Quantitative analysis of fucosylated glycoproteins by immobilized lectin-affinity fluorescent labeling.
Ziyuan GaoSufeng ChenJing DuZhen WuWei GeSong GaoZeyang ZhouXiaodong YangYufei XingMinhua ShiYunyun HuWen TangJun XiaXumin ZhangJunhong JiangShuang YangPublished in: RSC advances (2023)
Human biofluids are often used to discover disease-specific glycosylation, since abnormal changes in protein glycosylation can discern physiopathological states. Highly glycosylated proteins in biofluids make it possible to identify disease signatures. Glycoproteomic studies on saliva glycoproteins showed that fucosylation was significantly increased during tumorigenesis and that glycoproteins became hyperfucosylated in lung metastases, and tumor stage is associated with fucosylation. Quantification of salivary fucosylation can be achieved by mass spectrometric analysis of fucosylated glycoproteins or fucosylated glycans; however, the use of mass spectrometry is non-trivial for clinical practice. Here, we developed a high-throughput quantitative method, lectin-affinity fluorescent labeling quantification (LAFLQ), to quantify fucosylated glycoproteins without relying on mass spectrometry. Lectins with a specific affinity for fucoses are immobilized on the resin and effectively capture fluorescently labeled fucosylated glycoproteins, which are further quantitatively characterized by fluorescence detection in a 96-well plate. Our results demonstrated that serum IgG can be accurately quantified by lectin and fluorescence detection. Quantification in saliva showed significantly higher fucosylation in lung cancer patients compared to healthy controls or other non-cancer diseases, suggesting that this method has the potential to quantify stage-related fucosylation in lung cancer saliva.
Keyphrases
- capillary electrophoresis
- mass spectrometry
- high throughput
- label free
- clinical practice
- liquid chromatography
- high resolution
- quantum dots
- endothelial cells
- high performance liquid chromatography
- ionic liquid
- loop mediated isothermal amplification
- genome wide
- living cells
- squamous cell carcinoma
- papillary thyroid
- computed tomography
- dna methylation
- gas chromatography
- risk assessment
- gene expression
- binding protein
- cell surface
- tandem mass spectrometry