Mosyak L, Zhang Y, Glasfeld E, Haney S, Stahl M, Seehra J, Somers W S
Biological Chemistry, Wyeth Research, 87 Cambridge Park Drive, Cambridge, MA 02140, USA.
EMBO J. 2000 Jul 3;19(13):3179-91. doi: 10.1093/emboj/19.13.3179.
In Escherichia coli, FtsZ, a homologue of eukaryotic tubulins, and ZipA, a membrane-anchored protein that binds to FtsZ, are two essential components of the septal ring structure that mediates cell division. Recent data indicate that ZipA is involved in the assembly of the ring by linking FtsZ to the cytoplasmic membrane and that the ZipA-FtsZ interaction is mediated by their C-terminal domains. We present the X-ray crystal structures of the C-terminal FtsZ-binding domain of ZipA and a complex between this domain and a C-terminal fragment of FtsZ. The ZipA domain is a six-stranded beta-sheet packed against three alpha-helices and contains the split beta-alpha-beta motif found in many RNA-binding proteins. The uncovered side of the sheet incorporates a shallow hydrophobic cavity exposed to solvent. In the complex, the 17-residue FtsZ fragment occupies this entire cavity of ZipA and binds as an extended beta-strand followed by alpha-helix. An alanine-scanning mutagenesis analysis of the FtsZ fragment was also performed, which shows that only a small cluster of the buried FtsZ side chains is critical in binding to ZipA.
在大肠杆菌中,FtsZ(真核微管蛋白的同源物)和ZipA(一种与FtsZ结合的膜锚定蛋白)是介导细胞分裂的隔膜环结构的两个必需成分。最近的数据表明,ZipA通过将FtsZ连接到细胞质膜而参与环的组装,并且ZipA与FtsZ的相互作用由它们的C末端结构域介导。我们展示了ZipA的C末端FtsZ结合结构域以及该结构域与FtsZ的C末端片段之间复合物的X射线晶体结构。ZipA结构域是由三条α螺旋堆积而成的六股β折叠,并且包含许多RNA结合蛋白中发现的分裂β-α-β基序。折叠的未覆盖面包含一个暴露于溶剂的浅疏水腔。在复合物中,17个残基的FtsZ片段占据ZipA的整个腔,并作为延伸的β链随后是α螺旋结合。还对FtsZ片段进行了丙氨酸扫描诱变分析,结果表明只有一小簇埋藏的FtsZ侧链在与ZipA结合中起关键作用。