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量化无序蛋白质相分离的方法和策略

Methods and Strategies to Quantify Phase Separation of Disordered Proteins.

作者信息

Ceballos Alfredo Vidal, McDonald Charles J, Elbaum-Garfinkle Shana

机构信息

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.

出版信息

Methods Enzymol. 2018;611:31-50. doi: 10.1016/bs.mie.2018.09.037. Epub 2018 Nov 3.

DOI:10.1016/bs.mie.2018.09.037
PMID:30471691
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6688841/
Abstract

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.

摘要

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。

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Methods and Strategies to Quantify Phase Separation of Disordered Proteins.量化无序蛋白质相分离的方法和策略
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2
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本文引用的文献

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Protein Phase Separation: A New Phase in Cell Biology.蛋白质液-液相分离:细胞生物学的一个新领域。
Trends Cell Biol. 2018 Jun;28(6):420-435. doi: 10.1016/j.tcb.2018.02.004. Epub 2018 Mar 27.
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What lava lamps and vinaigrette can teach us about cell biology.熔岩灯和油醋汁能教给我们的细胞生物学知识。
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Phase behaviour of disordered proteins underlying low density and high permeability of liquid organelles.无序蛋白质的相行为是液体细胞器低密度和高通透性的基础。
Mol Biol Cell. 2024 Dec 1;35(12):ar154. doi: 10.1091/mbc.E24-03-0128. Epub 2024 Nov 13.
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Optical characterization of molecular interaction strength in protein condensates.蛋白质凝聚物中分子相互作用强度的光学表征
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Quantifying surface tension and viscosity in biomolecular condensates by FRAP-ID.通过 FRAP-ID 定量生物分子凝聚物中的表面张力和粘度。
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Fluorescent protein tags affect the condensation properties of a phase-separating viral protein.荧光蛋白标签会影响一种发生相分离的病毒蛋白的凝聚特性。
Mol Biol Cell. 2024 Jul 1;35(7):ar100. doi: 10.1091/mbc.E24-01-0013. Epub 2024 May 29.
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Targeting nucleic acid phase transitions as a mechanism of action for antimicrobial peptides.靶向核酸相转变作为抗菌肽作用机制。
Nat Commun. 2023 Nov 7;14(1):7170. doi: 10.1038/s41467-023-42374-4.
8
Intermolecular interactions underlie protein/peptide phase separation irrespective of sequence and structure at crowded milieu.分子间相互作用是蛋白质/肽相分离的基础,而与拥挤环境中的序列和结构无关。
Nat Commun. 2023 Oct 4;14(1):6199. doi: 10.1038/s41467-023-41864-9.
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Biomolecular condensates - extant relics or evolving microcompartments?生物分子凝聚物——现存的遗迹还是进化中的微型隔室?
Commun Biol. 2023 Jun 21;6(1):656. doi: 10.1038/s42003-023-04963-3.
10
Peroxisome biogenesis initiated by protein phase separation.蛋白液-液相分离起始的过氧化物酶体生物发生。
Nature. 2023 May;617(7961):608-615. doi: 10.1038/s41586-023-06044-1. Epub 2023 May 10.
Nat Chem. 2017 Nov;9(11):1118-1125. doi: 10.1038/nchem.2803. Epub 2017 Jun 26.
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Liquid phase condensation in cell physiology and disease.细胞生理学和疾病中的液相凝聚。
Science. 2017 Sep 22;357(6357). doi: 10.1126/science.aaf4382.
5
Structural and hydrodynamic properties of an intrinsically disordered region of a germ cell-specific protein on phase separation.生殖细胞特异性蛋白无规卷曲结构域的相分离的结构和流体力学性质
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6
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Biomolecular condensates: organizers of cellular biochemistry.生物分子凝聚物:细胞生物化学的组织者
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