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首页> 外文期刊>E3S Web of Conferences >Combining bioinformatic prediction and assay experiment to identify novel xanthine oxidase inhibitory peptides from Pacific bluefin tuna ( Thunnus Orientalis)
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Combining bioinformatic prediction and assay experiment to identify novel xanthine oxidase inhibitory peptides from Pacific bluefin tuna ( Thunnus Orientalis)

机译:结合生物信息预测和测定实验鉴定太平洋蓝鳍金枪鱼的新型黄嘌呤氧化酶抑制肽(<斜斜探> Thunnus Orientalis

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In this work, we aim to combine bioinformatic prediction with a special experiment to search xanthine oxidase (XOD) inhibitory peptides from myosin of Pacific bluefin tuna ( Thunnus Orientalis ). The program Peptide Cutter, Peptide Ranker, Peptide Property calculator, Toxin Pred, and Discovery Studio (DS) help us screen the probable sequence. The result indicated that peptide ICRK has the highest inhibition effect and the value of IC50 was 14.18 mg/mL. The IC50 of the other two peptides (FDAK and MMER) were 16.8mg/mL and 15.3 mg/mL respectively. Molecular simulation demonstrated that ICRK interacted with amino acid residues GLU802, PHE914, ALA1079, GLU1261, LYS771, LEU648, THR1010, VAL1011 and SER 876. The possible inhibition mechanism of peptides and enzyme was stated by DS. Peptide ICRK blocked the entrance to the hydrophobic channel and stopped xanthine going into the active site of XOD. MMER and FDAK have the similar mechanism with ICRK. Therefore, ICRK, FDAK and MMER can be considered as nature XOD inhibitory peptides and further utilized.
机译:在这项工作中,我们的目的是将生物信息预测与特殊实验相结合,以搜索来自太平洋蓝鳍金枪鱼(Thunnus Orientalis)的肌蛋白的三原氧化酶(XOD)抑制肽。程序肽切割器,肽排名蛋白,肽属性计算器,毒素PRED和Discovery Studio(DS)帮助我们筛选可能的序列。结果表明,肽ICRK具有最高的抑制作用,IC 50的值为14.18mg / ml。另外两个肽(FDAK和MMER)的IC 50分别为16.8mg / ml和15.3mg / ml。分子模拟表明,ICRK与氨基酸残基GLU802,PHE914,ALA1079,GLU1261,LYS771,LEU648,THR1010,VAL1011和SER 876相互作用。DS鉴定肽和酶的可能抑制机制。肽ICRK阻止了疏水通道的入口,并停止了XONTHINE进入XOD的活跃点。 MMER和FDAK具有ICRK的类似机制。因此,ICRK,FDAK和MMER可以被认为是自然XOD抑制肽并进一步使用。

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