Controlled and orthogonal partitioning of large particles into biomolecular condensates.
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ABSTRACT: Biomolecular condensates arising from liquid-liquid phase separation contribute to diverse cellular processes, such as gene expression. Partitioning of client molecules into condensates is critical to regulating the composition and function of condensates. Previous studies suggest that client size limits partitioning, with dextrans >5 nm excluded from condensates. Here, we asked whether larger particles, such as macromolecular complexes, can partition into condensates based on particle-condensate interactions. We sought to discover the biophysical principles that govern particle inclusion in or exclusion from condensates using polymer nanoparticles with tailored surface chemistries as models of macromolecular complexes. Particles coated with polyethylene glycol (PEG) did not partition into
SUBMITTER: Kelley FM
PROVIDER: S-EPMC11275771 | biostudies-literature | 2024 Jul
REPOSITORIES: biostudies-literature
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