Yap Moh Lan, Klose Thomas, Arisaka Fumio, Speir Jeffrey A, Veesler David, Fokine Andrei, Rossmann Michael G
Department of Biological Sciences, Purdue University, West Lafayette, IN 47907;
College of Bioresource Science, Nihon University, Fujisawa, Kanagawa 252-0880, Japan;
Proc Natl Acad Sci U S A. 2016 Mar 8;113(10):2654-9. doi: 10.1073/pnas.1601654113. Epub 2016 Feb 29.
Bacteriophage T4 consists of a head for protecting its genome and a sheathed tail for inserting its genome into a host. The tail terminates with a multiprotein baseplate that changes its conformation from a "high-energy" dome-shaped to a "low-energy" star-shaped structure during infection. Although these two structures represent different minima in the total energy landscape of the baseplate assembly, as the dome-shaped structure readily changes to the star-shaped structure when the virus infects a host bacterium, the dome-shaped structure must have more energy than the star-shaped structure. Here we describe the electron microscopy structure of a 3.3-MDa in vitro-assembled star-shaped baseplate with a resolution of 3.8 Å. This structure, together with other genetic and structural data, shows why the high-energy baseplate is formed in the presence of the central hub and how the baseplate changes to the low-energy structure, via two steps during infection. Thus, the presence of the central hub is required to initiate the assembly of metastable, high-energy structures. If the high-energy structure is formed and stabilized faster than the low-energy structure, there will be insufficient components to assemble the low-energy structure.
噬菌体T4由一个用于保护其基因组的头部和一个用于将其基因组插入宿主的带鞘尾部组成。尾部末端是一个多蛋白基板,在感染过程中,该基板的构象会从“高能”圆顶形转变为“低能”星形结构。尽管这两种结构代表了基板组装总能量态势中的不同最低点,但由于当病毒感染宿主细菌时圆顶形结构很容易转变为星形结构,所以圆顶形结构的能量肯定比星形结构更多。在此,我们描述了一种体外组装的3.3兆道尔顿星形基板的电子显微镜结构,分辨率为3.8埃。该结构与其他遗传和结构数据一起,揭示了在存在中心枢纽的情况下高能基板为何会形成,以及在感染过程中基板如何通过两个步骤转变为低能结构。因此,中心枢纽的存在是启动亚稳态高能结构组装所必需的。如果高能结构比低能结构形成和稳定得更快,那么用于组装低能结构的组件就会不足。