Sequencing technologies to measure translation in single cells

Michael VanInsberghe*, Alexander van Oudenaarden

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Translation is one of the most energy-intensive processes in a cell and, accordingly, is tightly regulated. Genome-wide methods to measure translation and the translatome and to study the complex regulation of protein synthesis have enabled unprecedented characterization of this crucial step of gene expression. However, technological limitations have hampered our understanding of translation control in multicellular tissues, rare cell types and dynamic cellular processes. Recent optimizations, adaptations and new techniques have enabled these measurements to be made at single-cell resolution. In this Progress, we discuss single-cell sequencing technologies to measure translation, including ribosome profiling, ribosome affinity purification and spatial translatome methods.

Original languageEnglish
Article numbere694
Pages (from-to)337-346
Number of pages10
JournalNature reviews molecular cell biology
Volume26
Issue number5
Early online date20 Jan 2025
DOIs
Publication statusPublished - May 2025

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