Wang Zhongyan, Liang Chunhui, Shang Yuna, He Shuangshuang, Wang Ling, Yang Zhimou
State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, and Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Nankai University, Tianjin 300071, P. R. China.
Chem Commun (Camb). 2018 Mar 13;54(22):2751-2754. doi: 10.1039/c8cc01082j.
We designed and synthesized three phosphorylated peptides as precursors of the same peptide Nap-YYY. We found that different precursors led to different materials with almost identical chemical compositions at the final stages. Only Nap-YpYY could form very uniform nanofibers in a stable supramolecular hydrogel by enzyme-instructed self-assembly (EISA) at the physiological temperature (37 °C). In contrast, de-phosphorylation of the other two precursors (Nap-pYYY and Nap-YYpY) resulted in diverse nanostructures in metastable hydrogels with precipitates. The formation of uniform nanomaterials in the stable hydrogels was due to the preorganization property of the precursor Nap-YpYY, which facilitated rapid folding and accelerated the kinetics of hydrogelation of the resulting peptide Nap-YYY generated by the EISA process. Our study demonstrated the importance of the precursor for the self-assembly of nanomaterials and provided a useful strategy to manipulate them.
我们设计并合成了三种磷酸化肽作为同一肽Nap-YYY的前体。我们发现不同的前体在最终阶段会导致具有几乎相同化学组成的不同材料。只有Nap-YpYY能够在生理温度(37°C)下通过酶促自组装(EISA)在稳定的超分子水凝胶中形成非常均匀的纳米纤维。相比之下,其他两种前体(Nap-pYYY和Nap-YYpY)的去磷酸化导致在含有沉淀物的亚稳水凝胶中形成多种纳米结构。稳定水凝胶中均匀纳米材料的形成归因于前体Nap-YpYY的预组织特性,这促进了快速折叠并加速了由EISA过程产生的所得肽Nap-YYY的水凝胶化动力学。我们的研究证明了前体对纳米材料自组装的重要性,并提供了一种操纵它们的有用策略。