Efficient cell-free translation from diverse human cell types

Cell-free translation systems are indispensable for studying protein synthesis, enabling researchers to explore translational regulation across different cell types. The difficulties in producing cell-free translation systems from different cell types limit the ability to study regulatory mechanisms that depend on different biological contexts. Here, we present a scalable method for preparing translation-competent lysates from a range of frequently used human cell lines using dual centrifugation. We optimized lysis conditions for adherent and suspension cells, producing high-quality lysates from HEK-293 (adherent and in suspension), HeLa, SH-SY5Y, and U2OS cells. Our results demonstrate that cell-specific factors influence translation efficiency, with adherent HeLa cells showing the highest activity. We also observed that sensitivity to lysis conditions varies between cell lines, underscoring the importance of fine-tuning parameters for efficient protein production. Our method provides a robust and adaptable approach for generating cell-type-specific lysates, broadening the application of in vitro translation systems in studying translational mechanisms.

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Publication Details

Journal
Journal of Biological Chemistry
Published
2025-05-28
DOI
https://doi.org/10.1016/j.jbc.2025.110307
Citations
2
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
1.61

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article

Efficient cell-free translation from diverse human cell types

Oliver Mühlemann, Jana Ziegelmüller, Alexander M. Hofer, Evangelos D. Karousis et al.
2 citations
Journal of Biological Chemistry
CRISPR and Genetic Engineering
1.61
article

Efficient cell-free translation from diverse human cell types

Oliver Mühlemann, Jana Ziegelmüller, Alexander M. Hofer, Evangelos D. Karousis, Nino Schwaller, Nikolaos Kouvelas, Priyanka Thambythurai
article en
2 citations

Abstract

Cell-free translation systems are indispensable for studying protein synthesis, enabling researchers to explore translational regulation across different cell types. The difficulties in producing cell-free translation systems from different cell types limit the ability to study regulatory mechanisms that depend on different biological contexts. Here, we present a scalable method for preparing translation-competent lysates from a range of frequently used human cell lines using dual centrifugation. We optimized lysis conditions for adherent and suspension cells, producing high-quality lysates from HEK-293 (adherent and in suspension), HeLa, SH-SY5Y, and U2OS cells. Our results demonstrate that cell-specific factors influence translation efficiency, with adherent HeLa cells showing the highest activity. We also observed that sensitivity to lysis conditions varies between cell lines, underscoring the importance of fine-tuning parameters for efficient protein production. Our method provides a robust and adaptable approach for generating cell-type-specific lysates, broadening the application of in vitro translation systems in studying translational mechanisms.

Journal of Biological ChemistryVol. 301(7)
University of Bern (CH), Bern University of Applied Sciences (CH)
National Science Foundation, University of Bern, Kanton Bern, Ministerul Cercetării, Inovării şi Digitalizării, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, UniBern Forschungsstiftung, Fondation Claude et Giuliana, Holcim Stiftung zur Förderung der Wissenschaftlichen Fortbildung
Openalex Percentile: Top 17%
CRISPR and Genetic Engineering
1.61
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