Department of Chemistry , University of Turin , Via P. Giuria 5 , 10125 Torino , Italy.
ACS Appl Mater Interfaces. 2019 Sep 11;11(36):32758-32768. doi: 10.1021/acsami.9b11559. Epub 2019 Sep 3.
Stable and efficient conjugates between antibodies and gold nanoparticles (GNP-Ab) are sought to develop highly sensitive and robust biosensors with applications in medicine, toxicology, food safety controls, and targeted drug delivery. Several strategies have been proposed for directing the antibody attachment to GNPs thus preserving antibody activity, including covalently coupling the antibody to a polymer grafted on GNP surface and exploiting the high affinity of bioreceptors as mediators for the binding. Both approaches also allow for shielding GNPs with a protective layer that guarantees the robustness of the conjugate. Notwithstanding, antibodies freely adsorb to GNP with high binding efficiency. The nonspecific adsorption is far more simple, fast, and inexpensive than any mediated coupling. Therefore, it is preferred for most applications, although it is considered to produce GNP-Ab with a limited activity. In this work, we compared three strategies for producing GNP-Ab, such as (i) covalent coupling mediated by a chemical layer, (ii) affinity-based binding mediated by a biomolecular layer composed of Staphylococcal protein A, and (iii) direct attachment via adsorption. The so-prepared GNP-Ab were employed as probes in a colorimetric lateral flow immunoassay (LFIA) for measuring salivary cortisol as a model biosensor that relies on the use of active GNP-Ab conjugates. Unexpectedly, the biosensors fabricated using the three probes were completely comparable in terms of their ability to measure salivary cortisol. Furthermore, we observed that the sensitivity of the LFIA primarily depended on the amount of the antibody bound to GNPs rather than on the method by which it was bound. The probes prepared using both the direct adsorption approach and mediated coupling via the biochemical mediator enabled development of point-of-care devices for the fast, sensitive, and reliable measurement of human salivary cortisol.
我们寻求将抗体与金纳米粒子(GNP-Ab)稳定且高效地连接,以开发具有医学、毒理学、食品安全控制和靶向药物输送等应用的高灵敏度和强稳健性生物传感器。已经提出了几种策略来指导抗体附着到 GNP 上,从而保持抗体的活性,包括将抗体共价偶联到接枝在 GNP 表面的聚合物上,以及利用生物受体的高亲和力作为结合的介导物。这两种方法还允许用保护层屏蔽 GNP,从而保证了结合物的稳健性。尽管如此,抗体仍会以高结合效率自由吸附到 GNP 上。非特异性吸附比任何介导的偶联都简单、快速且廉价。因此,尽管它被认为会产生活性有限的 GNP-Ab,但它仍然是大多数应用的首选。在这项工作中,我们比较了三种生产 GNP-Ab 的策略,例如:(i)通过化学层介导的共价偶联,(ii)由包含葡萄球菌蛋白 A 的生物分子层介导的基于亲和力的结合,以及(iii)通过吸附直接附着。制备的 GNP-Ab 被用作比色横向流动免疫分析(LFIA)的探针,以测量唾液皮质醇作为依赖于使用活性 GNP-Ab 结合物的模型生物传感器。出乎意料的是,基于这三种探针制备的生物传感器在测量唾液皮质醇的能力方面完全可比。此外,我们观察到 LFIA 的灵敏度主要取决于结合到 GNP 上的抗体量,而不是结合的方法。通过直接吸附方法和通过生化介导物介导的偶联制备的探针,能够开发用于快速、灵敏和可靠测量人唾液皮质醇的即时护理设备。