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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 andnhigh Raman activity, and on the basis of which, we havenemployed brilliant blue R-250 (BBR) and brilliant bluenG-250 (BBG) as surface-enhanced Raman scatteringn(SERS) labels to probe protein ligand recognitions. Thisnmethod differs from previously proposed methods in thatntarget proteins are labeled rapidly before biological rec-nognitions without procedures of separation and purifica-ntion, rather than attaching Raman labels to metal nano-nparticles, which significantly simplifies the Raman dyenlabeling procedure. In typical assays, ligand-functionalizednmetal nanoparticles assemble by target protein-specificnbindings and this assembly sequentially turns on electro-nmagnetic enhancement of Raman scattering of the pro-nposed labels. The method with its advantages of rapid-nness, high sensitivity, and spectral multiplexing has greatnpotential in probing protein protein and protein smallnmolecule recognitions not only in solution systems butnalso on flexible solid substrates.
机译:考马斯亮染料对蛋白质的亲和力高,拉曼活性高,在此基础上,我们采用了亮蓝色R-250(BBR)和亮蓝色nG-250(BBG)作为表面增强拉曼散射(SERS)标记来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,在进行生物识别之前,无需进行分离和纯化的步骤即可对目标蛋白进行快速标记,而不是将拉曼标记物附着于金属纳米粒子上,这大大简化了拉曼染料标记法。在典型的测定中,配体官能化的n金属纳米颗粒通过靶蛋白特异性结合而组装,并且该组装顺序地开启电磁增强了预先标记的拉曼散射。该方法具有快速,高灵敏度和光谱多路复用的优势,不仅在溶液系统中而且在柔性固体基质上,在探测蛋白质和蛋白质小分子识别方面具有巨大的潜力。

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  • 来源
    《Analytical Chemistry》 |2010年第10期|p.4102-4106|共5页
  • 作者单位

    State Key Laboratory of Supramolecular Structure and Materials, Jilin University, Changchun 130012, P. R. China,and Department of Chemistry, School of Science and Technology, Kwansei Gakuin University,Sanda, Hyogo 669-1337, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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