Department of Chemistry , Sungkyunkwan University , Suwon 16419 , South Korea.
ACS Chem Neurosci. 2019 Nov 20;10(11):4612-4618. doi: 10.1021/acschemneuro.9b00467. Epub 2019 Oct 11.
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.
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。