Dipartimento di Ing. Civile, Ambientale, del Territorio, Edile e di Chimica, Politecnico di Bari, Via Re David 200, 70126 Bari, Italy; INFN Sezione di Bari, I-70126 Bari, Italy.
Laboratory of Bio-inspired, Bionic, Nano, Meta Materials & Mechanics, Department of Civil, Environmental and Mechanical Engineering, University of Trento, Italy; School of Engineering and Materials Science, Queen Mary University of London, UK.
Acta Biomater. 2021 Oct 15;134:477-489. doi: 10.1016/j.actbio.2021.07.032. Epub 2021 Jul 22.
We propose a simple general framework to predict folding, native states, energy barriers, protein unfolding, as well as mutation induced diseases and other protein structural analyses. The model should not be considered as an alternative to classical approaches (Molecular Dynamics or Monte Carlo) because it neglects low scale details and rather focuses on global features of proteins and structural information. We aim at the description of phenomena that are out of the range of classical molecular modeling approaches due to the large computational cost: multimolecular interactions, cyclic behavior under variable external interactions, and similar. To demonstrate the effectiveness of the approach in a real case, we focus on the folding and unfolding behavior of tropoelastin and its mutations. Specifically, we derive a discrete mechanical model whose structure is deduced based on a coarse graining approach that allows us to group the amino acids sequence in a smaller number of `equivalent' masses. Nearest neighbor energy terms are then introduced to reproduce the interaction of such amino acid groups. Nearest and non-nearest neighbor energy terms, inter and intra functional blocks are phenomenologically added in the form of Morse potentials. As we show, the resulting system reproduces important properties of the folding-unfolding mechanical response, including the monotonic and cyclic force-elongation behavior, representing a physiologically important information for elastin. The comparison with the experimental behavior of mutated tropoelastin confirms the predictivity of the model. STATEMENT OF SIGNIFICANCE: Classical approaches to the study of phenomena at the molecular scale such as Molecular Dynamics (MD) represent an incredible tool to unveil mechanical and conformational properties of macromolecules, in particular for biological and medical applications. On the other hand, due to the computational cost, the time and spatial scales are limited. Focusing of the real case of tropoelastin, we propose a new approach based on a careful coarse graining of the system, able to describe the overall properties of the macromolecule and amenable of extension to larger scale effects (protein bundles, protein-protein interactions, cyclic loading). The comparison with tropoelastin behavior, also for mutations, is very promising.
我们提出了一个简单的通用框架,用于预测折叠、天然状态、能量障碍、蛋白质变性,以及突变引起的疾病和其他蛋白质结构分析。该模型不应被视为替代经典方法(分子动力学或蒙特卡罗方法),因为它忽略了小尺度细节,而是专注于蛋白质的全局特征和结构信息。我们的目标是描述由于计算成本过高而超出经典分子建模方法范围的现象:多分子相互作用、在可变外部相互作用下的循环行为等。为了在实际案例中证明该方法的有效性,我们专注于原弹性蛋白及其突变体的折叠和变性行为。具体来说,我们推导出了一个离散力学模型,其结构基于粗粒化方法推导得出,该方法允许我们将氨基酸序列分组为较少数量的“等效”质量。然后引入最近邻能量项来再现这些氨基酸基团的相互作用。最近邻和非最近邻能量项、内功能块和外功能块以 Morse 势的形式添加到系统中。正如我们所展示的,所得到的系统再现了折叠-变性力学响应的重要性质,包括单调和循环力-伸长行为,这是弹性蛋白的一个重要生理信息。与突变原弹性蛋白的实验行为的比较证实了该模型的可预测性。
在分子尺度上研究现象的经典方法,如分子动力学 (MD),是揭示生物大分子力学和构象特性的一种非常有用的工具,特别是对于生物和医学应用。另一方面,由于计算成本,时间和空间尺度是有限的。我们专注于原弹性蛋白的实际案例,提出了一种新的方法,该方法基于对系统的仔细粗粒化,能够描述大分子的整体特性,并能够扩展到更大的尺度效应(蛋白质束、蛋白质-蛋白质相互作用、循环加载)。与原弹性蛋白行为的比较,也包括突变体,是非常有前景的。