Advances in the Computational Design of Small-Molecule-Controlled Protein-Based Circuits for Synthetic Biology.

Biological sensor-actuators Rosetta cellular therapies computational protein design de novo design molecular sensors protein engineering protein–small-molecule interactions synthetic biological signaling systems synthetic biology

Journal

Proceedings of the IEEE. Institute of Electrical and Electronics Engineers
ISSN: 0018-9219
Titre abrégé: Proc IEEE Inst Electr Electron Eng
Pays: United States
ID NLM: 9879073

Informations de publication

Date de publication:
May 2022
Historique:
entrez: 19 12 2022
pubmed: 20 12 2022
medline: 20 12 2022
Statut: ppublish

Résumé

Synthetic biology approaches living systems with an engineering perspective and promises to deliver solutions to global challenges in healthcare and sustainability. A critical component is the design of biomolecular circuits with programmable input-output behaviors. Such circuits typically rely on a sensor module that recognizes molecular inputs, which is coupled to a functional output via protein-level circuits or regulating the expression of a target gene. While gene expression outputs can be customized relatively easily by exchanging the target genes, sensing new inputs is a major limitation. There is a limited repertoire of sensors found in nature, and there are often difficulties with interfacing them with engineered circuits. Computational protein design could be a key enabling technology to address these challenges, as it allows for the engineering of modular and tunable sensors that can be tailored to the circuit's application. In this article, we review recent computational approaches to design protein-based sensors for small-molecule inputs with particular focus on those based on the widely used Rosetta software suite. Furthermore, we review mechanisms that have been harnessed to couple ligand inputs to functional outputs. Based on recent literature, we illustrate how the combination of protein design and synthetic biology enables new sensors for diverse applications ranging from biomedicine to metabolic engineering. We conclude with a perspective on how strategies to address frontiers in protein design and cellular circuit design may enable the next generation of sense-response networks, which may increasingly be assembled from

Identifiants

pubmed: 36531560
doi: 10.1109/JPROC.2022.3157898
pmc: PMC9754107
mid: NIHMS1809761
doi:

Types de publication

Journal Article

Langues

eng

Pagination

659-674

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM110089
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM145236
Pays : United States

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Auteurs

Simon Kretschmer (S)

Department of Bioengineering and Therapeutic Sciences, University of California at San Francisco, San Francisco, CA 94158 USA, and affiliated with the California Quantitative Biosciences Institute (QBI) at UCSF, San Francisco, CA 94158 USA.

Tanja Kortemme (T)

Department of Bioengineering and Therapeutic Sciences, University of California at San Francisco, San Francisco, CA 94158 USA, and affiliated with the California Quantitative Biosciences Institute (QBI) at UCSF, San Francisco, CA 94158 USA.

Classifications MeSH