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Antibody-Directed Synthesis of Catalytic Nanoclusters for Bioanalytical Assays

机译:生物分析测定的催化纳米能器的抗体合成

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摘要

Synthesis of atomic nanoclusters (NCs) using proteins as a scaffold has attracted great attention. Usually, the synthetic conditions for the synthesis of NCs stabilized with proteins require extreme pH values or temperature. These harsh reaction conditions cause the denaturation of the proteins and end up in the loss of their biological functions. Until now, there are no examples of the use of antibodies as NC stabilizers. In this work, we present the first method for the synthesis of catalytic NCs that uses antibodies for the stabilization of NCs. Anti-BSA IgG was used as a model to demonstrate that it is possible to use an antibody as a scaffold for the synthesis of semiconductor and metallic NCs with catalytic properties. The synthesis of antibodies modified with NCs is carried out under nondenaturing conditions, which do not affect the antibody structure. The resulting antibodies still maintain the affinity for target antigens and protein G. The catalytic properties of the anti-BSA IgG modified with NCs can be used to the quantification of bovine serum albumin (BSA) in a direct sandwich enzyme-linked immunosorbent assay (ELISA).
机译:用蛋白质作为支架的原子纳米能器(NCS)的合成引起了极大的关注。通常,用蛋白质稳定的NCs合成的合成条件需要极端pH值或温度。这些恶劣的反应条件导致蛋白质的变性并最终丧失其生物学功能。到目前为止,没有使用抗体作为NC稳定剂的例子。在这项工作中,我们提出了合成催化NCS的第一种方法,该方法使用抗体稳定NCS。抗BSA IgG用作模型,以证明可以使用抗体作为合成具有催化性质的半导体和金属NC的支架。用NCS改性的抗体的合成在非生种条件下进行,其不会影响抗体结构。得到的抗体仍然保持对靶抗原和蛋白G.用NCS改性的抗BSA IgG的催化性能可用于定量直接夹心酶联免疫吸附试验中的牛血清白蛋白(BSA)(ELISA )。

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