Kou Songzi, Yang Xin, Yang Zhongguang, Liu Xiaotian, Wegner Seraphine V, Sun Fei
Biomedical Research Institute, Shenzhen Peking University-The Hong Kong University of Science and Technology Medical Center, Shenzhen 518036, China.
Division of Life Science, State Key Laboratory of Molecular Neuroscience, and Center of Systems Biology and Human Health, School of Science and Institute for Advanced Study, Hong Kong University of Science and Technology, Hong Kong SAR, China.
ACS Macro Lett. 2019 Jul 16;8(7):773-778. doi: 10.1021/acsmacrolett.9b00333. Epub 2019 Jun 11.
Although assembly of recombinant proteins by SpyTag/SpyCatcher chemistry has proven to be a versatile approach for creating bioactive hydrogels, the resulting Spy networks often exhibit weak mechanics due to the poor efficiency of interchain cross-linking. Here we leverage metal/ligand (i.e., cobalt/His6-tag) coordination interactions to modulate the bulk mechanics of the protein networks. The drastic difference between the Co and Co complexes in thermodynamic and kinetic properties enabled us to regulate the materials' properties and to immobilize and release recombinant proteins in a redox-dependent manner. The resulting hydrogels are capable of not only supporting cell growth and proliferation, but also influencing specific cell signaling via immobilized growth factors such as leukemia inhibitory factor (LIF). The integrated use of stimuli-responsive metal coordination and SpyTag/SpyCatcher chemistry opens up a new dimension for designing bioactive protein materials.
尽管通过SpyTag/SpyCatcher化学方法组装重组蛋白已被证明是创建生物活性水凝胶的一种通用方法,但由于链间交联效率低下,所得的Spy网络通常表现出较弱的力学性能。在此,我们利用金属/配体(即钴/His6标签)配位相互作用来调节蛋白质网络的整体力学性能。钴与钴配合物在热力学和动力学性质上的巨大差异使我们能够调节材料的性能,并以氧化还原依赖的方式固定和释放重组蛋白。所得的水凝胶不仅能够支持细胞生长和增殖,还能够通过固定化的生长因子如白血病抑制因子(LIF)影响特定的细胞信号传导。刺激响应性金属配位和SpyTag/SpyCatcher化学的综合应用为设计生物活性蛋白质材料开辟了一个新的维度。