Shapes of condensate droplets containing filaments

preprint OA: closed
Full text JSON View at publisher

Abstract

The interactions of droplets and filaments can lead to mutual deformations and complex combined behavior. Such interactions also occur within the cell, where biomolecular condensates, distinct liquid phases often composed of proteins, have been observed to structure and affect the organization of the cytoskeleton. In particular, biomolecular condensates have been shown to undergo characteristic deformations when cytoskeletal filaments are fully embedded within them. However, a full understanding of the underlying physical mechanisms is still missing. Here, we combine experiments with coarse-grained molecular dynamics simulations and analytical models to uncover the physical mechanisms that define emerging shapes of droplets containing filaments. We find that the surface tension of the liquid phase and the bending energy of the filament(s) suffice to accurately capture emerging shapes if the length of the filament is small compared to the liquid volume. As the volume fraction of filament(s) increases, wetting effects become increasingly important, setting physical constraints within which surface and bending energies compete to define the droplet shapes. We find that mutual deformations of condensate and filament extend accessible shapes beyond classical stability considerations, leading to structuring and entrapment of contained filaments. Shape deformations may further affect ripening dynamics that favor certain geometries. Our findings provide a physical framework for a better understanding of the possible roles of biomolecular condensates in cytoskeletal organization.
Full text 1,684 characters · extracted from oa-doi-fallback · click to expand
Abstract The interactions of droplets and filaments can lead to mutual deformations and complex combined behavior. Such interactions also occur within the cell, where biomolecular condensates, distinct liquid phases often composed of proteins, have been observed to structure and affect the organization of the cytoskeleton. In particular, biomolecular condensates have been shown to undergo characteristic deformations when cytoskeletal filaments are fully embedded within them. However, a full understanding of the underlying physical mechanisms is still missing. Here, we combine experiments with coarse-grained molecular dynamics simulations and analytical models to uncover the physical mechanisms that define emerging shapes of droplets containing filaments. We find that the surface tension of the liquid phase and the bending energy of the filament(s) suffice to accurately capture emerging shapes if the length of the filament is small compared to the liquid volume. As the volume fraction of filament(s) increases, wetting effects become increasingly important, setting physical constraints within which surface and bending energies compete to define the droplet shapes. We find that mutual deformations of condensate and filament extend accessible shapes beyond classical stability considerations, leading to structuring and entrapment of contained filaments. Shape deformations may further affect ripening dynamics that favor certain geometries. Our findings provide a physical framework for a better understanding of the possible roles of biomolecular condensates in cytoskeletal organization. Competing Interest Statement The authors have declared no competing interest.

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2026) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

Source provenance

europepmc
last seen: 2026-05-20T01:45:00.602351+00:00