MOSAIC: Codon Harmonization of Monte Carlo-Based Simulated Annealing for Linked Codons in Heterologous Protein Expression
Yoonho Jeong, Chengcheng Yang, Ryan Fernandez Medina Hariri, Jihoo Kim, Eok Kyun Lee, Younghoon Lee, Won June Kim, Seung Seo Lee, Insung S. Choi

TL;DR
This paper introduces MOSAIC, a Monte Carlo-based algorithm for linked codon harmonization that improves heterologous protein expression by better mimicking native translation rates.
Contribution
It presents a novel linked codon harmonization method using Monte Carlo simulated annealing, demonstrating improved protein expression in model systems.
Findings
Harmonized gene of RP S18 produced more protein than wild-type.
Harmonized gene yielded more soluble protein.
MOSAIC showed robust computational performance.
Abstract
Codon usage bias has a crucial impact on the translation efficiency and co-translational folding of proteins, necessitating the algorithmic development of codon optimization/harmonization methods, particularly for heterologous recombinant protein expression. Codon harmonization is especially valuable for proteins sensitive to translation rates, because it can potentially replicate native translation speeds, preserving proper folding and maintaining protein activity. This work proposes a Monte Carlo-based codon harmonization algorithm, MOSAIC (Monte Carlo-based Simulated Annealing for Linked Codons), for the harmonization of a set of linked codons, which differs from conventional codon harmonization, by focusing on the codon sets rather than individual ones. Our MOSAIC demonstrates robust computational performance on ribosomal proteins (S18, S15, S10, and L11) as model systems. Among…
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