影响细菌双组分信号转导反应调节蛋白与同源启动子DNA相互作用的化合物筛选。

Matthew G Erickson, Andrew T Ulijasz, Bernard Weisblum
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引用次数: 1

摘要

细菌信号转导系统可以作为药物靶点。信号转导靶标分为两组——传感器激酶和反应调节因子。先前报道的研究描述了被认为会使传感器激酶失活的撞击,但仔细检查后发现它在其他地方起作用;一个可能的原因是全长传感器激酶是完整的膜蛋白,其活性可能反映与细胞膜或膜组分的相互作用。我们描述了一个模型系统,而不是基于在均相反应中测试化合物和响应调节器之间的相互作用。在该系统中,反应调节因子- dna复合物的形成及其被测试化合物的抑制作用被荧光偏振测量。该模型系统应易于适应基于其他细菌双组分转导系统的药物发现。
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Screening for compounds that affect the interaction between bacterial two-component signal transduction response regulator protein and cognate promoter DNA.

Bacterial signal transduction systems can be used as drug targets. The signal transduction targets fall into two groups--sensor kinases and response regulators. Previously reported studies describe hits that were thought to inactivate sensor kinases but on closer examination were found to act elsewhere instead; a possible reason for this is that full-length sensor kinases are integral membrane proteins whose activity might reflect interaction with the cell membrane or with membrane components. We describe a model system that instead is based on the interaction between a test compound and a response regulator in a homogeneous phase reaction. In this system, response regulator-DNA complex formation and its inhibition by a test compound are measured by fluorescence polarization. The model system should be readily adaptable to drug discovery based on other bacterial two-component s transduction systems.

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