FB2026_03 , released September 17, 2026
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Citation
Fehr, A.N., GutiĆ©rrez-Medina, B., Asbury, C.L., Block, S.M. (2009). On the origin of kinesin limping.  Biophys. J. 97(6): 1663--1670.
FlyBase ID
FBrf0215155
Publication Type
Research paper
Abstract
Kinesin is a dimeric motor with twin catalytic heads joined to a common stalk. Kinesin molecules move processively along microtubules in a hand-over-hand walk, with the two heads advancing alternately. Recombinant kinesin constructs with short stalks have been found to "limp", i.e., exhibit alternation in the dwell times of successive steps. Limping behavior implies that the molecular rearrangements underlying even- and odd-numbered steps must differ, but the mechanism by which such rearrangements lead to limping remains unsolved. Here, we used an optical force clamp to measure individual, recombinant dimers and test candidate explanations for limping. Introducing a covalent cross-link into the stalk region near the heads had no effect on limping, ruling out possible stalk misregistration during coiled-coil formation as a cause. Limping was equally unaffected by mutations that produced 50-fold changes in stalk stiffness, ruling out models where limping arises from an asymmetry in torsional strain. However, limping was enhanced by perturbations that increased the vertical component of load on the motor, including increases in bead size or net load, and decreases in the stalk length. These results suggest that kinesin heads take different vertical trajectories during alternate steps, and that the rates for these motions are differentially sensitive to load.
PubMed ID
PubMed Central ID
PMC2749785 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Biophys. J.
    Title
    Biophysical Journal
    Publication Year
    1960-
    ISBN/ISSN
    0006-3495
    Data From Reference
    Genes (1)