Posey Ammon E, Bremer Anne, Erkamp Nadia A, Pant Avnika, Knowles Tuomas P J, Dai Yifan, Mittag Tanja, Pappu Rohit V
Department of Biomedical Engineering, Center for Biomolecular Condensates, James McKelvey School of Engineering, Washington University in St. Louis, St. Louis, Missouri 63130-4899, United States.
Department of Structural Biology, St. Jude Children's Research Hospital, Memphis, Tennessee 38103, United States.
J Am Chem Soc. 2024 Oct 16;146(41):28268-28281. doi: 10.1021/jacs.4c08946. Epub 2024 Oct 2.
Biomolecular condensates form via processes that combine phase separation and reversible associations of multivalent macromolecules. Condensates can be two- or multiphase systems defined by coexisting dense and dilute phases. Here, we show that solution ions partition asymmetrically across coexisting phases defined by condensates formed by intrinsically disordered proteins or homopolymeric RNA molecules. Our findings were enabled by direct measurements of the activities of cations and anions within coexisting phases of protein and RNA condensates. Asymmetries in ion partitioning between coexisting phases vary with protein sequence, macromolecular composition, salt concentration, and ion type. The Donnan equilibrium set up by the asymmetrical partitioning of solution ions generates interphase electric potentials known as Donnan and Nernst potentials. Our measurements show that the interphase potentials of condensates are of the same order of magnitude as membrane potentials of membrane-bound organelles. Interphase potentials quantify the degree to which microenvironments of coexisting phases are different from one another. Importantly, and based on condensate-specific interphase electric potentials, we reason that condensates are akin to capacitors that store charge. Interphase potentials should lead to electric double layers at condensate interfaces, thereby explaining recent observations of condensate interfaces being electrochemically active.
生物分子凝聚物通过多价大分子的相分离和可逆缔合相结合的过程形成。凝聚物可以是由共存的浓相和稀相定义的两相或多相系统。在这里,我们表明溶液离子在由内在无序蛋白质或同聚RNA分子形成的凝聚物所定义的共存相之间不对称分配。我们的发现得益于对蛋白质和RNA凝聚物共存相内阳离子和阴离子活性的直接测量。共存相之间离子分配的不对称性随蛋白质序列、大分子组成、盐浓度和离子类型而变化。溶液离子的不对称分配建立的唐南平衡产生了称为唐南电位和能斯特电位的相间电势。我们的测量表明,凝聚物的相间电势与膜结合细胞器的膜电位处于同一数量级。相间电势量化了共存相微环境彼此不同的程度。重要的是,基于特定凝聚物的相间电势,我们推断凝聚物类似于储存电荷的电容器。相间电势应导致凝聚物界面处形成双电层,从而解释了最近关于凝聚物界面具有电化学活性的观察结果。