Highly sensitive and specific graphene oxide-based FRET aptasensor for quantitative detection of human soluble growth stimulating gene protein 2

适体 指数富集配体系统进化 化学 费斯特共振能量转移 检出限 石墨烯 线性范围 生物传感器 靶蛋白 色谱法 分子生物学 基因 纳米技术 荧光 生物化学 核糖核酸 生物 量子力学 物理 材料科学
作者
Zhikun Zeng,Wenfeng Li,Jixuan Zhang,Zijian Hu,Junyi Wu,Guangming Ye,Yi Luo
出处
期刊:Talanta [Elsevier BV]
卷期号:271: 125629-125629 被引量:12
标识
DOI:10.1016/j.talanta.2024.125629
摘要

Soluble growth stimulation expressed gene 2 (sST2) is a new generation biomarker in the diagnosis and prognosis of heart failure (HF). Here, the sST2-specific aptamers were selected from a random ssDNA library with the full length of 88 nucleotides (nt) via target-immobilized magnetic beads (MB)-based systematic evolution of ligands by exponential enrichment (SELEX) technology. After eight rounds of selection, six aptamers with the most enrichment were selected. Among, the aptamer L1 showed the high-affinity binding to sST2 with the lowest Kd value (77.3 ± 0.05 nM), which was chosen as the optimal aptamer for further molecular docking. Then, the aptamer L1 was used to construct a graphene oxide (GO) - based fluorescence resonance energy transfer (FRET) biosensor for sST2, which exhibits a linear detection range of 0.1–100 μg/ml and a detection limit of 3.7 ng/ml. The aptasensor was applied to detect sST2 in real samples, with a good correlation and agreement with the traditional enzyme-linked immunosorbent assay (ELISA) when quantitative analyzing the sST2 concentration in serum samples from HF patients. The results show that not only an efficient strategy for screening the practicable aptamer, but also a rapid and sensitive detection platform for sST2 were established.
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