Related Experiment Video
Updated: Mar 31, 2026

Author Spotlight: Developing Synthetic Cells from Programmable Amphiphilic DNA Nanostructures
Published on: May 31, 2024
Biomolecular condensates: Dynamic organizers from cell physiology to engineered applications
1Chemical Biology Unit, Institute of Nano Science and Technology, Sector-81, Knowledge City, SAS Nagar, Punjab, 140306, India.
None:
Phase separation (PS) has emerged as a fundamental biophysical process that organizes essential cellular processes through the formation of biomolecular condensates. These dynamic membrane-less assemblies reversibly form and dissolve in response to environmental and physiological stimuli, including changes in concentration, pH, temperature, or light. Such responsiveness makes biomolecular condensates highly attractive platforms for engineering applications, including drug delivery, biosensing, stimuli-responsive nanomedicine, and gene or protein transfection. Physiological cues induce phase separation that selectively partitions biomolecules into dense phases increasing the local concentrations leading to enhanced catalytic effects. This concentration-driven organization is particularly advantageous for enzymatic systems, where condensate formation has been shown to accelerate reaction kinetics by several fold. In this review we discuss how insights from cellular condensates are being translated into engineered systems, with emerging applications in biocatalysis, drug delivery, and related biomedical applications.
Related Concept Videos
Chemistry of the Cell
Water
The polarity of the water molecule and its resulting hydrogen bonding makes water a unique substance with special properties that are intimately tied to the processes of life. Life originally evolved in an aqueous environment, and most of an organism’s cellular chemistry and metabolism occur inside the aqueous contents of the cell’s cytoplasm. Special properties of water are its high heat capacity...
Protein Dynamics in Living Cells
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...

