A stochastic model for microtubule motors describes the in vivo cytoplasmic transport of human adenovirus.
Cytoplasmic transport of organelles, nucleic acids and proteins on microtubules is usually bidirectional with dynein and kinesin motors mediating the delivery of cargoes in the cytoplasm. Here we combine live cell microscopy, single virus tracking and trajectory segmentation to systematically identi...
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2009-12-01
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Series: | PLoS Computational Biology |
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20041204/pdf/?tool=EBI |
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doaj-bceb26f9e3564446ac4dfcdff125b2462021-04-21T15:08:30ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582009-12-01512e100062310.1371/journal.pcbi.1000623A stochastic model for microtubule motors describes the in vivo cytoplasmic transport of human adenovirus.Mattia GazzolaChristoph J BurckhardtBasil BayatiMartin EngelkeUrs F GreberPetros KoumoutsakosCytoplasmic transport of organelles, nucleic acids and proteins on microtubules is usually bidirectional with dynein and kinesin motors mediating the delivery of cargoes in the cytoplasm. Here we combine live cell microscopy, single virus tracking and trajectory segmentation to systematically identify the parameters of a stochastic computational model of cargo transport by molecular motors on microtubules. The model parameters are identified using an evolutionary optimization algorithm to minimize the Kullback-Leibler divergence between the in silico and the in vivo run length and velocity distributions of the viruses on microtubules. The present stochastic model suggests that bidirectional transport of human adenoviruses can be explained without explicit motor coordination. The model enables the prediction of the number of motors active on the viral cargo during microtubule-dependent motions as well as the number of motor binding sites, with the protein hexon as the binding site for the motors.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20041204/pdf/?tool=EBI |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mattia Gazzola Christoph J Burckhardt Basil Bayati Martin Engelke Urs F Greber Petros Koumoutsakos |
spellingShingle |
Mattia Gazzola Christoph J Burckhardt Basil Bayati Martin Engelke Urs F Greber Petros Koumoutsakos A stochastic model for microtubule motors describes the in vivo cytoplasmic transport of human adenovirus. PLoS Computational Biology |
author_facet |
Mattia Gazzola Christoph J Burckhardt Basil Bayati Martin Engelke Urs F Greber Petros Koumoutsakos |
author_sort |
Mattia Gazzola |
title |
A stochastic model for microtubule motors describes the in vivo cytoplasmic transport of human adenovirus. |
title_short |
A stochastic model for microtubule motors describes the in vivo cytoplasmic transport of human adenovirus. |
title_full |
A stochastic model for microtubule motors describes the in vivo cytoplasmic transport of human adenovirus. |
title_fullStr |
A stochastic model for microtubule motors describes the in vivo cytoplasmic transport of human adenovirus. |
title_full_unstemmed |
A stochastic model for microtubule motors describes the in vivo cytoplasmic transport of human adenovirus. |
title_sort |
stochastic model for microtubule motors describes the in vivo cytoplasmic transport of human adenovirus. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Computational Biology |
issn |
1553-734X 1553-7358 |
publishDate |
2009-12-01 |
description |
Cytoplasmic transport of organelles, nucleic acids and proteins on microtubules is usually bidirectional with dynein and kinesin motors mediating the delivery of cargoes in the cytoplasm. Here we combine live cell microscopy, single virus tracking and trajectory segmentation to systematically identify the parameters of a stochastic computational model of cargo transport by molecular motors on microtubules. The model parameters are identified using an evolutionary optimization algorithm to minimize the Kullback-Leibler divergence between the in silico and the in vivo run length and velocity distributions of the viruses on microtubules. The present stochastic model suggests that bidirectional transport of human adenoviruses can be explained without explicit motor coordination. The model enables the prediction of the number of motors active on the viral cargo during microtubule-dependent motions as well as the number of motor binding sites, with the protein hexon as the binding site for the motors. |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20041204/pdf/?tool=EBI |
work_keys_str_mv |
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1714667950498119680 |