Single fluorogen imaging reveals distinct environmental and structural features of biomolecular condensates.

Tingting Wu, Matthew R King, Yuanxin Qiu, Mina Farag, Rohit V Pappu, Matthew D Lew
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Abstract

Biomolecular condensates are viscoelastic materials. Simulations predict that fluid-like condensations are defined by spatially inhomogeneous organization of the underlying molecules. Here, we test these predictions using single-fluorogen tracking and super-resolution imaging. Specifically, we leverage the localization and orientational preferences of freely diffusing fluorogens and the solvatochromic effect whereby specific fluorogens are turned on in response to condensate microenvironments. We deployed three different fluorogens to probe the microenvironments and molecular organization of different protein-based condensates. The spatiotemporal resolution and environmental sensitivity afforded by single-fluorogen imaging shows that the internal environments of condensates are more hydrophobic than coexisting dilute phases. Molecules within condensates are organized in a spatially inhomogeneous manner, and this gives rise to slow-moving nanoscale molecular clusters that coexist with fast-moving molecules. Fluorogens that localize preferentially to the interface help us map their distinct features. Our findings provide a structural and dynamical basis for the viscoelasticity of condensates.

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单荧光原成像揭示了生物分子凝聚物的独特环境和结构特征。
最近的计算表明,通过大分子相分离形成的生物分子凝聚物是一种网络流体,其特点是底层分子的空间组织不均匀。计算还表明,分子在凝聚态界面上具有独特的构象。在这里,我们使用高分辨率结构表征了由本质无序的朊病毒样低复杂性结构域(PLD)形成的凝聚态,从而验证了这些预测。我们利用自由扩散荧光素的定位和定向偏好以及溶解变色效应(即特定荧光素随凝聚微环境的物理化学特性而开启)来促进单分子追踪和超分辨率成像。我们使用了三种不同的荧光剂来探测 PLCD 凝聚物的内部微环境和分子组织。单荧光剂成像所提供的时空分辨率和环境灵敏度表明,凝聚体的内部环境比共存的稀释相更疏水。凝结物内部的分子以空间不均匀的方式组织起来,具有与快速移动分子共存的慢速移动纳米级分子簇或枢纽。最后,与内部相比,凝结物界面上的分子具有不同的取向偏好。我们的发现证实了计算预测,有助于为凝聚态粘弹性提供结构基础,并消除了蛋白质凝聚态是由均匀内部密度定义的各向同性液体的观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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