Abstract
The segregation of DNA prior to cell division is essential to the faithful inheritance of the genetic materials. In many bacteria, the segregation of the low-copy-number plasmids involves an active partition system composed of ParA ATPase and DNA-binding ParB protein, which stimulates the hydrolysis activity of ParA. Both in vivo and in vitro experiments have shown that the ParA/ParB system can drive the persistent movement of the plasmids in a directed fashion, just like a processive motor protein. However, the underlying mechanism remains unknown. We have developed the first theoretical model on ParA/ParB-mediated motility. We establish that the coupling between the ParA/ParB biochemistry and its mechanical action works as a robust engine. It powers the directed movement of plasmids, buffering against the diffusive motion. Our work thus sheds light on a new emergent phenomenon, in which elaborate mechanochemical couplings of non-motor proteins can work collectively to propel cargos to designated locations, an ingenious way shaped by evolution to cope with the lack of a processive motor protein in bacteria.
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