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Choosing orientation: influence of cargo geometry and ActA polarization on actin comet tails

Networks of polymerizing actin filaments can propel intracellular pathogens and drive movement of artificial particles in reconstituted systems. While biochemical mechanisms activating actin network assembly have been well characterized, it remains unclear how particle geometry and large-scale force...

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Autores principales: Lacayo, Catherine I., Soneral, Paula A. G., Zhu, Jie, Tsuchida, Mark A., Footer, Matthew J., Soo, Frederick S., Lu, Yu, Xia, Younan, Mogilner, Alexander, Theriot, Julie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279390/
https://www.ncbi.nlm.nih.gov/pubmed/22219381
http://dx.doi.org/10.1091/mbc.E11-06-0584
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author Lacayo, Catherine I.
Soneral, Paula A. G.
Zhu, Jie
Tsuchida, Mark A.
Footer, Matthew J.
Soo, Frederick S.
Lu, Yu
Xia, Younan
Mogilner, Alexander
Theriot, Julie A.
author_facet Lacayo, Catherine I.
Soneral, Paula A. G.
Zhu, Jie
Tsuchida, Mark A.
Footer, Matthew J.
Soo, Frederick S.
Lu, Yu
Xia, Younan
Mogilner, Alexander
Theriot, Julie A.
author_sort Lacayo, Catherine I.
collection PubMed
description Networks of polymerizing actin filaments can propel intracellular pathogens and drive movement of artificial particles in reconstituted systems. While biochemical mechanisms activating actin network assembly have been well characterized, it remains unclear how particle geometry and large-scale force balance affect emergent properties of movement. We reconstituted actin-based motility using ellipsoidal beads resembling the geometry of Listeria monocytogenes. Beads coated uniformly with the L. monocytogenes ActA protein migrated equally well in either of two distinct orientations, with their long axes parallel or perpendicular to the direction of motion, while intermediate orientations were unstable. When beads were coated with a fluid lipid bilayer rendering ActA laterally mobile, beads predominantly migrated with their long axes parallel to the direction of motion, mimicking the orientation of motile L. monocytogenes. Generating an accurate biophysical model to account for our observations required the combination of elastic-propulsion and tethered-ratchet actin-polymerization theories. Our results indicate that the characteristic orientation of L. monocytogenes must be due to polarized ActA rather than intrinsic actin network forces. Furthermore, viscoelastic stresses, forces, and torques produced by individual actin filaments and lateral movement of molecular complexes must all be incorporated to correctly predict large-scale behavior in the actin-based movement of nonspherical particles.
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spelling pubmed-32793902012-04-30 Choosing orientation: influence of cargo geometry and ActA polarization on actin comet tails Lacayo, Catherine I. Soneral, Paula A. G. Zhu, Jie Tsuchida, Mark A. Footer, Matthew J. Soo, Frederick S. Lu, Yu Xia, Younan Mogilner, Alexander Theriot, Julie A. Mol Biol Cell Articles Networks of polymerizing actin filaments can propel intracellular pathogens and drive movement of artificial particles in reconstituted systems. While biochemical mechanisms activating actin network assembly have been well characterized, it remains unclear how particle geometry and large-scale force balance affect emergent properties of movement. We reconstituted actin-based motility using ellipsoidal beads resembling the geometry of Listeria monocytogenes. Beads coated uniformly with the L. monocytogenes ActA protein migrated equally well in either of two distinct orientations, with their long axes parallel or perpendicular to the direction of motion, while intermediate orientations were unstable. When beads were coated with a fluid lipid bilayer rendering ActA laterally mobile, beads predominantly migrated with their long axes parallel to the direction of motion, mimicking the orientation of motile L. monocytogenes. Generating an accurate biophysical model to account for our observations required the combination of elastic-propulsion and tethered-ratchet actin-polymerization theories. Our results indicate that the characteristic orientation of L. monocytogenes must be due to polarized ActA rather than intrinsic actin network forces. Furthermore, viscoelastic stresses, forces, and torques produced by individual actin filaments and lateral movement of molecular complexes must all be incorporated to correctly predict large-scale behavior in the actin-based movement of nonspherical particles. The American Society for Cell Biology 2012-02-15 /pmc/articles/PMC3279390/ /pubmed/22219381 http://dx.doi.org/10.1091/mbc.E11-06-0584 Text en © 2012 Lacayo et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology.
spellingShingle Articles
Lacayo, Catherine I.
Soneral, Paula A. G.
Zhu, Jie
Tsuchida, Mark A.
Footer, Matthew J.
Soo, Frederick S.
Lu, Yu
Xia, Younan
Mogilner, Alexander
Theriot, Julie A.
Choosing orientation: influence of cargo geometry and ActA polarization on actin comet tails
title Choosing orientation: influence of cargo geometry and ActA polarization on actin comet tails
title_full Choosing orientation: influence of cargo geometry and ActA polarization on actin comet tails
title_fullStr Choosing orientation: influence of cargo geometry and ActA polarization on actin comet tails
title_full_unstemmed Choosing orientation: influence of cargo geometry and ActA polarization on actin comet tails
title_short Choosing orientation: influence of cargo geometry and ActA polarization on actin comet tails
title_sort choosing orientation: influence of cargo geometry and acta polarization on actin comet tails
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279390/
https://www.ncbi.nlm.nih.gov/pubmed/22219381
http://dx.doi.org/10.1091/mbc.E11-06-0584
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