Biology subjects

Sommer, J.-U.

Publications and source records attributed to Sommer, J.-U..

5 recordsLinked to original sources

bioRxiv2025

Born to Condense: Polysomes Drive Co-Translational Condensation of Biomolecular Condensate Proteins

Biomolecular condensates formed by protein liquid-liquid phase separation (LLPS) are ubiquitous in cells and play crucial roles in cellular regulation. While the physics and functions of LLPS are well studied, its interplay with protein synthesis - translation - remains largely unexplored. Here we introduce a theoretical framework for Co-Translational Condensation (CTC), in which nascent protein chains of polysomes - multiple ribosomes on one mRNA - interact with condensates, localizing translation to condensate surfaces. Using coarse-grained simulations, we show that protein domain architecture dictates the thermodynamics of CTC, consistent with a Langmuir adsorption model. Bioinformatic analysis of more than 7,500 proteins reveals that most condensate-associated proteins have architectures favoring CTC, with strong interaction regions of nascent chains exposed on polysomes. At the dynamical level, simulation and reaction-diffusion modeling reveal that CTC is kinetically feasible within typical polysome lifetimes, either through large polysomes nucleating new condensates or via diffusion to pre-existing condensates. As a case study, we demonstrate that CTC enhances post-translational modifications by minimizing unmodified intermediates. More broadly, we anticipate CTC may also influence protein folding, misfolding, and signal-integration latency. Together, our results establish CTC as a general mechanism coupling translation with phase separation, with broad implications for protein evolution, cellular organization, and synthetic biology.

biophysics↗

bioRxiv2025

Polymer-assisted condensation as key to chromatin localization

We put forward a novel mechanism to account for the experimentally observed positional shifts of chromosomes within the cell nucleus, which appear to be driven by compositional alterations in the nuclear lamina [Science 7, eabf6251 (2021)]. By considering chromatin as a biomolecular condensate we demonstrate that the adsorption of the chromatin-binding proteins at the lamina leads to a wetting of the condensate while spreading of the chromatin on the lamina is avoided. This leads to the non-monotonous density profile of the polymer with respect to the surface which can be explained by the competition between the tendency of the protein component to wet the surface and the conformational restrictions of the polymer near the impenetrable surface. A change in the composition of the lamina can lead to repositioning of chromatin towards the center of the nucleus. We explore various mechanisms by which lamina compositional shifts could lead to the dewetting of the condensate. Our theory not only offers an explanation for specific chromatin conformation experiments, but also contributes to the broader understanding of wetting onto responsive surfaces in multi-component systems.

biophysics↗

bioRxiv2024

The Impact of Coiled-Coil Domains on the Phase Behavior of Biomolecular Condensates

Spatial organization is fundamental to biological systems, with biomolecular condensates as a key subset. Many studies show that folded domains play important roles in condensate formation by facilitating interactions. However, little is known about how the presence of large structured elements impacts condensate formation. Using coarse-grained simulations, we investigated a model system of two multivalent proteins, one containing a coiled-coil domain (CCD), which undergoes liquid-liquid phase separation (LLPS). We found that CCDs promote LLPS by preventing loop-closure defects, enabling protein networking. Replacing the CCD with a flexible linker abolishes LLPS due to formation of oligomeric clusters. There is a critical length of the CCD where the system rapidly changes from no LLPS to LLPS at low concentrations. This highlights their potential in regulating condensate formation and properties. This study provides insights into the phase behavior of biomolecular condensates and offers a framework for designing synthetic condensates with tunable phase behaviors.

biophysics↗

bioRxiv2024

Assembling a true "Olympic Gel" from >16,000 combinatorial DNA rings

Olympic gels are an elusive form of soft matter, comprising a three-dimensional network of mechanically interlocked cyclic molecules. In the absence of defined network junctions, the high conformational freedom of the molecules was previously theorized to confer unique mechanical properties to Olympic gels, such as non-linear elasticity and unconventional swelling characteristics. However, the synthesis of an Olympic gel exhibiting these intriguing features is challenging, since unintended crosslinking and polymerization processes are often favored over cyclization. Here, we report the successful assembly of a true Olympic gel from a library of DNA rings comprising more than 16,000 distinct molecules. Each of these rings contains a unique sequence domain that can be enzymatically activated to produce reactive termini that favor intramolecular cyclization. We characterized the genetic, mechanical, and structural characteristics of the material by next-generation sequencing, oscillatory rheology, large-scale computational simulations, atomic force microscopy, and cryogenic electron microscopy. Our results confirm the formation of a stable Olympic gel, which exhibits unique swelling behavior and an elastic response that is exclusively determined by entanglements, yet persists on long time scales. By combining concepts from polymer physics, synthetic biology, and DNA nanotechnology, this new material class provides a flexible experimental platform for future studies into the effects of network topology on macroscopic material properties and its function as a carrier of genetic information in biological and biomimetic systems. This work moreover demonstrates that exotic material properties can emerge in systems with a high compositional complexity that is more reminiscent of biological than synthetic matter.

bioengineering↗

bioRxiv2021

Polymer-Assisted Condensation: A Mechanism for Hetero-Chromatin Formation and Epigenetic Memory

We consider the formation of droplets from a 2-component liquid mixture induced by a large polymer chain that has preferential solubility with one of the components. We assume that the liquid mixture is in a fully miscible state, but far above the critical interaction limit of the two species. We show that the polymer coil acts as a chemical potential trap, which can shift the mixture inside the polymer volume into the partially miscible state and thus triggers the formation of a polymer-bound droplet of the preferred solvent phase which we denote as polymer-assisted condensation (PAC). We propose a simple mean-field model which can predict the essential feature of PAC and perform molecular-dynamics simulations to show that the predicted phase behavior is robust against fluctuation effects. Our model aims to understand the formation of macromolecular condensates inside the cell nucleus, such as those formed by heterochromatin 1 (HP1). We propose that such droplets organize the spatial structure of chromatin into hetero- and euchromatin and ensure the propagation of epigenetic information through the cell generations.

biophysics↗