PT - JOURNAL ARTICLE AU - Loïc Chaubet AU - Abdullah R. Chaudhary AU - Hossein K. Heris AU - Allen J. Ehrlicher AU - Adam G. Hendricks TI - Dynamic actin crosslinking governs the cytoplasm’s transition to fluid-like behavior AID - 10.1101/774935 DP - 2020 Jan 01 TA - bioRxiv PG - 774935 4099 - http://biorxiv.org/content/early/2020/03/18/774935.short 4100 - http://biorxiv.org/content/early/2020/03/18/774935.full AB - Cells precisely control their mechanical properties to organize and differentiate into tissues. The architecture and connectivity of cytoskeletal filaments changes in response to mechanical and biochemical cues, allowing the cell to rapidly tune its mechanics from highly-crosslinked, elastic networks to weakly-crosslinked viscous networks. While the role of actin crosslinking in controlling actin network mechanics is well-characterized in purified actin networks, its mechanical role in the cytoplasm of living cells remains unknown. Here, we probe the frequency-dependent intracellular viscoelastic properties of living cells using multifrequency excitation and in situ optical trap calibration. At long timescales in the intracellular environment, we observe that the cytoskeleton becomes fluid-like. The mechanics are well-captured by a model in which actin filaments are dynamically connected by a single dominant crosslinker. A disease-causing point mutation (K255E) of the actin crosslinker α-actinin 4 (ACTN4) causes its binding kinetics to be insensitive to tension. Under normal conditions, the viscoelastic properties of wild type (WT) and K255E+/- cells are similar. However, when tension is reduced through myosin II inhibition, WT cells relax 3x faster to the fluid-like regime while K255E+/- cells are not affected. These results indicate that dynamic actin crosslinking enables the cytoplasm to flow at long timescales.