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Kinesin and Dynein Move a Peroxisome in Vivo: A Tug-of-War or Coordinated Movement?
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Fast vesicle transport in PC12 neurites: velocities and forces
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The force exerted by a single kinesin molecule against a viscous load
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Identification of a novel force-generating protein, kinesin, involved in microtubule-based motility
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Membrane trafficking, organelle transport, and the cytoskeleton
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Distinct Functions of Nucleotide-Binding/Hydrolysis Sites in the Four AAA Modules of Cytoplasmic Dynein
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Force generation of organelle transport measured in vivo by an infrared laser trap
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Direct observation of kinesin stepping by optical trapping interferometry
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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
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Visualizing infection of individual influenza viruses
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A Single-headed Recombinant Fragment of Dictyostelium Cytoplasmic Dynein Can Drive the Robust Sliding of Microtubules
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
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Drosophila EB1 is important for proper assembly, dynamics, and positioning of the mitotic spindle
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Axonal Membrane Proteins Are Transported in Distinct Carriers: A Two-Color Video Microscopy Study in Cultured Hippocampal Neurons
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Intracellular transport in neurons.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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How to Follow a Traveler with a Brownian Swagger
inferred← citeshttps://doi.org/10.1016/j.bpj.2018.04.006openalex-snapshot
PLANT: A Method for Detecting Changes of Slope in Noisy Trajectories
inferred← citeshttps://doi.org/10.1016/j.bpj.2018.11.016openalex-snapshot
Single-Nanoparticle Tracking with Angstrom Localization Precision and Microsecond Time Resolution
inferred← citeshttps://doi.org/10.1016/j.bpj.2020.01.045openalex-snapshot
Stochastic Model of T Cell Repolarization during Target Elimination I
inferred← citeshttps://doi.org/10.1016/j.bpj.2020.01.047openalex-snapshot
Processivity and Velocity for Motors Stepping on Periodic Tracks
inferred← citeshttps://doi.org/10.1016/j.bpj.2021.04.011openalex-snapshot
Glass-like characteristics of intracellular motion in human cells
inferred← citeshttps://doi.org/10.1016/j.bpj.2022.11.241openalex-snapshot
Nanometer-resolution long-term tracking of single cargos reveals dynein motor mechanisms
inferred← citeshttps://doi.org/10.1016/j.brainres.2008.03.014openalex-snapshot
Fewer active motors per vesicle may explain slowed vesicle transport in chick motoneurons after three days in vitro
inferred← citeshttps://doi.org/10.1016/j.cap.2022.09.002openalex-snapshot
High spatial and temporal resolution using upconversion nanoparticles and femtosecond pulsed laser in single particle tracking
inferred← citeshttps://doi.org/10.1016/j.cbpa.2008.08.008openalex-snapshot
Super-resolution microscopy by nanoscale localization of photo-switchable fluorescent probes
inferred← citeshttps://doi.org/10.1016/j.ceb.2005.06.003openalex-snapshot
The control of peroxisome number and size during division and proliferation
inferred← citeshttps://doi.org/10.1016/j.ceb.2007.11.006openalex-snapshot
Cargo transport: molecular motors navigate a complex cytoskeleton
inferred← citeshttps://doi.org/10.1016/j.ceb.2009.12.014openalex-snapshot
Coordination of molecular motors: from in vitro assays to intracellular dynamics
inferred← citeshttps://doi.org/10.1016/j.cell.2006.02.018openalex-snapshot
A Superhighway to Virus Infection
inferred← citeshttps://doi.org/10.1016/j.cell.2006.05.046openalex-snapshot
Single-Molecule Analysis of Dynein Processivity and Stepping Behavior
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.cell.2011.01.021openalex-snapshot
Stable Kinesin and Dynein Assemblies Drive the Axonal Transport of Mammalian Prion Protein Vesicles
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.12.051openalex-snapshot
A Genome-wide RNAi Screen for Microtubule Bundle Formation and Lysosome Motility Regulation in Drosophila S2 Cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110433openalex-snapshot
Modulation of the cell membrane lipid milieu by peroxisomal β-oxidation induces Rho1 signaling to trigger inflammatory responses
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111140openalex-snapshot
A sphingolipid-mTORC1 nutrient-sensing pathway regulates animal development by an intestinal peroxisome relocation-based gut-brain crosstalk
inferred← citeshttps://doi.org/10.1016/j.chembiol.2015.04.014openalex-snapshot
Optogenetic Control of Molecular Motors and Organelle Distributions in Cells
inferred← citeshttps://doi.org/10.1016/j.chembiol.2015.05.002openalex-snapshot
Light Moves Mountains in the Cell
inferred← citeshttps://doi.org/10.1016/j.chemphys.2013.06.020openalex-snapshot
Collective THz dynamics in living Escherichia coli cells
inferred← citeshttps://doi.org/10.1016/j.chempr.2025.102742openalex-snapshot
Structure-performance relationships for catalysis-driven molecular machinery
inferred← citeshttps://doi.org/10.1016/j.cpc.2008.06.008openalex-snapshot
An objective, model-independent method for detection of non-uniform steps in noisy signals
inferred← citeshttps://doi.org/10.1016/j.cplett.2008.03.098openalex-snapshot
Progress in single-molecule tracking spectroscopy
inferred← citeshttps://doi.org/10.1016/j.cub.2005.10.047openalex-snapshot
APLIP1, a Kinesin Binding JIP-1/JNK Scaffold Protein, Influences the Axonal Transport of Both Vesicles and Mitochondria in Drosophila
inferred← citeshttps://doi.org/10.1016/j.cub.2006.05.055openalex-snapshot
Guidance of Bidirectional Motor Complexes by mRNA Cargoes through Control of Dynein Number and Activity
inferred← citeshttps://doi.org/10.1016/j.cub.2007.04.025openalex-snapshot
Cargo Transport: Two Motors Are Sometimes Better Than One
inferred← citeshttps://doi.org/10.1016/j.cub.2008.07.027openalex-snapshot
Stepping, Strain Gating, and an Unexpected Force-Velocity Curve for Multiple-Motor-Based Transport
inferred← citeshttps://doi.org/10.1016/j.cub.2010.03.018openalex-snapshot
Bidirectional Transport: Matchmaking for Motors
inferred← citeshttps://doi.org/10.1016/j.cub.2012.11.009openalex-snapshot
Intracellular Transport: New Tools Provide Insights into Multi-motor Transport
inferred← citeshttps://doi.org/10.1016/j.cub.2013.01.008openalex-snapshot
The Microtubule-Binding Protein Ensconsin Is an Essential Cofactor of Kinesin-1
inferred← citeshttps://doi.org/10.1016/j.devcel.2005.11.016openalex-snapshot
Polarized Transport of Frizzled along the Planar Microtubule Arrays in Drosophila Wing Epithelium
inferred← citeshttps://doi.org/10.1016/j.devcel.2012.09.022openalex-snapshot
Visualizing Cell Structure and Function with Point-Localization Superresolution Imaging
inferred← citeshttps://doi.org/10.1016/j.ejcb.2007.05.005openalex-snapshot
Intracellular objects tracking
inferred← citeshttps://doi.org/10.1016/j.ejcb.2010.08.005openalex-snapshot
The native structure of cytoplasmic dynein at work translocating vesicles in Paramecium
inferred← citeshttps://doi.org/10.1016/j.febslet.2007.05.041openalex-snapshot
Quantitative single particle tracking of NGF–receptor complexes: Transport is bidirectional but biased by longer retrograde run lengths
inferred← citeshttps://doi.org/10.1016/j.febslet.2009.11.035openalex-snapshot
Single molecule approaches to transcription factor kinetics in living cells
inferred← citeshttps://doi.org/10.1016/j.febslet.2015.07.038openalex-snapshot
Asymmetries in kinesin‐2 and cytoplasmic dynein contributions to melanosome transport
inferred← citeshttps://doi.org/10.1016/j.isci.2026.114875openalex-snapshot
Kinesin-1 is highly flexible and adopts an open conformation in the absence of cargo
inferred← citeshttps://doi.org/10.1016/j.jbiomech.2009.09.006openalex-snapshot
The mechanochemistry of integrated motor protein complexes
inferred← citeshttps://doi.org/10.1016/j.jbiomech.2015.09.043openalex-snapshot
Effects of wild type tau and disease-linked tau mutations on microtubule organization and intracellular trafficking
inferred← citeshttps://doi.org/10.1016/j.jmb.2020.166765openalex-snapshot
Competitive Microtubule Binding of PEX14 Coordinates Peroxisomal Protein Import and Motility
inferred← citeshttps://doi.org/10.1016/j.jtbi.2008.12.011openalex-snapshot
A quantitative examination of the role of cargo-exerted forces in axonal transport
inferred← citeshttps://doi.org/10.1016/j.jtbi.2012.01.019openalex-snapshot
Cargo distributions differentiate pathological axonal transport impairments
inferred← citeshttps://doi.org/10.1016/j.jtbi.2015.01.010openalex-snapshot
Axonal transport cargo motor count versus average transport velocity: Is fast versus slow transport really single versus multiple motor transport?
inferred← citeshttps://doi.org/10.1016/j.jtbi.2018.11.022openalex-snapshot
Slow and fast grouping of cargo velocities in axonal transport due to single versus multi-motor transport
inferred← citeshttps://doi.org/10.1016/j.mbs.2010.10.003openalex-snapshot
Comparison of active transport in neuronal axons and dendrites
inferred← citeshttps://doi.org/10.1016/j.mbs.2011.04.008openalex-snapshot
Modeling bidirectional transport of quantum dot nanoparticles in membrane nanotubes
inferred← citeshttps://doi.org/10.1016/j.medengphy.2015.03.003openalex-snapshot
Effects of particle uptake, encapsulation, and localization in cancer cells on intracellular applications
inferred← citeshttps://doi.org/10.1016/j.molcel.2006.10.017openalex-snapshot
Single-Molecule Biology: What Is It and How Does It Work?
inferred← citeshttps://doi.org/10.1016/j.nbd.2024.106594openalex-snapshot
Patient-specific mutation of Dync1h1 in mice causes brain and behavioral deficits
inferred← citeshttps://doi.org/10.1016/j.neuron.2008.05.029openalex-snapshot
Localized Regulation of Axonal RanGTPase Controls Retrograde Injury Signaling in Peripheral Nerve
inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2016.09.006openalex-snapshot
In vivo cardiac nano-imaging: A new technology for high-precision analyses of sarcomere dynamics in the heart
inferred← citeshttps://doi.org/10.1016/j.physa.2006.05.019openalex-snapshot
Molecular motor traffic: From biological nanomachines to macroscopic transport
inferred← citeshttps://doi.org/10.1016/j.physa.2007.03.022openalex-snapshot
Computational modelling of the stochastic dynamics of kinesin biomolecular motors
inferred← citeshttps://doi.org/10.1016/j.physd.2009.01.005openalex-snapshot
Cooperativity of multiple kinesin-1 motors mechanically coupled through a shared load
inferred← citeshttps://doi.org/10.1016/j.physe.2009.08.010openalex-snapshot
Cooperative behavior of molecular motors: Cargo transport and traffic phenomena
inferred← citeshttps://doi.org/10.1016/j.physrep.2015.07.001openalex-snapshot
Intracellular transport driven by cytoskeletal motors: General mechanisms and defects
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2017.10.003openalex-snapshot
Nano- and neurotoxicology: An emerging discipline
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