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Effects of desolvation barriers and sidechains on local-nonlocal coupling and chevron behaviors in coarse-grained models of protein folding

机译:去溶剂化障碍和侧链对蛋白质折叠粗粒模型中局部-非局部偶联和人字形行为的影响

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Local-nontocal coupling is an organizational principle in protein folding. It envisions a cooperative energetic interplay between local conformational preferences and favorable nonlocal contacts. Previous theoretical studies by our group showed that two classes of native-centric coarse-grained models can capture the experimentally observed high degrees of protein folding cooperativity and diversity in folding rates. These models either embody an explicit local-nonlocal coupling mechanism or incorporate desolvation barriers in the models' pairwise interactions. Here a conceptual connection is made between these two paradigmatic coarse-grained interaction schemes by showing that desolvation barriers enhance local-nonlocal coupling. Furthermore, we find that a class of coarse-grained protein models with a single-site representation of sidechains also increases local-nonlocal coupling relative to mainchain models without sidechains. Enhanced local-nonlocal coupling generally leads to higher folding cooperativity and chevron plots with more linear folding arms. For the sidechain models studied, the chevron plot simulated with entirely native-centric intrachain interactions behaves very similarly to the corresponding chevron plots simulated with interactions that are partly modulated by sequence-and denaturant-dependent transfer free energies. In these essentially native-centric models, the mild chevron rollovers in the simulated folding arm are caused by occasionally populated intermediates as well as the movement of the unfolded and putative folding transition states. The strength and limitation of the models are analyzed by comparison with experiment. New formulations of sidechain models that may provide a physical account for nonnative interactions are also explored.
机译:局部-非分子偶联是蛋白质折叠中的组织原理。它设想了局部构象偏好与有利的非局部接触之间的合作性能量相互作用。我们小组先前的理论研究表明,两类以本机为中心的粗粒度模型可以捕获实验观察到的高度蛋白质折叠协同性和折叠率多样性。这些模型要么体现了显式的局部-非局部耦合机制,要么在模型的成对相互作用中纳入了去溶剂化障碍。在这里,通过证明去溶剂化障碍增强了局部-非局部耦合,在这两个范式的粗粒相互作用方案之间建立了概念上的联系。此外,我们发现,相对于没有侧链的主链模型,一类具有侧链单点表示的粗粒度蛋白质模型也增加了局部-非局部偶联。增强的局部-非局部耦合通常会导致更高的折叠协作性和带有更多线性折叠臂的V形图。对于所研究的侧链模型,使用完全以本机为中心的链内交互作用模拟的人字形图的行为与通过交互作用模拟的相应人字形图的行为非常相似,该交互作用部分受依赖于序列和变性剂的转移自由能的调节。在这些本质上以自然为中心的模型中,模拟折叠臂中的人字形轻度翻转是由偶尔填充的中间体以及未折叠和假定的折叠过渡状态的移动引起的。通过与实验比较,分析了模型的强度和局限性。还探索了可能为非本地交互提供物理解释的侧链模型的新公式。

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