TY - JOUR
T1 - Kinesin and dynein-dynactin at intersecting microtubules
T2 - Motor density affects dynein function
AU - Ross, Jennifer L.
AU - Shuman, Henry
AU - Holzbaur, Erika L.F.
AU - Goldman, Yale E.
N1 - Funding Information:
This work was supported by the National Institutes of Health (NIH) project program grant P01-AR-051174 to the Pennsylvania Muscle Institute, National Science Foundation grant NSEC DMR04-25780 to the Penn Nano/Bio Interface Center, and by NIH GM068591 to E.L.F.H. J.L.R. was supported by an NIH National Research Service Award grant 1F32GM075754-01. The authors have no competing interests.
PY - 2008/4/15
Y1 - 2008/4/15
N2 - Kinesin and cytoplasmic dynein are microtubule-based motor proteins that actively transport material throughout the cell. Microtubules can intersect at a variety of angles both near the nucleus and at the cell periphery, and the behavior of molecular motors at these intersections has implications for long-range transport efficiency and accuracy. To test motor function at microtubule intersections, crossovers were arranged in vitro using flow to orient successive layers of filaments. Single kinesin and cytoplasmic dynein-dynactin molecules fused with green-fluorescent protein, and artificial bead cargos decorated with multiple motors, were observed while they encountered intersections. Single kinesins tend to cross intersecting microtubules, whereas single dynein-dynactins have a more varied response. For bead cargos, kinesin motion is independent of motor number. Dynein beads with high motor numbers pause, but their actions become more varied as the motor number decreases. These results suggest that regulating the number of active dynein molecules could change a motile cargo into one that is anchored at an intersection, consistent with dynein's proposed transport and tethering functions in the cell.
AB - Kinesin and cytoplasmic dynein are microtubule-based motor proteins that actively transport material throughout the cell. Microtubules can intersect at a variety of angles both near the nucleus and at the cell periphery, and the behavior of molecular motors at these intersections has implications for long-range transport efficiency and accuracy. To test motor function at microtubule intersections, crossovers were arranged in vitro using flow to orient successive layers of filaments. Single kinesin and cytoplasmic dynein-dynactin molecules fused with green-fluorescent protein, and artificial bead cargos decorated with multiple motors, were observed while they encountered intersections. Single kinesins tend to cross intersecting microtubules, whereas single dynein-dynactins have a more varied response. For bead cargos, kinesin motion is independent of motor number. Dynein beads with high motor numbers pause, but their actions become more varied as the motor number decreases. These results suggest that regulating the number of active dynein molecules could change a motile cargo into one that is anchored at an intersection, consistent with dynein's proposed transport and tethering functions in the cell.
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U2 - 10.1529/biophysj.107.120014
DO - 10.1529/biophysj.107.120014
M3 - Article
C2 - 18227130
AN - SCOPUS:43149117264
SN - 0006-3495
VL - 94
SP - 3115
EP - 3125
JO - Biophysical Journal
JF - Biophysical Journal
IS - 8
ER -