大肠杆菌在细胞分裂时,FtsZ(Filamentous temperature-sensitive protein Z)蛋白会在细胞中部潜在位点聚合形成Z环,而MinC蛋白会抑制Z环形成,从而控制细胞分裂。本研究将min C与fts Z目的基因克隆到合适的载体中,并导入到大肠杆菌中进行表达,采用亲和层析和分子筛纯化的方法得到MinC/FtsZ复合物蛋白进行晶体筛选。通过FtsZ、MinC分别单独转化、表达纯化后混合和FtsZ、MinC共转化法两种方法得到FtsZ/MinC蛋白复合物,并分别对其进行晶体筛选。实验结果表明,在适宜的表达条件下,利用分别转化、纯化再混合的方法得到的FtsZ和MinC蛋白复合比例约为1∶1;混合时加入GTP和Mg Cl2可以促进复合物聚集态更单一,通过晶体筛选初步得到形状为针状的FtsZ/MinC复合蛋白晶体,为MinC/FtsZ复合物的结构解析提供实验基础。
In Escherichia coli,cell division occurs when Z-ring forms at the mid-site of cell through polymerization of FtsZ. The Z-ring formation is inhibited by MinC,resulting in regulation of cell division. Herein,min C and fts Z were cloned into vectors containing different antibiotics to express recombinant proteins,then MinC and FtsZ were purified by affinity chromatography and gel filtration chromatography. Two different methods,binding MinC and FtsZ after being expressed and purified respectively,and co-transformation,co-expression and co-purification of MinC and FtsZ were tried to gain MinC/FtsZ complex for crystal screen. Results showed that with appropriate conditions,through the way of binding MinC and FtsZ after being expressed and purified respectively,MinC/FtsZ complex were in the proportion of 1∶ 1. The addition of GTP and MgCl_2 helped improve the protein state of MinC/FtsZ complex,and needle shape of MinC/FtsZ complex was observed after crystal screen. This study provides experimental basis for structural analysis of MinC/FtsZ complex.