Suppr超能文献

近红外表面等离子体共振相成像和纳米粒子增强表面等离子体共振相成像在寡核苷酸和适体微阵列的超灵敏蛋白质和 DNA 生物传感中的应用。

Near infrared surface plasmon resonance phase imaging and nanoparticle-enhanced surface plasmon resonance phase imaging for ultrasensitive protein and DNA biosensing with oligonucleotide and aptamer microarrays.

机构信息

Department of Chemistry, University of California-Irvine, Irvine, California 92697, USA.

出版信息

Anal Chem. 2012 Jan 3;84(1):440-5. doi: 10.1021/ac202863k. Epub 2011 Dec 15.

Abstract

The techniques of surface plasmon resonance-phase imaging (SPR-PI) and nanoparticle-enhanced SPR-PI have been implemented for the multiplexed bioaffinity detection of proteins and nucleic acids. The SPR-PI experiments utilized a near-infrared 860 nm light emitting diode (LED) light source and a wedge depolarizer to create a phase grating on a four-element single-stranded DNA (ssDNA) microarray; bioaffinity adsorption onto the various microarray elements was detected via multiplexed real time phase shift measurements. In a first set of demonstration experiments, an ssDNA aptamer microarray was used to directly detect thrombin at concentrations down to 100 pM with SPR-PI. Two different ssDNA aptamers were used in these experiments with two different Langmuir adsorption coefficients, K(A1) = 4.4 × 10(8) M(-1) and K(A2) = 1.2 × 10(8) M(-1). At concentrations below 1 nM, the equilibrium phase shifts observed upon thrombin adsorption vary linearly with concentration with a slope that is proportional to the appropriate Langmuir adsorption coefficient. The observed detection limit of 100 pM is approximately 20 times more sensitive than that observed previously with SPRI. In a second set of experiments, two short ssDNA oligonucleotides (38mers) were simultaneously detected at concentrations down to 25 fM using a three-sequence hybridization format that employed 120 nm DNA-modified silica nanoparticles to enhance the SPR-PI signal. In this first demonstration of nanoparticle-enhanced SPR-PI, the adsorbed silica nanoparticles provided a greatly enhanced phase shift upon bioaffinity adsorption due to a large increase in the real component of the interfacial refractive index from the adsorbed nanoparticle. As in the case of SPR-PI, the detection limit of 25 fM for nanoparticle-enhanced SPR-PI is approximately 20 times more sensitive than that observed previously with nanoparticle-enhanced SPRI.

摘要

表面等离子体共振-相成像(SPR-PI)和纳米粒子增强 SPR-PI 技术已被用于蛋白质和核酸的多重生物亲和力检测。SPR-PI 实验利用近红外 860nm 发光二极管(LED)光源和楔形去偏振器在四元件单链 DNA(ssDNA)微阵列上创建相位光栅;通过多路实时相移测量检测各种微阵列元件上的生物亲和力吸附。在一组演示实验中,使用 ssDNA 适体微阵列通过 SPR-PI 直接检测凝血酶,浓度低至 100pM。在这些实验中使用了两种不同的 ssDNA 适体,它们的 Langmuir 吸附系数分别为 K(A1)=4.4×10(8)M(-1)和 K(A2)=1.2×10(8)M(-1)。在低于 1nM 的浓度下,凝血酶吸附后观察到的平衡相移与浓度呈线性变化,斜率与适当的 Langmuir 吸附系数成正比。观察到的 100pM 检测限比以前使用 SPRI 观察到的检测限敏感约 20 倍。在第二组实验中,使用三序列杂交格式在低至 25fM 的浓度下同时检测两种短 ssDNA 寡核苷酸(38 个碱基),该格式使用 120nm 修饰 DNA 的硅纳米粒子增强 SPR-PI 信号。在纳米粒子增强 SPR-PI 的首次演示中,由于吸附纳米粒子使界面折射率的实部大大增加,因此在生物亲和力吸附后,吸附的硅纳米粒子提供了大大增强的相移。与 SPRI 一样,纳米粒子增强 SPR-PI 的 25fM 检测限比以前使用纳米粒子增强 SPRI 观察到的检测限敏感约 20 倍。

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