A propagating ATPase gradient drives transport of surface-confined cellular cargo.
A propagating ATPase gradient drives transport of surface-confined cellular cargo.
复制标题
传播的 ATP 酶梯度驱动表面限制的细胞货物的运输。
DOI:
10.1073/pnas.1401025111
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发表时间:
2014
影响因子:
11.1
通讯作者:
Mizuuchi,Kiyoshi
中科院分区:
文献类型:
--
作者:
Vecchiarelli,AnthonyG;Neuman,KeirC;Mizuuchi,Kiyoshi
The faithful segregation of duplicated genetic material into daughter cells is critical to all organisms. In many bacteria, the segregation of chromosomes involves transport of “centromere-like” loci over the main body of the chromosome, the nucleoid, mediated by a two-protein partition system: a nonspecific DNA-binding ATPase, ParA, and an ATPase stimulator, ParB, which binds to the centromere-like loci. These systems have previously been proposed to function through a filament-based mechanism, analogous to actin- or microtubule-based movement. Here, we reconstituted the F-plasmid partition system using a DNA-carpeted flow cell as an artificial nucleoid surface and magnetic beads coated with plasmid partition complexes as surface-confined cargo. This minimal system recapitulated directed cargo motion driven by a surface ATPase gradient that propagated with the cargo. The dynamics are consistent with a diffusion-ratchet model, whereby the cargo dynamically establishes, and interacts with, a concentration gradient of the ATPase. A chemophoresis force ensues as the cargo perpetually chases the ATPase gradient, allowing the cargo to essentially “surf” the nucleoid on a continuously traveling wave of the ATPase. Demonstration of this non–filament-based motility mechanism in a biological context establishes a distinct class of motor system used for the transport and positioning of large cellular cargo.