Schneewind O, Mihaylova-Petkov D, Model P
Department of Microbiology and Immunology, UCLA School of Medicine 90024.
EMBO J. 1993 Dec;12(12):4803-11. doi: 10.1002/j.1460-2075.1993.tb06169.x.
Staphylococcal protein A is anchored to the cell wall, a unique cellular compartment of Gram-positive bacteria. The sorting signal sufficient for cell wall anchoring consists of an LPXTG motif, a C-terminal hydrophobic domain and a charged tail. Homologous sequences are found in many surface proteins of Gram-positive bacteria and we explored the universality of these sequences to serve as cell wall sorting signals. We show that several signals are able to anchor fusion proteins to the staphylococcal cell wall. Some signals do not sort effectively, but acquire sorting activity once the spacing between the LPXTG motif and the charged tail has been increased to span the same length as in protein A. Thus, signals for cell wall anchoring in Gram-positive bacteria are as universal as signal (leader) sequences.
葡萄球菌蛋白A锚定在细胞壁上,细胞壁是革兰氏阳性菌特有的细胞区室。足以实现细胞壁锚定的分选信号由一个LPXTG基序、一个C端疏水结构域和一个带电荷的尾部组成。在革兰氏阳性菌的许多表面蛋白中都发现了同源序列,我们探索了这些序列作为细胞壁分选信号的普遍性。我们发现,几种信号能够将融合蛋白锚定到葡萄球菌细胞壁上。一些信号分选效率不高,但一旦LPXTG基序与带电荷尾部之间的间距增加到与蛋白A中的长度相同,就会获得分选活性。因此,革兰氏阳性菌中用于细胞壁锚定的信号与信号(前导)序列一样具有普遍性。