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首页> 外文期刊>Analytical chemistry >Coomassie Brilliant Dyes as Surface-Enhanced Raman Scattering Probes for Protein-Ligand Recognitions
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Coomassie Brilliant Dyes as Surface-Enhanced Raman Scattering Probes for Protein-Ligand Recognitions

机译:考马斯亮染料作为用于蛋白质配体识别的表面增强拉曼散射探针

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摘要

Coomassie brilliant dyes have high affinity to proteins and high Raman activity, and on the basis of which, we have employed brilliant blue R-250 (BBR) and brilliant blue G-250 (BBG) as surface-enhanced Raman scattering (SERS) labels to probe protein-ligand recognitions. This method differs from previously proposed methods in that target proteins are labeled rapidly before biological recognitions without procedures of separation and purification, rather than attaching Raman labels to metal nano-particles, which significantly simplifies the Raman dye labeling procedure. In typical assays, ligand-functionalized metal nanoparticles assemble by target protein-specific bindings and this assembly sequentially turns on electromagnetic enhancement of Raman scattering of the proposed labels. The method with its advantages of rapidness, high sensitivity, and spectral multiplexing has great potential in probing protein-protein and protein-small molecule recognitions not only in solution systems but also on flexible solid substrates.
机译:考马斯亮丽染料对蛋白质具有高亲和力,并具有很高的拉曼活性,在此基础上,我们使用了亮蓝R-250(BBR)和亮蓝G-250(BBG)作为表面增强拉曼散射(SERS)标签探测蛋白质-配体识别。该方法与先前提出的方法的不同之处在于,在不进行分离和纯化步骤的情况下,无需进行分离和纯化的过程即可在生物识别之前快速标记目标蛋白,而不是将拉曼标记物附着到金属纳米颗粒上,这大大简化了拉曼染料标记过程。在典型的测定中,配体官能化的金属纳米粒子通过靶蛋白特异性结合而组装,并且该组装顺序地开启所提议标记的拉曼散射的电磁增强。该方法具有快速,高灵敏度和光谱多路复用的优点,不仅在溶液系统中而且在柔性固体基质上,在探测蛋白质-蛋白质和蛋白质-小分子识别方面都具有巨大的潜力。

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