癌胚抗原
胶体金
检出限
材料科学
枚举
抗原
纳米颗粒
免疫分析
分子印迹
扫描电子显微镜
纳米技术
蛋白质阵列分析
抗体
色谱法
化学
癌症
生物
免疫学
选择性
催化作用
DNA微阵列
生物化学
组合数学
基因表达
基因
复合材料
遗传学
数学
作者
Xin Zhou,Chih‐Tsung Yang,Qiaoshu Xu,Zhichao Lou,Zhengfeng Xu,Benjamin Thierry,Ning Gu
标识
DOI:10.1021/acsami.8b19055
摘要
Currently, it remains challenging to count protein-biomarker molecules present in a small droplet of biological samples. Herein, we propose a gold nanoparticle (GNP) probe-assisted sandwich-counting strategy that relies on a GNP probe, an antibody-functionalized chip to "count" antigen molecules using a scanning electron microscope. Both standard carcinoembryonic antigen (CEA) and two real CEA-related tumor samples (tumor tissues and serum) were assayed to demonstrate the proof-of-concept of the counting strategy. Results show that our method is excellently correlative with enzyme-linked immuno-sorbent assay (ELISA) that is widely used in clinics for antigen or antibody detection and the limit of detection of our enumeration strategy reaches down to 0.045 ng/mL, which is ∼40 times more sensitive than the conventional ELISA. Therefore, our GNP probe-assisted sandwich-counting strategy has the potential to be used for quantification of protein biomarkers at ultralow concentrations in early tumor specimens and detection of target proteins in much diluted concentrations.
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