Synthesis and Assembly of Hepatitis B Virus-Like Particles in a Pichia pastoris Cell-Free System

Virus-like particles (VLPs) are supramolecular protein assemblies with the potential for unique and exciting applications in synthetic biology and medicine. Despite the attention VLPs have gained thus far, considerable limitations still persist in their production. Poorly scalable manufacturing tech...

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Main Authors: Alex J. Spice, Rochelle Aw, Daniel G. Bracewell, Karen M. Polizzi
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-02-01
Series:Frontiers in Bioengineering and Biotechnology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fbioe.2020.00072/full
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author Alex J. Spice
Alex J. Spice
Rochelle Aw
Rochelle Aw
Daniel G. Bracewell
Karen M. Polizzi
Karen M. Polizzi
author_facet Alex J. Spice
Alex J. Spice
Rochelle Aw
Rochelle Aw
Daniel G. Bracewell
Karen M. Polizzi
Karen M. Polizzi
author_sort Alex J. Spice
collection DOAJ
description Virus-like particles (VLPs) are supramolecular protein assemblies with the potential for unique and exciting applications in synthetic biology and medicine. Despite the attention VLPs have gained thus far, considerable limitations still persist in their production. Poorly scalable manufacturing technologies and inconsistent product architectures continue to restrict the full potential of VLPs. Cell-free protein synthesis (CFPS) offers an alternative approach to VLP production and has already proven to be successful, albeit using extracts from a limited number of organisms. Using a recently developed Pichia pastoris-based CFPS system, we have demonstrated the production of the model Hepatitis B core antigen VLP as a proof-of-concept. The VLPs produced in the CFPS system were found to have comparable characteristics to those previously produced in vivo and in vitro. Additionally, we have developed a facile and rapid synthesis, assembly and purification methodology that could be applied as a rapid prototyping platform for vaccine development or synthetic biology applications. Overall the CFPS methodology allows far greater throughput, which will expedite the screening of optimal assembly conditions for more robust and stable VLPs. This approach could therefore support the characterization of larger sample sets to improve vaccine development efficiency.
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spelling doaj.art-135577779d2848fda05dce69ca0542822022-12-22T03:14:50ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852020-02-01810.3389/fbioe.2020.00072494686Synthesis and Assembly of Hepatitis B Virus-Like Particles in a Pichia pastoris Cell-Free SystemAlex J. Spice0Alex J. Spice1Rochelle Aw2Rochelle Aw3Daniel G. Bracewell4Karen M. Polizzi5Karen M. Polizzi6Department of Chemical Engineering, Imperial College London, London, United KingdomThe Imperial College Centre for Synthetic Biology Imperial College London, London, United KingdomDepartment of Chemical Engineering, Imperial College London, London, United KingdomThe Imperial College Centre for Synthetic Biology Imperial College London, London, United KingdomDepartment of Biochemical Engineering, University College London, London, United KingdomDepartment of Chemical Engineering, Imperial College London, London, United KingdomThe Imperial College Centre for Synthetic Biology Imperial College London, London, United KingdomVirus-like particles (VLPs) are supramolecular protein assemblies with the potential for unique and exciting applications in synthetic biology and medicine. Despite the attention VLPs have gained thus far, considerable limitations still persist in their production. Poorly scalable manufacturing technologies and inconsistent product architectures continue to restrict the full potential of VLPs. Cell-free protein synthesis (CFPS) offers an alternative approach to VLP production and has already proven to be successful, albeit using extracts from a limited number of organisms. Using a recently developed Pichia pastoris-based CFPS system, we have demonstrated the production of the model Hepatitis B core antigen VLP as a proof-of-concept. The VLPs produced in the CFPS system were found to have comparable characteristics to those previously produced in vivo and in vitro. Additionally, we have developed a facile and rapid synthesis, assembly and purification methodology that could be applied as a rapid prototyping platform for vaccine development or synthetic biology applications. Overall the CFPS methodology allows far greater throughput, which will expedite the screening of optimal assembly conditions for more robust and stable VLPs. This approach could therefore support the characterization of larger sample sets to improve vaccine development efficiency.https://www.frontiersin.org/article/10.3389/fbioe.2020.00072/fullcell-free protein synthesisvirus-like particlesPichia pastorissynthetic biologyhepatitis B core antigen
spellingShingle Alex J. Spice
Alex J. Spice
Rochelle Aw
Rochelle Aw
Daniel G. Bracewell
Karen M. Polizzi
Karen M. Polizzi
Synthesis and Assembly of Hepatitis B Virus-Like Particles in a Pichia pastoris Cell-Free System
Frontiers in Bioengineering and Biotechnology
cell-free protein synthesis
virus-like particles
Pichia pastoris
synthetic biology
hepatitis B core antigen
title Synthesis and Assembly of Hepatitis B Virus-Like Particles in a Pichia pastoris Cell-Free System
title_full Synthesis and Assembly of Hepatitis B Virus-Like Particles in a Pichia pastoris Cell-Free System
title_fullStr Synthesis and Assembly of Hepatitis B Virus-Like Particles in a Pichia pastoris Cell-Free System
title_full_unstemmed Synthesis and Assembly of Hepatitis B Virus-Like Particles in a Pichia pastoris Cell-Free System
title_short Synthesis and Assembly of Hepatitis B Virus-Like Particles in a Pichia pastoris Cell-Free System
title_sort synthesis and assembly of hepatitis b virus like particles in a pichia pastoris cell free system
topic cell-free protein synthesis
virus-like particles
Pichia pastoris
synthetic biology
hepatitis B core antigen
url https://www.frontiersin.org/article/10.3389/fbioe.2020.00072/full
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