# Molecular Motors Orchestrate Pause-and-Run Dynamics to Facilitate Intracellular Transport

**Authors:** Yusheng Shen, Kassandra M. Ori-McKenney

PMC · DOI: 10.3390/biom16020221 · Biomolecules · 2026-02-02

## TL;DR

Molecular motors actively control pauses during intracellular transport, revealing a new principle that helps cells move cargo efficiently.

## Contribution

The discovery that pauses in intracellular transport are active, motor-driven states governed by a quantitative law.

## Key findings

- Pauses during intracellular transport are active and driven by molecular motors, not passive drifting.
- A quantitative law (Deff ∝ v²) links the diffusivity during pauses to the velocity during runs across different motors and cargo.
- Reduced motor engagement leads to slower transport and longer pauses, impairing cargo delivery.

## Abstract

Intracellular transport is essential for cellular organization and function. This process is driven by molecular motors that ferry cargo along microtubules, but is characterized by intermittent motility, where cargoes switch between directed runs and prolonged pauses. The fundamental nature of these pauses has remained a mystery, specifically whether they are periods of motor detachment and passive drifting or states of active motor engagement. By combining single-particle tracking with large-scale motion analysis, we discovered that pauses are not passive. Instead, they are active, motor-driven states. We uncovered a unifying quantitative law: the diffusivity of a vesicle during a pause scales with the square of its velocity during a run. This parabolic relationship, Deff ∝ v2, holds true for both kinesin and dynein motors, different cargo types, and a variety of cellular perturbations. We show that this coupling arises because the number of engaged motors governs motility in both states. When we reduce motor engagement, vesicles move more slowly and become trapped in longer, less mobile pauses, collectively causing them to fail to reach their destination. Our work redefines transport pauses as an essential, motor-driven part of microtubule-based cargo delivery, revealing a quantitative principle that contributes to robust cargo transport through the crowded cellular environment.

## Linked entities

- **Proteins:** Khc (Kinesin heavy chain), Dhc64C (Dynein heavy chain 64C)

## Full-text entities

- **Genes:** KIF5B [NCBI Gene 477968], SVBP (small vasohibin binding protein) [NCBI Gene 374969] {aka CCDC23, NEDAHM, SPG94}, TUBA1B (tubulin alpha 1b) [NCBI Gene 10376] {aka K-ALPHA-1}, KIF5B (kinesin family member 5B) [NCBI Gene 3799] {aka HEL-S-61, KINH, KNS, KNS1, UKHC}, RAB6A (RAB6A, member RAS oncogene family) [NCBI Gene 5870] {aka RAB6}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, RAB6A (RAB6A, member RAS oncogene family) [NCBI Gene 608330], VASH2 (vasohibin 2) [NCBI Gene 79805], MAP7 (microtubule associated protein 7) [NCBI Gene 9053] {aka E-MAP-115, EMAP115}, KIF13B (kinesin family member 13B) [NCBI Gene 23303] {aka GAKIN}, VASH1 (vasohibin 1) [NCBI Gene 22846] {aka KIAA1036, TTCP 1}, RAB5A (RAB5A, member RAS oncogene family) [NCBI Gene 5868] {aka RAB5}, KIF1B (kinesin family member 1B) [NCBI Gene 23095] {aka CMT2, CMT2A, CMT2A1, HMSNII, KLP, NBLST1}, KIF1C (kinesin family member 1C) [NCBI Gene 10749] {aka LTXS1, SATX2, SAX2, SPAX2, SPG58}, ABRA (actin binding Rho activating protein) [NCBI Gene 137735] {aka STARS}
- **Diseases:** injury to (MESH:D014947)
- **Chemicals:** NaCl (MESH:D012965), methanol (MESH:D000432), DMEM (-), MgCl2 (MESH:D015636), HEPES (MESH:D006531), penicillin (MESH:D010406), Alexa Fluor 488 (MESH:C000711379), streptomycin (MESH:D013307), D-mannitol (MESH:D008353), polystyrene (MESH:D011137), CO2 (MESH:D002245), ATP (MESH:D000255), PBS (MESH:D007854), CaCl2 (MESH:D002122), KCl (MESH:D011189), DMSO (MESH:D004121)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Mycoplasma (genus) [taxon 2093], Cytomegalovirus (genus) [taxon 10358]
- **Mutations:** C168A
- **Cell lines:** S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232), BEAS-2B — Homo sapiens (Human), Transformed cell line (CVCL_0168)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937800/full.md

## References

78 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937800/full.md

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Source: https://tomesphere.com/paper/PMC12937800