Determination of proteins with Alizarin Red S by Rayleigh light scattering technique |
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Authors: | Zhong Hui Li Na Zhao Fenglin Li Ke An |
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Affiliation: | a Department of Chemistry, Huaiyin Normal College, Jiangsu 223001, China b Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Department of Chemistry, Peking University, Beijing 100871, China |
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Abstract: | A new protein determination method by enhanced Rayleigh light scattering (RLS) technique has been developed. In acid condition (pH=3.60), RLS of 1,2-dihydroxyanthraquinone-3-sulfonate (Alizarin Red S) can be greatly enhanced by addition of proteins, resulting in two characteristic peaks, 360 and 505 nm, respectively. The new protein assay is based on the RLS enhancement and spectrum change. The optimum condition for the reaction was investigated. The linear range is 0.20-24.9 μg ml−1 for BSA and 0.20-15.5 μg ml−1 for HSA. The detection limits (S/N=3) are 9.59 ng ml−1 for BSA and 9.51 ng ml−1 for HSA. The results of determination for human serum samples were comparable to those obtained by Bradford method. The binding stoichiometry was determined. |
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Keywords: | Rayleigh light scattering (RLS) Alizarin Red S Protein Determination |
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