糖基化
化学
聚糖
计算生物学
凝集素
背景(考古学)
PD-L1
糖蛋白
免疫系统
免疫疗法
生物化学
免疫学
生物
古生物学
作者
Mengjiao Huang,Lin Zhu,Siyin Kang,Fude Chen,Xinyu Wei,Liyuan Lin,Xiaofeng Chen,Wei Wang,Zhi Zhu,Chaoyong Yang,Yanling Song
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2021-11-23
卷期号:93 (48): 15958-15963
被引量:21
标识
DOI:10.1021/acs.analchem.1c03287
摘要
Immune checkpoint therapy has provided a weapon against cancer, but its response rate has been extremely low due to the lack of effective predictors. Herein, we developed a FRET strategy based on lectin for glycan labeling and an aptamer for PD-L1 antigen recognition for visualization of PD-L1-specific glycosylation (FLAG). The FLAG strategy combines the PD-L1 aptamer, which efficiently labels the PD-L1 polyantigen with smaller steric hindrance than the PD-L1 antibody, and metabolism-free lectin labeling for glycosylation. As a result, the FLAG strategy enables in situ visualization of PD-L1-specific glycosylation on the tissue section while maintaining the spatial context and tissue architecture. Due to nonmetabolic labeling, the FLAG strategy revealed that the tissue level of PD-L1-specific glycosylation is correlated with the efficacy of PD-1/PD-L1 therapy. Overall, the FLAG strategy provides a powerful tool for revealing the significance of PD-L1 glycosylation, offering the unprecedented potential for immunophenotypic differential analysis to predict the immunotherapy response.
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