Department of Chemical and Biomolecular Engineering, University of Notre Dame, University of Notre Dame, Notre Dame, IN 46556, USA.
Nanoscale. 2017 Jun 29;9(25):8684-8694. doi: 10.1039/c7nr03096g.
Small dimensions of gold nanoparticles (AuNPs) necessitate antibodies to be immobilized in an oriented fashion in order to conserve their antigen binding activity for proper function. In this study, we used the previously described UV-NBS method to site-specifically incorporate a thioctic acid (TA) functionality into antibodies at the conserved nucleotide-binding site (NBS). Modified antibodies were immobilized on the AuNP surface in an oriented manner utilizing the newly incorporated TA functionality while maintaining the antibody structure and activity. The resulting antibody functionalized AuNPs via the UV-NBS method demonstrated significantly enhanced antigen detection capabilities and improved antigen detection sensitivity with a high level of selectivity when compared to other commonly used AuNP functionalization methods. Our results demonstrate that the limit of detection (LOD) for AuNPs functionalized via the UV-NBS method was 55 pM PSA, which is 40, 851, and 5873-fold improved over the other immobilization methods: EDC-NHS, thiol reduction, and ionic interaction, respectively. Consequently, the UV-NBS method provides a universal, site-specific functionalization method that generates highly sensitive and more stable antibody functionalized AuNPs which are amenable to any available detection and treatment assay with potential significant implications.
小尺寸的金纳米粒子(AuNPs)需要将抗体定向固定,以保持其抗原结合活性,从而发挥正常功能。在这项研究中,我们使用了先前描述的 UV-NBS 方法,在保守的核苷酸结合位点(NBS)处将硫辛酸(TA)功能特异性地掺入抗体中。修饰后的抗体利用新掺入的 TA 功能在 AuNP 表面上以定向方式固定,同时保持抗体的结构和活性。与其他常用的 AuNP 功能化方法相比,通过 UV-NBS 方法制备的抗体功能化 AuNPs 具有显著增强的抗原检测能力和更高的抗原检测灵敏度,具有高水平的选择性。我们的结果表明,通过 UV-NBS 方法功能化的 AuNPs 的检测限(LOD)为 55 pM PSA,与其他固定化方法(EDC-NHS、巯基还原和离子相互作用)相比,分别提高了 40、851 和 5873 倍。因此,UV-NBS 方法提供了一种通用的、特异性的功能化方法,生成了高度敏感和更稳定的抗体功能化 AuNPs,适用于任何现有的检测和治疗分析,具有潜在的重要意义。