2025
2.
David Goh; Deepti Kannan; Pradeep Natarajan; Andriy Goychuk; Arup K. Chakraborty
RNA gradients can guide condensates toward promoters: Implications for enhancer–promoter contacts and condensate-promoter kissing Journal Article
In: The Journal of Chemical Physics, vol. 163, no. 10, pp. 104905, 2025, ISSN: 0021-9606, 1089-7690.
Abstract | Links | BibTeX | Tags: Biological Physics, Biomolecular Interactions, Chromatin, Gene transcription, Phase transitions, Polymers, Protein-Protein-Interactions, Reentrant, Ribonucleic Acid, Simulation
@article{goh_rna_2025,
title = {RNA gradients can guide condensates toward promoters: Implications for enhancer–promoter contacts and condensate-promoter kissing},
author = {David Goh and Deepti Kannan and Pradeep Natarajan and Andriy Goychuk and Arup K. Chakraborty},
url = {https://pubs.aip.org/jcp/article/163/10/104905/3362007/RNA-gradients-can-guide-condensates-toward},
doi = {10.1063/5.0277838},
issn = {0021-9606, 1089-7690},
year = {2025},
date = {2025-09-01},
urldate = {2026-05-29},
journal = {The Journal of Chemical Physics},
volume = {163},
number = {10},
pages = {104905},
abstract = {We study how protein condensates respond to a site of active RNA transcription (i.e., a gene promoter) due to electrostatic protein–RNA interactions. Our results indicate that condensates can show directed motion toward the promoter, driven by gradients in the RNA concentration. Analytical theory, consistent with simulations, predicts that the droplet velocity has a non-monotonic dependence on the distance to the promoter. We explore the consequences of this gradient-sensing mechanism for enhancer–promoter (E–P) communication using polymer simulations of the intervening chromatin chain. Directed motion of enhancer-bound condensates can, together with loop extrusion by cohesin, collaboratively increase the enhancer–promoter contact probability. Finally, we investigate under which conditions condensates can exhibit oscillations in their morphology and in the distance to the promoter. Oscillatory dynamics are caused by a delayed response of transcription to condensate-promoter contact and negative feedback from the accumulation of RNA at the promoter, which results in charge repulsion.},
keywords = {Biological Physics, Biomolecular Interactions, Chromatin, Gene transcription, Phase transitions, Polymers, Protein-Protein-Interactions, Reentrant, Ribonucleic Acid, Simulation},
pubstate = {published},
tppubtype = {article}
}
We study how protein condensates respond to a site of active RNA transcription (i.e., a gene promoter) due to electrostatic protein–RNA interactions. Our results indicate that condensates can show directed motion toward the promoter, driven by gradients in the RNA concentration. Analytical theory, consistent with simulations, predicts that the droplet velocity has a non-monotonic dependence on the distance to the promoter. We explore the consequences of this gradient-sensing mechanism for enhancer–promoter (E–P) communication using polymer simulations of the intervening chromatin chain. Directed motion of enhancer-bound condensates can, together with loop extrusion by cohesin, collaboratively increase the enhancer–promoter contact probability. Finally, we investigate under which conditions condensates can exhibit oscillations in their morphology and in the distance to the promoter. Oscillatory dynamics are caused by a delayed response of transcription to condensate-promoter contact and negative feedback from the accumulation of RNA at the promoter, which results in charge repulsion.
2018
1.
Andriy Goychuk; David B. Brückner; Andrew W. Holle; Joachim P. Spatz; Chase P. Broedersz; Erwin Frey
Morphology and Motility of Cells on Soft Substrates Miscellaneous
2018, (Version Number: 2).
Abstract | Links | BibTeX | Tags: Biological Physics, Cell Behavior, Cell Migration, Cell Polarization, Cellular Potts Model, Mechanobiology, Simulation, Traction Force
@misc{goychuk_morphology_2018,
title = {Morphology and Motility of Cells on Soft Substrates},
author = {Andriy Goychuk and David B. Brückner and Andrew W. Holle and Joachim P. Spatz and Chase P. Broedersz and Erwin Frey},
url = {https://arxiv.org/abs/1808.00314},
doi = {10.48550/ARXIV.1808.00314},
year = {2018},
date = {2018-01-01},
urldate = {2026-05-29},
publisher = {arXiv},
abstract = {Recent experiments suggest that the interplay between cells and the mechanics of their substrate gives rise to a diversity of morphological and migrational behaviors. Here, we develop a Cellular Potts Model of polarizing cells on a visco-elastic substrate. We compare our model with experiments on endothelial cells plated on polyacrylamide hydrogels to constrain model parameters and test predictions. Our analysis reveals that morphology and migratory behavior are determined by an intricate interplay between cellular polarization and substrate strain gradients generated by traction forces exerted by cells (self-haptotaxis).},
note = {Version Number: 2},
keywords = {Biological Physics, Cell Behavior, Cell Migration, Cell Polarization, Cellular Potts Model, Mechanobiology, Simulation, Traction Force},
pubstate = {published},
tppubtype = {misc}
}
Recent experiments suggest that the interplay between cells and the mechanics of their substrate gives rise to a diversity of morphological and migrational behaviors. Here, we develop a Cellular Potts Model of polarizing cells on a visco-elastic substrate. We compare our model with experiments on endothelial cells plated on polyacrylamide hydrogels to constrain model parameters and test predictions. Our analysis reveals that morphology and migratory behavior are determined by an intricate interplay between cellular polarization and substrate strain gradients generated by traction forces exerted by cells (self-haptotaxis).