Department of Chemical Engineering, University of Florida, 1006 Center Drive, Gainesville, Florida 32611, United States.
Department of Chemical and Biomedical Engineering, FAMU-FSU, Tallahassee, Florida 32310, United States.
Biomacromolecules. 2024 Sep 9;25(9):6127-6134. doi: 10.1021/acs.biomac.4c00807. Epub 2024 Aug 6.
We present a straightforward strategy for constructing giant, multicompartmentalized vesicles using recombinant fusion proteins. Our method leverages the self-assembly of globule-zipper-elastin-like polypeptide fusion protein complexes in aqueous conditions, eliminating the need for organic solvents and chemical conjugation. By employing the thin-film rehydration method, we have successfully encapsulated a diverse range of bioactive macromolecules and engineered organelle-like compartments─ranging from soluble proteins and coacervate droplets to vesicles─within these protein-assembled giant vesicles. This approach also facilitates the integration of water-soluble block copolymers, enhancing the structural stability and functional versatility of the vesicles. Our results suggest that these multicompartment giant protein vesicles not only mimic the complex architecture of living cells but also support biochemically distinct reactions regulated by functionally folded proteins, providing a robust model for studying cellular processes and designing microreactor systems. This work highlights the transformative potential of self-assembling recombinant fusion proteins in artificial cell design.
我们提出了一种使用重组融合蛋白构建大型多室囊泡的简单策略。我们的方法利用了球蛋白-拉链-弹性蛋白样多肽融合蛋白复合物在水相条件下的自组装,无需有机溶剂和化学偶联。通过采用薄膜水化方法,我们已经成功地将各种生物活性大分子和工程细胞器样隔室——从可溶性蛋白和凝聚体液滴到囊泡——封装在这些蛋白组装的大型囊泡内。这种方法还促进了水溶性嵌段共聚物的整合,增强了囊泡的结构稳定性和功能多样性。我们的结果表明,这些多室巨型蛋白囊泡不仅模拟了活细胞的复杂结构,还支持由功能折叠蛋白调节的生化反应,为研究细胞过程和设计微反应系统提供了一个强大的模型。这项工作突出了自组装重组融合蛋白在人工细胞设计中的变革潜力。