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Multi-line split DNA synthesis: a novel combinatorial method to make high quality peptide libraries

BACKGROUND: We developed a method to make a various high quality random peptide libraries for evolutionary protein engineering based on a combinatorial DNA synthesis. RESULTS: A split synthesis in codon units was performed with mixtures of bases optimally designed by using a Genetic Algorithm progra...

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Detalles Bibliográficos
Autores principales: Tabuchi, Ichiro, Soramoto, Sayaka, Ueno, Shingo, Husimi, Yuzuru
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC520752/
https://www.ncbi.nlm.nih.gov/pubmed/15341664
http://dx.doi.org/10.1186/1472-6750-4-19
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author Tabuchi, Ichiro
Soramoto, Sayaka
Ueno, Shingo
Husimi, Yuzuru
author_facet Tabuchi, Ichiro
Soramoto, Sayaka
Ueno, Shingo
Husimi, Yuzuru
author_sort Tabuchi, Ichiro
collection PubMed
description BACKGROUND: We developed a method to make a various high quality random peptide libraries for evolutionary protein engineering based on a combinatorial DNA synthesis. RESULTS: A split synthesis in codon units was performed with mixtures of bases optimally designed by using a Genetic Algorithm program. It required only standard DNA synthetic reagents and standard DNA synthesizers in three lines. This multi-line split DNA synthesis (MLSDS) is simply realized by adding a mix-and-split process to normal DNA synthesis protocol. Superiority of MLSDS method over other methods was shown. We demonstrated the synthesis of oligonucleotide libraries with 10(16 )diversity, and the construction of a library with random sequence coding 120 amino acids containing few stop codons. CONCLUSIONS: Owing to the flexibility of the MLSDS method, it will be able to design various "rational" libraries by using bioinformatics databases.
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spelling pubmed-5207522004-10-01 Multi-line split DNA synthesis: a novel combinatorial method to make high quality peptide libraries Tabuchi, Ichiro Soramoto, Sayaka Ueno, Shingo Husimi, Yuzuru BMC Biotechnol Methodology Article BACKGROUND: We developed a method to make a various high quality random peptide libraries for evolutionary protein engineering based on a combinatorial DNA synthesis. RESULTS: A split synthesis in codon units was performed with mixtures of bases optimally designed by using a Genetic Algorithm program. It required only standard DNA synthetic reagents and standard DNA synthesizers in three lines. This multi-line split DNA synthesis (MLSDS) is simply realized by adding a mix-and-split process to normal DNA synthesis protocol. Superiority of MLSDS method over other methods was shown. We demonstrated the synthesis of oligonucleotide libraries with 10(16 )diversity, and the construction of a library with random sequence coding 120 amino acids containing few stop codons. CONCLUSIONS: Owing to the flexibility of the MLSDS method, it will be able to design various "rational" libraries by using bioinformatics databases. BioMed Central 2004-09-01 /pmc/articles/PMC520752/ /pubmed/15341664 http://dx.doi.org/10.1186/1472-6750-4-19 Text en Copyright © 2004 Tabuch et al; licensee BioMed Central Ltd.
spellingShingle Methodology Article
Tabuchi, Ichiro
Soramoto, Sayaka
Ueno, Shingo
Husimi, Yuzuru
Multi-line split DNA synthesis: a novel combinatorial method to make high quality peptide libraries
title Multi-line split DNA synthesis: a novel combinatorial method to make high quality peptide libraries
title_full Multi-line split DNA synthesis: a novel combinatorial method to make high quality peptide libraries
title_fullStr Multi-line split DNA synthesis: a novel combinatorial method to make high quality peptide libraries
title_full_unstemmed Multi-line split DNA synthesis: a novel combinatorial method to make high quality peptide libraries
title_short Multi-line split DNA synthesis: a novel combinatorial method to make high quality peptide libraries
title_sort multi-line split dna synthesis: a novel combinatorial method to make high quality peptide libraries
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC520752/
https://www.ncbi.nlm.nih.gov/pubmed/15341664
http://dx.doi.org/10.1186/1472-6750-4-19
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