Imaging specific cell-surface sialylation using DNA dendrimer-assisted FRET

被引:4
作者
Tang, Jinlu [1 ]
Li, Bo [1 ,2 ]
Qi, Cuihua [1 ]
Wang, Zhaoting [1 ]
Yin, Kai [1 ]
Guo, Linyan [1 ]
Zhang, Weihang [1 ]
Yuan, Baoyin [1 ,2 ,3 ]
机构
[1] Zhengzhou Univ, Sch Basic Med Sci, Zhengzhou 450001, Henan, Peoples R China
[2] Henan Prov Cooperat Innovat Ctr Canc Chemoprevent, Zhengzhou 450001, Henan, Peoples R China
[3] Zhengzhou Univ, State Key Lab Esophageal Canc Prevent & Treatment, Zhengzhou 450052, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Cell-surface sialylation; DNA dendrimer; FRET; MOE; Aptamer; ROLLING CIRCLE AMPLIFICATION; CHEMICAL BIOLOGY; SIALIC ACIDS; APTAMERS; GLYCANS; GLYCOSYLATION; CHEMISTRY; SELECTION; PROBES;
D O I
10.1016/j.talanta.2022.123399
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Sialylation plays a vital role in multiple different physiologic processes, aberrant sialylation is highly related to disease development. Especially in cancer development, changed states of specific cell-surface sialylation implies rich cancer-related information. Therefore, it is necessary to image specific cell-surface sialylation for better understanding biological functions of sialylation. To meet this purpose, we designed a DNA dendrimer-assisted fluorescence resonance energy transfer (FRET) strategy in this work. By labeling multiple FRET donors and acceptors on the target molecules through metabolic oligosaccharide engineering (MOE) and targeted recognition of aptamer-tethered DNA dendrimer, the FRET was significantly improved. With the DNA dendrimer-assisted FRET strategy, specific imaging of cell-surface sialylation on SMMC-7721 and CEM cells were successfully achieved. The obtained FRET signal intensity was approximately four times higher than the control without the assistance of DNA dendrimer. Moreover, this method is competent to monitor changed states of PTK7-specific sialylation induced by tunicamycin. The proposed imaging strategy may provide a powerful tool to explore the physiological roles of specific cell-surface sialylation and the related mechanism of diseases.
引用
收藏
页数:7
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