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A Gold Nanoparticle Platform for Protein—Protein Interactions and Drug Discovery

机译:用于蛋白质—蛋白质相互作用和药物发现的金纳米颗粒平台

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Gold nanoparticles hold great promise for studying protein—protein interactions because of their intrinsic optical properties. Pink when in a homogeneous suspension, the solution turns blue-gray when particles are drawn close together, for example, when immobilized proteins specifically interact with each other. However, the nanoparticle stability, size, and method of protein attachment contribute to the unreliable outcome of current assays. To overcome these hurdles, we developed novel and reliable methods first to synthesize homogenous particles of optimal diameter and second to apply a heterologous NTA-Ni-SAM coating for controlled orientation and optimal presentation of histidine-tagged proteins. Both methods were proven to greatly enhance assay sensitivity and specificity by increasing the signal and minimizing the nonspecific binding. Our assay reproducibly detected known protein—protein interactions and unambiguously identified small molecules that inhibited them. We believe our gold nanoparticle bioassay is a versatile and trustworthy new platform for analyzing protein—protein interactions and high-throughput screening of small-molecule inhibitors.
机译:金纳米粒子因其固有的光学特性而在研究蛋白质之间相互作用方面具有广阔的前景。在均匀悬浮液中呈粉红色时,当粒子靠近在一起时(例如,固定的蛋白质之间特异性地相互作用),溶液会变成蓝灰色。但是,纳米颗粒的稳定性,大小和蛋白质附着方法导致了当前测定的不可靠结果。为了克服这些障碍,我们开发了新颖且可靠的方法,首先合成了最佳直径的均质颗粒,其次应用了异源NTA-Ni-SAM涂层来控制取向和组氨酸标签蛋白的最佳表达。两种方法都被证明可以通过增加信号并最大程度地减少非特异性结合来大大提高检测灵敏度和特异性。我们的测定法可重复检测已知的蛋白质-蛋白质相互作用,并明确鉴定出抑制它们的小分子。我们相信,我们的金纳米颗粒生物测定法是一种多功能且值得信赖的新平台,可用于分析蛋白质-蛋白质相互作用和小分子抑制剂的高通量筛选。

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