Theuer C, Kasturi S, Pastan I
Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
Biochemistry. 1994 May 17;33(19):5894-900. doi: 10.1021/bi00185a029.
The translocation of PE from the extracytosolic compartment to the cytosol during the intoxication of mammalian cells is mediated by domain II of the toxin. We have shown previously that within domain II amino acids 280-313 of PE promote their own export from mammalian microsomes following signal sequence-directed membrane insertion. In this study, we attempted to target full-length PE into mammalian microsomes using the preprocecropin signal sequence, but found that translocation was arrested to generate a transmembrane protein. "Stop transfer" required the presence of amino acids 280-313 of PE, and the first 313 amino acids of PE were sufficient to generate a transmembrane protein (N-terminus-in/C-terminus-out). The mechanism of stop transfer appears to be different from that described previously because amino acids 280-313 of PE are not highly hydrophobic and do contain many charged residues. In addition, the transmembrane segment appeared to be influenced by the cytoplasmic domain of the transmembrane proteins.
在哺乳动物细胞中毒期间,PE从细胞外区室向细胞质的转运由毒素的结构域II介导。我们之前已经表明,在结构域II内,PE的氨基酸280 - 313在信号序列引导的膜插入后促进其自身从哺乳动物微粒体中输出。在本研究中,我们试图使用前原杀菌肽信号序列将全长PE靶向到哺乳动物微粒体中,但发现转运被阻断以产生一种跨膜蛋白。“停止转运”需要PE的氨基酸280 - 313的存在,并且PE的前313个氨基酸足以产生一种跨膜蛋白(N端在内/C端在外)。停止转运的机制似乎与先前描述的不同,因为PE的氨基酸280 - 313并非高度疏水,并且确实含有许多带电荷的残基。此外,跨膜区段似乎受到跨膜蛋白细胞质结构域的影响。