...
【24h】

Arresting an Unusual Amide Tautomer Using Divalent Cations

机译:使用二数阳离子逮捕一个不寻常的酰胺互变异构体

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Ion-specific effects on peptides and proteins are key to biomolecular structure and stability. The subtle roles of the cations are far less understood, compared to the pronounced effects of the anions on proteins. Most importantly, divalent cations such as Ca2+ and Mg2+ are crucial to several biological functions. Herein, we demonstrate that an amide-iminolate equilibrium is triggered by the binding of the divalent cations to the amide oxygen in aqueous solution. The excellent agreement between the experimental and theoretical results confirms the arrest of an unusual amide tautomer by the divalent cations, which is a rarely known phenomenon that might open up an array of applications in chemistry and biology.
机译:对肽和蛋白质的离子特异性效果是生物分子结构和稳定性的关键。 与蛋白质阴离子的发明效应相比,阳离子的微妙角色远不太清楚。 最重要的是,如CA2 +和MG2 +等二价阳离子对若干生物学功能至关重要。 在此,我们证明通过二价阳离子与酰胺水溶液中的酰胺氧的结合引发酰胺 - ininolate平衡。 实验和理论结果之间的良好一致性证实了二价阳离子的不寻常的酰胺互变异构成,这是一个很少已知的现象,可能在化学和生物学中开辟一系列应用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号