...
首页> 外文期刊>International Journal of Molecular Sciences >Influence of Secondary-Structure Folding on the Mutually Exclusive Folding Process of GL5/I27 Protein: Evidence from Molecular Dynamics Simulations
【24h】

Influence of Secondary-Structure Folding on the Mutually Exclusive Folding Process of GL5/I27 Protein: Evidence from Molecular Dynamics Simulations

机译:二级结构折叠对GL5 / I27蛋白互斥折叠过程的影响:来自分子动力学模拟的证据。

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Mutually exclusive folding proteins are a class of multidomain proteins in which the host domain remains folded while the guest domain is unfolded, and both domains achieve exchange of their folding status by a mutual exclusive folding (MEF) process. We carried out conventional and targeted molecular dynamics simulations for the mutually exclusive folding protein of GL5/I27 to address the MEF transition mechanisms. We constructed two starting models and two targeted models, i.e., the starting models GL5/I27-S and GL5/I27-ST in which the first model involves the host domain GL5 and the secondary-structure unfolded guest domain I27-S, while the second model involves the host domain GL5 and the secondary/tertiary-structure extending guest domain I27-ST, and the target models GL5-S/I27 and GL5-ST/I27 in which GL5-S and GL5-ST represent the secondary-structure unfolding and the secondary/tertiary-structure extending, respectively. We investigated four MEF transition processes from both starting models to both target models. Based on structural changes and the variations of the radius of gyration ( R g ) and the fractions of native contacts ( Q ), the formation of the secondary structure of the I27-guest domain induces significant extending of the GL5-host domain; but the primary shrinking of the tertiary structure of the I27-guest domain causes insignificant extending of the GL5-host domain during the processes. The results indicate that only formation of the secondary structure in the I27-guest domain provides the main driving force for the mutually exclusive folding/unfolding between the I27-guest and GL5-host domains. A special structure as an intermediate with both host and guest domains being folded at the same time was found, which was suggested by the experiment. The analysis of hydrogen bonds and correlation motions supported the studied transition mechanism with the dynamical “tug-of-war” phenomenon.
机译:互斥折叠蛋白是一类多结构域蛋白,其中宿主结构域保持折叠而来宾结构域未折叠,并且两个结构域通过互斥折叠(MEF)过程实现其折叠状态的交换。我们对GL5 / I27的互斥折叠蛋白进行了常规和有针对性的分子动力学模拟,以解决MEF过渡机制。我们构建了两个起始模型和两个目标模型,即起始模型GL5 / I27-S和GL5 / I27-ST,其中第一个模型涉及主机域GL5和二级结构展开的来宾域I27-S,而第二个模型涉及主机域GL5和扩展来宾域I27-ST的二级/三级结构,以及目标模型GL5-S / I27和GL5-ST / I27,其中GL5-S和GL5-ST表示二级结构展开和二级/三级结构分别扩展。我们研究了从两个初始模型到两个目标模型的四个MEF过渡过程。基于结构变化以及回转半径(R g)和固有接触分数(Q)的变化,I27-客体域二级结构的形成诱导了GL5-宿主域的显着延伸。但是I27-guest域的三级结构的一次收缩会导致GL5-host域在此过程中的扩展不明显。结果表明,仅在I27-来宾域中二级结构的形成为I27-来宾域和GL5-宿主域之间的互斥折叠/展开提供了主要驱动力。实验表明,发现了一种特殊的结构作为中间结构,该结构同时折叠了主域和来宾域。氢键和相关运动的分析支持了带有动态“拔河”现象的过渡机制。

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