Suppr超能文献

由于组氨酸互变异构效应导致 Aβ 成熟纤维的结构和结合特性。

Structural and Binding Properties on Aβ Mature Fibrils Due to the Histidine Tautomeric Effect.

机构信息

Department of Chemistry , Sungkyunkwan University , Suwon 16419 , South Korea.

出版信息

ACS Chem Neurosci. 2019 Nov 20;10(11):4612-4618. doi: 10.1021/acschemneuro.9b00467. Epub 2019 Oct 11.

Abstract

Many studies have focused on histidine behaviors in misfolding diseases. However, histidine behaviors on mature fibrils are still unknown. In the current study, we investigated mature fibrils with various histidine states to understand the structural properties of the histidine tautomeric effect on mature fibrils. Our results show that substituting chain 1 with different histidine states affects Aβ structural properties in A2, D7-G9, H14-Q15, S26-N27, and G33-G37 regions. The binding free energies with substituted fibrils were influenced not only along the axial direction, but also between duplex fibrils. Our results suggest that substituted (εδδ) preferentially disturbed the stability among the current mature fibrils. Further, H-bonded network differences indicate that twisted morphologies in mature fibrils are derived from the position and orientation of the imidazole ring in histidines. Our current study helps to elucidate histidine behaviors on mature fibrils, which will present opportunities to understand the misfolding mechanisms.

摘要

许多研究都集中在错误折叠疾病中的组氨酸行为上。然而,对于成熟原纤维上的组氨酸行为仍不清楚。在本研究中,我们研究了具有各种组氨酸状态的成熟原纤维,以了解组氨酸互变异构效应对成熟原纤维的结构特性的影响。我们的结果表明,用不同的组氨酸状态取代链 1 会影响 Aβ 在 A2、D7-G9、H14-Q15、S26-N27 和 G33-G37 区域的结构特性。取代原纤维的结合自由能不仅受到轴向的影响,而且还受到双股原纤维之间的影响。我们的结果表明,取代的(εδδ)优先扰乱了当前成熟原纤维之间的稳定性。此外,氢键网络差异表明,成熟原纤维中的扭曲形态源于组氨酸中咪唑环的位置和取向。我们目前的研究有助于阐明成熟原纤维上的组氨酸行为,这将为理解错误折叠机制提供机会。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验