Flechsig Holger
Department of Mathematical and Life Sciences, Graduate School of Science, Hiroshima University, Higashi-Hiroshima, Hiroshima, Japan.
Biophys J. 2017 Aug 8;113(3):558-571. doi: 10.1016/j.bpj.2017.06.043.
Allosteric effects often underlie the activity of proteins, and elucidating generic design aspects and functional principles unique to allosteric phenomena represent a major challenge. Here an approach consisting of the in silico design of synthetic structures, which, as the principal element of allostery, encode dynamical long-range coupling among two sites, is presented. The structures are represented by elastic networks, similar to coarse-grained models of real proteins. A strategy of evolutionary optimization was implemented to iteratively improve allosteric coupling. In the designed structures, allosteric interactions were analyzed in terms of strain propagation, and simple pathways that emerged during evolution were identified as signatures through which long-range communication was established. Moreover, robustness of allosteric performance with respect to mutations was demonstrated. As it turned out, the designed prototype structures reveal dynamical properties resembling those found in real allosteric proteins. Hence, they may serve as toy models of complex allosteric systems, such as proteins. Application of the developed modeling scheme to the allosteric transition in the myosin V molecular motor was also demonstrated.
别构效应通常是蛋白质活性的基础,阐明别构现象独特的通用设计方面和功能原理是一项重大挑战。本文提出了一种方法,该方法包括合成结构的计算机设计,这些结构作为别构的主要元素,编码两个位点之间的动态长程耦合。这些结构由弹性网络表示,类似于真实蛋白质的粗粒度模型。实施了进化优化策略以迭代改善别构耦合。在设计的结构中,根据应变传播分析别构相互作用,并将进化过程中出现的简单途径识别为建立长程通信的特征。此外,还证明了别构性能相对于突变的稳健性。事实证明,设计的原型结构揭示了与真实别构蛋白质中发现的动态特性相似的特性。因此,它们可以作为复杂别构系统(如蛋白质)的简化模型。还展示了所开发的建模方案在肌球蛋白V分子马达别构转变中的应用。