Deich J, Judd E M, McAdams H H, Moerner W E
Department of Chemistry, Stanford University, Stanford, CA 94305, USA.
Proc Natl Acad Sci U S A. 2004 Nov 9;101(45):15921-6. doi: 10.1073/pnas.0404200101. Epub 2004 Nov 2.
The bacterium Caulobacter crescentus divides asymmetrically as part of its normal life cycle. This asymmetry is regulated in part by the membrane-bound histidine kinase PleC, which localizes to one pole of the cell at specific times in the cell cycle. Here, we track single copies of PleC labeled with enhanced yellow fluorescent protein (EYFP) in the membrane of live Caulobacter cells over a time scale of seconds. In addition to the expected molecules immobilized at one cell pole, we observed molecules moving throughout the cell membrane. By tracking the positions of these molecules for several seconds, we determined a diffusion coefficient (D) of 12 +/- 2 x 10(-3) microm(2)/s for the mobile copies of PleC not bound at the cell pole. This D value is maintained across all cell cycle stages. We observe a reduced D at poles containing localized PleC-EYFP; otherwise D is independent of the position of the diffusing molecule within the bacterium. We did not detect any directional bias in the motion of the PleC-EYFP molecules, implying that the molecules are not being actively transported.
新月柄杆菌在其正常生命周期中进行不对称分裂。这种不对称性部分受膜结合组氨酸激酶PleC调控,PleC在细胞周期的特定时间定位于细胞的一极。在此,我们在数秒的时间尺度上追踪活的新月柄杆菌细胞膜中用增强型黄色荧光蛋白(EYFP)标记的单个PleC拷贝。除了预期固定在一个细胞极的分子外,我们还观察到分子在整个细胞膜上移动。通过追踪这些分子的位置数秒,我们确定未结合在细胞极的PleC移动拷贝的扩散系数(D)为12±2×10⁻³ 微米²/秒。这个D值在所有细胞周期阶段都保持不变。我们观察到在含有定位的PleC-EYFP的极处D值降低;否则,D与细菌内扩散分子的位置无关。我们未检测到PleC-EYFP分子运动中的任何方向偏向,这意味着这些分子不是在被主动运输。