Mehra V, Khanna H, Chandra R, Singh Y
Centre for Biochemical Technology, Mall Road, Delhi-110007, India and Ambedkar Centre for Biomedical Research, University of Delhi, Delhi-110007, India.
Biotechnol Appl Biochem. 2001 Apr;33(2):71-4. doi: 10.1042/ba20000072.
PA63, the proteolytically activated 63 kDa fragment of protective antigen (PA, 83 kDa), mediates translocation of lethal factor (LF) and oedema factor into the cytosol. The N-terminal 254 amino acids of LF (LFn) are required for binding to PA63 and mediating translocation of active ligands fused to either the N- or C-terminus. Here we report translocation of a 19 kDa antigen of Mycobacterium tuberculosis into the cytosol of mammalian cells when fused to the C-terminus of LFn (LFn-19kDa). The fusion protein was non-toxic to J774A.1 macrophage cells in combination with PA and retained the ability to bind to PA63 when incubated with Chinese hamster ovary K1 cells. The data show the efficacy of anthrax toxin to mediate translocation of M. tuberculosis antigens into the cytosol of mammalian cells and may prove useful in delivering proteins and peptides carrying immunodominant mycobacterial antigens into the cytosol.
PA63是保护性抗原(PA,83 kDa)经蛋白水解激活后的63 kDa片段,介导致死因子(LF)和水肿因子进入胞质溶胶。LF的N端254个氨基酸对于与PA63结合以及介导与N端或C端融合的活性配体的转运是必需的。在此我们报告,当与LFn(LFn-19kDa)的C端融合时,结核分枝杆菌的一种19 kDa抗原能够转运至哺乳动物细胞的胞质溶胶中。该融合蛋白与PA联合使用时对J774A.1巨噬细胞无毒,并且与中国仓鼠卵巢K1细胞孵育时保留了与PA63结合的能力。这些数据表明炭疽毒素介导结核分枝杆菌抗原转运至哺乳动物细胞胞质溶胶中的有效性,并且可能在将携带免疫显性分枝杆菌抗原的蛋白质和肽递送至胞质溶胶中方面证明是有用的。