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The identification of a novel SIRT6 modulator from Trigonella foenum-graecum using ligand fishing with protein coated magnetic beads

机译:使用配体包被和蛋白包被的磁珠钓鱼从三角叶草中鉴定出新型SIRT6调节剂

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摘要

SIRT6 is a histone deacetylase that has been proposed as a potential therapeutic target for metabolic disorders and the prevention of age-associated diseases. Thus the identification of compounds that modulate SIRT6 activity could be of great therapeutic importance. We have previously developed an H3K9 deacetylation guided assay with SIRT6 coated magnetic beads (SIRT6-MB). With the developed assay, we identified quercetin, naringenin and vitexin as SIRT6 inhibitors from T. foenum-graecum seed extract using a candidate approach. Currently, the predominant method for the identification of active compounds from a plant extract is carried out through a dereplication process. A novel targeted approach for the direct identification of active compounds from a complex matrix could save time and resources. Herein, we report the application of the SIRT6-MB for ‘fishing’ experiments utilizing T. foenum-graecum seed extract. In which orientin, and seventeen other compounds were identified as SIRT6 binders. This is the first use of this method for ‘fishing’ out active ligands from a botanical matrix, and sets the basis for the identification of active compounds from a complex matrix.
机译:SIRT6是一种组蛋白脱乙酰基酶,已被提议作为代谢紊乱和与年龄相关疾病的预防的潜在治疗靶标。因此,鉴定调节SIRT6活性的化合物可能具有重要的治疗意义。我们之前已经开发出了带有SIRT6涂层磁珠(SIRT6-MB)的H3K9脱乙酰基引导测定。通过开发的测定方法,我们使用一种候选方法从槲皮草种子提取物中鉴定出槲皮素,柚皮素和葡萄胎蛋白为SIRT6抑制剂。当前,从植物提取物中鉴定活性化合物的主要方法是通过去复制过程进行的。从复杂基质中直接鉴定活性化合物的新型靶向方法可以节省时间和资源。在此,我们报告了SIRT6-MB在利用镰刀T-草种子提取物进行“捕捞”实验中的应用。其中其中Orientin和其他17种化合物被确定为SIRT6粘合剂。这是该方法首次用于从植物基质中“捕捞”出活性配体,并为从复杂基质中鉴定出活性化合物奠定了基础。

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