Leikina Eugenia, Ramos Corinne, Markovic Ingrid, Zimmerberg Joshua, Chernomordik Leonid V
Laboratory of Cellular and Molecular Biophysics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892-1855, USA.
EMBO J. 2002 Nov 1;21(21):5701-10. doi: 10.1093/emboj/cdf559.
The refolding of the prototypic fusogenic protein hemagglutinin (HA) at the pH of fusion is considered to be a concerted and irreversible discharge of a loaded spring, with no distinct intermediates between the initial and final conformations. Here, we show that HA refolding involves reversible conformations with a lifetime of minutes. After reneutralization, low pH-activated HA returns from the conformations wherein both the fusion peptide and the kinked loop of the HA2 subunit are exposed, but the HA1 subunits have not yet dissociated, to a structure indistinguishable from the initial one in functional, biochemical and immunological characteristics. The rate of the transition from reversible conformations to irreversible refolding depends on the pH and on the presence of target membrane. Importantly, recovery of the initial conformation is blocked by the interactions between adjacent HA trimers. The existence of the identified reversible stage of refolding can be crucial for allowing multiple copies of HA to synchronize their release of conformational energy, as required for fusion.
在融合pH值下,原型融合蛋白血凝素(HA)的重折叠被认为是一个加载弹簧的协同且不可逆的释放过程,在初始构象和最终构象之间没有明显的中间体。在这里,我们表明HA重折叠涉及寿命为数分钟的可逆构象。重新中和后,低pH激活的HA从融合肽和HA2亚基的扭结环均暴露但HA1亚基尚未解离的构象,转变为在功能、生化和免疫特性上与初始结构无法区分的结构。从可逆构象到不可逆重折叠的转变速率取决于pH值和靶膜的存在。重要的是,相邻HA三聚体之间的相互作用会阻止初始构象的恢复。所确定的重折叠可逆阶段的存在对于允许多个HA拷贝同步释放融合所需的构象能量可能至关重要。