LAUSR

Abstract Transcriptional factor-based biosensor has been widely used to reprogram and adjust cellular activity to the changing environment. These biosensors translate an internal cellular signal to a transcriptional reporter output. Previous examples have demonstrated transcriptional factor (TF) cross-talk could lead to complex gene expression dynamics. In this report, we formulated a mechanism-based kinetic model to simulate and predict how TF cross-talk reshape the transcriptional dynamics of an engineered biosensor. Our model comprises TF cross-talk and Hill-type equation to quantify the degree of gene repression and de-repression; it also accounts for protein degradation, cell growth (dilution) effect and the carrying capacity of the system. Our simulation fits well with the biphasic parabolic gene expression pattern of an experimentally validated malonyl-CoA sensor. We discovered that exponential growth could lead to hysteresis in the TF cross-talk model. With Logistic growth to limit the carrying capacity, we find that bimodal gene expression pattern could arise, and this phenomenon is rooted in the hysteresis characteristics of the TF cross-talk model. The computational insights obtained in this study will guide us to design accurate, sensitive TF-based biosensors and may serve as a diagnostic platform to troubleshoot the complex transcriptional dynamics in biosensor design. The computational framework developed here will also provide an educational toolbox for synthetic biologist and biochemical/biomolecular engineering students to understand biosystem design and transcriptional regulation.