关于PFOA如何降低α-螺旋,破坏基质结合,并在模型球状蛋白中创建结合口袋的原子和分子洞察
Anju Yadav1, Lela Vuković1,2,3, Mahesh Narayan1
1Department of Chemistry and Biochemistry, The University of Texas at El Paso, El Paso, Texas 79968, United States.
Journal of the American Chemical Society
|April 24, 2024
概括
和多基物质 (PFAS) 改变了牛奶蛋白的结构和功能. 酸与β- 乳糖球蛋白 (BLG) 的结合会产生新的囊,损害蛋白质活性,并揭示PFAS的分子机制.
科学领域:
- 环境化学
- 生物化学
- 毒理学
背景情况:
- 和多基物质 (PFAS) 是具有重大健康风险的普遍环境污染物.
- PFAS与蛋白质等生物分子相互作用的分子机制尚不清楚.
研究的目的:
- 为了研究 perfluorooctanoic 酸 (PFOA) 和牛奶蛋白β-乳球蛋白 (BLG) 之间的分子相互作用.
- 阐明PFOA结合如何影响BLG在原子层面的结构和功能.
主要方法:
- 循环二色谱测定二次结构变化.
- 用于评估蛋白质功能障碍的疏水探针结合测试.
- 导向分子动力学和雨采样模拟用于原子级相互作用分析.
主要成果:
- PFOA诱导了剂量依赖的α-性损失,并改变了BLG中的β-片含量.
- PFOA的结合减弱了疏水探针的结合,表明功能受损.
- 计算模型显示PFOA通过残留物展开和分子间相互作用在BLG中形成一种新的,能量有利的结合口袋.
结论:
- 结合PFOA显著调节球状蛋白BLG的结构和功能.
- 这项研究为PFAS与蛋白质相互作用提供了新的原子层面的洞察力,有助于理解改变的生物结果.
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