Cell
Volume 184, Issue 19, 16 September 2021, Pages 4886-4903.e21
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Article
Dual film-like organelles enable spatial separation of orthogonal eukaryotic translation

https://doi.org/10.1016/j.cell.2021.08.001Get rights and content
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Highlights

  • 2D phase separation was utilized to design orthogonal enzymes

  • Film-like organelles maintained distinct suppressor tRNA microenvironments

  • Dual film-like synthetic organelles enabled orthogonal translation in eukaryotes

  • Cells were equipped with two expanded genetic codes in addition to the canonical one

Summary

Engineering new functionality into living eukaryotic systems by enzyme evolution or de novo protein design is a formidable challenge. Cells do not rely exclusively on DNA-based evolution to generate new functionality but often utilize membrane encapsulation or formation of membraneless organelles to separate distinct molecular processes that execute complex operations. Applying this principle and the concept of two-dimensional phase separation, we develop film-like synthetic organelles that support protein translation on the surfaces of various cellular membranes. These sub-resolution synthetic films provide a path to make functionally distinct enzymes within the same cell. We use these film-like organelles to equip eukaryotic cells with dual orthogonal expanded genetic codes that enable the specific reprogramming of distinct translational machineries with single-residue precision. The ability to spatially tune the output of translation within tens of nanometers is not only important for synthetic biology but has implications for understanding the function of membrane-associated protein condensation in cells.

Keywords

synthetic biology
synthetic biomolecular condensates
2D phase separation
enzyme engineering
orthogonal translation
genetic code expansion
membrane signaling

Data and code availability

  • All data are available in the main text or the supplementary materials. Raw data reported in this paper will be shared by the lead contact upon request.

  • This paper does not report original code.

  • Any additional information required to reanalyze the data reported in this paper is available from the lead contact upon request.

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