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Protein-specific Raman imaging of glycosylation on single cells with zone-controllable SERS effect

机译:具有区域可控SERS效应的单细胞糖基化的蛋白质特异性拉曼成像

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摘要

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 via 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 in situ 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.
机译:提出了一种区域可控的SERS效应,用于使用两种新设计的纳米探针在细胞表面进行蛋白质特异性糖基化的拉曼成像。使用拉曼信号分子和二苯并环辛炔胺将10 nm Au纳米粒子功能化制备的信号探针显示出微不足道的SERS效果,并且可以通过点击反应识别并连接叠氮化物标记的聚糖。底物探针是适体修饰的30或40 nm Au纳米颗粒,可以特异性识别靶蛋白,从而在靶蛋白上创建有效的SERS区。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,可以产生有效的SERS信号。该方法已成功用于MCF-7细胞表面目标蛋白EpCAM上唾液酸的原位成像,并用于监测药物治疗过程中蛋白特异性糖基化的表达变化。区域控制的概念也可用于测量细胞表面糖蛋白之间的距离。该协议在揭示糖基化相关的生物过程中显示出希望。

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