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...
Autores principales: | , , , , , |
---|---|
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 |