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首页> 外文期刊>ACS nano >Luminescent lanthanide-functionalized gold nanoparticles: Exploiting the interaction with bovine serum albumin for potential sensing applications
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Luminescent lanthanide-functionalized gold nanoparticles: Exploiting the interaction with bovine serum albumin for potential sensing applications

机译:发光镧系元素官能化的金纳米颗粒:利用与牛血清白蛋白的相互作用来进行潜在的传感应用

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As luminescent surface-functionalized gold nanoparticles emerged as potential powerful analytical tools in the biomedical fields, understanding the interaction of such systems with proteins has become crucial. In the present study, the interaction of luminescent water-soluble gold nanoparticles (AuNP-1·Eu-nta), obtained through the self-assembly of a naphthalene β-diketone antenna with a Eu(III) cyclen complex tethered to the gold surface via a C12 alkyl thiol spacer, with bovine serum albumin (BSA) was investigated. The changes in the UV-visible absorption and fluorescence spectra of both the antenna and protein, as well as in the time-resolved Eu(III)-centered emission, of the resulting self-assembly were monitored, at physiological pH, as a function of the BSA concentration. We demonstrate that the Eu(III) emission arising from the self-assembly on the AuNP surface is almost completely quenched upon addition of BSA. Binding constant determination clearly showed that the sensitizing antenna was not displaced and that the quenching was the result of the interaction between the antenna and BSA. Detailed spectroscopic studies performed on the nta-BSA system brought a better insight in the strength of such interaction as well as its effect on the protein secondary structure. Finally, the information gathered on each system resulted in applying AuNP-1·Eu-nta-BSA for the luminescent detection of drugs via the perturbation of the nta-BSA interaction. Competitive titrations using ibuprofen and warfarin showed that nta was located in the binding site II of BSA and that the presence of warfarin, a site I drug, did not interfere with the detection of site II ibuprofen.
机译:随着发光表面功能化的金纳米粒子在生物医学领域中成为潜在的强大分析工具,了解此类系统与蛋白质的相互作用已变得至关重要。在本研究中,发光的水溶性金纳米粒子(AuNP-1·Eu-nta)的相互作用是通过将萘β-二酮天线与Eu(III)周期复合物束缚在金表面上而自组装而获得的通过C12烷基硫醇间隔基,与牛血清白蛋白(BSA)一起进行了研究。在生理pH值下,监测天线和蛋白质的紫外-可见吸收光谱和荧光光谱以及时间分辨的以Eu(III)为中心的发射的自组装的变化, BSA浓度。我们证明了由于自组装在AuNP表面上产生的Eu(III)发射几乎在添加BSA后被完全淬灭。结合常数的确定清楚地表明,敏化天线没有移位,淬灭是天线和BSA之间相互作用的结果。在nta-BSA系统上进行的详细光谱研究为这种相互作用的强度及其对蛋白质二级结构的影响提供了更好的见识。最后,在每个系统上收集的信息导致通过干扰nta-BSA相互作用将AuNP-1·Eu-nta-BSA应用于发光检测药物。使用布洛芬和华法林的竞争性滴定表明,nta位于BSA的结合位点II,而华法林(一种位点I的药物)的存在不干扰对位点II布洛芬的检测。

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