Cell Motility and the Cytoskeleton · 1997 · 26 citations · 10 references
Natural SciencesBiophysicsCell BiologyCell BiophysicsCytoskeletonMolecular BiophysicsCytoskeletal MechanicsCytoskeleton DynamicsMicrotubule-associated ProteinsMolecular MotorsMotor ProteinsGliding LocomotionGliding MotilityKinesin MotilityKinesin MotorsKinesin-mediated MotilityMicroscopic ObservationMicrotubule DynamicsMicrotubule-based Motility
We studied the effect of alkaline-earth metal ions on the kinesin-driven gliding of microtubules, using a narrow glass chamber enabling the exchange of buffer components without interrupting microscopic observation. Under standard conditions (0.5 mM Mg2+), microtubules were found to glide at a mean velocity of about 0.6 micron/s. Motility was widely ceased after removing Mg2+. Subsequent addition of Ca2+ restored motility (maximal mean gliding velocity measured: 0.26 micron/s at 2.5 mM Ca2+). Also in the presence of Sr2+ or Ba2+ a slow gliding could be observed (0.025 micron/s and 0.014 micron/s, respectively, at 0.5 mM). After removal of Ca2+, Sr2+, or Ba2+ and re-addition of Mg2+, the gliding velocities reached approximately the values determined under standard conditions. Motility was not changed when 0.5 mM Ca2+, Sr2+, or Ba2+ were applied together with Mg2+. Microtubule gliding stopped after substitution of 0.5 mM BeCl2 for Mg2+. When both BeCl2 and Mg2+ were present, the mean gliding velocity was reduced to 0.29 micron/s. In addition, many microtubules were released from the kinesin coated glass surface, indicating that the beryllium salt disorders the binding between kinesin and microtubules. Our results confirm that Mg2+ is the most suitable cofactor for kinesin driven microtubule motility. However, they also demonstrate that brain kinesin can generate motility when Ca2+ was substituted for Mg2+.
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A protein factor essential for microtubule assembly.
Murray Weingarten, Arthur H. Lockwood, S Y Hwo et al. · Proceedings of the National Academy of Sciences · 1975 · 3.1K citations · Full text