Endotoxin-Free E. coli-Based Cell-Free Protein Synthesis: Pre-Expression Endotoxin Removal Approaches for on-Demand Cancer Therapeutic Production.


Journal

Biotechnology journal
ISSN: 1860-7314
Titre abrégé: Biotechnol J
Pays: Germany
ID NLM: 101265833

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 12 03 2018
revised: 12 06 2018
pubmed: 20 7 2018
medline: 15 6 2019
entrez: 20 7 2018
Statut: ppublish

Résumé

Approximately one third of protein therapeutics are produced in Escherichia coli, targeting a wide variety of diseases. However, due to immune recognition of endotoxin (a lipid component in the E. coli cell membrane), these protein products must be extensively purified before application to avoid adverse reactions such as septic shock. E. coli-based cell-free protein synthesis (CFPS), which has emerged as a promising platform for the development and production of enhanced protein therapeutics, provides a unique opportunity to remove endotoxins prior to protein expression due to its open environment and the absence of live cells. Pre-expression endotoxin removal from CFPS reagents could simplify downstream processing, potentially enabling on-demand production of unique protein therapeutics. Herein, three strategies for removing endotoxins from E. coli cell lysate are evaluated: Triton X-114 two-phase extraction, polylysine affinity chromatography, and extract preparation from genetically engineered, endotoxin-free ClearColi cells. It is demonstrated that current protocols for endotoxin removal treatments insufficiently reduce endotoxin and significantly reduce protein synthesis yields. Further, the first adaptation of ClearColi cells to prepare cell-free extract with high protein synthesis capability is demonstrated. Finally, production of the acute lymphoblastic leukemia therapeutic crisantaspase from reduced-endotoxin extract and endotoxin-free ClearColi extract is demonstrated.

Identifiants

pubmed: 30024107
doi: 10.1002/biot.201800271
doi:

Substances chimiques

Endotoxins 0
Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1800271

Subventions

Organisme : National Science Foundation Graduate Research Fellowship Program
ID : 1247046
Organisme : National Science Foundation CBET Division CAREER Award
ID : 1254148

Informations de copyright

© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Auteurs

Kristen M Wilding (KM)

Chemical Engineering, Brigham Young University, 350 Clyde, Provo, UT 84602, USA.

John P Hunt (JP)

Chemical Engineering, Brigham Young University, 350 Clyde, Provo, UT 84602, USA.

Joshua W Wilkerson (JW)

Chemical Engineering, Brigham Young University, 350 Clyde, Provo, UT 84602, USA.

Parker J Funk (PJ)

Chemical Engineering, Brigham Young University, 350 Clyde, Provo, UT 84602, USA.

Rebecca L Swensen (RL)

Chemical Engineering, Brigham Young University, 350 Clyde, Provo, UT 84602, USA.

William C Carver (WC)

Chemical Engineering, Brigham Young University, 350 Clyde, Provo, UT 84602, USA.

Michael L Christian (ML)

Chemical Engineering, Brigham Young University, 350 Clyde, Provo, UT 84602, USA.

Bradley C Bundy (BC)

Chemical Engineering, Brigham Young University, 350 Clyde, Provo, UT 84602, USA.

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Classifications MeSH