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DNA 折纸金纳米棒二聚体纳米天线:实现用于单个癌症生物标志物 SERS 检测的可寻址光学热点。

DNA origami-templated gold nanorod dimer nanoantennas: enabling addressable optical hotspots for single cancer biomarker SERS detection.

机构信息

Institute of Nano Science and Technology, Sector-81, Mohali, Punjab-140306, India.

出版信息

Nanoscale. 2024 Aug 15;16(32):15128-15140. doi: 10.1039/d4nr01110d.

Abstract

The convergence of DNA origami and surface-enhanced Raman spectroscopy (SERS) has opened a new avenue in bioanalytical sciences, particularly in the detection of single-molecule proteins. This breakthrough has enabled the development of advanced sensor technologies for diagnostics. DNA origami offers a highly controllable framework for the precise positioning of nanostructures, resulting in superior SERS signal amplification. In our investigation, we have successfully designed and synthesized DNA origami-based gold nanorod monomer and dimer assemblies. Moreover, we have evaluated the potential of dimer assemblies for label-free detection of a single biomolecule, namely epidermal growth factor receptor (EGFR), a crucial biomarker in cancer research. Our findings have revealed that the significant Raman amplification generated by DNA origami-assembled gold nanorod dimer nanoantennas facilitates the label-free identification of Raman peaks of single proteins, which is a prime aim in biomedical diagnostics. The present work represents a significant advancement in leveraging plasmonic nanoantennas to realize single protein SERS for the detection of various cancer biomarkers with single-molecule sensitivity.

摘要

DNA 折纸术和表面增强拉曼光谱 (SERS) 的融合为生物分析科学开辟了新途径,特别是在单分子蛋白质检测方面。这一突破使用于诊断的先进传感器技术得以发展。DNA 折纸术为纳米结构的精确定位提供了高度可控的框架,从而实现了卓越的 SERS 信号放大。在我们的研究中,我们成功设计并合成了基于 DNA 折纸术的金纳米棒单体和二聚体组装体。此外,我们评估了二聚体组装体在无标记检测单个生物分子(即表皮生长因子受体,EGFR)方面的潜力,EGFR 是癌症研究中的关键生物标志物。我们的研究结果表明,DNA 折纸术组装的金纳米棒二聚体纳米天线产生的显著拉曼增强有助于无标记识别单个蛋白质的拉曼峰,这是生物医学诊断中的主要目标。本工作代表着利用等离子体纳米天线实现单分子 SERS 的重要进展,可实现对各种癌症生物标志物的单分子灵敏度检测。

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