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An mRNA-protein Fusion at N-terminus for Evolutionary Protein Engineering

A novel method to link a nascent protein (phenotype) to its mRNA (genotype) covalently through the N-terminus was developed. The mRNA harboring amber stop codon at just downstream of initiation site was hybridized with hydrazide-modified ssDNA at upstream of coding region and was ligated to the DNA....

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Detalles Bibliográficos
Autores principales: Ueno, Shingo, Arai, Hidenao, Suzuki, Miho, Husimi, Yuzuru
Formato: Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1975775/
https://www.ncbi.nlm.nih.gov/pubmed/17848981
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author Ueno, Shingo
Arai, Hidenao
Suzuki, Miho
Husimi, Yuzuru
author_facet Ueno, Shingo
Arai, Hidenao
Suzuki, Miho
Husimi, Yuzuru
author_sort Ueno, Shingo
collection PubMed
description A novel method to link a nascent protein (phenotype) to its mRNA (genotype) covalently through the N-terminus was developed. The mRNA harboring amber stop codon at just downstream of initiation site was hybridized with hydrazide-modified ssDNA at upstream of coding region and was ligated to the DNA. This construct was then modified with 4-acetyl-phenylalanyl amber suppressor tRNA. This modified construct was fused with the nascent protein via the phenylalanine derivative when the mRNA uses the amber suppressor tRNA to decode the amber stop codon. The obtained fusion molecule was used successfully in selective enrichment experiments. It will be applicable for high-through-put screening in evolutionary protein engineering. In contrast to fusion molecules generated by other methods in which the protein is linked to genotype molecule through the C- terminus, our fusion molecule will serve to select a protein for which the C-terminus is essential to be active.
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spelling pubmed-19757752007-09-11 An mRNA-protein Fusion at N-terminus for Evolutionary Protein Engineering Ueno, Shingo Arai, Hidenao Suzuki, Miho Husimi, Yuzuru Int J Biol Sci Research Paper A novel method to link a nascent protein (phenotype) to its mRNA (genotype) covalently through the N-terminus was developed. The mRNA harboring amber stop codon at just downstream of initiation site was hybridized with hydrazide-modified ssDNA at upstream of coding region and was ligated to the DNA. This construct was then modified with 4-acetyl-phenylalanyl amber suppressor tRNA. This modified construct was fused with the nascent protein via the phenylalanine derivative when the mRNA uses the amber suppressor tRNA to decode the amber stop codon. The obtained fusion molecule was used successfully in selective enrichment experiments. It will be applicable for high-through-put screening in evolutionary protein engineering. In contrast to fusion molecules generated by other methods in which the protein is linked to genotype molecule through the C- terminus, our fusion molecule will serve to select a protein for which the C-terminus is essential to be active. Ivyspring International Publisher 2007-08-29 /pmc/articles/PMC1975775/ /pubmed/17848981 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Ueno, Shingo
Arai, Hidenao
Suzuki, Miho
Husimi, Yuzuru
An mRNA-protein Fusion at N-terminus for Evolutionary Protein Engineering
title An mRNA-protein Fusion at N-terminus for Evolutionary Protein Engineering
title_full An mRNA-protein Fusion at N-terminus for Evolutionary Protein Engineering
title_fullStr An mRNA-protein Fusion at N-terminus for Evolutionary Protein Engineering
title_full_unstemmed An mRNA-protein Fusion at N-terminus for Evolutionary Protein Engineering
title_short An mRNA-protein Fusion at N-terminus for Evolutionary Protein Engineering
title_sort mrna-protein fusion at n-terminus for evolutionary protein engineering
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1975775/
https://www.ncbi.nlm.nih.gov/pubmed/17848981
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