Biomaterial Assembly Guided by Biochemical Reactions
Friday, February 9, 2024 11am to 12pm
About this Event
29 Oxford Street, Cambridge, MA 02138
Complex cellular behaviors such as motion and division are directed by far-from-equilibrium chemical reaction networks that regulate self-assembly, driving a cell to states that, without control by these networks, would be inaccessible. Could one design analogous biochemical reaction networks to control the dynamic behavior of synthetic materials? To do so, we must understand how materials assemble and behave when their dynamics are coupled to biomolecular reaction dynamics.
By coupling simple relatively simple chemical reactions to self-assembly processes, one can impose feedback regulation or trap materials in chosen metastable states. More complex networks could switch materials between many different metastable states and guide the transitions between them. Using examples of DNA and colloid self-assembly and shape-change in soft hydrogel films, I will discuss how we might construct “programmable” DNA and enzyme networks that can drive such multistate switching. These in vitro genetic regulatory networks are composed of interchangeable parts, so they can emulate the dynamics of a large class of feedforward and recurrent artificial neural networks. They can also faithfully propagate and amplify information, and handle the load imposed by when they are coupled to an assembly process. In vitro genetic regulatory networks could thus allow us to explore a broad range of dynamic material behaviors by design.