Department of Bioengineering, University of California, Berkeley, Berkeley, CA, USA.
Division of Biological Systems and Engineering, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
Nat Protoc. 2017 Sep;12(9):1999-2013. doi: 10.1038/nprot.2017.085. Epub 2017 Aug 31.
Large-scale fabrication of precisely defined nanostructures with tunable functions is critical to the exploitation of nanoscience and nanotechnology for production of electronic devices, energy generators, biosensors, and bionanomedicines. Although self-assembly processes have been developed to exploit biological molecules for functional materials, the resulting nanostructures and functions are still very limited, and scalable synthesis is far from being realized. Recently, we have established a bacteriophage-based biomimetic process, called 'self-templating assembly'. We used bacteriophage as a nanofiber model system to exploit its liquid crystalline structure for the creation of diverse hierarchically organized structures. We have also demonstrated that genetic modification of functional peptides of bacteriophage results in structures that can be used as soft and hard tissue-regenerating materials, biosensors, and energy-generating materials. Here, we describe a comprehensive protocol to perform genetic engineering of phage, liter-scale amplification, purification, and self-templating assembly, and suggest approaches for characterizing hierarchical phage nanostructures using optical microscopy, atomic-force microscopy (AFM), and scanning electron microscopy (SEM). We also discuss sources of contamination, common mistakes during the fabrication process, and quality-control measures to ensure reproducible material production. The protocol takes ∼8-10 d to complete.
大规模制造具有可调功能的精确定义的纳米结构对于开发纳米科学和纳米技术以生产电子设备、能源发生器、生物传感器和生物纳米医学至关重要。尽管已经开发出自组装过程来利用生物分子制造功能材料,但由此产生的纳米结构和功能仍然非常有限,并且可扩展的合成还远未实现。最近,我们建立了一种基于噬菌体的仿生仿生过程,称为“自模板组装”。我们使用噬菌体作为纳米纤维模型系统,利用其液晶结构来创建各种层次化的结构。我们还证明,噬菌体功能肽的遗传修饰导致可以用作软组织和硬组织再生材料、生物传感器和能源生成材料的结构。在这里,我们描述了一种全面的方案,用于执行噬菌体的基因工程、大量扩增、纯化和自模板组装,并提出了使用光学显微镜、原子力显微镜 (AFM) 和扫描电子显微镜 (SEM) 来表征分层噬菌体纳米结构的方法。我们还讨论了污染的来源、制造过程中的常见错误以及质量控制措施,以确保可重复的材料生产。该方案大约需要 8-10 天才能完成。