Fluorescent protein lifetimes report densities and phases of nuclear condensates during embryonic stem-cell differentiation.
Ontology highlight
ABSTRACT: Fluorescent proteins (FP) are frequently used for studying proteins inside cells. In advanced fluorescence microscopy, FPs can report on additional intracellular variables. One variable is the local density near FPs, which can be useful in studying densities within cellular bio-condensates. Here, we show that a reduction in fluorescence lifetimes of common monomeric FPs reports increased levels of local densities. We demonstrate the use of this fluorescence-based variable to report the distribution of local densities within heterochromatin protein 1α (HP1α) in mouse embryonic stem cells (ESCs), before and after early differentiation. We find that local densities within HP1α condensates in pluripotent ESCs are heterogeneous and cannot be explained by a single liquid phase. Early differentia
SUBMITTER: Joron K
PROVIDER: S-EPMC10423231 | biostudies-literature | 2023 Aug
REPOSITORIES: biostudies-literature
ACCESS DATA