METHODE DE DETECTION DE L'INTERNALISATION DE PROTEINES MEMBRANAIRES
    2.
    发明公开
    METHODE DE DETECTION DE L'INTERNALISATION DE PROTEINES MEMBRANAIRES 有权
    方法检测蛋白质内膜

    公开(公告)号:EP2329272A2

    公开(公告)日:2011-06-08

    申请号:EP09740420.6

    申请日:2009-07-30

    IPC分类号: G01N33/566 G01N33/58

    摘要: A method for detecting the internalization of a transmembrane protein of interest expressed at the surface of a cell, comprising the following steps: a) labelling the protein of interest with a fluorescent metal complex, the lifetime of which is greater than 0.1 ms; b) adding to the reaction medium a composition capable of causing the internalization of the protein of interest; c) adding to the reaction medium a modulating agent selected from: a. a fluorescent or nonfluorescent FRET acceptor compound compatible with said fluorescent metal complex, the final concentration of which in the reaction medium is greater than 10
    ‑7 M; b. a reducing agent, the redox potential of which is less than +0.1 V and preferably between 0.25 and 0.75 V; c. an agent which binds specifically, by noncovalent bonding, with the fluorescent metal complex; d. a metal ion which competes with the rare earth so as to form a nonfluorescent metal complex; d) measuring the luminescence emitted by the reaction medium at the emission wavelength of the fluorescent metal complex and/or at the emission wavelength of the modulating compound when said compound is a fluorescent acceptor compound; e) comparing the signal measured in step d) with a reference signal measured on cells having been subjected only to steps a) and c). Use: Method for detecting membrane protein internalization.

    摘要翻译: 一种检测细胞表面表达的感兴趣的跨膜蛋白的内化的方法,包括以下步骤:a)用荧光金属配合物标记感兴趣的蛋白质,其寿命大于0.1ms; b)向反应介质中加入能够引起感兴趣蛋白质内化的组合物; c)向反应介质中加入选自以下的调节剂:a。 与所述荧光金属配合物相容的荧光或非荧光FRET受体化合物,其在反应介质中的最终浓度大于10 -7 M; 湾 还原剂,其氧化还原电位低于+ 0.1V,优选在0.25和0.75V之间; C。 通过非共价键特异性结合荧光金属配合物的试剂; d。 与稀土竞争以形成无荧光金属络合物的金属离子; d)当所述化合物是荧光受体化合物时,在荧光金属络合物的发射波长处和/或在调制化合物的发射波长处测量由反应介质发射的发光; e)将步骤d)中测得的信号与仅在经过步骤a)和c)的细胞上测量的参考信号进行比较。 用途:检测膜蛋白内在化的方法。