip surface, and the resulting SPR image was analyzed. Upon increased His(6)-RB concentration in the spotting solution, the SPR signal intensity increased proportionally, indicating that His(6)-RB bound to GST-E7 in a concentration-dependent manner. The His(6)-RB/GST-E7 interaction was challenged by spotting the His(6)-RB solution in the presence of a RB binding peptide (PepC) derived from a motif on E7. The SPR imaging data showed that PepC inhibited the His(6)-RB/GST-E7 interaction in a concentration-dependent manner. Our results show that the SPR imaging-based protein array chip can be applied to screen small molecule inhibitors that target protein-protein interaction.

Papillomavirus E7 Proteins↗

PubMed2005

Surface plasmon resonance imaging-based protein array chip system for monitoring a hexahistidine-tagged protein during expression and purification.

A surface plasmon resonance imaging-based Ni(2+)-iminodiacetic acid-coated gold chip system was developed to enable specific detection of a hexahistidine-tagged recombinant protein in crude extracts or in column chromatography fractions. This system is especially advantageous for high-throughput analysis of multiple proteins.

Escherichia coli↗