Ceballos Alfredo Vidal, McDonald Charles J, Elbaum-Garfinkle Shana
Structural Biology Initiative, CUNY Advanced Science Research Center, New York, NY, United States; Ph.D Program in Biochemistry, The Graduate Center, CUNY, New York, NY, United States.
Structural Biology Initiative, CUNY Advanced Science Research Center, New York, NY, United States; Ph.D Program in Biochemistry, The Graduate Center, CUNY, New York, NY, United States; Ph.D Program in Biology, The Graduate Center, CUNY, New York, NY, United States.
Methods Enzymol. 2018;611:31-50. doi: 10.1016/bs.mie.2018.09.037. Epub 2018 Nov 3.
Phase separation has emerged as a new paradigm currently revolutionizing our understanding of cell biology and intracellular organization. Disordered protein domains have recently been demonstrated as integral drivers of phase separation into condensed liquids with emergent material properties. Using in vitro model systems employing purified protein components is necessary to interrogate the molecular mechanisms underlying phase separation; however, these systems pose many experimental challenges. In this chapter we describe general strategies for purifying, handling, imaging, and characterizing the phase behavior of disordered proteins. We further outline methods for the purification of the model P granule protein LAF-1, the construction of phase diagrams, and the quantification of liquid droplet fusion or coalescence.
相分离已成为一种新的范式,正在彻底改变我们对细胞生物学和细胞内组织的理解。最近已证明,无序蛋白质结构域是相分离成具有新兴物质特性的凝聚液体的重要驱动因素。使用含有纯化蛋白质成分的体外模型系统来探究相分离背后的分子机制是必要的;然而,这些系统带来了许多实验挑战。在本章中,我们描述了纯化、处理、成像和表征无序蛋白质相行为的一般策略。我们还概述了模型P颗粒蛋白LAF-1的纯化方法、相图的构建以及液滴融合或合并的定量方法。