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Method and apparatus for detecting enzymatic activity using molecules that change electrophoretic mobility

机译:使用改变电泳迁移率的分子检测酶活性的方法和装置

摘要

The activity of intracellular chemical reactions of molecules is measured by the use of fluorescently labeled substrate molecules that undergo a change in electrophoretic mobility upon chemical reaction such as that catalyzed by an enzyme. Specificity is achieved by using labeled substrate molecules that can be acted upon only by specific enzymes. Thus the activity of a specific enzyme or class of enzymes can be determined. Measurements are made with the intracellular presence of such substrate molecules, at some time of interest, typically after exposure of the cell to a stimulus that activates a particular enzymatic pathway. To ensure accuracy, measurements must be made in a timely manner so as to minimize chemical reactions occurring subsequent to the time of interest. Fast controllable laser lysis is used to obtain the contents of a single cell into which reporter substrate molecules have been introduced. The cell contents are then subjected to capillary electrophoresis and enzymatic activity is determined by comparing amounts of substrate molecules to amounts of enzymatically altered substrate molecules which are separated by the electrophoresis and identified by the presence of a fluorescent label.
机译:分子的细胞内化学反应的活性是通过使用荧光标记的底物分子来测量的,所述底物分子在化学反应(例如酶催化的反应)后发生电泳迁移率变化。通过使用标记的底物分子可以实现特异性,该底物分子只能被特定的酶作用。因此,可以确定特定酶或酶类别的活性。通常在细胞暴露于激活特定酶促途径的刺激下,在感兴趣的某个时间用此类底物分子在细胞内的存在进行测量。为了确保准确性,必须及时进行测量,以最大程度地减少感兴趣的时间之后发生的化学反应。快速可控的激光裂解用于获得已引入报道分子底物分子的单个细胞的内含物。然后将细胞内容物进行毛细管电泳,并通过将底物分子的量与通过电泳分离并通过荧光标记的存在进行鉴定的酶促改变的底物分子的量进行比较来确定酶活性。

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