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Dynein catch bond as a mediator of codependent bidirectional cellular transport

https://doi.org/10.1101/250175
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cm.970100130openalex-snapshot
Microtubule‐associated organelle and vesicle transport in fibroblasts
inferredcites →https://doi.org/10.1007/s10955-008-9651-7openalex-snapshot
Motility States of Molecular Motors Engaged in a Stochastic Tug-of-War
inferredcites →https://doi.org/10.1016/0021-9991(76)90041-3openalex-snapshot
A general method for numerically simulating the stochastic time evolution of coupled chemical reactions
inferredcites →https://doi.org/10.1016/0092-8674(91)90264-yopenalex-snapshot
Kinesin heavy chain is essential for viability and neuromuscular functions in Drosophila, but mutants show no defects in mitosis
inferredcites →https://doi.org/10.1016/0370-1573(94)90015-9openalex-snapshot
Reentrant phase transitions in multicomponent liquid mixtures
inferredcites →https://doi.org/10.1016/j.bpj.2010.02.037openalex-snapshot
Bidirectional Transport by Molecular Motors: Enhanced Processivity and Response to External Forces
inferredcites →https://doi.org/10.1016/j.bpj.2010.07.055openalex-snapshot
Probing Intracellular Motor Protein Activity Using an Inducible Cargo Trafficking Assay
inferredcites →https://doi.org/10.1016/j.bpj.2012.06.038openalex-snapshot
Measuring Molecular Motor Forces In Vivo: Implications for Tug-of-War Models of Bidirectional Transport
inferredcites →https://doi.org/10.1016/j.cell.2006.05.046openalex-snapshot
Single-Molecule Analysis of Dynein Processivity and Stepping Behavior
inferredcites →https://doi.org/10.1016/j.cell.2007.10.016openalex-snapshot
Force-Induced Bidirectional Stepping of Cytoplasmic Dynein
inferredcites →https://doi.org/10.1016/j.cell.2008.10.021openalex-snapshot
Consequences of Motor Copy Number on the Intracellular Transport of Kinesin-1-Driven Lipid Droplets
inferredcites →https://doi.org/10.1016/j.cell.2008.11.046openalex-snapshot
The Mechanism of Ca2+-Dependent Regulation of Kinesin-Mediated Mitochondrial Motility
inferredcites →https://doi.org/10.1016/j.cell.2010.02.035openalex-snapshot
LIS1 and NudE Induce a Persistent Dynein Force-Producing State
inferredcites →https://doi.org/10.1016/j.cell.2011.01.021openalex-snapshot
Stable Kinesin and Dynein Assemblies Drive the Axonal Transport of Mammalian Prion Protein Vesicles
inferredcites →https://doi.org/10.1016/j.cell.2012.11.044openalex-snapshot
Molecular Adaptations Allow Dynein to Generate Large Collective Forces inside Cells
inferredcites →https://doi.org/10.1016/j.cell.2013.05.020openalex-snapshot
Dynein Motion Switches from Diffusive to Directed upon Cortical Anchoring
inferredcites →https://doi.org/10.1016/j.cub.2003.08.032openalex-snapshot
A Determinant for Directionality of Organelle Transport in Drosophila Embryos
inferredcites →https://doi.org/10.1016/j.cub.2003.10.027openalex-snapshot
Switching between Microtubule- and Actin-Based Transport Systems in Melanophores Is Controlled by cAMP Levels
inferredcites →https://doi.org/10.1016/j.cub.2004.06.045openalex-snapshot
Bidirectional Transport along Microtubules
inferredcites →https://doi.org/10.1016/j.cub.2005.06.062openalex-snapshot
Regulation of Lipid-Droplet Transport by the Perilipin Homolog LSD2
inferredcites →https://doi.org/10.1016/j.cub.2005.10.039openalex-snapshot
Building Complexity: An In Vitro Study of Cytoplasmic Dynein with In Vivo Implications
inferredcites →https://doi.org/10.1016/j.cub.2010.02.058openalex-snapshot
Motor Coordination via a Tug-of-War Mechanism Drives Bidirectional Vesicle Transport
inferredcites →https://doi.org/10.1016/j.neuron.2012.02.025openalex-snapshot
Dynactin Is Required for Transport Initiation from the Distal Axon
inferredcites →https://doi.org/10.1016/j.tcb.2013.06.003openalex-snapshot
Teamwork in microtubule motors
inferredcites →https://doi.org/10.1016/s0074-7696(08)60339-3openalex-snapshot
Polarized Intracellular Particle Transport: Saltatory Movements and Cytoplasmic Streaming
inferredcites →https://doi.org/10.1016/s0092-8674(00)80947-2openalex-snapshot
Developmental Regulation of Vesicle Transport in Drosophila Embryos: Forces and Kinetics
inferredcites →https://doi.org/10.1016/s0960-9822(03)00237-9openalex-snapshot
Dynactin: Coordinating Motors with Opposite Inclinations
inferredcites →https://doi.org/10.1021/j100540a008openalex-snapshot
Exact stochastic simulation of coupled chemical reactions
inferredcites →https://doi.org/10.1023/a:1020300319224openalex-snapshot
Mechanical Properties of a Single-Headed Processive Motor, Inner-Arm Dynein Subspecies-c of ChlamydomonasStudied at the Single Molecule Level
inferredcites →https://doi.org/10.1038/35036345openalex-snapshot
Force production by single kinesin motors
inferredcites →https://doi.org/10.1038/71338openalex-snapshot
Dynactin increases the processivity of the cytoplasmic dynein motor
inferredcites →https://doi.org/10.1038/nature02293openalex-snapshot
Cytoplasmic dynein functions as a gear in response to load
inferredcites →https://doi.org/10.1038/nature03528openalex-snapshot
Mechanics of the kinesin step
inferredcites →https://doi.org/10.1038/ncomms2037openalex-snapshot
Rotational dynamics of cargos at pauses during axonal transport
inferredcites →https://doi.org/10.1038/nrm3853openalex-snapshot
Bidirectional cargo transport: moving beyond tug of war
inferredcites →https://doi.org/10.1039/b900760copenalex-snapshot
Enhancement of cargo processivity by cooperating molecular motors
inferredcites →https://doi.org/10.1039/c5sm01609fopenalex-snapshot
Collective dynamics of processive cytoskeletal motors
inferredcites →https://doi.org/10.1073/pnas.0406598101openalex-snapshot
Cooperative extraction of membrane nanotubes by molecular motors
inferredcites →https://doi.org/10.1073/pnas.0408114101openalex-snapshot
Transport of Drosophila fragile X mental retardation protein-containing ribonucleoprotein granules by kinesin-1 and cytoplasmic dynein
inferredcites →https://doi.org/10.1073/pnas.0501570102openalex-snapshot
Monte Carlo modeling of single-molecule cytoplasmic dynein
inferredcites →https://doi.org/10.1073/pnas.0507363102openalex-snapshot
Cooperative cargo transport by several molecular motors
inferredcites →https://doi.org/10.1073/pnas.0508511103openalex-snapshot
Overlapping hand-over-hand mechanism of single molecular motility of cytoplasmic dynein
inferredcites →https://doi.org/10.1073/pnas.061029798openalex-snapshot
Herpesviruses use bidirectional fast-axonal transport to spread in sensory neurons
inferredcites →https://doi.org/10.1073/pnas.0706825105openalex-snapshot
Tug-of-war as a cooperative mechanism for bidirectional cargo transport by molecular motors
inferredcites →https://doi.org/10.1073/pnas.0906524106openalex-snapshot
Tug-of-war between dissimilar teams of microtubule motors regulates transport and fission of endosomes
inferredcites →https://doi.org/10.1073/pnas.1015839108openalex-snapshot
Transient binding of dynein controls bidirectional long-range motility of early endosomes
inferredcites →https://doi.org/10.1073/pnas.1107841108openalex-snapshot
Mechanical stochastic tug-of-war models cannot explain bidirectional lipid-droplet transport
inferredcites →https://doi.org/10.1073/pnas.1219961110openalex-snapshot
In vivo optical trapping indicates kinesin’s stall force is reduced by dynein during intracellular transport
inferredcites →https://doi.org/10.1073/pnas.79.15.4818openalex-snapshot
Microinjection into an identified axon to study the mechanism of fast axonal transport.
inferredcites →https://doi.org/10.1073/pnas.94.22.12180openalex-snapshot
The interaction between cytoplasmic dynein and dynactin is required for fast axonal transport
inferredcites →https://doi.org/10.1073/pnas.94.8.3720openalex-snapshot
Regulated bidirectional motility of melanophore pigment granules along microtubules in vitro
inferredcites →https://doi.org/10.1083/jcb.121.2.305openalex-snapshot
Products of endocytosis and autophagy are retrieved from axons by regulated retrograde organelle transport.
inferredcites →https://doi.org/10.1083/jcb.137.1.113openalex-snapshot
Molecular Requirements for Bi-directional Movement of Phagosomes Along Microtubules
inferredcites →https://doi.org/10.1083/jcb.141.2.443openalex-snapshot
Kinesin Light Chains Are Essential for Axonal Transport in Drosophila
inferredcites →https://doi.org/10.1083/jcb.144.4.657openalex-snapshot
Microtubule-dependent Plus- and Minus End–directed Motilities Are Competing Processes for Nuclear Targeting of Adenovirus
inferredcites →https://doi.org/10.1083/jcb.148.5.945openalex-snapshot
Dynein-Mediated Cargo Transport in Vivo
inferredcites →https://doi.org/10.1083/jcb.200105055openalex-snapshot
Interactions and regulation of molecular motors in Xenopus melanophores
inferredcites →https://doi.org/10.1083/jcb.200109047openalex-snapshot
Coordination of opposite-polarity microtubule motors
inferredcites →https://doi.org/10.1083/jcb.200203150openalex-snapshot
Visualization of the intracellular behavior of HIV in living cells
inferredcites →https://doi.org/10.1083/jcb.200210066openalex-snapshot
Dynactin is required for bidirectional organelle transport
inferredcites →https://doi.org/10.1083/jcb.200908075openalex-snapshot
Opposite-polarity motors activate one another to trigger cargo transport in live cells
inferredcites →https://doi.org/10.1083/jcb.201104076openalex-snapshot
High-resolution imaging reveals indirect coordination of opposite motors and a role for LIS1 in high-load axonal transport
inferredcites →https://doi.org/10.1083/jcb.201302078openalex-snapshot
JIP1 regulates the directionality of APP axonal transport by coordinating kinesin and dynein motors
inferredcites →https://doi.org/10.1085/jgp.50.6.223openalex-snapshot
Structural Aspects of Saltatory Particle Movement
inferredcites →https://doi.org/10.1088/0953-8984/25/46/463101openalex-snapshot
Motor proteins and molecular motors: how to operate machines at the nanoscale
inferredcites →https://doi.org/10.1088/1478-3967/1/2/r01openalex-snapshot
Hither and yon: a review of bi-directional microtubule-based transport
inferredcites →https://doi.org/10.1088/1478-3975/3/1/005openalex-snapshot
Finite-particle tracking reveals submicroscopic-size changes of mitochondria during transport in mitral cell dendrites
inferredcites →https://doi.org/10.1088/1478-3975/5/4/046004openalex-snapshot
Dynamic kinesin-1 clustering on microtubules due to mutually attractive interactions
inferredcites →https://doi.org/10.1091/mbc.10.11.3717openalex-snapshot
Cytoplasmic Dynein, the Dynactin Complex, and Kinesin Are Interdependent and Essential for Fast Axonal Transport
inferredcites →https://doi.org/10.1091/mbc.10.12.4107openalex-snapshot
Role of Dynactin in Endocytic Traffic: Effects of Dynamitin Overexpression and Colocalization with CLIP-170
inferredcites →https://doi.org/10.1091/mbc.11.2.419openalex-snapshot
Reconstitution of ATP-dependent Movement of Endocytic Vesicles Along Microtubules In Vitro: An Oscillatory Bidirectional Process
inferredcites →https://doi.org/10.1091/mbc.e05-06-0526openalex-snapshot
Kinesin-1 and Dynein Are the Primary Motors for Fast Transport of Mitochondria in Drosophila Motor Axons
inferredcites →https://doi.org/10.1091/mbc.e06-08-0695openalex-snapshot
Dynactin Is Required for Coordinated Bidirectional Motility, but Not for Dynein Membrane Attachment
inferredcites →https://doi.org/10.1091/mbc.e09-04-0304openalex-snapshot
Tight Functional Coupling of Kinesin-1A and Dynein Motors in the Bidirectional Transport of Neurofilaments
inferredcites →https://doi.org/10.1091/mbc.e10-03-0233openalex-snapshot
Huntingtin coordinates the dynein-mediated dynamic positioning of endosomes and lysosomes
inferredcites →https://doi.org/10.1093/genetics/144.3.1075openalex-snapshot
Kinesin Mutations Cause Motor Neuron Disease Phenotypes by Disrupting Fast Axonal Transport in Drosophila
inferredcites →https://doi.org/10.1103/physreve.73.050902openalex-snapshot
Force-induced deformations and stability of biological bonds
inferredcites →https://doi.org/10.1103/physreve.94.032403openalex-snapshot
Effect of catch bonding on transport of cellular cargo by dynein motors
inferredcites →https://doi.org/10.1242/jcs.00672openalex-snapshot
Interaction of the actin cytoskeleton with microtubules regulates secretory organelle movement near the plasma membrane in human endothelial cells
inferredcites →https://doi.org/10.1242/jcs.053850openalex-snapshot
The axonal transport of mitochondria
inferredcites →https://doi.org/10.1242/jcs.106.3.955openalex-snapshot
Regulation of vesicle transport in CV-1 cells and extracts
inferredcites →https://doi.org/10.1242/jcs.110.13.1453openalex-snapshot
Microtubule-dependent transport of secretory vesicles visualized in real time with a GFP-tagged secretory protein
inferredcites →https://doi.org/10.1242/jcs.1991.supplement_14.21openalex-snapshot
Kinesin interactions with membrane bounded organelles in vivo and in vitro
inferredcites →https://doi.org/10.1242/jeb.00263openalex-snapshot
Mitochondrial movement and positioning in axons: the role of growth factor signaling
inferredcites →https://doi.org/10.1529/biophysj.106.097881openalex-snapshot
Transport of Beads by Several Kinesin Motors
inferredcites →https://doi.org/10.2741/a118openalex-snapshot
The pattern and mechanism of mitochondrial transport in axons
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