Terashima Hiroyuki, Abe-Yoshizumi Rei, Kojima Seiji, Homma Michio
Division of Biological Science, Graduate School of Science, Nagoya University, Chikusa-Ku, Nagoya 464-8602, Japan.
J Biochem. 2008 Nov;144(5):635-42. doi: 10.1093/jb/mvn110. Epub 2008 Sep 6.
Flagellar motor proteins, PomA and PomB, are essential for converting the sodium motive force into rotational energy in the Na(+)-driven flagella motor of Vibrio alginolyticus. PomA and PomB, which are cytoplasmic membrane proteins, together comprise the stator complex of the motor and form a Na(+) channel. We tried to synthesize PomA and PomB by using the cell-free protein synthesis system, PURESYSTEM. We succeeded in doing so in the presence of liposomes, and showed an interaction between them using the pull-down assay. It seems likely that the proteins are inserted into liposomes and assembled spontaneously. The N-terminal region of in vitro synthesized PomB appeared to be lost, but this problem was suppressed by fusing GFP to the N-terminus of PomB or by mutagenesis at Pro-11 or Pro-12. A structural change of the N-terminal region of PomB by these modifications may prevent cleavage during protein synthesis in PURESYSTEM. The mutations did not affect the functioning of the motor. Using this system, biochemical analysis of PomA and PomB can be performed easily and efficiently.
鞭毛运动蛋白PomA和PomB对于在溶藻弧菌的Na⁺驱动鞭毛马达中将钠动力转化为旋转能量至关重要。PomA和PomB是细胞质膜蛋白,共同构成马达的定子复合体并形成一个Na⁺通道。我们尝试使用无细胞蛋白质合成系统PURESYSTEM合成PomA和PomB。我们在脂质体存在的情况下成功做到了这一点,并使用下拉分析法显示了它们之间的相互作用。蛋白质似乎插入脂质体并自发组装。体外合成的PomB的N端区域似乎缺失了,但通过将绿色荧光蛋白(GFP)融合到PomB的N端或在Pro-11或Pro-12处进行诱变,这个问题得到了抑制。通过这些修饰对PomB N端区域的结构改变可能会防止在PURESYSTEM中蛋白质合成过程中的切割。这些突变不影响马达的功能。使用这个系统,可以轻松高效地对PomA和PomB进行生化分析。