Mashaghi Alireza, van Wijk Roeland J, Tans Sander J
FOM Institute AMOLF, Science Park 104, 1098 XG Amsterdam, the Netherlands.
FOM Institute AMOLF, Science Park 104, 1098 XG Amsterdam, the Netherlands.
Structure. 2014 Sep 2;22(9):1227-1237. doi: 10.1016/j.str.2014.06.015. Epub 2014 Aug 7.
Folded biomolecules display a bewildering structural complexity and diversity. They have therefore been analyzed in terms of generic topological features. For instance, folded proteins may be knotted, have beta-strands arranged into a Greek-key motif, or display high contact order. In this perspective, we present a method to formally describe the topology of all folded linear chains and hence provide a general classification and analysis framework for a range of biomolecules. Moreover, by identifying the fundamental rules that intrachain contacts must obey, the method establishes the topological constraints of folded linear chains. We also briefly illustrate how this circuit topology notion can be applied to study the equivalence of folded chains, the engineering of artificial RNA structures and DNA origami, the topological structure of genomes, and the role of topology in protein folding.
折叠的生物分子展现出令人眼花缭乱的结构复杂性和多样性。因此,人们从一般拓扑特征的角度对它们进行了分析。例如,折叠的蛋白质可能会打结,具有排列成希腊钥匙基序的β链,或者呈现出高接触序。从这个角度出发,我们提出了一种形式化描述所有折叠线性链拓扑结构的方法,从而为一系列生物分子提供一个通用的分类和分析框架。此外,通过确定链内接触必须遵循的基本规则,该方法确立了折叠线性链的拓扑约束。我们还简要说明了这种电路拓扑概念如何应用于研究折叠链的等效性、人工RNA结构和DNA折纸的工程设计、基因组的拓扑结构以及拓扑结构在蛋白质折叠中的作用。