首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Four-color alternating-laser excitation single-molecule fluorescence spectroscopy for next-generation biodetection assays
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Four-color alternating-laser excitation single-molecule fluorescence spectroscopy for next-generation biodetection assays

机译:四色交替激光激发单分子荧光光谱法用于下一代生物检测测定

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BACKGROUND: Single-molecule detection (SMD) technologies are well suited for clinical diagnostic applications by offering the prospect of minimizing precious patient sample requirements while maximizing clinical information content. Not yet available, however, is a universal SMD-based platform technology that permits multiplexed detection of both nucleic acid and protein targets and that is suitable for automation and integration into the clinical laboratory work flow. METHODS: We have used a sensitive, specific, quantitative, and cost-effective homogeneous SMD method that has high single-well multiplexing potential and uses alternating-laser excitation (ALEX) fluorescenceaided molecule sorting extended to 4 colors (4c-ALEX). Recognition molecules are tagged with different-color fluorescence dyes, and coincident confocal detection of ≥2 colors constitutes a positive target-detection event. The virtual exclusion of the majority of sources of background noise eliminates washing steps. Sorting molecules with multidimensional probe stoichiometries (S) and single-molecule fluorescence resonance energy transfer efficiencies (E) allows differentiation of numerous targets simultaneously. RESULTS: We show detection, differentiation, and quantification-in a single well-of (a) 25 different fluorescently labeled DNAs; (b) 8 bacterial genetic markers, including 3 antibiotic drug-resistance determinants found in 11 septicemia-causing Staphylococcus and Enterococcus strains; and (c) 6 tumor markers present in blood. CONCLUSIONS: The results demonstrate assay utility for clinical molecular diagnostic applications by means of multiplexed detection of nucleic acids and proteins and suggest potential uses for early diagnosis of cancer and infectious and other diseases, as well as for personalized medicine. Future integration of additional technology components to minimize preanalytical sample manipulation while maximizing throughput should allow development of a user-friendly ("sample in, answer out") point-of-care platform for next-generation medical diagnostic tests that offer considerable savings in costs and patient sample.
机译:背景:单分子检测(SMD)技术非常适合于临床诊断应用,因为它提供了将患者宝贵的样本需求最小化而将临床信息含量最大化的前景。但是,尚不存在一种通用的基于SMD的平台技术,该技术允许对核酸和蛋白质靶标进行多重检测,并且适合于自动化和集成到临床实验室工作流程中。方法:我们已经使用了一种灵敏,特异性,定量且经济高效的均质SMD方法,该方法具有很高的单井多路复用潜力,并且使用了交替激光激发(ALEX)荧光分子分选技术,扩展了4种颜色(4c-ALEX)。识别分子用不同颜色的荧光染料标记,并且同时共聚焦检测≥2种颜色构成阳性目标检测事件。实际上排除了大多数背景噪声源,从而消除了清洗步骤。具有多维探针化学计量比(S)和单分子荧光共振能量转移效率(E)的分子可以同时区分众多目标。结果:我们在(a)25个不同的荧光标记DNA的单个孔中显示了检测,区分和定量; (b)在11种引起败血病的葡萄球菌和肠球菌菌株中发现了8种细菌遗传标记,包括3种抗生素耐药性决定因素; (c)血液中存在6种肿瘤标志物。结论:结果证明了通过核酸和蛋白质的多重检测在临床分子诊断应用中的测定实用性,并提出了在癌症,传染病和其他疾病的早期诊断以及个性化药物中的潜在用途。未来集成其他技术组件以最大程度地减少分析前样品的处理,同时最大程度地提高通量,应该可以为下一代医学诊断测试开发一种用户友好型(即时输入,“出样”)即时护理平台,从而节省大量成本和病人样本。

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