聚结(物理)
融合
化学物理
表面张力
静电学
乳状液
Zeta电位
静电
化学
表面电荷
纳米技术
材料科学
热力学
物理
物理化学
哲学
纳米颗粒
天体生物学
量子力学
生物化学
语言学
作者
Timothy J. Welsh,Georg Krainer,Jorge R. Espinosa,Jerelle A. Joseph,Akshay Sridhar,Marcus Jahnel,William E. Arter,Kadi L. Saar,Simon Alberti,Rosana Collepardo‐Guevara,Tuomas P. J. Knowles
标识
DOI:10.1101/2020.04.20.047910
摘要
Abstract Liquid–liquid phase separation underlies the formation of biological condensates. Physically, such systems are microemulsions which have a general propensity to fuse and coalesce; however, many condensates persist as independent droplets inside cells. This stability is crucial for their functioning, but the physicochemical mechanisms that control the emulsion stability of condensates remain poorly understood. Here, by combining single-condensate zeta potential measurements, optical microscopy, tweezer experiments, and multiscale molecular modelling, we investigate how the forces that sustain condensates impact their stability against fusion. By comparing PR 25 :PolyU and FUS condensates, we show that a higher condensate surface charge correlates with a lower fusion propensity, and that this behavior can be inferred from their zeta potentials. We reveal that overall stabilization against fusion stems from a combination of repulsive forces between condensates and the effects that surface electrostatics have on lowering surface tension, thus shedding light on the molecular determinants of condensate coalescence.
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