Abstract
Engineering cell fate is fundamental for optimizing stem cell-based therapies aimed at replacing cells in patients suffering from trauma or disease. By timely administering molecular regulators—such as transcription factors, RNAs, or small molecules—in a process that mimics in vivo embryonic development, stem cell differentiation can be guided toward a specific cell fate. A significant challenge in scaling up these therapies is that such differentiation strategies often result in mixed cellular populations. While synthetic biology approaches have been proposed to increase the yield of desired cell types, designing gene circuits that effectively redirect cell fate decisions requires mechanistic insight into the dynamics of endogenous regulatory networks that govern decision-making. In this work, we present a biomolecular adaptive controller based on an Incoherent Feedforward Loop (IFFL)-like topology designed to favor a specific cell fate. This controller requires minimal knowledge of the endogenous network as it exhibits adaptive, non-reference-based behavior. The synthetic circuit operates through a sequestration mechanism and a delay introduced by an intermediate species, producing an output that asymptotically approximates a discrete temporal derivative of its input, provided there is a sufficiently fast sequestration rate. By allowing the controller to actuate over a target species involved in the decision-making process, a tunable, synthetic bias is created that favors the production of the desired species with minimal alteration to the overall equilibrium landscape of the endogenous network. Through theoretical and computational analysis, we provide design guidelines for the controller’s optimal operation, evaluate its performance under parametric perturbations, and extend its applicability to various examples of common multistable systems in biology.
Competing Interest Statement
The authors have declared no competing interest.
