Department of Microbiology and Molecular Genetics and Medicine, Harvard Medical School, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2011 Feb 1;108(5):1868-73. doi: 10.1073/pnas.1018965108. Epub 2011 Jan 24.
The protective antigen (PA) moiety of anthrax toxin forms oligomeric pores that translocate the enzymatic moieties of the toxin--lethal factor (LF) and edema factor (EF)--across the endosomal membrane of mammalian cells. Here we describe site-directed spin-labeling studies that identify interactions of LF with the prepore and pore conformations of PA. Our results reveal a direct interaction between the extreme N terminus of LF (residues 2-5) and the Φ-clamp, a structure within the lumen of the pore that catalyzes translocation. Also, consistent with a recent crystallographic model, we find that, upon binding of the translocation substrate to PA, LF helix α1 separates from helices α2 and α3 and binds in the α-clamp of PA. These interactions, together with the binding of the globular part of the N-terminal domain of LF to domain 1' of PA, indicate that LF interacts with the PA pore at three distinct sites. Our findings elucidate the state from which translocation of LF and EF proceeds through the PA pore.
炭疽毒素的保护性抗原(PA)部分形成寡聚体孔,将毒素的酶部分——致死因子(LF)和水肿因子(EF)——穿过哺乳动物细胞的内体膜。在这里,我们描述了定点自旋标记研究,这些研究确定了 LF 与 PA 的前孔和孔构象的相互作用。我们的结果揭示了 LF 的极端 N 端(残基 2-5)与 Φ 夹之间的直接相互作用,Φ 夹是孔腔中的一种结构,催化易位。此外,与最近的晶体结构模型一致,我们发现,在将易位底物与 PA 结合后,LF 螺旋 α1 与 α2 和 α3 分离,并结合在 PA 的 α 夹中。这些相互作用,以及 LF 的 N 端结构域的球形部分与 PA 的域 1'的结合,表明 LF 与 PA 孔在三个不同的位点相互作用。我们的发现阐明了 LF 和 EF 通过 PA 孔易位的状态。