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一种用于测量多组分生物分子凝聚物组成的无标记方法。

A label-free method for measuring the composition of multicomponent biomolecular condensates.

作者信息

McCall Patrick M, Kim Kyoohyun, Shevchenko Anna, Ruer-Gruß Martine, Peychl Jan, Guck Jochen, Shevchenko Andrej, Hyman Anthony A, Brugués Jan

机构信息

Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.

Max Planck Institute for the Physics of Complex Systems, Dresden, Germany.

出版信息

Nat Chem. 2025 Sep 3. doi: 10.1038/s41557-025-01928-3.

Abstract

Many subcellular compartments are biomolecular condensates made of multiple components, often including several distinct proteins and nucleic acids. However, current tools to measure condensate composition are limited and cannot capture this complexity quantitatively because they either require fluorescent labels, which can perturb composition, or can distinguish only one or two components. Here we describe a label-free method based on quantitative phase imaging and analysis of tie-lines and refractive index to measure the composition of reconstituted condensates with multiple components. We first validate the method empirically in binary mixtures, revealing sequence-encoded density variation and complex ageing dynamics for condensates composed of full-length proteins. We then use analysis of tie-lines and refractive index to simultaneously resolve the concentrations of five macromolecular solutes in multicomponent condensates containing RNA and constructs of multiple RNA-binding proteins. Our measurements reveal an unexpected decoupling of density and composition, highlighting the need to determine molecular stoichiometry in multicomponent condensates. We foresee this approach enabling the study of compositional regulation of condensate properties and function.

摘要

许多亚细胞区室是由多种成分构成的生物分子凝聚物,通常包括几种不同的蛋白质和核酸。然而,目前用于测量凝聚物组成的工具有限,无法定量捕捉这种复杂性,因为它们要么需要荧光标记(这可能会干扰组成),要么只能区分一两种成分。在此,我们描述了一种基于定量相成像以及对连接线和折射率进行分析的无标记方法,用于测量含有多种成分的重组凝聚物的组成。我们首先在二元混合物中通过实验验证了该方法,揭示了由全长蛋白质组成的凝聚物的序列编码密度变化和复杂的老化动力学。然后,我们利用对连接线和折射率的分析,同时解析了含有RNA和多种RNA结合蛋白构建体的多组分凝聚物中五种大分子溶质的浓度。我们的测量结果揭示了密度和组成之间意想不到的解耦,突出了确定多组分凝聚物中分子化学计量比的必要性。我们预计这种方法将有助于研究凝聚物性质和功能的组成调控。

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