Chen Yunlong, Ding Lin, Song Wanyao, Yang Min, Ju Huangxian
State Key Laboratory of Analytical Chemistry for Life Science , School of Chemistry and Chemical Engineering , Nanjing University , Nanjing 210023 , P. R. China . Email:
Department of Pharmaceutical & Biological Chemistry , UCL School of Pharmacy , University College London , London WC1N 1AX , UK.
Chem Sci. 2016 Jan 1;7(1):569-574. doi: 10.1039/c5sc03560k. Epub 2015 Oct 16.
A zone-controllable SERS effect is presented for Raman imaging of protein-specific glycosylation on a cell surface using two types of newly designed nanoprobes. The signal probe, prepared using a Raman signal molecule and dibenzocyclooctyne-amine to functionalize a 10 nm Au nanoparticle, exhibits a negligible SERS effect and can recognize and link the azide-tagged glycan a click reaction. The substrate probe, an aptamer modified 30 or 40 nm Au nanoparticles, can specifically recognize the target protein to create an efficient SERS zone on the target protein. By controlling the size of the substrate probe to match the expression zone of the protein-specific glycan, an efficient SERS signal can be generated. This method has been successfully used for imaging of sialic acids on the target protein EpCAM on an MCF-7 cell surface and for the monitoring of the expression variation of protein-specific glycosylation during drug treatment. The concept of zone control can also be used to measure the distance between glycoproteins on a cell surface. This protocol shows promise in uncovering glycosylation-related biological processes.
利用两种新设计的纳米探针,展示了一种用于细胞表面蛋白质特异性糖基化拉曼成像的区域可控表面增强拉曼散射(SERS)效应。信号探针是用拉曼信号分子和二苯并环辛炔胺对10纳米金纳米颗粒进行功能化制备的,其SERS效应可忽略不计,并且可以通过点击反应识别并连接叠氮标记的聚糖。底物探针是一种适配体修饰的30或40纳米金纳米颗粒,能够特异性识别靶蛋白,在靶蛋白上创建一个高效的SERS区域。通过控制底物探针的大小以匹配蛋白质特异性聚糖的表达区域,可以产生高效的SERS信号。该方法已成功用于MCF-7细胞表面靶蛋白上皮细胞黏附分子(EpCAM)上唾液酸的成像,以及药物治疗期间蛋白质特异性糖基化表达变化的监测。区域控制的概念还可用于测量细胞表面糖蛋白之间的距离。该方案在揭示糖基化相关生物学过程方面显示出前景。