Physiology and pharmacological targeting of phase separation.
Fangfang WangYouwei ZhangPublished in: Journal of biomedical science (2024)
Liquid-liquid phase separation (LLPS) in biology describes a process by which proteins form membraneless condensates within a cellular compartment when conditions are met, including the concentration and posttranslational modifications of the protein components, the condition of the aqueous solution (pH, ionic strength, pressure, and temperature), and the existence of assisting factors (such as RNAs or other proteins). In these supramolecular liquid droplet-like inclusion bodies, molecules are held together through weak intermolecular and/or intramolecular interactions. With the aid of LLPS, cells can assemble functional sub-units within a given cellular compartment by enriching or excluding specific factors, modulating cellular function, and rapidly responding to environmental or physiological cues. Hence, LLPS is emerging as an important means to regulate biology and physiology. Yet, excessive inclusion body formation by, for instance, higher-than-normal concentrations or mutant forms of the protein components could result in the conversion from dynamic liquid condensates into more rigid gel- or solid-like aggregates, leading to the disruption of the organelle's function followed by the development of human disorders like neurodegenerative diseases. In summary, well-controlled formation and de-formation of LLPS is critical for normal biology and physiology from single cells to individual organisms, whereas abnormal LLPS is involved in the pathophysiology of human diseases. In turn, targeting these aggregates or their formation represents a promising approach in treating diseases driven by abnormal LLPS including those neurodegenerative diseases that lack effective therapies.
Keyphrases
- induced apoptosis
- endothelial cells
- cell cycle arrest
- aqueous solution
- ionic liquid
- signaling pathway
- induced pluripotent stem cells
- protein protein
- pluripotent stem cells
- energy transfer
- cancer therapy
- high throughput
- binding protein
- body mass index
- drug delivery
- tyrosine kinase
- sensitive detection
- cell proliferation
- living cells
- wound healing
- gram negative
- risk assessment
- pi k akt