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Single-molecule imaging of stochastic interactions that drive dynein activation and cargo movement in cells

Tirumala, NA and Redpath, GMI and Skerhut, SV and Dolai, P and Kapoor-Kaushik, N and Ariotti, N and Vijay Kumar, K and Ananthanarayanan, V (2024) Single-molecule imaging of stochastic interactions that drive dynein activation and cargo movement in cells. In: The Journal of cell biology, 223 (3).

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Official URL: https://doi.org/10.1083/jcb.202210026

Abstract

Cytoplasmic dynein 1 (dynein) is the primary minus end-directed motor protein in most eukaryotic cells. Dynein remains in an inactive conformation until the formation of a tripartite complex comprising dynein, its regulator dynactin, and a cargo adaptor. How this process of dynein activation occurs is unclear since it entails the formation of a three-protein complex inside the crowded environs of a cell. Here, we employed live-cell, single-molecule imaging to visualize and track fluorescently tagged dynein. First, we observed that only �30 of dynein molecules that bound to the microtubule (MT) engaged in minus end-directed movement, and that too for a short duration of �0.6 s. Next, using high-resolution imaging in live and fixed cells and using correlative light and electron microscopy, we discovered that dynactin and endosomal cargo remained in proximity to each other and to MTs. We then employed two-color imaging to visualize cargo movement effected by single motor binding. Finally, we performed long-term imaging to show that short movements are sufficient to drive cargo to the perinuclear region of the cell. Taken together, we discovered a search mechanism that is facilitated by dynein's frequent MT binding-unbinding kinetics: (i) in a futile event when dynein does not encounter cargo anchored in proximity to the MT, dynein dissociates and diffuses into the cytoplasm, (ii) when dynein encounters cargo and dynactin upon MT binding, it moves cargo in a short run. Several of these short runs are undertaken in succession for long-range directed movement. In conclusion, we demonstrate that dynein activation and cargo capture are coupled in a step that relies on the reduction of dimensionality to enable minus end-directed transport in cellulo and that complex cargo behavior emerges from stochastic motor-cargo interactions. © 2024 Tirumala et al.

Item Type: Journal Article
Publication: The Journal of cell biology
Additional Information: The copyright for this article belongs to author.
Keywords: cytoplasmic dynein; dynactin; dynein adenosine triphosphatase; microtubule associated protein, endosome; genetics; metabolism; microtubule; single molecule imaging, Cytoplasmic Dyneins; Dynactin Complex; Dyneins; Endosomes; Microtubule-Associated Proteins; Microtubules; Single Molecule Imaging
Department/Centre: Division of Interdisciplinary Sciences > Centre for Biosystems Science and Engineering
Date Deposited: 01 Mar 2024 06:23
Last Modified: 01 Mar 2024 06:23
URI: https://eprints.iisc.ac.in/id/eprint/83886

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