Suppr超能文献

通过 DNA 引导的多功能 DNA-金纳米粒子的固定化制备的多模式等离子体生物传感纳米结构。

Multimodal plasmonic biosensing nanostructures prepared by DNA-directed immobilization of multifunctional DNA-gold nanoparticles.

机构信息

Nanobiotechnology for Diagnostics (Nb4D), IQAC-CSIC, Spain; CIBER de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), Jordi Girona 18-26, 08034 Barcelona, Spain.

Nanobiotechnology for Diagnostics (Nb4D), IQAC-CSIC, Spain; CIBER de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), Jordi Girona 18-26, 08034 Barcelona, Spain.

出版信息

Biosens Bioelectron. 2017 Apr 15;90:13-22. doi: 10.1016/j.bios.2016.11.022. Epub 2016 Nov 11.

Abstract

Biofunctional multimodal plasmonic nanostructures suitable for multiplexed localized surface plasmon resonance (LSPR) biosensing have been created by DNA-directed immobilization (DDI) of two distinct multifunctional biohybrid gold nanoparticles. Gold nanoparticles (AuNP) of distinct sizes, and therefore showing distinct plasmon resonant peaks (RP), have been biofunctionalized and codified with two different single stranded-DNA (ssDNA) chains. One of these oligonucleotide chains has been specifically designed to direct each AuNP to a distinct location of the surface of a DNA microarray chip through specific hybridization with complementary oligonucleotide strands. Scanning Electron Microscopy (SEM) has been used to demonstrate selective immobilization of each AuNP on distinct spots. The second ssDNA chain of the AuNPs provides the possibility to introduce by hybridization distinct types of bioactive molecules or bioreceptors, on a reversible manner. In this work, hapten-oligonucleotide bioconjugate probes, with sequences complementary to the second ssDNA linked to the AuNP, have been synthesized and used to create multiplexed hapten-biofuncionalized plasmonic nanostructures. The oligonucleotide probes consist on anabolic androgenic steroid haptens (AAS) covalently linked to specifically designed oligonucleotide sequences. The biofunctionality of these plasmonic nanostructures has been demonstrated by fluorescent microarray immunoassay and LSPR measurements, recording the shift of the RP produced after the antibody binding to the corresponding hapten-oligonucleotide probes immobilized on the nanostructured surface. Preliminary data show that this approach could allow manufacturing multifunctional multimodal LSPR chips for multiplexed analysis of different substances reaching very good detectability. Thus, small molecular weigh, analytes such as stanozolol (ST,) could be detected at concentrations in the low nM range. The results here presented open the door for an easy way to construct site-encoded multiplexed multimodal LSPR sensor transducers, combining the DDI strategies with multimodal biohybrid nanoparticles showing distinct optical properties.

摘要

通过 DNA 定向固定化 (DDI) 将两种不同的多功能生物杂交金纳米粒子固定在合适的位置,制造出适用于多重局部表面等离子体共振 (LSPR) 生物传感的生物功能化多模态等离子体纳米结构。不同尺寸的金纳米粒子 (AuNP) 具有不同的等离子体共振峰 (RP),并通过两条不同的单链 DNA (ssDNA) 链进行生物功能化和编码。其中一条寡核苷酸链经过专门设计,通过与互补寡核苷酸链特异性杂交,将每个 AuNP 引导到 DNA 微阵列芯片表面的特定位置。扫描电子显微镜 (SEM) 已被用于证明每个 AuNP 在特定位置的选择性固定化。AuNP 的第二条 ssDNA 链提供了以可逆方式引入不同类型的生物活性分子或生物受体的可能性。在这项工作中,合成了与 AuNP 连接的第二 ssDNA 互补的半抗原寡核苷酸生物缀合物探针,并用于创建多重半抗原生物功能化等离子体纳米结构。寡核苷酸探针由与特定设计的寡核苷酸序列共价连接的合成代谢雄激素类固醇半抗原 (AAS) 组成。通过荧光微阵列免疫分析和 LSPR 测量记录了抗体与固定在纳米结构表面上的相应半抗原-寡核苷酸探针结合后产生的 RP 的位移,证明了这些等离子体纳米结构的生物功能性。初步数据表明,这种方法可以制造多功能多模态 LSPR 芯片,用于对不同物质进行多重分析,达到非常好的检测灵敏度。因此,可以在低 nM 范围内检测到低分子量的分析物,如司坦唑醇 (ST)。这里呈现的结果为构建基于位置编码的多重多模态 LSPR 传感器转换器提供了一种简单的方法,该方法将 DDI 策略与具有不同光学特性的多模态生物杂交纳米粒子相结合。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验