PT  - JOURNAL ARTICLE
AU  - Daniel S.W. Lee
AU  - Ned S. Wingreen
AU  - Clifford P. Brangwynne
TI  - Chromatin Mechanics Dictates Subdiffusion and Coarsening Dynamics of Embedded Condensates
AID  - 10.1101/2020.06.03.128561
DP  - 2020 Jan 01
TA  - bioRxiv
PG  - 2020.06.03.128561
4099  - http://biorxiv.org/content/early/2020/06/04/2020.06.03.128561.short
4100  - http://biorxiv.org/content/early/2020/06/04/2020.06.03.128561.full
AB  - DNA is organized into chromatin, a complex polymeric material which stores information and controls gene expression. An emerging mechanism for biological organization, particularly within the crowded nucleus, is biomolecular phase separation into condensed droplets of protein and nucleic acids. However, the way in which chromatin impacts the dynamics of phase separation and condensate formation is poorly understood. Here, we utilize a powerful optogenetic strategy to examine the interplay of droplet coarsening with the surrounding viscoelastic chromatin network. We demonstrate that droplet growth dynamics are directly inhibited by the chromatin-dense environment, which gives rise to an anomalously slow coarsening exponent, β∼0.12, contrasting with the classical prediction of β∼ 1/3. Using scaling arguments and simulations, we show how this arrested growth can arise due to subdiffusion of individual condensates, predicting β∼α/3, where α is the diffusion exponent. Tracking the fluctuating motion of condensates within chromatin reveals a subdiffusive exponent, α∼0.5, which explains the anomalous coarsening behavior and is also consistent with Rouse-like dynamics arising from the entangled chromatin. Our findings have implications for the biophysical regulation of the size and shape of biomolecular condensates, and suggest that condensate emulsions can be used to probe the viscoelastic mechanical environment within living cells.Competing Interest StatementThe authors have declared no competing interest.