Biomedical subjects

Benyu Su

Publications and source records attributed to Benyu Su.

5 recordsLinked to original sources

PubMed2005

Resonance light scattering technique for the determination of protein with rutin and cetylpyridine bromide system.

A new resonance light scattering (RLS) assay of protein is presented. In Tris-NaOH (pH = 10.93) buffer, the RLS of rutin-cetylpyridine bromide (CPB) system can be greatly enhanced by protein, including bovine serum albumin (BSA) and human serum albumin (HSA). The enhanced RLS intensities are in proportion to the concentration of proteins in the range of 5 x 10(-9) to 2.5 x 10(-6) g ml(-1) for BSA and 2.5 x 10(-8) to 3.5 x 10(-6) g ml(-1) for HSA. The detection limits (S/N = 3) are 3.0 ng ml(-1) for BSA and 10.0 ng ml(-1) for HSA. Samples are determined satisfactorily.

Animals↗

PubMed2004

The fluorescence enhancement effect of the Tb-Gd-guanosine-5'-triphosphate-phen system and its analytical application.

It has been found that Tb(3+) can react with guanosine-5'-triphosphate (GTP) and o-phenanthroline (phen), resulting in the intrinsic fluorescence of Tb(3+). This fluorescence can be enhanced by adding La(3+), Gd(3+), Lu(3+), Sc(3+), Y(3+), and so on, among which Gd(3+) produces the greatest enhancement. These are new co-luminescence systems. The experiments indicate under optimum conditions, the fluorescence intensity of the Tb-Gd-GTP-phen system is proportional to the concentration of GTP over the range 1x10(-9) to 3x10(-5) mol/l. The detection limit is 3.1x10(-10) mol/l. The proposed method provides the most sensitive fluorimetry of GTP so far. The mechanism of the Tb-Gd-GTP-phen system has also been studied. The data indicates that there is a large congeries of Tb-Gd-GTP-phen, and the fluorescence enhancement of the Tb-Gd-GTP-phen system is considered to originate from intramolecular and intermocular energy transfers, and the energy-insulating sheath of the Gd complex.

Gadolinium↗

PubMed2004

Study on the interaction between nucleic acids and cationic surfactants.

The interactions of nucleic acids and cationic surfactants (cetylpyridine bromide (CPB) and cetyltrimethylammonium bromide (CTMAB)) in aqueous solution have been studied using the techniques of resonance light scattering (RLS) spectroscopy, the absorption spectroscopy, zeta potential assay and NMR assignment measurement. It is considered that CPB or CTMAB can assemble on the surface of nucleic acid via electrostatic and hydrophobic forces, which results in the formation of large associate of nucleic acid-cationic surfactant and RLS enhancement of nucleic acid. Besides these forces, the pi-pi stacking force between CPB and nucleic acid also exists in the associate. In comparison with CTMAB, CPB has larger enhancement on RLS of nucleic acid, which is attributed to that the enhancement of the former is only due to the absorption of the bases of nucleic acid, while the enhancement of the latter is own to the synergetic resonance caused by the absorption of both bases of nucleic acid and the pyridyl in CPB. These results have important implication for understanding the influence of surfactants on nucleic acid functionality in life science.

Bromides↗

PubMed2004

Study on the fluorescent enhancement effect in terbium-gadolinium-protein-sodium dodecyl benzene sulfonate system and its application on sensitive detection of protein at nanogram level.

The co-luminescence effect in a terbium-gadolinium-protein-sodium dodecyl benzene sulfonate (SDBS) system is reported here. Based on it, the sensitive quantitative analysis of protein at nanogram levels is established. The co-luminescence mechanism is studied using fluorescence, resonance light scattering (RLS), absorption spectroscopy and NMR measurement. It is considered that protein could be unfolded by SDBS, then a efficacious intramolecular fluorescent energy transfer occurs from unfolded protein to rare earth ions through SDBS acting as a "transfer bridge" to enhance the emission fluorescence of Tb3+ in this ternary complex of Tb-SDBS-BSA, where energy transfer from protein to SDBS by aromatic ring stacking is the most important step. Cooperating with the intramolecular energy transfer above is the intermolecular energy transfer between the simultaneous existing complexes of both Tb3+ and Gd3+. The fluorescence quantum yield is increased by an energy-insulating sheath, which is considered to be another reason for the resulting enhancement of the fluorescence. Förster theory is used to calculate the distribution of enhancing factors and has led to a greater understanding of the mechanisms of energy transfer.

Absorption↗

PubMed2004

Study of the reaction between the nucleic acid and Y-BPMPHD-CTMAB complex and its analytical application.

The fluorescence quenching of the Y-BPMPHD-CTMAB by nucleic acids is reported. It is considered that the Y-BPMPHD-CTMAB can form a large complex with nucleic acid through the electrostatic attraction in the pH range of 4.2-6.8. Under optimal conditions, the difference of fluorescence intensity between the system without and with nucleic acids is proportional to the concentration of nucleic acids over the range of 4.5 x 10(-8)-1.2 x 10(-5) g/mL for fsDNA and 3.2 x 10(-8)-3.0 x 10(-5) g/mL for yRNA, respectively. The detection limits are 14.0 ng/mL for fsDNA and 21.0 ng/mL for yRNA. The method is applied for the determination of nucleic acids in actual sample, and the result obtained is satisfactory.

Buffers↗