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Development of a high throughput screening assay for inhibitors of hedgehog-heparin interactions

机译:刺猬与肝素相互作用抑制剂的高通量筛选测定方法的开发

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Abstract: The activity of hedgehog ligand is mediated in part by interactions with heparin and heparan sulfate proteoglycans. In order to identify inhibitors that block the interaction of hedgehog with heparin, we have developed a simple and robust high throughput assay based on fluorescence polarization. This assay utilizing fluorescein-labeled heparin binding to sonic hedgehog N-terminal domain (ShhN) protein was developed and optimized in a 384-well format. ShhN bound to fluorescein-labeled heparin with high affinity (KD = 99 nM) and the interaction was shown to be stable over time and tolerant to dimethyl sulfoxide (DMSO). A panel of unlabeled heparins of varying molecular weights was tested in the assay, with lower IC50 values correlating with heparins of increasing size. The assay was automated into two simple steps, and validation with whole DMSO plates yielded a Z’ factor of 0.56, indicating a robust assay for high throughput screening. We predict that this assay will be suitable for identifying chemical probes of hedgehog ligand-heparin interactions. Further, compounds that disrupt the ShhN interaction with heparin and/or heparan sulfate proteoglycans may be considered as potential therapeutics for those cancers driven by Hh ligand overexpression.
机译:摘要:刺猬配体的活性部分是通过与肝素和硫酸乙酰肝素蛋白聚糖的相互作用来介导的。为了鉴定阻断刺猬与肝素相互作用的抑制剂,我们开发了一种基于荧光偏振的简单而强大的高通量测定方法。利用荧光素标记的肝素与声波刺猬N末端域(ShhN)蛋白的结合,开发了该测定法,并以384孔格式进行了优化。 ShhN以高亲和力(KD = 99 nM)与荧光素标记的肝素结合,并且该相互作用显示出随时间推移稳定并耐受二甲基亚砜(DMSO)。在该测定法中测试了一组不同分子量的未标记肝素,较低的IC50值与大小增加的肝素相关。该测定法被自动化为两个简单的步骤,并且使用整个DMSO板进行验证得出的Z'因子为0.56,这表明该方法可用于高通量筛选。我们预测该测定将适合于鉴定刺猬配体-肝素相互作用的化学探针。另外,破坏ShhN与肝素和/或硫酸乙酰肝素蛋白聚糖的相互作用的化合物可以被认为是由Hh配体过表达驱动的那些癌症的潜在治疗剂。

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