Pimental Ruth-Anne L, Christensen Kenneth A, Krantz Bryan A, Collier R John
Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, MA 02115, USA.
Biochem Biophys Res Commun. 2004 Sep 10;322(1):258-62. doi: 10.1016/j.bbrc.2004.07.105.
The 83 kDa protective antigen (PA(83)) component of anthrax toxin, after proteolytic activation, self-associates to form ring-shaped heptamers (PA(63)) that bind and aid delivery of the Edema Factor (EF) and Lethal Factor (LF) components to the cytosol. Here we show using fluorescence (Förster) resonance energy transfer that a molecule of PA(63) can bind EF and LF simultaneously. We labeled EF and LF with an appropriate donor/acceptor pair and found quenching of the donor and an increase in sensitized emission of the acceptor when, and only when, a mixture of the labeled proteins was combined with PA(63). Addition of unlabeled PA(63)-binding domain of LF to the mixture competitively displaced labeled EF and LF, causing a loss of energy transfer. In view of the known maximum occupancy of 3 ligand molecules per PA(63), these findings indicate that PA, EF, and LF can form mixtures of liganded toxin complexes containing both EF and LF.
炭疽毒素的83 kDa保护性抗原(PA(83))成分经蛋白水解激活后,会自我缔合形成环形七聚体([PA(63)]7),该七聚体可结合水肿因子(EF)和致死因子(LF)成分并协助其递送至胞质溶胶。在此,我们利用荧光(Förster)共振能量转移表明,一个[PA(63)]7分子可同时结合EF和LF。我们用合适的供体/受体对标记了EF和LF,并且发现,只有当标记蛋白的混合物与[PA(63)]7混合时,供体才会发生淬灭且受体的敏化发射会增强。向混合物中添加未标记的LF的PA(63)结合结构域会竞争性取代标记的EF和LF,导致能量转移丧失。鉴于已知每个[PA(63)]7的最大配体分子占有率为3个,这些发现表明,PA、EF和LF可形成同时含有EF和LF的配体化毒素复合物混合物。