Mathews M A, Tang H L, Blair D F
Department of Biochemistry, University of Utah, Salt Lake City, Utah 84112, USA.
J Bacteriol. 1998 Nov;180(21):5580-90. doi: 10.1128/JB.180.21.5580-5590.1998.
The FliM protein of Escherichia coli is required for the assembly and function of flagella. Genetic analyses and binding studies have shown that FliM interacts with several other flagellar proteins, including FliN, FliG, phosphorylated CheY, other copies of FliM, and possibly MotA and FliF. Here, we examine the effects of a set of linker insertions and partial deletions in FliM on its binding to FliN, FliG, CheY, and phospho-CheY and on its functions in flagellar assembly and rotation. The results suggest that FliM is organized into multiple domains. A C-terminal domain of about 90 residues binds to FliN in coprecipitation experiments, is most stable when coexpressed with FliN, and has some sequence similarity to FliN. This C-terminal domain is joined to the rest of FliM by a segment (residues 237 to 247) that is poorly conserved, tolerates linker insertion, and may be an interdomain linker. Binding to FliG occurs through multiple segments of FliM, some in the C-terminal domain and others in an N-terminal domain of 144 residues. Binding of FliM to CheY and phospho-CheY was complex. In coprecipitation experiments using purified FliM, the protein bound weakly to unphosphorylated CheY and more strongly to phospho-CheY, in agreement with previous reports. By contrast, in experiments using FliM in fresh cell lysates, the protein bound to unphosphorylated CheY about as well as to phospho-CheY. Determinants for binding CheY occur both near the N terminus of FliM, which appears most important for binding to the phosphorylated protein, and in the C-terminal domain, which binds more strongly to unphosphorylated CheY. Several different deletions and linker insertions in FliM enhanced its binding to phospho-CheY in coprecipitation experiments with protein from cell lysates. This suggests that determinants for binding phospho-CheY may be partly masked in the FliM protein as it exists in the cytoplasm. A model is proposed for the arrangement and function of FliM domains in the flagellar motor.
大肠杆菌的FliM蛋白是鞭毛组装和功能所必需的。遗传分析和结合研究表明,FliM与其他几种鞭毛蛋白相互作用,包括FliN、FliG、磷酸化的CheY、FliM的其他拷贝,可能还有MotA和FliF。在此,我们研究了FliM中一组连接子插入和部分缺失对其与FliN、FliG、CheY和磷酸化CheY的结合以及对其在鞭毛组装和旋转中的功能的影响。结果表明,FliM被组织成多个结构域。在共沉淀实验中,一个约90个残基的C末端结构域与FliN结合,与FliN共表达时最稳定,并且与FliN有一些序列相似性。这个C末端结构域通过一段保守性较差、耐受连接子插入且可能是结构域间连接子的片段(残基237至247)与FliM的其余部分相连。与FliG的结合通过FliM的多个片段发生,一些在C末端结构域,另一些在一个144个残基的N末端结构域。FliM与CheY和磷酸化CheY的结合很复杂。在使用纯化的FliM进行的共沉淀实验中,该蛋白与未磷酸化的CheY弱结合,与磷酸化的CheY结合更强,这与先前的报道一致。相比之下,在使用新鲜细胞裂解物中的FliM进行的实验中,该蛋白与未磷酸化的CheY的结合程度与与磷酸化的CheY的结合程度相当。结合CheY的决定因素既存在于FliM的N末端附近,这似乎对与磷酸化蛋白的结合最为重要,也存在于C末端结构域,该结构域与未磷酸化的CheY结合更强。在与细胞裂解物中的蛋白进行的共沉淀实验中,FliM中的几种不同缺失和连接子插入增强了其与磷酸化CheY的结合。这表明,在细胞质中存在的FliM蛋白中,结合磷酸化CheY的决定因素可能部分被掩盖。我们提出了一个关于鞭毛马达中FliM结构域的排列和功能的模型。