Zhang Yitao, Malamakal Roy M, Chenoweth David M
Department of Chemistry, University of Pennsylvania, 231 South 34thStreet, Philadelphia, PA 19104 (USA).
Angew Chem Int Ed Engl. 2015 Sep 7;54(37):10826-32. doi: 10.1002/anie.201504459. Epub 2015 Jul 23.
Chirality is a property of asymmetry important to both physical and abstract systems. Understanding how molecular systems respond to perturbations in their chiral building blocks can provide insight into diverse areas such as biomolecular self-assembly, protein folding, drug design, materials, and catalysis. Despite the fundamental importance of stereochemical preorganization in nature and designed materials, the ramifications of replacing chiral centers with stereodynamic atomic mimics in the context of biomolecular systems is unknown. Herein, we demonstrate that replacement of a single amino acid stereocenter with a stereodynamic nitrogen atom has profound consequences on the self-assembly of a biomolecular system. Our results provide insight into how the fundamental biopolymers of life would behave if their chiral centers were not configurationally stable, highlighting the vital importance of stereochemistry as a pre-organizing element in biomolecular folding and assembly events.
手性是一种对物理系统和抽象系统都很重要的不对称属性。了解分子系统如何响应其手性构建单元中的扰动,可以为生物分子自组装、蛋白质折叠、药物设计、材料和催化等不同领域提供见解。尽管立体化学预组织在自然界和设计材料中具有根本重要性,但在生物分子系统中用立体动态原子模拟物取代手性中心的影响尚不清楚。在此,我们证明用一个立体动态氮原子取代单个氨基酸立体中心会对生物分子系统的自组装产生深远影响。我们的结果提供了关于生命的基本生物聚合物如果其手性中心在构型上不稳定会如何表现的见解,突出了立体化学作为生物分子折叠和组装事件中的预组织元素的至关重要性。