College of Biological Science and Engineering , Fuzhou University , Fuzhou 350116 , P. R. China.
Department of Medical Oncology , Fujian Medical University Union Hospital , Fuzhou 350001 , P. R. China.
J Am Chem Soc. 2018 Dec 5;140(48):16589-16595. doi: 10.1021/jacs.8b08442. Epub 2018 Nov 19.
The visualization of glycosylation states of specific proteins in vivo is of great importance for uncovering their roles in disease development. However, the ubiquity of glycosylation makes probing the glycans on a certain protein as difficult as looking for a needle in a haystack. Herein, we demonstrate a proximity-induced hybridization chain reaction (HCR) strategy for amplified visualization of protein-specific glycosylation. The strategy relies on designing two kinds of DNA probes, glycan conversion probes and protein recognition probes, which are attached to glycans and target proteins, respectively. Upon sequential binding to the targets, the proximity-induced hybridization between two probes occurs, which leads to the structure-switching of protein recognition probes, followed by triggering of HCR assembly. This strategy has been used to visualize tyrosine-protein kinase 7-specific sialic acid in living CEM cells and zebrafish and to monitor its variation during drug treatment. It provides a potential tool for investigating protein-specific glycosylation and researching the relation between dynamic glycans state and disease process.
在体内可视化特定蛋白质的糖基化状态对于揭示它们在疾病发展中的作用非常重要。然而,糖基化的普遍性使得探测特定蛋白质上的聚糖就像在干草堆中寻找一根针一样困难。在此,我们展示了一种基于邻近诱导杂交链式反应(HCR)的策略,用于放大可视化蛋白质特异性糖基化。该策略依赖于设计两种 DNA 探针,即糖基化转换探针和蛋白质识别探针,它们分别附着在聚糖和靶蛋白上。在依次与靶标结合后,两个探针之间发生邻近诱导杂交,导致蛋白质识别探针的结构转换,随后触发 HCR 组装。该策略已用于可视化活 CEM 细胞和斑马鱼中酪氨酸蛋白激酶 7 特异性唾液酸,并监测其在药物治疗过程中的变化。它为研究蛋白质特异性糖基化和研究动态糖状态与疾病过程之间的关系提供了一种潜在的工具。