Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2019 Oct 15;20(20):2653-2665.
doi: 10.1002/cbic.201900272. Epub 2019 Aug 22.

Characterization of Gene Circuit Parts Based on Multiobjective Optimization by Using Standard Calibrated Measurements

Affiliations

Characterization of Gene Circuit Parts Based on Multiobjective Optimization by Using Standard Calibrated Measurements

Yadira Boada et al. Chembiochem. .

Abstract

Standardization and characterization of biological parts is necessary for the further development of bottom-up synthetic biology. Herein, an easy-to-use methodology that embodies both a calibration procedure and a multiobjective optimization approach is proposed to characterize biological parts. The calibration procedure generates values for specific fluorescence per cell expressed as standard units of molecules of equivalent fluorescein per particle. The use of absolute standard units enhances the characterization of model parameters for biological parts by bringing measurements and estimations results from different sources into a common domain, so they can be integrated and compared faithfully. The multiobjective optimization procedure exploits these concepts by estimating the values of the model parameters, which represent biological parts of interest, while considering a varied range of experimental and circuit contexts. Thus, multiobjective optimization provides a robust characterization of them. The proposed calibration and characterization methodology can be used as a guide for good practices in dry and wet laboratories; thus allowing not only portability between models, but is also useful for generating libraries of tested and well-characterized biological parts.

Keywords: DNA; bioinformatics; fluorescence; gene technology; synthetic biology.

PubMed Disclaimer

References

    1. ERA SynBio Report, ERA SynBio 2014, https://bbsrc.ukri.org/documents/1404-era-synbio-strategic-vision-pdf/.
    1. R. Kojima, M. Fussenegger, ChemBioChem 2019, 20, 994-1002.
    1. P. Schwille, J. Spatz, K. Landfester, E. Bodenschatz, S. Herminghaus, V. Sourjik, T. J. Erb, P. Bastiaens, R. Lipowsky, A. Hyman, P. Dabrock, J.-C. Baret, T. Vidakovic-Koch, P. Bieling, R. Dimova, H. Mutschler, T. Robinson, T.-Y. D. Tang, S. Wegner, K. Sundmacher, Angew. Chem. Int. Ed. 2018, 57, 13382-13392;
    1. Angew. Chem. 2018, 130, 13566-13577.
    1. B. Canton, A. Labno, D. Endy, Nat. Biotechnol. 2008, 26, 787-793.

Publication types

MeSH terms

LinkOut - more resources