School of Chemistry and Biomolecular Sciences Research Complex, University of St Andrews and EaStCHEM, North Haugh, St Andrews, Fife, Scotland KY16 9ST, UK.
Molecules. 2013 Sep 23;18(9):11639-57. doi: 10.3390/molecules180911639.
The yeast three-hybrid (Y3H) approach shows considerable promise for the unbiased identification of novel small molecule-protein interactions. In recent years, it has been successfully used to link a number of bioactive molecules to novel protein binding partners. However despite its potential importance as a protein target identification method, the Y3H technique has not yet been widely adopted, in part due to the challenges associated with the synthesis of the complex chemical inducers of dimerisation (CIDs). The development of a modular approach using potentially "off the shelf" synthetic components was achieved and allowed the synthesis of a family of four triazole-containing CIDs, MTX-Cmpd2.2-2.5. These CIDs were then compared using the Y3H approach with three of them giving a strong positive interaction with a known target of compound 2, TgCDPK1. These results showed that the modular nature of our synthetic strategy may help to overcome the challenges currently encountered with CID synthesis and should contribute to the Y3H approach reaching its full potential as an unbiased target identification strategy.
酵母三杂交(Y3H)方法为非偏性鉴定新型小分子-蛋白质相互作用提供了很大的前景。近年来,它已成功地将许多生物活性分子与新型蛋白质结合伙伴联系起来。然而,尽管该方法作为一种蛋白质靶标鉴定方法具有重要意义,但 Y3H 技术尚未得到广泛采用,部分原因是与复杂的二聚化诱导物(CID)的合成相关的挑战。通过使用潜在的“现成”合成组件实现了模块化方法的开发,并允许合成一系列含有四唑的 CID,MTX-Cmpd2.2-2.5。然后使用 Y3H 方法对这些 CID 进行比较,其中三个与已知化合物 2 的靶标 TgCDPK1 产生强烈的阳性相互作用。这些结果表明,我们的合成策略的模块化性质可能有助于克服 CID 合成中目前遇到的挑战,并有助于 Y3H 方法充分发挥其作为非偏性靶标鉴定策略的潜力。