Kuo S C, McGrath J L
Department of Biomedical Engineering, The Johns Hopkins University, Baltimore, Maryland 21205, USA.
Nature. 2000 Oct 26;407(6807):1026-9. doi: 10.1038/35039544.
The actin-based motility of the bacterium, Listeria monocytogenes, is a model system for understanding motile cell functions involving actin polymerization. Although the biochemical and genetic aspects of Listeria motility have been intensely studied, biophysical data are sparse. Here we have used high-resolution laser tracking to follow the trailing ends of Listeria moving in the lamellae of COS7 cells. We found that pauses during motility occur frequently and that episodes of step-like motion often show pauses spaced at about 5.4 nm, which corresponds to the spatial periodicity of F-actin. We occasionally observed smaller steps (<3 nm), as well as periods of motion with no obvious pauses. Clearly, bacteria do not sense cytoplasmic viscoelasticity because they fluctuate 20 times less than adjacent lipid droplets. Instead, bacteria bind their own actin 'tails, and the anchoring proteins can 'step' along growing filaments within the actin tail. Because positional fluctuations are unusually small, the forces of association and propulsion must be very strong. Our data disprove the brownian ratchet models and limit alternative models, such as the 'elastic' brownian ratchet or the 'molecular' ratchet.
单核细胞增生李斯特菌基于肌动蛋白的运动性是理解涉及肌动蛋白聚合的运动细胞功能的一个模型系统。尽管对李斯特菌运动性的生化和遗传方面已进行了深入研究,但生物物理数据却很稀少。在此,我们利用高分辨率激光追踪技术来跟踪在COS7细胞薄片中移动的李斯特菌的尾部。我们发现运动过程中频繁出现停顿,且阶梯状运动的片段常常显示停顿间隔约为5.4纳米,这与F-肌动蛋白的空间周期性相对应。我们偶尔也观察到更小的步长(<3纳米)以及无明显停顿的运动时期。显然,细菌无法感知细胞质的粘弹性,因为它们的波动比相邻的脂滴小20倍。相反,细菌会结合自身的肌动蛋白“尾巴”,且锚定蛋白能够沿着肌动蛋白尾巴内正在生长的细丝“行走”。由于位置波动异常小,结合力和推进力必定非常强大。我们的数据反驳了布朗棘轮模型,并限制了其他替代模型,如“弹性”布朗棘轮或“分子”棘轮。