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Kozak sequence libraries for systematically characterizing transgenes across expression levels.

Created on 21 Jul 2026

Authors

Nidhi Shukla, Nisha D Kamath, John C Snell, Anna M Bruchez, Kenneth A Matreyek

Published in

Nucleic acids research. Volume 54. Issue 14. Jul 17, 2026.

Abstract

Typical mammalian overexpression systems test protein sequence variants with little control over expression levels and steady-state protein abundances, hindering interpretations of how protein sequence and expression converge to yield phenotypic outcomes. We explored the translation initiation sequence, commonly referred to as the Kozak sequence, as a means to systematically modulate protein steady-state abundance and cellular function. We performed sort-seq on a randomized library of the 6 nt preceding the start codon, amounting to 4042 sequences, with a single sequence integrated at a shared genomic integration site in each HEK 293T cell. Calibrating the scores revealed a ∼100-fold range of protein steady-state abundances possible through manipulation of the Kozak sequence. We identified human germline variants with predicted expression-reducing Kozak substitutions in disease-associated genes. Modulating the cell surface abundance of the host cell receptor ACE2 controlled the rate at which those cells became infected by SARS-like coronavirus spike pseudotyped particles. We demonstrated the potential of the approach by simultaneously testing Kozak libraries with a small panel of coding variants for ACE2 and STIM1. This approach lays the methodological groundwork for linking the causal relationships between protein sequence, abundance, and functional outcome.

PMID:
42475684
Bibliographic data and abstract were imported from PubMed on 21 Jul 2026.

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