Daube Shirley S, Arad Talmon, Bar-Ziv Roy
Kimmel Center for Nanoscale Science, Chemical Research Support, Department of Materials and Interfaces, The Weizmann Institute of Science, Rehovot, Israel 76100.
Nano Lett. 2007 Mar;7(3):638-41. doi: 10.1021/nl062560n. Epub 2007 Feb 2.
We used a cell-free transcription/translation system to synthesize structural proteins of the T4 bacteriophage. We focused on two proteins that participate in the formation of the virus tail tube assembly. Synthesized separately, the proteins assembled into their in vivo forms, namely one polymerized into rigid hollow nanotubes approximately 20 nm thick and hundreds of nanometers long, the other assembled into 10 nm tube-capping hexameric rings. Co-synthesis of the two proteins, however, revealed a novel structure of a nanodoughnut with an outer diameter of approximately 50 nm and thickness of approximately 20 nm. Cell-free co-synthesis and assembly of T4 structural proteins can be extended in a combinatorial fashion. The addition of other structural genes offers control of native nanoassemblies and may reveal ones not observable by mixing purified components.
我们使用无细胞转录/翻译系统来合成T4噬菌体的结构蛋白。我们聚焦于两种参与病毒尾管组装形成的蛋白质。分别合成时,这些蛋白质组装成它们在体内的形式,即一种聚合成约20纳米厚、数百纳米长的刚性中空纳米管,另一种组装成10纳米的管帽六聚体环。然而,这两种蛋白质的共合成揭示了一种外径约50纳米、厚度约20纳米的新型纳米甜甜圈结构。T4结构蛋白的无细胞共合成和组装可以以组合方式扩展。添加其他结构基因可实现对天然纳米组装体的控制,并可能揭示通过混合纯化成分无法观察到的组装体。