Department of Anesthesiology, Weill Cornell Medicine, New York City, NY, USA.
Department of Physiology and Biophysics, Weill Cornell Medicine, New York City, NY, USA.
Nat Commun. 2022 Aug 26;13(1):5039. doi: 10.1038/s41467-022-32757-4.
Perforin-2 (PFN2, MPEG1) is a pore-forming protein that acts as a first line of defense in the mammalian immune system, rapidly killing engulfed microbes within the phagolysosome in macrophages. PFN2 self-assembles into hexadecameric pre-pore rings that transition upon acidification into pores damaging target cell membranes. Here, using high-speed atomic force microscopy (HS-AFM) imaging and line-scanning and molecular dynamics simulation, we elucidate PFN2 pre-pore to pore transition pathways and dynamics. Upon acidification, the pre-pore rings (pre-pore-I) display frequent, 1.8 s, ring-opening dynamics that eventually, 0.2 s, initiate transition into an intermediate, short-lived, ~75 ms, pre-pore-II state, inducing a clockwise pre-pore-I to pre-pore-II propagation. Concomitantly, the first pre-pore-II subunit, undergoes a major conformational change to the pore state that propagates also clockwise at a rate ~15 s. Thus, the pre-pore to pore transition is a clockwise hand-over-hand mechanism that is accomplished within ~1.3 s. Our findings suggest a clockwise mechanism of membrane insertion that with variations may be general for the MACPF/CDC superfamily.
穿孔素 2(PFN2,MPEG1)是一种形成孔的蛋白,在哺乳动物免疫系统中作为第一道防线,迅速杀死巨噬细胞吞噬体中的吞噬微生物。PFN2 自我组装成十六聚体的预孔环,在酸化时转变为破坏靶细胞膜的孔。在这里,我们使用高速原子力显微镜(HS-AFM)成像和线扫描以及分子动力学模拟,阐明了 PFN2 预孔到孔的转变途径和动力学。在酸化时,预孔环(预孔-I)显示出频繁的 1.8s 的环打开动力学,最终在 0.2s 时引发进入短暂的中间状态75ms 的预孔-II 状态,诱导顺时针预孔-I 到预孔-II 的传播。同时,第一个预孔-II 亚基经历主要构象变化到孔状态,以15s 的速率也顺时针传播。因此,预孔到孔的转变是一个顺时针的逐步机制,在~1.3s 内完成。我们的发现表明了一种顺时针的膜插入机制,这种机制可能在 MACPF/CDC 超家族中具有普遍性。