Interferometric Nano-sensing for Biochemical Analysis

用于生化分析的干涉纳米传感

• 批准号: 6970011
• 负责人: DARRYL J. BORNHOP
• 金额: $ 22.23万
• 依托单位: VANDERBILT UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-07-01 至 2009-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6970011
• 关键词: analytical chemistry; interferometry; microfluidics; protein binding; technology /technique development

DESCRIPTION (provided by applicant): Protein - protein and ligand - substrate interactions are central to understanding basic cellular function and for evaluating therapeutics. However, the tools available to quantify these interactions without modifying the proteins or ligands have important limitations. Surface immobilization of the substrate, receptor, or protein or the attachment of a signaling fluorophore influences molecular interactions. It is desirable to eliminate the need for the surface chemistry normally used in binding assays, since it presents persistent problems including: complicated kinetics due to surface bound targets, lack of durability and longevity, high cost, non-specific binding, and difficulty in quantification of the immobilized targets. The ability to perform pure liquid - phase molecular binding analysis in a mu-TAS format would eliminate many of the problems that arise from the surface chemistry, while facilitating small volume samples to be studied. Preliminary observations presented here indicate that molecular interactions, such as protein - protein or ligand - substrate binding, can be studied in the absence of these perturbations, at high sensitivity, in picoliter volumes and in free-solution using on-chip interferometric backscatter detection (OCIBD). The proposed technology uses a simple and inexpensive optical train to facilitate these homogeneous, label-free measurements. OCIBD monitors minute refractive index changes within a microfluidics channel formed in silica or PDMS. OCIBD performed in a non-modified PDMS channel has recently facilitated quantification of reversible and irreversible protein - protein binding without a fluorescent label, the direct measurement of DNA interactions and fluorescent tag perturbations on delta/G. These determinations were performed in picoliter volumes and at attomolar levels and confirmed by Isothermal Titration Calorimetry (ITC). It has been possible to quantify reaction kinetics and binding affinities (Ko) for protein-IgG label-free in free-solution, with detection limits of 4 attomoles for IgG. Recently it has been possible to detect 10,800 molecules of IL-2 with backscattering interferometry. This proposal expands on these results, culminating a multiplexed OCIBD for homogeneous (free-solution) molecular interaction assays.

描述（由申请人提供）：蛋白质-蛋白质和配体-底物相互作用是理解基本细胞功能和评价治疗的核心。然而，在不修饰蛋白质或配体的情况下量化这些相互作用的工具具有重要的局限性。底物、受体或蛋白质的表面固定或信号荧光团的附着影响分子相互作用。期望消除对通常用于结合测定的表面化学的需要，因为它存在持续的问题，包括：由于表面结合的靶而导致的复杂动力学、缺乏耐久性和寿命、高成本、非特异性结合以及难以定量固定的靶。以mu-TAS形式进行纯液相分子结合分析的能力将消除许多由表面化学引起的问题，同时便于研究小体积样品。这里提出的初步观察表明，分子间的相互作用，如蛋白质-蛋白质或配体-底物结合，可以在没有这些扰动的情况下，在高灵敏度，在皮升体积和自由溶液中使用芯片上干涉反向散射检测（OCIBD）进行研究。所提出的技术使用一个简单而廉价的光学火车，以促进这些均匀的，无标记的测量。OCIBD监测在二氧化硅或PDMS中形成的微流体通道内的微小折射率变化。在未修饰的PDMS通道中进行的OCIBD最近促进了在没有荧光标记的情况下可逆和不可逆的蛋白质-蛋白质结合的定量、DNA相互作用的直接测量和δ/G上的荧光标记扰动。这些测定以皮升体积和阿摩尔水平进行，并通过等温滴定量热法（ITC）进行确认。它已经可以量化反应动力学和结合亲和力（Ko）的蛋白质-IgG标记的自由溶液中，检测限为4阿托摩尔的IgG。最近，已经可以用反向散射干涉法检测10，800个IL-2分子。该建议扩展了这些结果，最终多重OCIBD同质（自由溶液）分子相互作用测定。