Cytoplasmic dynein functions as a gear in response to load
Roop Mallik,
Brian C. Carter,
Stephanie A. Lex,
Stephen J. King and
Steven P. Gross ()
Additional contact information
Roop Mallik: University of California Irvine
Brian C. Carter: University of California Irvine
Stephanie A. Lex: University of Missouri-Kansas City
Stephen J. King: University of Missouri-Kansas City
Steven P. Gross: University of California Irvine
Nature, 2004, vol. 427, issue 6975, 649-652
Abstract:
Abstract Cytoskeletal molecular motors belonging to the kinesin and dynein families transport cargos (for example, messenger RNA, endosomes, virus) on polymerized linear structures called microtubules in the cell1. These ‘nanomachines’ use energy obtained from ATP hydrolysis to generate force2, and move in a step-like manner on microtubules. Dynein3,4,5 has a complex and fundamentally different structure from other motor families. Thus, understanding dynein's force generation can yield new insight into the architecture and function of nanomachines. Here, we use an optical trap6 to quantify motion of polystyrene beads driven along microtubules by single cytoplasmic dynein motors. Under no load, dynein moves predominantly with a mixture of 24-nm and 32-nm steps. When moving against load applied by an optical trap, dynein can decrease step size to 8 nm and produce force up to 1.1 pN. This correlation between step size and force production is consistent with a molecular gear mechanism. The ability to take smaller but more powerful strokes under load—that is, to shift gears—depends on the availability of ATP. We propose a model whereby the gear is downshifted through load-induced binding of ATP at secondary sites in the dynein head.
Date: 2004
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DOI: 10.1038/nature02293
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