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Simple quantitative fluorescent assay method for determining the activity of transport proteins of interest

机译:用于确定目标转运蛋白活性的简单定量荧光测定方法

摘要

The invention relates to a simple quantitative fluorescent assay method for determining the activity of transport proteins, more specifically multi-drug resistance associated proteins (MRPs). The method of the invention is performed on a well sealed culture of polarized cells expressing a transport protein of interest grown to confluency on a permeable support, said confluent cell culture forming well separated apical and basolateral compartments. The cells are contacted with a cell permeable non-fluorescent derivative of a fluorescent compound (e.g. calcein AM) in one compartment and, after a certain period of incubation, the fluorescence intensity detected in a sample taken from the opposite compartment is indicative of the activity of the transport protein of interest expressed in the cells. The invention also concerns methods for the qualitative and quantitative determination of inhibitors and activators of transport proteins of interest and methods for assessing basolateral and/or apical localization of plasma membrane bound transport proteins of interest in polarized cells.
机译:本发明涉及一种简单的定量荧光测定法,该测定法用于测定转运蛋白,特别是多药耐药相关蛋白(MRP)的活性。本发明的方法在极化细胞的密封良好的培养物中进行,所述极化细胞表达在转运性支持物上生长至汇合的感兴趣的转运蛋白,所述汇合的细胞培养物形成良好分离的顶端和基底外侧区室。在一个隔室中将细胞与荧光化合物(例如钙黄绿素AM)的可渗透细胞的非荧光衍生物接触,经过一定时间的培养,从相对隔室中采集的样品中检测到的荧光强度表明了该活性在细胞中表达的目的转运蛋白的表达。本发明还涉及定性和定量确定目的转运蛋白的抑制剂和活化剂的方法,以及评估极化细胞中目的膜结合转运蛋白的基底外侧和/或顶端定位的方法。

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