IBIVU - Deptartment of Computer Science, VU University, Amsterdam, The Netherlands.
Deptartment of Chemistry, University of Cambridge, Cambridge, United Kingdom.
PLoS One. 2014 Jan 15;9(1):e85185. doi: 10.1371/journal.pone.0085185. eCollection 2014.
The ability of many proteins to convert from their functional soluble state to amyloid fibrils can be attributed to inter-molecular beta strand formation. Such amyloid formation is associated with neurodegenerative disorders like Alzheimer's and Parkinson's. Molecular modelling can play a key role in providing insight into the factors that make proteins prone to fibril formation. However, fully atomistic models are computationally too expensive to capture the length and time scales associated with fibril formation. As the ability to form fibrils is the rule rather than the exception, much insight can be gained from the study of coarse-grained models that capture the key generic features associated with amyloid formation. Here we present a simple lattice model that can capture both protein folding and beta strand formation. Unlike standard lattice models, this model explicitly incorporates the formation of hydrogen bonds and the directionality of side chains. The simplicity of our model makes it computationally feasible to investigate the interplay between folding, amorphous aggregation and fibril formation, and maintains the capability of classic lattice models to simulate protein folding with high specificity. In our model, the folded proteins contain structures that resemble naturally occurring beta-sheets, with alternating polar and hydrophobic amino acids. Moreover, fibrils with intermolecular cross-beta strand conformations can be formed spontaneously out of multiple short hydrophobic peptide sequences. Both the formation of hydrogen bonds in folded structures and in fibrils is strongly dependent on the amino acid sequence, indicating that hydrogen-bonding interactions alone are not strong enough to initiate the formation of beta sheets. This result agrees with experimental observations that beta sheet and amyloid formation is strongly sequence dependent, with hydrophobic sequences being more prone to form such structures. Our model should open the way to a systematic study of the interplay between the factors that lead to amyloid formation.
许多蛋白质从其功能可溶性状态转变为淀粉样纤维的能力可归因于分子间β链形成。这种淀粉样形成与阿尔茨海默病和帕金森病等神经退行性疾病有关。分子建模可以在提供有关使蛋白质易于形成纤维的因素的见解方面发挥关键作用。然而,全原子模型在计算上过于昂贵,无法捕捉与纤维形成相关的长度和时间尺度。由于形成纤维是规则而不是例外,因此可以从研究捕获与淀粉样形成相关的关键通用特征的粗粒度模型中获得很多见解。在这里,我们提出了一个简单的晶格模型,该模型可以同时捕获蛋白质折叠和β链形成。与标准晶格模型不同,该模型明确包含氢键的形成和侧链的方向性。我们的模型简单,使研究折叠、无定形聚集和纤维形成之间的相互作用在计算上变得可行,并保持经典晶格模型模拟蛋白质折叠的高特异性的能力。在我们的模型中,折叠的蛋白质包含类似于天然存在的β-折叠的结构,其中交替出现极性和疏水性氨基酸。此外,由多个短疏水性肽序列自发形成具有分子间交叉β-链构象的纤维。折叠结构和纤维中氢键的形成强烈依赖于氨基酸序列,这表明氢键相互作用本身不足以引发β-片层的形成。这一结果与实验观察结果一致,即β片层和淀粉样形成强烈依赖于序列,疏水性序列更容易形成这种结构。我们的模型应该为系统研究导致淀粉样形成的因素之间的相互作用开辟道路。