Related Experiment Video
Updated: Aug 25, 2025

Author Spotlight: Developing Synthetic Cells from Programmable Amphiphilic DNA Nanostructures
Published on: May 31, 2024
Engineering DNA-based synthetic condensates with programmable material properties, compositions, and functionalities
Sungho Do1, Chanseok Lee2, Taehyun Lee1
1Department of Mechanical Engineering, Seoul National University, Seoul 08826, Republic of Korea.
Abstract:
Biomolecular condensates participate in diverse cellular processes, ranging from gene regulation to stress survival. Bottom-up engineering of synthetic condensates advances our understanding of the organizing principle of condensates. It also enables the synthesis of artificial systems with novel functions. However, building synthetic condensates with a predictable organization and function remains challenging. Here, we use DNA as a building block to create synthetic condensates that are assembled through phase separation. The programmability of intermolecular interactions between DNA molecules enables the control over various condensate properties including assembly, composition, and function. Similar to the way intracellular condensates are organized, DNA clients are selectively partitioned into cognate condensates. We demonstrate that the synthetic condensates can accelerate DNA strand displacement reactions and logic gate operation by concentrating specific reaction components. We envision that the DNA-based condensates could help the realization of the high-order functions required to build more life-like artificial systems.
Related Concept Videos
Synthetic Biology
Golden rice
Golden rice is a genetically modified...
DNA as a Genetic Template
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
DNA Topoisomerases
Types and Mechanism of action
Topoisomerases are divided into two main types. ...
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

