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The inhibitory action of SQDG (sulfoquinovosyl diacylglycerol) from spinach on Cdtl-geminin interaction

机译:菠菜中SQDG(磺基喹喔酰基二酰基甘油)对Cdtl-Geminin相互作用的抑制作用

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A human replication initiation protein, Cdtl, is a central player in the cell cycle regulation of DNA replication, and geminin down-regulates Cdtl function by direct binding. It has been demonstrated that Cdtl hyperfunction resulting from Cdtl-geminin imbalance, for example, by geminin silencing with small interfering RNA, induces DNA re-replication and eventual cell death in some cancer-derived cell lines. We established a high throughput screening system based on a modified enzyme linked immunosorbent assay to identify compounds that interfere with human Cdtl-geminin binding. Using this system, we screened inhibitors from natural materials containing food components, and found that a glycolipid, sulfoquinovosyl diacylglycerol (SQDG), from spinach can inhibit Cdtl -geminin interaction in vitro, with 50% inhibition observed at concentrations of 1.79 ug/ml. Other major glycolipids, such as monogalactosyl diacylglycerol (MGDG) and digalactosyl diacylglycerol (DGDG) from spinach, had no influence. Surface plasmon resonance analysis demonstrated that SQDG bound selectively to Cdtl, but did not interact with geminin. Using three-dimensional computer modeling analysis, SQDG was considered to interact with the geminin interaction interface on Cdtl, and the sulfate group of SQDG was assumed to make hydrogen bonds with the residue of Arg346 of Cdtl. These data could help to further understanding of the structure and function of Cdtl. In addition, SQDG could be a clue to developing more appropriate inhibitors of Cdtl-geminin interactions.
机译:人类复制起始蛋白Cdtl在DNA复制的细胞周期调控中起着核心作用,而胚芽蛋白则通过直接结合来下调Cdtl功能。已经证明由Cdtl-双倍体蛋白失衡导致的Cdt1功能亢进,例如通过用小的干扰RNA使双倍体蛋白沉默而引起,在某些癌症来源的细胞系中诱导DNA再复制和最终细胞死亡。我们基于修饰的酶联免疫吸附测定法建立了高通量筛选系统,以鉴定干扰人Cdtl-Geminin结合的化合物。使用该系统,我们从含有食品成分的天然材料中筛选了抑制剂,发现菠菜中的糖脂,磺基喹喔酰基二酰基甘油(SQDG)可以在体外抑制Cdtl-双倍蛋白的相互作用,在1.79 ug / ml的浓度下观察到50%的抑制作用。其他主要糖脂,如菠菜中的单半乳糖基二酰基甘油(MGDG)和二半乳糖基二酰基甘油(DGDG),则没有影响。表面等离子体共振分析表明SQDG选择性绑定到Cdtl,但不与geminin相互作用。使用三维计算机建模分析,认为SQDG与Cdtl上的geminin相互作用界面相互作用,并且假定SQDG的硫酸根与Cdtl的Arg346残基形成氢键。这些数据可以帮助进一步了解Cdtl的结构和功能。此外,SQDG可能是开发更合适的Cdtl-geminin相互作用抑制剂的线索。

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