Department of Chemistry, Syracuse University, Syracuse, New York 13244, United States.
Department of Chemistry, Pennsylvania State University, University Park, Pennsylvania 16802, United States.
J Am Chem Soc. 2024 Feb 28;146(8):5383-5392. doi: 10.1021/jacs.3c12791. Epub 2024 Feb 14.
Although post-translational lipidation is prevalent in eukaryotes, its impact on the liquid-liquid phase separation of disordered proteins is still poorly understood. Here, we examined the thermodynamic phase boundaries and kinetics of aqueous two-phase system (ATPS) formation for a library of elastin-like polypeptides modified with saturated fatty acids of different chain lengths. By systematically altering the physicochemical properties of the attached lipids, we were able to correlate the molecular properties of lipids to changes in the thermodynamic phase boundaries and the kinetic stability of droplets formed by these proteins. We discovered that increasing the chain length lowers the phase separation temperature in a sigmoidal manner due to alterations in the unfavorable interactions between protein and water and changes in the entropy of phase separation. Our kinetic studies unveiled remarkable sensitivity to lipid length, which we propose is due to the temperature-dependent interactions between lipids and the protein. Strikingly, we found that the addition of just a single methylene group is sufficient to allow tuning of these interactions as a function of temperature, with proteins modified with C7-C9 lipids exhibiting non-Arrhenius dependence in their phase separation, a behavior that is absent for both shorter and longer fatty acids. This work advances our theoretical understanding of protein-lipid interactions and opens avenues for the rational design of lipidated proteins in biomedical paradigms, where precise control over the phase separation is pivotal.
尽管翻译后脂质化在真核生物中很普遍,但它对无序蛋白质的液-液相分离的影响仍知之甚少。在这里,我们研究了一系列带有不同链长饱和脂肪酸的弹性蛋白样多肽的水相两相间系统 (ATPS) 形成的热力学相界和动力学。通过系统改变附着脂质的物理化学性质,我们能够将脂质的分子性质与这些蛋白质形成的液滴的热力学相界和动力学稳定性的变化相关联。我们发现,由于蛋白质与水之间的不利相互作用的改变以及相分离熵的变化,链长的增加以类正弦方式降低相分离温度。我们的动力学研究对脂质长度表现出显著的敏感性,我们提出这是由于脂质与蛋白质之间的温度依赖性相互作用。引人注目的是,我们发现只需添加一个亚甲基即可根据温度调节这些相互作用,带有 C7-C9 脂质修饰的蛋白质在相分离中表现出非 Arrhenius 依赖性,而对于较短和较长的脂肪酸则不存在这种行为。这项工作推进了我们对蛋白质-脂质相互作用的理论理解,并为生物医学范例中脂质化蛋白质的合理设计开辟了途径,在这些范例中,相分离的精确控制至关重要。