Comparing homogeneous and heterogeneous sticker-spacer condensates with matched scaffold density, sticker fraction, and sticker-sticker interaction strength identifies mesoscale organization as an important physical factor controlling both molecular selectivity and transport in biomolecular condensates, with implications for the biochemical functions of both natural and engineered systems.
Abstract
Growing experimental and computational evidence suggests that many condensates exhibit heterogeneous internal organization at mesoscopic length scales. How such mesoscale organization influences client selectivity and transport, however, remains poorly understood. Here, we use coarsegrained molecular dynamics simulations to compare homogeneous and heterogeneous sticker-spacer condensates with matched scaffold density, sticker fraction, and sticker-sticker interaction strength. We find that the two condensates exhibit markedly different client partitioning profiles and transport dynamics. In the heterogeneous condensate, clients sample distinct local microenvironments in a size-dependent manner, leading to pronounced differences in their transfer free energy compared with the homogeneous condensate. The heterogeneous internal organization also generates local environments with different mobilities and constraints, giving rise to transient subdiffusion and non-Gaussian displacement distributions in client motion. Our results identify mesoscale organization as an important physical factor controlling both molecular selectivity and transport in biomolecular condensates, with implications for the biochemical functions of both natural and engineered systems.
The Condensate Code is refined as a testable thermodynamic state map that integrates continuous cellular inputs, intrinsic molecular grammar and boundary conditions to govern measurable material states and a continuum from electrostatic coacervates to viscoelastic networks is highlighted.
Yao-Yao Hou, Ling-Yun Jing, Kan Sun et al.· Communications Biology· 0 citations
Biomolecular condensates formed by intrinsically disordered proteins require molecular models that accurately describe proteins in both dilute solution and condensed phases. Explicit-solvent coarse-grained models offer an attractive balance between chemical resolution and computational efficiency. Yet, it remains uncle...
Fran Bačić Toplek, L. Borges-Araújo, Kresten Lindorff-Larsen et al.· bioRxiv· 0 citations
The interactions among condensate-forming biomolecules dictate both the specificity and properties of these condensates, including their fluid-like nature and material exchange dynamics among condensate droplets. While interaction specificity is typically associated with mean interaction lifetimes, the role of interact...
B. Debnath, P. Katira· Biophysical Journal· 1 citation
It is found that affinity governs the phase boundary, resistance to chemical perturbation, and molecular mobility of condensates in vitro and in human cells and is shown to be a quantitative determinant of condensate phase behavior, internal dynamics and biochemical output.
Andres Reyna, Madyson O. Briggs, Alexander F. Russell et al.· bioRxiv· 0 citations
Focusing on interfacial rheology, with particular attention to mechanical hysteresis, it is discussed how dynamic interfacial observables may provide experimentally accessible indicators of how lipid assemblies accumulate, dissipate, and reorganize lateral stresses, and how such responses may become linked to membrane...
M. E. Villanueva· The European Physical Journa...· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.