Cargando…

Association of high pressure and alkaline condition for solubilization of inclusion bodies and refolding of the NS1 protein from zika virus

BACKGROUND: Proteins in inclusion bodies (IBs) present native-like secondary structures. However, chaotropic agents at denaturing concentrations, which are widely used for IB solubilization and subsequent refolding, unfold these secondary structures. Removal of the chaotropes frequently causes reagg...

Descripción completa

Detalles Bibliográficos
Autores principales: Rosa da Silva, Cleide Mara, Chura-Chambi, Rosa Maria, Ramos Pereira, Lennon, Cordeiro, Yraima, de Souza Ferreira, Luís Carlos, Morganti, Ligia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291932/
https://www.ncbi.nlm.nih.gov/pubmed/30541520
http://dx.doi.org/10.1186/s12896-018-0486-2
_version_ 1783380309086044160
author Rosa da Silva, Cleide Mara
Chura-Chambi, Rosa Maria
Ramos Pereira, Lennon
Cordeiro, Yraima
de Souza Ferreira, Luís Carlos
Morganti, Ligia
author_facet Rosa da Silva, Cleide Mara
Chura-Chambi, Rosa Maria
Ramos Pereira, Lennon
Cordeiro, Yraima
de Souza Ferreira, Luís Carlos
Morganti, Ligia
author_sort Rosa da Silva, Cleide Mara
collection PubMed
description BACKGROUND: Proteins in inclusion bodies (IBs) present native-like secondary structures. However, chaotropic agents at denaturing concentrations, which are widely used for IB solubilization and subsequent refolding, unfold these secondary structures. Removal of the chaotropes frequently causes reaggregation and poor recovery of bioactive proteins. High hydrostatic pressure (HHP) and alkaline pH are two conditions that, in the presence of low level of chaotropes, have been described as non-denaturing solubilization agents. In the present study we evaluated the strategy of combination of HHP and alkaline pH on the solubilization of IB using as a model an antigenic form of the zika virus (ZIKV) non-structural 1 (NS1) protein. RESULTS: Pressure-treatment (2.4 kbar) of NS1-IBs at a pH of 11.0 induced a low degree of NS1 unfolding and led to solubilization of the IBs, mainly into monomers. After dialysis at pH 8.5, NS1 was refolded and formed soluble oligomers. High (up to 68 mg/liter) NS1 concentrations were obtained by solubilization of NS1-IBs at pH 11 in the presence of arginine (Arg) with a final yield of approximately 80% of total protein content. The process proved to be efficient, quick and did not require further purification steps. Refolded NS1 preserved biological features regarding reactivity with antigen-specific antibodies, including sera of ZIKV-infected patients. The method resulted in an increase of approximately 30-fold over conventional IB solubilization-refolding methods. CONCLUSIONS: The present results represent an innovative non-denaturing protein refolding process by means of the concomitant use of HHP and alkaline pH. Application of the reported method allowed the recovery of ZIKV NS1 at a condition that maintained the antigenic properties of the protein. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12896-018-0486-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6291932
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-62919322018-12-17 Association of high pressure and alkaline condition for solubilization of inclusion bodies and refolding of the NS1 protein from zika virus Rosa da Silva, Cleide Mara Chura-Chambi, Rosa Maria Ramos Pereira, Lennon Cordeiro, Yraima de Souza Ferreira, Luís Carlos Morganti, Ligia BMC Biotechnol Research Article BACKGROUND: Proteins in inclusion bodies (IBs) present native-like secondary structures. However, chaotropic agents at denaturing concentrations, which are widely used for IB solubilization and subsequent refolding, unfold these secondary structures. Removal of the chaotropes frequently causes reaggregation and poor recovery of bioactive proteins. High hydrostatic pressure (HHP) and alkaline pH are two conditions that, in the presence of low level of chaotropes, have been described as non-denaturing solubilization agents. In the present study we evaluated the strategy of combination of HHP and alkaline pH on the solubilization of IB using as a model an antigenic form of the zika virus (ZIKV) non-structural 1 (NS1) protein. RESULTS: Pressure-treatment (2.4 kbar) of NS1-IBs at a pH of 11.0 induced a low degree of NS1 unfolding and led to solubilization of the IBs, mainly into monomers. After dialysis at pH 8.5, NS1 was refolded and formed soluble oligomers. High (up to 68 mg/liter) NS1 concentrations were obtained by solubilization of NS1-IBs at pH 11 in the presence of arginine (Arg) with a final yield of approximately 80% of total protein content. The process proved to be efficient, quick and did not require further purification steps. Refolded NS1 preserved biological features regarding reactivity with antigen-specific antibodies, including sera of ZIKV-infected patients. The method resulted in an increase of approximately 30-fold over conventional IB solubilization-refolding methods. CONCLUSIONS: The present results represent an innovative non-denaturing protein refolding process by means of the concomitant use of HHP and alkaline pH. Application of the reported method allowed the recovery of ZIKV NS1 at a condition that maintained the antigenic properties of the protein. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12896-018-0486-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-12 /pmc/articles/PMC6291932/ /pubmed/30541520 http://dx.doi.org/10.1186/s12896-018-0486-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Article
Rosa da Silva, Cleide Mara
Chura-Chambi, Rosa Maria
Ramos Pereira, Lennon
Cordeiro, Yraima
de Souza Ferreira, Luís Carlos
Morganti, Ligia
Association of high pressure and alkaline condition for solubilization of inclusion bodies and refolding of the NS1 protein from zika virus
title Association of high pressure and alkaline condition for solubilization of inclusion bodies and refolding of the NS1 protein from zika virus
title_full Association of high pressure and alkaline condition for solubilization of inclusion bodies and refolding of the NS1 protein from zika virus
title_fullStr Association of high pressure and alkaline condition for solubilization of inclusion bodies and refolding of the NS1 protein from zika virus
title_full_unstemmed Association of high pressure and alkaline condition for solubilization of inclusion bodies and refolding of the NS1 protein from zika virus
title_short Association of high pressure and alkaline condition for solubilization of inclusion bodies and refolding of the NS1 protein from zika virus
title_sort association of high pressure and alkaline condition for solubilization of inclusion bodies and refolding of the ns1 protein from zika virus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291932/
https://www.ncbi.nlm.nih.gov/pubmed/30541520
http://dx.doi.org/10.1186/s12896-018-0486-2
work_keys_str_mv AT rosadasilvacleidemara associationofhighpressureandalkalineconditionforsolubilizationofinclusionbodiesandrefoldingofthens1proteinfromzikavirus
AT churachambirosamaria associationofhighpressureandalkalineconditionforsolubilizationofinclusionbodiesandrefoldingofthens1proteinfromzikavirus
AT ramospereiralennon associationofhighpressureandalkalineconditionforsolubilizationofinclusionbodiesandrefoldingofthens1proteinfromzikavirus
AT cordeiroyraima associationofhighpressureandalkalineconditionforsolubilizationofinclusionbodiesandrefoldingofthens1proteinfromzikavirus
AT desouzaferreiraluiscarlos associationofhighpressureandalkalineconditionforsolubilizationofinclusionbodiesandrefoldingofthens1proteinfromzikavirus
AT morgantiligia associationofhighpressureandalkalineconditionforsolubilizationofinclusionbodiesandrefoldingofthens1proteinfromzikavirus