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    • 5. 发明申请
    • Method for the rapid taxonomic identification of pathogenic microorganisms and their toxic proteins
    • 用于快速分类鉴定病原微生物及其有毒蛋白质的方法
    • US20060257929A1
    • 2006-11-16
    • US11273356
    • 2005-11-14
    • Linda PowersWalther EllisChristopher Lloyd
    • Linda PowersWalther EllisChristopher Lloyd
    • G01N33/53
    • G01N33/54353
    • The present invention describes a method for the rapid binding of pathogenic microorganisms and their toxic proteins with ligands that have been covalently tethered at some distance from the surface of a substrate. Ligands directed to microbes are covalently attached to the substrate surface by tethers that are between 35 Å and 50 Å in length for optimal binding efficacy. Ligands directed to capture and concentrate proteinaceous materials are covalently attached to the substrate surface by tethers that are between 35 Å and 50 Å in length for optimum assay kinetics. The ligands described herein include heme compounds, siderophores, polysaccharides, and peptides specific for toxic proteins, outer membrane proteins and conjugated lipids. Non-binding components of the solution to be analyzed are separated from the bound fraction and binding is confirmed by detection of the analyte via microscopy, fluorescence, epifluorescence, luminescence, phosphorescence, radioactivity, or optical absorbance. By patterning numerous ligands in an array on a substrate surface it is possible to taxonomically identify the microorganism by analysis of the binding pattern of the sample to the array.
    • 本发明描述了一种用于将病原微生物及其毒性蛋白质与已经在与基底表面一定距离共价连接的配体快速结合的方法。 针对微生物的配体通过长度在35埃和50埃之间的系链共价连接到基质表面,以获得最佳的结合效力。 用于捕获和浓缩蛋白质材料的配体通过长度在35Å和50之间的系链共价连接到基底表面,以获得最佳的测定动力学。 本文所述的配体包括血红素化合物,铁载体,多糖和对毒性蛋白质,外膜蛋白质和缀合脂质有特异性的肽。 要分析的溶液的非结合组分与结合部分分离,通过显微镜,荧光,落射荧光,发光,磷光,放射性或光吸收检测分析物来确认结合。 通过在基板表面上阵列中的许多配体图案,可以通过分析样品与阵列的结合模式来分类学地鉴定微生物。