Abstract

Cell division in eukaryotes requires the regulated assembly of the spindle apparatus. The proper organization of microtubules within the spindle is driven by motor proteins that exert forces to slide filaments, while non-motor proteins crosslink filaments into higher order motifs such as overlapping bundles. It is not clear how active and passive forces are integrated to produce regulated mechanical outputs within spindles. Here we employ simultaneous optical trapping and TIRF microscopy to directly measure the frictional forces produced by the mitotic crosslinking protein PRC1 that resist microtubule sliding.

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