Escherichia coli‐based cell‐free synthesis of virus‐like particles

Virus‐like particles (VLP) have received considerable attention for vaccine, drug delivery, gene therapy and material science applications. Although the number of unique VLP and their applications are rapidly growing, the positive impact of VLP applications is limited by the current diverse, expensive, and typically low‐yielding production technologies available. These technologies, when scaled, often result in structurally and compositionally inconsistent products. We present Escherichia coli‐based cell‐free protein synthesis as a production technology to overcome many of the limitations of current VLP production processes. Using this technique, the MS2 bacteriophage coat protein VLP was produced at a yield 14 times the best published production yield. Also, a C‐terminally truncated Hepatitis B core protein VLP was produced at similarly high yields (6 × 1013 VLP/mL). These VLP were found to have comparable characteristics to those produced in vivo. The scalability of this technology was tested without loss in production yields. To our knowledge, this is the first time a prokaryote‐based in vitro transcription/translation system has generated a virus‐like particle. Biotechnol. Bioeng. 2008;100: 28–37. Biotechnol. Bioeng. 2008;100: 28–37. © 2007 Wiley Periodicals, Inc.

[1]  J. Dunn,et al.  ompT encodes the Escherichia coli outer membrane protease that cleaves T7 RNA polymerase during purification , 1988, Journal of bacteriology.

[2]  D. Peabody,et al.  Encapsidation of heterologous RNAs by bacteriophage MS2 coat protein. , 1993, Nucleic acids research.

[3]  Bruce E. Gnade,et al.  Cowpea Mosaic Virus as a Scaffold for 3-D Patterning of Gold Nanoparticles , 2004 .

[4]  V. Erdmann,et al.  The potentials of the in vitro protein biosynthesis system. , 1995, Journal of biotechnology.

[5]  K. Woodrow,et al.  Rapid expression of functional genomic libraries. , 2006, Journal of proteome research.

[6]  Daisuke Kiga,et al.  An engineered Escherichia coli tyrosyl–tRNA synthetase for site-specific incorporation of an unnatural amino acid into proteins in eukaryotic translation and its application in a wheat germ cell-free system , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[7]  Barbara Elaine Rothengass Advocating for the quadravalent HPV vaccination, Gardasil, by Merck. , 2007, International journal of pediatric otorhinolaryngology.

[8]  G. Rohrmann,et al.  Physical, Biochemical, and Immunological Properties of Coliphage MS-2 Particles , 1970, Journal of virology.

[9]  D. Peabody A Viral Platform for Chemical Modification and Multivalent Display , 2003, Journal of nanobiotechnology.

[10]  P. Wingfield,et al.  Hepatitis core antigen produced in Escherichia coli: subunit composition, conformational analysis, and in vitro capsid assembly. , 1995, Biochemistry.

[11]  P. Bonner Intermediates of Bacteriophage MS2 Assembly In Vivo , 1974, Journal of virology.

[12]  Trevor Douglas,et al.  Viruses: Making Friends with Old Foes , 2006, Science.

[13]  J. Fastrez,et al.  Production in Saccharomycescerevisiae of MS2 virus-like particles packaging functional heterologous mRNAs. , 2005, Journal of biotechnology.

[14]  C. Suttle Viruses in the sea , 2005, Nature.

[15]  Sai T Reddy,et al.  Targeting dendritic cells with biomaterials: developing the next generation of vaccines. , 2006, Trends in immunology.

[16]  A. Spirin,et al.  Cell-free synthesis and affinity isolation of proteins on a nanomole scale. , 2000, BioTechniques.

[17]  G. Jennings,et al.  Virus‐Like Particles: Combining Innate and Adaptive Immunity for Effective Vaccination , 2004 .

[18]  Trevor Douglas,et al.  Paramagnetic viral nanoparticles as potential high‐relaxivity magnetic resonance contrast agents , 2005, Magnetic resonance in medicine.

[19]  Daniel I. Lipin,et al.  Towards the preparative and large-scale precision manufacture of virus-like particles. , 2005, Trends in biotechnology.

[20]  A. Jegerlehner,et al.  Virus-Like Particles as a Modular System for Novel Vaccines , 2003, Intervirology.

[21]  J. Swartz,et al.  Efficient and scalable method for scaling up cell free protein synthesis in batch mode. , 2005, Biotechnology and bioengineering.

[22]  M. Jewett,et al.  Rapid Expression and Purification of 100 nmol Quantities of Active Protein Using Cell‐Free Protein Synthesis , 2008, Biotechnology progress.

[23]  D. Peabody,et al.  Role of the coat Protein-RNA interaction in the life cycle of bacteriophage MS2 , 1997, Molecular and General Genetics MGG.

[24]  P. Pumpens,et al.  HBV Core Particles as a Carrier for B Cell/T Cell Epitopes , 2001, Intervirology.

[25]  B. Böttcher,et al.  Native display of complete foreign protein domains on the surface of hepatitis B virus capsids. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[26]  P. Stockley,et al.  Cell-specific delivery of bacteriophage-encapsidated ricin A chain. , 1995, Bioconjugate chemistry.

[27]  J. Phillips,et al.  Stability of the recombinant hepatitis B core antigen , 1992, Journal of clinical microbiology.

[28]  Jacob M Hooker,et al.  Interior surface modification of bacteriophage MS2. , 2004, Journal of the American Chemical Society.

[29]  Joseph D Puglisi,et al.  Quantitative polysome analysis identifies limitations in bacterial cell-free protein synthesis. , 2005, Biotechnology and bioengineering.

[30]  M. Bachmann,et al.  Therapeutic vaccines for nicotine dependence. , 2006, Current opinion in molecular therapeutics.

[31]  P. Stockley,et al.  Multiple presentation of foreign peptides on the surface of an RNA-free spherical bacteriophage capsid. , 1993, The Journal of general virology.

[32]  J. Swartz,et al.  Streamlining Escherichia Coli S30 Extract Preparation for Economical Cell‐Free Protein Synthesis , 2008, Biotechnology progress.

[33]  Walter Gilbert,et al.  Hepatitis B virus genes and their expression in E. coli , 1979, Nature.

[34]  D. Hoover,et al.  DNAWorks: an automated method for designing oligonucleotides for PCR-based gene synthesis. , 2002, Nucleic acids research.

[35]  J. Swartz,et al.  An Economical Method for Cell‐Free Protein Synthesis using Glucose and Nucleoside Monophosphates , 2008, Biotechnology progress.

[36]  M. Jewett,et al.  Mimicking the Escherichia coli cytoplasmic environment activates long‐lived and efficient cell‐free protein synthesis , 2004, Biotechnology and bioengineering.

[37]  Peter G Stockley,et al.  Engineering thermal stability in RNA phage capsids via disulphide bonds. , 2005, Journal of nanoscience and nanotechnology.

[38]  P. Wingfield,et al.  Dimorphism of hepatitis B virus capsids is strongly influenced by the C-terminus of the capsid protein. , 1996, Biochemistry.

[39]  A. Zlotnick,et al.  Weak protein-protein interactions are sufficient to drive assembly of hepatitis B virus capsids. , 2002, Biochemistry.

[40]  G. Stubbs,et al.  Inorganic–Organic Nanotube Composites from Template Mineralization of Tobacco Mosaic Virus , 1999 .

[41]  K. C. Klein,et al.  Comparing capsid assembly of primate lentiviruses and hepatitis B virus using cell-free systems. , 2005, Virology.

[42]  L. Gold,et al.  Interactions of Escherichia coli RNA with bacteriophage MS2 coat protein: genomic SELEX. , 2000, Nucleic acids research.

[43]  Chris J. Adams,et al.  RNA Bacteriophage Capsid-Mediated Drug Delivery and Epitope Presentation , 2003, Intervirology.