Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published October 2, 2015 | Published + Supplemental Material
Journal Article Open

Rapid cell-free forward engineering of novel genetic ring oscillators

Abstract

While complex dynamic biological networks control gene expression in all living organisms, the forward engineering of comparable synthetic networks remains challenging. The current paradigm of characterizing synthetic networks in cells results in lengthy design-build-test cycles, minimal data collection, and poor quantitative characterization. Cell-free systems are appealing alternative environments, but it remains questionable whether biological networks behave similarly in cell-free systems and in cells. We characterized in a cell-free system the 'repressilator,' a three-node synthetic oscillator. We then engineered novel three, four, and five-gene ring architectures, from characterization of circuit components to rapid analysis of complete networks. When implemented in cells, our novel 3-node networks produced population-wide oscillations and 95% of 5-node oscillator cells oscillated for up to 72 hours. Oscillation periods in cells matched the cell-free system results for all networks tested. An alternate forward engineering paradigm using cell-free systems can thus accurately capture cellular behavior.

Additional Information

© 2015 Niederholtmeyer et al. This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited. Received June 29, 2015. Accepted October 1, 2015. Published October 2, 2015. We thank Yin He, Transcriptic, Inc. and Holly Rees for cloning assistance, Jan Kostecki and Stephen Mayo for protein purification and size exclusion chromatography assistance, Rohit Sharma and Marcella Gomez for initial testing and modeling of oscillators in vitro, Kyle Martin for laboratory assistance, Adam Abate, Tanja Kortemme, and Charles Craik for laboratory space and equipment, Matthieu Delincé, Joachim De Jonghe, Marc Spaltenstein, John McKinney and Jin Park for mother machine material and assistance, Tim Chang and Benjamin Alderete for CellASIC assistance, and Michael Elowitz for insights and scientific support. This work was supported in part by EPFL and the Defense Advanced Research Projects Agency (DARPA/MTO) Living Foundries program, contract number HR0011-12-C-0065 (DARPA/CMO). Z.Z.S. is also supported by a UCLA/Caltech Medical Scientist Training Program fellowship, Z.Z.S and E.Y by a National Defense Science and Engineering Graduate fellowship, and Y.H. by a JSPS Fellowship for Research Abroad. The views and conclusions contained in this document are those of the authors and should not be interpreted as representing officially policies, either expressly or implied, of the Defense Advanced Research Projects Agency or the U.S. Government.

Attached Files

Published - 14490644573328_1..pdf

Supplemental Material - elife09771_Supplemental_files.zip

Files

14490644573328_1..pdf
Files (48.4 MB)
Name Size Download all
md5:1da2ac84ea7ce4dae92770f735d556e1
2.5 MB Preview Download
md5:2755aadae79cd0963bc3879f608c7be2
45.9 MB Preview Download

Additional details

Created:
August 20, 2023
Modified:
October 24, 2023