SEC-seq reveals translation-focused metabolic strategies for high IgG productivity in clonal CHO cells

Jasmine Tat, Fides D. Lay, Jennitte Stevens, Nathan E. Lewis

bioRxiv, April 2026

https://doi.org/10.64898/2026.04.14.718270


Abstract

Chinese hamster ovary (CHO) cells are the dominant host for therapeutic protein production, yet intra- and inter-clonal heterogeneity in manufacturing phenotypes, and the underlying metabolic and secretory circuitry, remain poorly defined at single-cell resolution. Here, we apply secretion encoded single-cell sequencing (SEC-seq) to simultaneously measure transcriptomes and secreted IgG in single-cells from a parental production cell line and five CHO clones, each varying in cell-specific productivity. IgG mRNA and recombinant protein secretion are only moderately correlated across single cells, indicating that transcription alone does not explain intra-clonal secretion heterogeneity. By integrating SEC-seq with single-cell metabolic and secretory task scoring, we find that CHO cells accommodating recombinant protein expression burden have more active translation-associated pathways and suppressed energy-intensive endogenous secreted protein processing. Three high-secreting clones converge on this translation-focused state but differ in their subpopulation composition and energy/redox programs coupled to IgG output: one highly productive clone shows a low-growth, glycolytic, NAD/one-carbon–associated and UPR-activated program; a second shows increased oxidative phosphorylation and fatty-acid β-oxidation, and a third shows higher lipid-uptake with modest central carbon metabolism. Genes such as Aldoa, Ndufab1, Acsl5, Mthfd2 showed clone-specific correlations with IgG, linking glycolysis, mitochondrial respiration, fatty-acid metabolism, and redox to secretion. Together, these results demonstrate that SEC-seq can resolve IgG-coupled metabolic-secretory wiring within and between CHO clones, providing a framework to identify subpopulation and circuit features to engineer or select for improved recombinant protein production.

SEC-seq workflow using Nanovials and oligo-barcoded antibodies to simultaneously measure IgG secretion and gene expression in individual CHO cells.
 

Topics

SEC-seq, Cell Line Development, Antibody Secretion

Cell Types

Clonal Chinese hamster ovary (CHO) cells

Secretion Targets

IgG

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