How Spatially Modulated Activity Reshapes Active Polymer Conformations

Fuente: arXiv
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Autores principales: Malgaretti, Paolo, Locatelli, Emanuele
Formato: Preprint
Publicado: 2025
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author Malgaretti, Paolo
Locatelli, Emanuele
author_facet Malgaretti, Paolo
Locatelli, Emanuele
contents Active polymers are driven out of equilibrium by internal forces and exhibit conformational properties that differ fundamentally from those of passive chains. Here we study how spatially modulated tangential activity reshapes the conformations of semiflexible polymers. Using a continuum Rouse model with bending rigidity, we develop a systematic expansion in the limit of weak activity and derive analytical expressions for mode correlations, gyration radius, and end-to-end distance under sinusoidally varying propulsion. We show that spatially structured activity breaks self-similar scaling and induces a mode-dependent transition between polymer shrinking and swelling. Uniform or low-mode forcing produces compact, globule-like conformations, whereas higher modes generate alternating stretched and compressed segments, leading to globally swollen chains. Different polymer sizes respond differently to activity, allowing for conformations that are compact in gyration radius yet extended in end-to-end distance. Langevin dynamics simulations quantitatively confirm the theoretical predictions. Our results demonstrate that even weak, patterned activity provides a powerful mechanism to control polymer conformations far from equilibrium.
format Preprint
id arxiv_https___arxiv_org_abs_2512_14478
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle How Spatially Modulated Activity Reshapes Active Polymer Conformations
Malgaretti, Paolo
Locatelli, Emanuele
Soft Condensed Matter
Active polymers are driven out of equilibrium by internal forces and exhibit conformational properties that differ fundamentally from those of passive chains. Here we study how spatially modulated tangential activity reshapes the conformations of semiflexible polymers. Using a continuum Rouse model with bending rigidity, we develop a systematic expansion in the limit of weak activity and derive analytical expressions for mode correlations, gyration radius, and end-to-end distance under sinusoidally varying propulsion. We show that spatially structured activity breaks self-similar scaling and induces a mode-dependent transition between polymer shrinking and swelling. Uniform or low-mode forcing produces compact, globule-like conformations, whereas higher modes generate alternating stretched and compressed segments, leading to globally swollen chains. Different polymer sizes respond differently to activity, allowing for conformations that are compact in gyration radius yet extended in end-to-end distance. Langevin dynamics simulations quantitatively confirm the theoretical predictions. Our results demonstrate that even weak, patterned activity provides a powerful mechanism to control polymer conformations far from equilibrium.
title How Spatially Modulated Activity Reshapes Active Polymer Conformations
topic Soft Condensed Matter
url https://arxiv.org/abs/2512.14478