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Kapasiawala, M.

Publications and source records attributed to Kapasiawala, M..

2 recordsLinked to original sources

Metabolomics-informed coarse-grained model enables prediction of cell-free protein expression dynamics

Cell-free expression systems have gained considerable attention for their potential in biomanufac-turing, biosensing, and circuit prototyping. All these endeavors make use of the innate metabolic activity of cell lysates. However, our knowledge of the underlying nature of cell-free metabolism remains lacking. In this work, we use non-targeted mass spectrometry to generate time-course measurements of small molecules in E. coli cell lysates (metabolomics) during cell-free protein synthesis (CFPS) to show that the majority of E. colis metabolism is active in cell lysate. Fur-thermore, these data indicate that protein synthesis is a relatively small metabolic burden on cell lysates compared to the background metabolism, and that the build-up of multiple metabolic waste products is fundamentally responsible for stopping cell-free protein expression as opposed to depletion of fuel sources. We use these insights coupled with high-throughput CFPS experiments to develop a foundational coarse-grained mechanistic model of CFPS which we show can be easily recalibrated using Bayesian parameter inference techniques to provide accurate models across hundreds of novel experimental conditions. This work provides new experimental insights into the effects of cell-free metabolism on CFPS and establishes a novel framework for leveraging existing CFPS models in new experimental contexts, opening the avenue to future cell-free applications aimed at building complex systems, from multilayered biological circuits to synthetic biological cells.

synthetic biology↗

Probing metabolism in an E. coli-based cell-free system reveals a trade-off between transcription and translation

Cell-free transcription-translation (TX-TL) systems have been used for diverse applications, but their performance and scope are limited by variability and poor predictability. To understand the drivers of this variability, we explored the effects of metabolic perturbations to an E. coli Rosetta2 TX-TL system. We targeted three classes of molecules: energy molecules, in the form of nucleotide triphosphates (NTPs); central carbon "fuel" molecules, which regenerate NTPs; and magnesium ions (Mg2+). Using malachite green mRNA aptamer (MG aptamer) and destabilized enhanced Green Fluorescent Protein (deGFP) as transcriptional and translational readouts, respectively, we report the presence of a trade-off between optimizing total protein yield and optimizing total mRNA yield, as measured by integrating the area under the curve for mRNA time-course dynamics. We found that a systems position along the trade-off curve is strongly determined by Mg2+ concentration, fuel type and concentration, and cell lysate batch, and that variability can be reduced by modulating these components. Our results further suggest the trade-off arises from limitations in translation regulation and inefficient energy regeneration. This work advances our understanding of the effects of fuel and energy metabolism on TX-TL in cell-free systems and lays a foundation for improving TX-TL performance, lifetime, standardization, and prediction. For Table of Contents Use Only O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=74 SRC="FIGDIR/small/533877v4_ufig1.gif" ALT="Figure 1"> View larger version (16K): org.highwire.dtl.DTLVardef@d6ffd7org.highwire.dtl.DTLVardef@1368a05org.highwire.dtl.DTLVardef@19f5b31org.highwire.dtl.DTLVardef@11c14c0_HPS_FORMAT_FIGEXP M_FIG C_FIG

synthetic biology↗