School of Pharmacy, Guangdong Medical University, Dongguan, 523808, China.
Department of Electron Microscopy, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Nijenborgh 7, 9747, AG, Groningen, The Netherlands.
Macromol Rapid Commun. 2018 Jul;39(13):e1800099. doi: 10.1002/marc.201800099. Epub 2018 May 28.
Dynamic proteoids are dynamic covalent analogues of proteins which are generated through the reversible polymerization of amino-acid- or peptide-derived monomers. The authors design and prepare a series of dynamic proteoids based on the reversible polycondensation of six types of dipeptide hydrazides bearing different categories of side chains. The polymerization and structures of biodynamers generated by H-NMR spectroscopy, light scattering and cryo-transmission-electron microscopy are studied. This study shows that the presence of aromatic rings in the side chains plays the most essential role in determining the extent of the polymerization and organization into resultant nanostructures through π-π-stacking interactions, hydroxyl groups have a less favorable influence via hydrogen bonds, whereas a high density of positive charge blocks the generation of biodynamers due to electrostatic repulsions. These findings set the stage for the rational design and synthesis of dynamic proteoids as novel biofunctional materials.
动态蛋白类似物是蛋白质的动态共价类似物,通过氨基酸或肽衍生单体的可逆聚合生成。作者设计并制备了一系列基于带有不同侧链类别的六种二肽酰肼的可逆缩聚反应的动态蛋白类似物。通过 H-NMR 光谱、光散射和低温透射电子显微镜研究了由 H-NMR 光谱、光散射和低温透射电子显微镜生成的生物动态聚合物的聚合和结构。该研究表明,侧链中环的存在通过 π-π 堆积相互作用在决定聚合程度和组织成所得纳米结构方面起着最关键的作用,羟基通过氢键的影响较小,而高浓度的正电荷由于静电排斥作用阻止了生物动态聚合物的生成。这些发现为作为新型生物功能材料的动态蛋白类似物的合理设计和合成奠定了基础。