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由内源性酶催化实现的相分离凝聚微滴的液-凝胶转变。

Liquid-to-gel transitions of phase-separated coacervate microdroplets enabled by endogenous enzymatic catalysis.

作者信息

Liu Jian, Li Junbo, Huang Yan, Li Tong, Xu Cheng, Tao Zhengyu, Ji Wei, Huang Xin

机构信息

Center for Innovative Research in Synthetic Chemistry and Resource Utilization, College of Chemistry, Chemical Engineering and Resource Utilization, Northeast Forestry University, Harbin 150040, PR China.

Center for Innovative Research in Synthetic Chemistry and Resource Utilization, College of Chemistry, Chemical Engineering and Resource Utilization, Northeast Forestry University, Harbin 150040, PR China.

出版信息

J Colloid Interface Sci. 2025 Aug 15;692:137486. doi: 10.1016/j.jcis.2025.137486. Epub 2025 Mar 31.

Abstract

Biomolecular condensates formed by liquid-liquid phase separation (LLPS) play a crucial role in organizing biochemical processes within living cells. The phase transition of these condensates from a functional liquid-like state to a pathological gel-like or solid-like state is believed to be linked to cellular dysfunction and various diseases. Here, we present a biomimetic model to demonstrate that endogenous enzyme-catalyzed crosslinking within condensate-mimicked coacervate microdroplets can promote a liquid-to-gel phase transition. We identify the transformation in physical characteristics of the densely packed microdroplets including reduced internal mobility, increased storage modulus, selective blocking of large nanoparticles, and enhanced salt resistance. The reversible dynamics of gel-like microdroplets mediated by ionic strength exhibited a limited release and recapture of sequestered positively charged guest molecules. Furthermore, we validate that the phase transition contributes to a restricted biochemical process through an enzymatic cascade. Overall, this work represents an adaptive in vitro platform for exploring the phase transitions associated with the physiological functions of biomolecular condensates and offers chemical insights and perspectives for investigating potential mechanisms involved in phase transitions.

摘要

由液-液相分离(LLPS)形成的生物分子凝聚物在组织活细胞内的生化过程中起着至关重要的作用。这些凝聚物从功能性的液态转变为病理性的凝胶状或固态被认为与细胞功能障碍和各种疾病有关。在此,我们提出了一个仿生模型,以证明在模拟凝聚物的凝聚微滴内的内源性酶催化交联可以促进液-凝胶相转变。我们确定了紧密堆积的微滴在物理特性上的转变,包括内部流动性降低、储能模量增加、对大纳米颗粒的选择性阻断以及耐盐性增强。由离子强度介导的凝胶状微滴的可逆动力学表现出对隔离的带正电客体分子的有限释放和重新捕获。此外,我们验证了相转变通过酶级联反应导致生化过程受限。总体而言,这项工作代表了一个用于探索与生物分子凝聚物生理功能相关的相转变的适应性体外平台,并为研究相转变所涉及的潜在机制提供了化学见解和观点。

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