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Highly Efficient Synthesis and Assay of Protein‐Imprinted Nanogels by Using Magnetic Templates

机译:磁性模板高效合成和印迹蛋白质印迹纳米凝胶

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摘要

We report an approach integrating the synthesis of protein‐imprinted nanogels (“plastic antibodies”) with a highly sensitive assay employing templates attached to magnetic carriers. The enzymes trypsin and pepsin were immobilized on amino‐functionalized solgel‐coated magnetic nanoparticles (magNPs). Lightly crosslinked fluorescently doped polyacrylamide nanogels were subsequently produced by high‐dilution polymerization of monomers in the presence of the magNPs. The nanogels were characterised by a novel competitive fluorescence assay employing identical protein‐conjugated nanoparticles as ligands to reversibly immobilize the corresponding nanogels. Both nanogels exhibited K d<10 pM for their respective target protein and low cross‐reactivity with five reference proteins. This agrees with affinities reported for solid‐phase‐synthesized nanogels prepared using low‐surface‐area glass‐bead supports. This approach simplifies the development and production of plastic antibodies and offers direct access to a practical bioassay.
机译:我们报告了一种方法,该方法将蛋白质印迹纳米凝胶(“塑料抗体”)的合成与采用附着于磁性载体的模板的高灵敏度测定方法相结合。胰蛋白酶和胃蛋白酶固定在氨基官能化的溶胶凝胶包被的磁性纳米颗粒(magNPs)上。轻交联的荧光掺杂聚丙烯酰胺纳米凝胶随后通过在magNPs存在下高稀释度聚合单体而制得。纳米凝胶通过新颖的竞争荧光测定法进行表征,该测定法使用相同的蛋白质偶联纳米颗粒作为配体可逆地固定相应的纳米凝胶。两种纳米凝胶各自的靶蛋白均显示K d <10 pM,并且与五种参考蛋白的交叉反应性低。这与使用低表面积玻璃珠载体制备的固相合成纳米凝胶的亲和力相一致。这种方法简化了塑料抗体的开发和生产,并提供了直接进行实际生物测定的途径。

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