Visualizing liquid-liquid phase separation and protein aggregates

Liquid-liquid phase separation (LLPS) facilitates functionally-relevant proteins to gather in high concentrations at specific locations. Several interacting proteins encapsulated in the membraneless droplets tend to form abnormal protein aggregates which are linked to numerous pathological diseases. Thus direct observation of LLPS, successive protein aggregates and the potential conversion processes is significant for understanding associated cell function and pathology. In this review, we firstly introduce the techniques for imaging LLPS, including in vitro reconstitution and intracellular visualizing strategies. Then we elaborate recent advances in the development of the imaging approaches for protein aggregates, followed by highlighting the monitor of protein conformational changes during aggregation process. Furthermore, the similarities and differences are discussed along with these state-of-the-art technologies. Finally, the major challenges and potential in exploration of detection methods for visualizing LLPS and protein aggregates are also pointed out. With these advances, it is becoming possible both to 'see' independent state of LLPS or protein aggregates, and realize the real-time monitor of the whole process.

Authors

Institutions

Publication Details

Journal
Communications Chemistry
Published
2025-11-25
DOI
https://doi.org/10.1038/s42004-025-01756-z
Citations
1
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
0.81

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Visualizing liquid-liquid phase separation and protein aggregates

Da‐Chuan Yin, Xi Chen, Cao Xiaowen, Xiong Jia et al.
1 citations
Communications Chemistry
RNA Research and Splicing
0.81
article

Visualizing liquid-liquid phase separation and protein aggregates

Da‐Chuan Yin, Xi Chen, Cao Xiaowen, Xiong Jia, Jing Xue, Weihong Guo
article en
1 citations

Abstract

Liquid-liquid phase separation (LLPS) facilitates functionally-relevant proteins to gather in high concentrations at specific locations. Several interacting proteins encapsulated in the membraneless droplets tend to form abnormal protein aggregates which are linked to numerous pathological diseases. Thus direct observation of LLPS, successive protein aggregates and the potential conversion processes is significant for understanding associated cell function and pathology. In this review, we firstly introduce the techniques for imaging LLPS, including in vitro reconstitution and intracellular visualizing strategies. Then we elaborate recent advances in the development of the imaging approaches for protein aggregates, followed by highlighting the monitor of protein conformational changes during aggregation process. Furthermore, the similarities and differences are discussed along with these state-of-the-art technologies. Finally, the major challenges and potential in exploration of detection methods for visualizing LLPS and protein aggregates are also pointed out. With these advances, it is becoming possible both to 'see' independent state of LLPS or protein aggregates, and realize the real-time monitor of the whole process.

Communications ChemistryVol. 8(1)
Northwestern Polytechnical University (CN), Affiliated Hospital of Shaanxi University of Chinese Medicine (CN), Shaanxi University of Chinese Medicine (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 21%
RNA Research and Splicing
0.81
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.