Charge sensitive optical detection for high throughput study of small molecules

用于小分子高通量研究的电荷敏感光学检测

基本信息

批准号：
8728790
负责人：
NONGJIAN TAO
金额：
$ 19.3万
依托单位：
ARIZONA STATE UNIVERSITY-TEMPE CAMPUS
依托单位国家：
美国
项目类别：
财政年份：
2012
资助国家：
美国
起止时间：
2012-09-19 至 2016-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8728790
关键词：
Address Antibodies Attention Binding Biochemical Biochemical Reaction Biological Markers Biological Models Biomedical Research Cell division Cell physiology Charge Detection Diagnosis Diagnostics Research Dimensions Disease Drug Industry Drug Targeting Dyes Electrons Enzymes Equipment Event Family Fiber Fluorescence Fluorescent Dyes Genomics Human Ionic Strengths Label Lead Letters Malignant Neoplasms Measurement Measures Membrane Proteins Methods Microscope Molecular Molecular Probes Monitor Mutate Noise Optics Pharmaceutical Preparations Phosphorylation Phosphotransferases Play Positioning Attribute Post-Translational Protein Processing Process Proliferating Proteins Proteomics Reaction Research Role Screening for cancer Signaling Protein Solutions Surface System Techniques Technology Variant Viscosity base cancer cell cancer initiation cancer therapy dalton design drug candidate drug development frontier high throughput screening inorganic phosphate metabolomics new technology optical fiber prevent screening small molecule success theories tool tumor progression

项目摘要

DESCRIPTION (provided by applicant): High-throughput detection of small molecules and post translational protein modifications that involve small molecule biochemical reactions are critical for understanding the mechanisms underlying cancer initiation and progression, for discovering proper biomarkers that enable early cancer detection, and for screening drug candidates for effective cancer treatment. The most widely used technology uses fluorescence labels, which is problematic for small molecules whose sizes are comparable to those of the fluorescent dyes. Various label- free techniques have been developed, but their sensitivity diminishes with the size of the molecules, making it extremely challenging to detect small molecules. To address the need, a charge sensitive optical detection will be developed in this project. The technology is particularly suitable for the detection of small molecules, and biochemical interactions that involve small mass changes. The detection method uses optical probes that compatible with the standard microplate technology, making it attractive for high-throughput detection. The success of the project will lead to a new detection technology to measure small molecule interactions, such as drug-target interactions, membrane protein signaling, protein phosphorylation and other post translational modifications, oxidative and reduction reactions that involves charge transfer. Many of these processes are highly important for the research, diagnostic and treatment of cancer.

描述（由申请人提供）：涉及小分子生化反应的小分子和翻译后蛋白质修饰的高通量检测对于了解癌症发生和进展的机制、发现能够进行早期癌症检测的适当生物标志物以及筛选至关重要有效治疗癌症的候选药物。最广泛使用的技术使用荧光标记，这对于尺寸与荧光染料相当的小分子来说是有问题的。各种无标记技术已经被开发出来，但它们的灵敏度随着分子大小的增加而降低，使得检测小分子变得极具挑战性。为了满足这一需求，该项目将开发电荷敏感光学检测装置。该技术特别适合检测小分子以及涉及小质量变化的生化相互作用。该检测方法使用与标准微孔板技术兼容的光学探针，使其对高通量检测具有吸引力。该项目的成功将催生一种新的检测技术来测量小分子相互作用，例如药物-靶点相互作用、膜蛋白信号传导、蛋白质磷酸化和其他翻译后修饰、涉及电荷转移的氧化和还原反应。其中许多过程对于癌症的研究、诊断和治疗非常重要。