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    Modeling Bidirectional Transport of New and Used Organelles in Fast Axonal Transport in Neurons

    Source: Journal of Heat Transfer:;2011:;volume( 133 ):;issue: 001::page 11007
    Author:
    A. V. Kuznetsov
    DOI: 10.1115/1.4002304
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: This paper develops a model for simulating transport of newly synthesized material from the neuron body toward the synapse of the axon as well as transport of misfolded and aggregated proteins back to the neuron body for recycling. The model demonstrates that motor-assisted transport, much similar to diffusion, can occur due to a simple concentration difference between the cell body and the synapse; organelles heading to the synapse do not need to attach preferably to plus-end-directed molecular motors, same as organelles heading to the neuron body for recycling do not need to attach preferably to minus-end-directed molecular motors. The underlying mechanics of molecular-motor-assisted transport is such that organelles would be transported to the right place even if new and used organelles had the same probability of attachment to plus-end-directed (and minus-end-directed) motors. It is also demonstrated that the axon with organelle traps and a region with a reversed microtubule polarity would support much smaller organelle fluxes of both new and used organelles than a healthy axon. The flux of organelles is shown to decrease as the width of organelle traps increases.
    keyword(s): Diffusion (Physics) , Engines , Flux (Metallurgy) , Modeling , Boundary-value problems , Equations , Probability , Proteins , Molecular motors , Recycling , Traffic AND Motors ,
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      Modeling Bidirectional Transport of New and Used Organelles in Fast Axonal Transport in Neurons

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    https://yetl.yabesh.ir/yetl1/handle/yetl/146790
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    contributor authorA. V. Kuznetsov
    date accessioned2017-05-09T00:45:17Z
    date available2017-05-09T00:45:17Z
    date copyrightJanuary, 2011
    date issued2011
    identifier issn0022-1481
    identifier otherJHTRAO-27904#011007_1.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/146790
    description abstractThis paper develops a model for simulating transport of newly synthesized material from the neuron body toward the synapse of the axon as well as transport of misfolded and aggregated proteins back to the neuron body for recycling. The model demonstrates that motor-assisted transport, much similar to diffusion, can occur due to a simple concentration difference between the cell body and the synapse; organelles heading to the synapse do not need to attach preferably to plus-end-directed molecular motors, same as organelles heading to the neuron body for recycling do not need to attach preferably to minus-end-directed molecular motors. The underlying mechanics of molecular-motor-assisted transport is such that organelles would be transported to the right place even if new and used organelles had the same probability of attachment to plus-end-directed (and minus-end-directed) motors. It is also demonstrated that the axon with organelle traps and a region with a reversed microtubule polarity would support much smaller organelle fluxes of both new and used organelles than a healthy axon. The flux of organelles is shown to decrease as the width of organelle traps increases.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleModeling Bidirectional Transport of New and Used Organelles in Fast Axonal Transport in Neurons
    typeJournal Paper
    journal volume133
    journal issue1
    journal titleJournal of Heat Transfer
    identifier doi10.1115/1.4002304
    journal fristpage11007
    identifier eissn1528-8943
    keywordsDiffusion (Physics)
    keywordsEngines
    keywordsFlux (Metallurgy)
    keywordsModeling
    keywordsBoundary-value problems
    keywordsEquations
    keywordsProbability
    keywordsProteins
    keywordsMolecular motors
    keywordsRecycling
    keywordsTraffic AND Motors
    treeJournal of Heat Transfer:;2011:;volume( 133 ):;issue: 001
    contenttypeFulltext
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