Weerathunge Pabudi, Ramanathan Rajesh, Shukla Ravi, Sharma Tarun Kumar, Bansal Vipul
Ian Potter NanoBioSensing Facility, NanoBiotechnology Research Laboratory, School of Applied Science, RMIT University , GPO Box 2476 V, Melbourne Victoria 3001, Australia.
Anal Chem. 2014 Dec 16;86(24):11937-41. doi: 10.1021/ac5028726. Epub 2014 Oct 28.
This study addresses the need for rapid pesticide (acetamiprid) detection by reporting a new colorimetric biosensing assay. Our approach combines the inherent peroxidase-like nanozyme activity of gold nanoparticles (GNPs) with high affinity and specificity of an acetamiprid-specific S-18 aptamer to detect this neurotoxic pesticide in a highly rapid, specific, and sensitive manner. It is shown that the nanozyme activity of GNPs can be inhibited by its surface passivation with target-specific aptamer molecules. Similar to an enzymatic competitive inhibition process, in the presence of a cognate target, these aptamer molecules leave the GNP surface in a target concentration-dependent manner, reactivating GNP nanozyme activity. This reversible inhibition of the GNP nanozyme activity can either be directly visualized in the form of color change of the peroxidase reaction product or can be quantified using UV-visible absorbance spectroscopy. This approach allowed detection of 0.1 ppm acetamiprid within an assay time of 10 min. This reversible nanozyme activation/inhibition strategy may in principle be universally applicable for the detection of a range of environmental or biomedical molecules of interest.
本研究通过报告一种新的比色生物传感测定法,满足了快速检测农药(啶虫脒)的需求。我们的方法将金纳米颗粒(GNPs)固有的类过氧化物酶纳米酶活性与啶虫脒特异性S-18适配体的高亲和力和特异性相结合,以高度快速、特异和灵敏的方式检测这种神经毒性农药。结果表明,通过用靶标特异性适配体分子对GNPs进行表面钝化,可以抑制其纳米酶活性。类似于酶竞争性抑制过程,在存在同源靶标的情况下,这些适配体分子以靶标浓度依赖的方式离开GNP表面,重新激活GNP纳米酶活性。GNP纳米酶活性的这种可逆抑制既可以以过氧化物酶反应产物颜色变化的形式直接观察到,也可以使用紫外可见吸收光谱法进行定量。这种方法能够在10分钟的测定时间内检测到0.1 ppm的啶虫脒。这种可逆的纳米酶激活/抑制策略原则上可能普遍适用于检测一系列感兴趣的环境或生物医学分子。