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基于 DNA 链置换的表面增强拉曼散射-荧光双模纳米探针用于活细胞中血管内皮生长因子的定量和成像。

DNA strand displacement based surface-enhanced Raman scattering-fluorescence dual-mode nanoprobes for quantification and imaging of vascular endothelial growth factor in living cells.

机构信息

School of Chemistry, Sun Yat-sen University, Guangzhou, 510006, China.

School of Chemistry, Sun Yat-sen University, Guangzhou, 510006, China.

出版信息

Biosens Bioelectron. 2022 May 15;204:114069. doi: 10.1016/j.bios.2022.114069. Epub 2022 Feb 10.

DOI:10.1016/j.bios.2022.114069
PMID:35182835
Abstract

Vascular endothelial growth factor (VEGF) is an important over-expressed growth protein during cell proliferation process, which has been regarded as a pivotal biomarker of several cancers mainly including malignant melanoma (MM). The development of accurate quantification analysis combined with imaging technology for biomarkers in complex biological system is significantly essential. In this study, surface-enhanced Raman scattering-fluorescence (SERS-FL) dual-mode nanoprobes based on Au nanoparticles modified magnetic FeO nanoparticles (FeO/AuNPs) were fabricated for in situ quantification and imaging of VEGF in living cells. Dual-mode SERS quantification-FL imaging was achieved through "off-on" mode of SERS and FL signals based on DNA strand displacement strategy. The stellate FeO/Au endowed the great magnetic separation function for SERS quantification-FL imaging performance. Under the optimum conditions, the SERS quantification mode for trace VEGF in cell lysis samples achieved the good linearity in the range of 0.01-50.0 ng/mL with an excellent limit of detection of 2.3 pg/mL (S/N = 3). The FL imaging mode could achieve the selective detection of trace VEGF distributing in living tumor cells. The developed dual-mode SERS-FL method could provide accurate quantification and imaging results, which was highly expected to have broad application for the selective, sensitive and accurate analysis of biomarkers in complex cell or other real biological samples.

摘要

血管内皮生长因子(VEGF)是细胞增殖过程中重要的过表达生长蛋白,已被视为多种癌症的关键生物标志物,主要包括恶性黑色素瘤(MM)。在复杂生物体系中,结合成像技术对生物标志物进行准确的定量分析是非常重要的。在本研究中,基于金纳米粒子修饰的磁性 FeO 纳米粒子(FeO/AuNPs)的表面增强拉曼散射-荧光(SERS-FL)双模纳米探针被制备用于活细胞中 VEGF 的原位定量和成像。通过基于 DNA 链置换策略的 SERS 和 FL 信号的“关-开”模式实现双模 SERS 定量-FL 成像。星形 FeO/Au 赋予了 SERS 定量-FL 成像性能优异的磁性分离功能。在最佳条件下,细胞裂解样品中痕量 VEGF 的 SERS 定量模式在 0.01-50.0ng/mL 的范围内具有良好的线性关系,检测限为 2.3pg/mL(S/N = 3)。FL 成像模式能够选择性地检测到分布在活肿瘤细胞中的痕量 VEGF。所开发的双模 SERS-FL 方法能够提供准确的定量和成像结果,有望广泛应用于复杂细胞或其他真实生物样品中生物标志物的选择性、灵敏和准确分析。

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