Unlocking the Secrets of Neuronal Biomolecular Condensates!

Published on March 24, 2023

Imagine a bustling marketplace where groups of people gather and interact, forming distinct and functional communities. In a similar way, biomolecular condensates are dynamic gatherings of proteins and nucleic acids inside cells, allowing them to carry out specific functions without the need for membranes. However, these condensates are fragile and can be disrupted by genetic risks and other factors, leading to the development of neurodegenerative diseases. It’s like a peaceful village suddenly falling into chaos! Recent research has revealed that the abnormal transition of biomolecular condensates can trigger the buildup of disease-associated proteins, contributing to the progression of neurodegeneration. Moreover, specific condensates located in synapses and along neuronal processes act like specialized communities with liquid-like properties. These neuronal biomolecular condensates undergo changes in composition and function as part of the neurodegenerative process. To fully comprehend their role, further investigation is necessary. So, put on your scientist hats and dive into the fascinating world of neuronal biomolecular condensates! Discover groundbreaking studies that shed light on their pivotal involvement in neurological disorders and unravel the mysteries within.

Biomolecular condensates are subcellular organizations where functionally related proteins and nucleic acids are assembled through liquid-liquid phase separation, allowing them to develop on a larger scale without a membrane. However, biomolecular condensates are highly vulnerable to disruptions from genetic risks and various factors inside and outside the cell and are strongly implicated in the pathogenesis of many neurodegenerative diseases. In addition to the classical view of the nucleation-polymerization process that triggers the protein aggregation from the misfolded seed, the pathologic transition of biomolecular condensates can also promote the aggregation of proteins found in the deposits of neurodegenerative diseases. Furthermore, it has been suggested that several protein or protein-RNA complexes located in the synapse and along the neuronal process are neuron-specific condensates displaying liquid-like properties. As their compositional and functional modifications play a crucial role in the context of neurodegeneration, further research is needed to fully understand the role of neuronal biomolecular condensates. In this article, we will discuss recent findings that explore the pivotal role of biomolecular condensates in the development of neuronal defects and neurodegeneration.

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