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Detection of biomolecular microarrays without fluorescent-labeling agents

机译:没有荧光标记剂的生物分子微阵列检测

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We developed an optical oblique-incidence reflectivity difference (OI-RD) scanning microscope for imaging microarrays of label-free protein and DNA. Such a microscope complements currently widely used fluorescence-based optical microscopes by offering the capability to detect biochemical activities of DNA and protein molecules without the influence of fluorescent-labeling molecules. The specific activity and function of protein molecules are particularly subject to binding of small or large foreign molecules either directly through conformational change in the protein molecule itself or indirectly through properties of the attached molecules. We show that an OI-RD microscope can be used to: 1) detect binding reactions on microarrays without labeling, 2) quantitatively measure the optical properties of microarray spots, and 3) detect microarrays submerged in solution (which will enable OI-RD to monitor reaction kinetics on microarrays in reactive solutions). Furthermore, using both OI-RD and fluorescence images of an immunoglobulin-G (IgG) protein microarray, we observed that labeled and unlabeled IgG molecules deposited on the microarray substrate exhibit different wetting behaviors, and a mixture of the two tends to segregate into labeled and unlabeled regions. This illustrates potentially undesirable effects of fluorescent-labeling agents on protein properties that are of interest.
机译:我们开发了一种光学斜入射反射率差(OI-RD)扫描显微镜,用于成像无标签蛋白质和DNA的微阵列。这种显微镜通过提供检测DNA和蛋白质分子的生化活性而不受荧光标记分子影响的能力,对当前广泛使用的基于荧光的光学显微镜进行了补充。蛋白质分子的比活性和功能特别是直接通过蛋白质分子本身的构象变化或通过所连接分子的性质间接地与小或大外来分子结合。我们显示OI-RD显微镜可用于:1)在未标记的情况下检测微阵列上的结合反应,2)定量测量微阵列点的光学性质,和3)在溶液中浸没的微阵列(这将使OI-RD能够监测反应溶液中微阵列的反应动力学)。此外,使用免疫球蛋白G(IgG)蛋白微阵列的OI-RD和荧光图像,我们观察到沉积在微阵列基质上的标记和未标记的IgG分子表现出不同的润湿行为,并且两者的混合物倾向于分离成标记的和未标记的区域。这说明了荧光标记剂对感兴趣的蛋白质特性的潜在不良影响。

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