Wang Shuhe, Allmendinger Lars, Huc Ivan
Department of Pharmacy, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, 81377, München, Germany.
Angew Chem Int Ed Engl. 2024 Nov 25;63(48):e202413252. doi: 10.1002/anie.202413252. Epub 2024 Oct 29.
Abiotic aromatic foldamer sequences have been previously shown to fold in helix-turn-helix motifs in organic solvents. Using simple computational tools, a new helix-turn-helix motif was designed that bears additional hydrogen bond donor OH groups to promote its aggregation into a genuine, trimeric, abiotic quaternary structure. This sequence was synthesized and its self-assembly in solution was investigated by Nuclear Magnetic Resonance (NMR), Circular Dichroism (CD) and Molecular Dynamics (MD) simulations. The existence of two stable discrete aggregates was evidenced, one assigned to the initially designed trimer, the other to a dimer including multiple water molecules. The two species may be quantitatively interconverted upon changing the water content of the solution or the temperature. These results represent important steps in the design of protein-like abiotic architectures.
非生物芳香折叠体序列此前已被证明在有机溶剂中能折叠成螺旋-转角-螺旋基序。利用简单的计算工具,设计了一种新的螺旋-转角-螺旋基序,其带有额外的氢键供体OH基团,以促进其聚集成真正的三聚体非生物四级结构。合成了该序列,并通过核磁共振(NMR)、圆二色性(CD)和分子动力学(MD)模拟研究了其在溶液中的自组装。证实了存在两种稳定的离散聚集体,一种被指定为最初设计的三聚体,另一种为包含多个水分子的二聚体。改变溶液的含水量或温度时,这两种物种可能会定量地相互转化。这些结果代表了类蛋白质非生物结构设计中的重要步骤。