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使用蛋白包被磁珠进行配体垂钓,从胡芦巴中鉴定一种新型SIRT6调节剂。

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

作者信息

Singh N, Ravichandran S, Spelman K, Fugmann S D, Moaddel R

机构信息

Biomedical Research Center, National institute on Aging, National Institutes of Health, 251 Bayview Boulevard, Suite 100, Baltimore, MD 21224, USA.

Advanced Biomedical Computing Center, Information Systems Program, Frederick National Laboratory for Cancer Research (FNLCR), Frederick, MD 21702, USA.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Oct 1;968:105-11. doi: 10.1016/j.jchromb.2014.03.016. Epub 2014 Mar 15.

Abstract

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.

摘要

SIRT6是一种组蛋白脱乙酰酶,已被提议作为代谢紊乱和预防与年龄相关疾病的潜在治疗靶点。因此,鉴定调节SIRT6活性的化合物可能具有重大的治疗意义。我们之前开发了一种用包被有SIRT6的磁珠(SIRT6-MB)进行的H3K9去乙酰化导向检测方法。利用这种开发的检测方法,我们采用候选方法从胡芦巴种子提取物中鉴定出槲皮素、柚皮素和牡荆素作为SIRT6抑制剂。目前,从植物提取物中鉴定活性化合物的主要方法是通过去重复过程进行。一种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在利用胡芦巴种子提取物进行“垂钓”实验中的应用。其中,荭草素和其他十七种化合物被鉴定为SIRT6结合剂。这是首次使用这种方法从植物基质中“钓出”活性配体,并为从复杂基质中鉴定活性化合物奠定了基础。

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Pharmacophore model of the quercetin binding site of the SIRT6 protein.SIRT6蛋白槲皮素结合位点的药效团模型。
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