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Haowen Huang

Publications and source records attributed to Haowen Huang.

2 recordsLinked to original sources

Label-free reading of microarray-based proteins with high throughput surface plasmon resonance imaging.

A simple method is presented discriminating proteins at a gold surface by using an emerging technology, surface plasmon resonance (SPR) imaging. As a high throughput method, the protein array of bovine serum albumin (BSA), poly-l-lysine (PL), casein and lactate dehydrogenase (LDG) was fabricated and SPR imaging enables detection from different kinds of proteins immobilized on the sensor surface. These proteins can be discriminated directly by various reflected intensity or changing the incident angular position of light. Denaturation of these immobilized proteins on SPR sensor by interacting with denaturant 6M GdnHCl solution was also performed and obvious changes in reflected intensity were occurred after denaturation. The observation of denaturation of these proteins further supported the fact that different proteins could be discriminated on protein array before denaturation. On the other hand, the procedure of denaturation provided useful information that any change of molecular structure with the progress of denaturation would result in change of SPR signal. Excellent reproducibility with a chip-to-chip for label-free discriminating various proteins was achieved.

Image Enhancement↗

Chiral recognition of dextran sulfate with D- and L-cystine studied by multiwavelength surface plasmon resonance.

A multiwavelength surface plasmon resonance (mwSPR) approach has been developed to study the chiral discrimination between D- and L-cystine (Cys). A monolayer of the two enantiomers was separately assembled on a pair of gold films of about 50 nm in thickness and their resonance wavelength shifts, Deltalambda, were measured under a continuous flow of an identical chiral probe solution. Dextran sulfate (DS) was found to be an excellent chiral probe because it has rich chiral centers and is large enough to produce sensitive mwSPR response. The chiral discrimination was investigated either by Deltalambda(max), the maximum resonance wavelength shift in recognition equilibrium, or by recognition kinetics (Deltalambda vs time). The equilibrium data showed that D-Cys yielded always the smaller Deltalambda(max) as compared to L-Cys at pH 5.0 or above. This differentiation was enlarged by raising the probe content and became naught at pH <4.5. The kinetic results showed that, as pH increased from 5.0 to 7.5, the non-equilibrium Deltalambda for D-Cys rose above the level for L-Cys at the first 30s of recognition but came back gradually to its equilibrium position after about 150 s, with crossing at 50--150 s depending on DS concentration. This phenomenon was thought to be the result of molecular orientation adjustment after DS binding to D-Cys. Both kinetic and thermodynamic mechanisms were thus considered to be deeply involved in the investigated chiral recognition system.

Cystine↗