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mRNA codon optimization with quantum computers
Reverse translation of polypeptide sequences to expressible mRNA constructs is a NP-hard combinatorial optimization problem. Each amino acid in the protein sequence can be represented by as many as six codons, and the process of selecting the combination that maximizes probability of expression is t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8555812/ https://www.ncbi.nlm.nih.gov/pubmed/34714834 http://dx.doi.org/10.1371/journal.pone.0259101 |
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author | Fox, Dillion M. Branson, Kim M. Walker, Ross C. |
author_facet | Fox, Dillion M. Branson, Kim M. Walker, Ross C. |
author_sort | Fox, Dillion M. |
collection | PubMed |
description | Reverse translation of polypeptide sequences to expressible mRNA constructs is a NP-hard combinatorial optimization problem. Each amino acid in the protein sequence can be represented by as many as six codons, and the process of selecting the combination that maximizes probability of expression is termed codon optimization. This work investigates the potential impact of leveraging quantum computing technology for codon optimization. A Quantum Annealer (QA) is compared to a standard genetic algorithm (GA) programmed with the same objective function. The QA is found to be competitive in identifying optimal solutions. The utility of gate-based systems is also evaluated using a simulator resulting in the finding that while current generations of devices lack the hardware requirements, in terms of both qubit count and connectivity, to solve realistic problems, future generation devices may be highly efficient. |
format | Online Article Text |
id | pubmed-8555812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-85558122021-10-30 mRNA codon optimization with quantum computers Fox, Dillion M. Branson, Kim M. Walker, Ross C. PLoS One Research Article Reverse translation of polypeptide sequences to expressible mRNA constructs is a NP-hard combinatorial optimization problem. Each amino acid in the protein sequence can be represented by as many as six codons, and the process of selecting the combination that maximizes probability of expression is termed codon optimization. This work investigates the potential impact of leveraging quantum computing technology for codon optimization. A Quantum Annealer (QA) is compared to a standard genetic algorithm (GA) programmed with the same objective function. The QA is found to be competitive in identifying optimal solutions. The utility of gate-based systems is also evaluated using a simulator resulting in the finding that while current generations of devices lack the hardware requirements, in terms of both qubit count and connectivity, to solve realistic problems, future generation devices may be highly efficient. Public Library of Science 2021-10-29 /pmc/articles/PMC8555812/ /pubmed/34714834 http://dx.doi.org/10.1371/journal.pone.0259101 Text en © 2021 Fox et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Fox, Dillion M. Branson, Kim M. Walker, Ross C. mRNA codon optimization with quantum computers |
title | mRNA codon optimization with quantum computers |
title_full | mRNA codon optimization with quantum computers |
title_fullStr | mRNA codon optimization with quantum computers |
title_full_unstemmed | mRNA codon optimization with quantum computers |
title_short | mRNA codon optimization with quantum computers |
title_sort | mrna codon optimization with quantum computers |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8555812/ https://www.ncbi.nlm.nih.gov/pubmed/34714834 http://dx.doi.org/10.1371/journal.pone.0259101 |
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