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METHOD AND APPARATUS FOR DETECTING ENZYMATIC ACTIVITY USING MOLECULES THAT CHANGE ELECTROPHORETIC MOBILITY

机译:用改变电泳移动性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 (114) that undergo a change in electrophoretic mobility upon chemical reaction such as that catalyzed by an enzyme (112). Specificity is achieved by using labeled substrate molecules (114) that can be acted upon only by specific enzymes (112). Thus, the activity of a specific enzyme (112) or class of enzymes can be determined. Measurements are made with the intracellular presence of such substrate molecules (114), at some time of interest, typically after exposure of the cell (46) to a stimulus (118) 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 (46) into which reporter substrate molecules (114) have been introduced. The cell contents are then subjected to capillary eletrophoresis (22) and enzymatic activity is determined by comparing amounts of substrate molecules (114) to amounts of enzymatically altered substrate molecules (128) which are separated by the electrophoresis and identified by the presence of a fluorescent label.
机译:通过使用荧光标记的底物分子(114)来测量分子的细胞内化学反应的活性,所述底物分子在化学反应(例如由酶(112)催化的)后发生电泳迁移率的变化。通过使用仅能被特异性酶(112)作用的标记的底物分子(114)来实现特异性。因此,可以确定特定酶(112)或酶类别的活性。通常在细胞(46)暴露于激活特定酶促途径的刺激物(118)之后,在感兴趣的某个时间用此类底物分子(114)的细胞内存在进行测量。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。使用快速可控的激光裂解来获得已向其中引入报告物底物分子(114)的单个细胞(46)的内含物。然后将细胞内容物进行毛细管电泳(22),并通过比较底物分子(114)的量与酶促修饰的底物分子(128)的量来确定酶活性,所述底物分子经电泳分离并通过荧光的存在进行鉴定标签。

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