Cargando…

Design and implementation of a high yield production system for recombinant expression of peptides

BACKGROUND: Making peptide pharmaceuticals involves challenging processes where many barriers, which include production and manufacture, need to be overcome. A non common but interesting research area is related to peptides with intracellular targets, which opens up new possibilities, allowing the m...

Descripción completa

Detalles Bibliográficos
Autores principales: Rodríguez, Vida, Asenjo, Juan A, Andrews, Barbara A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022411/
https://www.ncbi.nlm.nih.gov/pubmed/24885242
http://dx.doi.org/10.1186/1475-2859-13-65
_version_ 1782316401643487232
author Rodríguez, Vida
Asenjo, Juan A
Andrews, Barbara A
author_facet Rodríguez, Vida
Asenjo, Juan A
Andrews, Barbara A
author_sort Rodríguez, Vida
collection PubMed
description BACKGROUND: Making peptide pharmaceuticals involves challenging processes where many barriers, which include production and manufacture, need to be overcome. A non common but interesting research area is related to peptides with intracellular targets, which opens up new possibilities, allowing the modulation of processes occurring within the cell or interference with signaling pathways. However, if the bioactive sequence requires fusion to a carrier peptide to allow access into the cell, the resulting peptide could be such a length that traditional production could be difficult. The goal of the present study was the development of a flexible recombinant expression and purification system for peptides, as a contribution to the discovery and development of these potentially new drugs. RESULTS: In this work, a high throughput recombinant expression and purification system for production of cell penetrating peptides in Escherichia coli has been designed and implemented. The system designed produces target peptides in an insoluble form by fusion to a hexahistidine tagged ketosteroid isomerase which is then separated by a highly efficient thrombin cleavage reaction procedure. The expression system was tested on the anticancer peptides p53pAnt and PNC27. These peptides comprise the C-terminal region and the N-terminal region of the protein p53, respectively, fused by its carboxyl terminal extreme to the cell penetrating peptide Penetratin. High yields of purified recombinant fused peptides were obtained in both cases; nevertheless, thrombin cleavage reaction was successful only for p53pAnt peptide release. The features of the system, together with the procedure developed, allow achievement of high production yields of over 30 mg of highly pure p53pAnt peptide per g of dry cell mass. It is proposed that the system could be used for production of other peptides at a similar yield. CONCLUSIONS: This study provides a system suitable for recombinant production of peptides for scientific research, including biological assays.
format Online
Article
Text
id pubmed-4022411
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-40224112014-05-16 Design and implementation of a high yield production system for recombinant expression of peptides Rodríguez, Vida Asenjo, Juan A Andrews, Barbara A Microb Cell Fact Research BACKGROUND: Making peptide pharmaceuticals involves challenging processes where many barriers, which include production and manufacture, need to be overcome. A non common but interesting research area is related to peptides with intracellular targets, which opens up new possibilities, allowing the modulation of processes occurring within the cell or interference with signaling pathways. However, if the bioactive sequence requires fusion to a carrier peptide to allow access into the cell, the resulting peptide could be such a length that traditional production could be difficult. The goal of the present study was the development of a flexible recombinant expression and purification system for peptides, as a contribution to the discovery and development of these potentially new drugs. RESULTS: In this work, a high throughput recombinant expression and purification system for production of cell penetrating peptides in Escherichia coli has been designed and implemented. The system designed produces target peptides in an insoluble form by fusion to a hexahistidine tagged ketosteroid isomerase which is then separated by a highly efficient thrombin cleavage reaction procedure. The expression system was tested on the anticancer peptides p53pAnt and PNC27. These peptides comprise the C-terminal region and the N-terminal region of the protein p53, respectively, fused by its carboxyl terminal extreme to the cell penetrating peptide Penetratin. High yields of purified recombinant fused peptides were obtained in both cases; nevertheless, thrombin cleavage reaction was successful only for p53pAnt peptide release. The features of the system, together with the procedure developed, allow achievement of high production yields of over 30 mg of highly pure p53pAnt peptide per g of dry cell mass. It is proposed that the system could be used for production of other peptides at a similar yield. CONCLUSIONS: This study provides a system suitable for recombinant production of peptides for scientific research, including biological assays. BioMed Central 2014-05-07 /pmc/articles/PMC4022411/ /pubmed/24885242 http://dx.doi.org/10.1186/1475-2859-13-65 Text en Copyright © 2014 Rodríguez et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Rodríguez, Vida
Asenjo, Juan A
Andrews, Barbara A
Design and implementation of a high yield production system for recombinant expression of peptides
title Design and implementation of a high yield production system for recombinant expression of peptides
title_full Design and implementation of a high yield production system for recombinant expression of peptides
title_fullStr Design and implementation of a high yield production system for recombinant expression of peptides
title_full_unstemmed Design and implementation of a high yield production system for recombinant expression of peptides
title_short Design and implementation of a high yield production system for recombinant expression of peptides
title_sort design and implementation of a high yield production system for recombinant expression of peptides
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022411/
https://www.ncbi.nlm.nih.gov/pubmed/24885242
http://dx.doi.org/10.1186/1475-2859-13-65
work_keys_str_mv AT rodriguezvida designandimplementationofahighyieldproductionsystemforrecombinantexpressionofpeptides
AT asenjojuana designandimplementationofahighyieldproductionsystemforrecombinantexpressionofpeptides
AT andrewsbarbaraa designandimplementationofahighyieldproductionsystemforrecombinantexpressionofpeptides