Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Cold Spring Harb Perspect Biol. 2010 Apr;2(4):a000307. doi: 10.1101/cshperspect.a000307. Epub 2010 Mar 3.
Like their eukaryotic counterparts, bacterial cells have a highly organized internal architecture. Here, we address the question of how proteins localize to particular sites in the cell and how they do so in a dynamic manner. We consider the underlying mechanisms that govern the positioning of proteins and protein complexes in the examples of the divisome, polar assemblies, cytoplasmic clusters, cytoskeletal elements, and organelles. We argue that geometric cues, self-assembly, and restricted sites of assembly are all exploited by the cell to specifically localize particular proteins that we refer to as anchor proteins. These anchor proteins in turn govern the localization of a whole host of additional proteins. Looking ahead, we speculate on the existence of additional mechanisms that contribute to the organization of bacterial cells, such as the nucleoid, membrane microdomains enriched in specific lipids, and RNAs with positional information.
与真核生物类似,细菌细胞具有高度组织化的内部结构。在这里,我们探讨了蛋白质如何在细胞中定位到特定的位置,以及它们如何以动态的方式进行定位。我们考虑了控制蛋白质和蛋白质复合物在分裂体、极性组装体、细胞质簇、细胞骨架元件和细胞器中的定位的基本机制。我们认为,几何线索、自组装和受限的组装位点都被细胞利用,以特异性地定位我们称之为锚定蛋白的特定蛋白质。这些锚定蛋白反过来又控制着一大批其他蛋白质的定位。展望未来,我们推测存在其他有助于细菌细胞组织的机制,例如拟核、富含特定脂质的膜微区以及具有位置信息的 RNA。