Bioorganic and Biophysical Chemistry Laboratory, Linnaeus University Centre for Biomaterials Chemistry, Department of Chemistry and Biomedical Sciences, Linnaeus University, 391 82, Kalmar, Sweden.
Department of Biomedical Sciences and Biofilms-Research Center for Biointerfaces (BRCB), Faculty of Health and Society, Malmö University, 205 06, Malmö, Sweden.
Angew Chem Int Ed Engl. 2019 Jan 14;58(3):727-730. doi: 10.1002/anie.201805772. Epub 2018 Nov 15.
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 <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.
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”)的合成与一种高度敏感的测定法相结合,该测定法使用附着在磁性载体上的模板。将酶胰蛋白酶和胃蛋白酶固定在氨基功能化溶胶-凝胶涂覆的磁性纳米颗粒(magNP)上。随后,在 magNP 的存在下,通过单体在高稀释度下聚合来产生轻度交联的荧光掺杂聚丙烯酰胺纳米凝胶。通过使用相同的蛋白质缀合纳米颗粒作为配体来可逆固定相应的纳米凝胶的新型竞争性荧光测定法对纳米凝胶进行了表征。两种纳米凝胶对其各自的靶蛋白的 K <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报道的亲和力一致。该方法简化了塑料抗体的开发和生产,并提供了对实用生物测定法的直接访问。