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    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/26419


    Title: Preparation of fractioned DNA aptamer-Pt complex through ultrafiltration and the colorimetric sensing of thrombin
    Authors: Higuchi,A;Yang,ST;Siao,YD;Hsieh,PV;Fukushima,H;Chang,Y;Chen,WY
    Contributors: 化學工程與材料工程學系
    Keywords: SINGLE-NUCLEOTIDE POLYMORPHISMS;PEROXIDASE-ACTIVITY;NANOPARTICLES;SENSORS;RECOGNITION;BIOCATALYST;SELECTION;DNAZYMES;ENZYMES;PROBES
    Date: 2009
    Issue Date: 2010-06-29 17:27:37 (UTC+8)
    Publisher: 中央大學
    Abstract: DNA aptamers were combined with platinum complexes to form DNA-Pt complexes, which exhibited peroxidase enzymatic activity while retaining the specific binding ability of aptamers. The DNA-Pt complexes were fractioned by size through ultrafiltration membranes having several molecular weight cut-offs, and the peroxidase enzymatic activities of these fractions were compared. The enzymatic activity was highest in the filtrate of DNA-Pt complex solutions prepared with cisplatin and K-2[PtCl4] after ultrafiltration through membranes having MWCO = 300,000. These showed 1.2-fold and 1.6-fold higher activity, respectively, than the corresponding unfractioned complexes. Sandwich-type DNAzyme-linked aptamer assays (DLAAs) using unfractioned or fractioned DNA-Pt complexes successfully detected the target protein thrombin. DLAAs incorporating a DNA-Pt (K-2[PtCl4]) complex fractioned through ultrafiltration membranes having MWCO = 300,000 showed the highest sensitivity among DLAAs made using fractioned DNA-Pt complexes, and had a 13-fold higher sensitivity than those made with unfractioned DNA-Pt complexes. (c) 2008 Elsevier B.V. All rights reserved.
    Relation: JOURNAL OF MEMBRANE SCIENCE
    Appears in Collections:[化學工程與材料工程研究所] 期刊論文

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