Impact of physicochemical parameters on in vitro assembly and disassembly kinetics of recombinant triple‐layered rotavirus‐like particles

Virus‐like particles constitute potentially relevant vaccine candidates. Nevertheless, their behavior in vitro and assembly process needs to be understood in order to improve their yield and quality. In this study we aimed at addressing these issues and for that purpose triple‐ and double‐layered rotavirus‐like particles (TLP 2/6/7 and DLP 2/6, respectively) size and zeta potential were measured using dynamic light scattering at different physicochemical conditions, namely pH, ionic strength, and temperature. Both TLP and DLP were stable within a pH range of 3–7 and at 5–25°C. Aggregation occurred at 35–45°C and their disassembly became evident at 65°C. The isoelectric points of TLP and DLP were 3.0 and 3.8, respectively. In vitro kinetics of TLP disassembly was monitored. Ionic strength, temperature, and the chelating agent employed determined disassembly kinetics. Glycerol (10%) stabilized TLP by preventing its disassembly. Disassembled TLP was able to reassemble by dialysis at high calcium conditions. VP7 monomers were added to DLP in the presence of calcium to follow in vitro TLP assembly kinetics; its assembly rate being mostly affected by pH. Finally, DLP and TLP were found to coexist under certain conditions as determined from all reaction products analyzed by capillary electrophoresis. Overall, these results contribute to the design of new strategies for the improvement of TLP yield and quality by reducing the VP7 detachment from TLP. Biotechnol. Bioeng. 2009; 104: 674–686 © 2009 Wiley Periodicals, Inc.

[1]  P M Alves,et al.  Downstream processing of triple layered rotavirus like particles. , 2007, Journal of biotechnology.

[2]  Mauricio G Mateu,et al.  In Vitro Disassembly of a Parvovirus Capsid and Effect on Capsid Stability of Heterologous Peptide Insertions in Surface Loops* , 2004, Journal of Biological Chemistry.

[3]  W. D. Wilson,et al.  The influence of ionic strength on the interaction of viruses with charged surfaces under environmental conditions. , 2006, Journal of colloid and interface science.

[4]  M. Stanley,et al.  Expression of human papillomavirus type 16 L1 protein in Escherichia coli: denaturation, renaturation, and self-assembly of virus-like particles in vitro. , 1998, Virology.

[5]  J. Pipas,et al.  Chaperone-mediated in vitro assembly of Polyomavirus capsids , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[6]  J. Mena,et al.  Quantification of rotavirus-like particles by gel permeation chromatography. , 2005, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[7]  P. Cruz,et al.  Removal of envelope protein-free retroviral vectors by anion-exchange chromatography to improve product quality. , 2008, Journal of separation science.

[8]  R. Zinkernagel,et al.  The influence of antigen organization on B cell responsiveness. , 1993, Science.

[9]  M. Lorrot,et al.  Ionic Strength- and Temperature-Induced KCa Shifts in the Uncoating Reaction of Rotavirus Strains RF and SA11: Correlation with Membrane Permeabilization , 2002, Journal of Virology.

[10]  P. Dormitzer,et al.  Assembly of Highly Infectious Rotavirus Particles Recoated with Recombinant Outer Capsid Proteins , 2006, Journal of Virology.

[11]  K. Jansen,et al.  Disassembly and reassembly of yeast-derived recombinant human papillomavirus virus-like particles (HPV VLPs). , 2006, Journal of pharmaceutical sciences.

[12]  A. Lenhoff,et al.  Sorption processes in ion-exchange chromatography of viruses. , 2007, Journal of chromatography. A.

[13]  M J Doktycz,et al.  Automated image analysis of atomic force microscopy images of rotavirus particles. , 2006, Ultramicroscopy.

[14]  D. Volkin,et al.  Stabilization of human papillomavirus virus-like particles by non-ionic surfactants. , 2005, Journal of pharmaceutical sciences.

[15]  T. Vedvick,et al.  Conformational Stability and Disassembly of Norwalk Virus-like Particles , 2006, Journal of Biological Chemistry.

[16]  A. Kamen,et al.  Stability of Serum‐Free and Purified Baculovirus Stocks under Various Storage Conditions , 2006, Biotechnology progress.

[17]  S. Stahl,et al.  A theoretical model successfully identifies features of hepatitis B virus capsid assembly. , 1999, Biochemistry.

[18]  J. Mccormick,et al.  Hydrodynamic diameters of RNA tumor viruses. Studies by laser beat frequency light scattering spectroscopy of avian myeloblastosis and Rauscher murine leukemia viruses. , 1975, Biochemistry.

[19]  M. Grace,et al.  Comparative thermal stabilities of recombinant adenoviruses and hexon protein. , 2005, Biochimica et biophysica acta.

[20]  H. Petry,et al.  Characterization of virus-like particle assembly for DNA delivery using asymmetrical flow field-flow fractionation and light scattering. , 2008, Analytical biochemistry.

[21]  R. Glass,et al.  Immunogenicity of a thermally inactivated rotavirus vaccine in mice , 2008, Human vaccines.

[22]  H. Handa,et al.  Purification and characterization of virus-like particles and pentamers produced by the expression of SV40 capsid proteins in insect cells. , 1996, Biochimica et biophysica acta.

[23]  A. Zlotnick,et al.  Mechanism of capsid assembly for an icosahedral plant virus. , 2000, Virology.

[24]  G. Bai,et al.  Thermodynamics of micellization of alkylimidazolium surfactants in aqueous solution , 2008 .

[25]  James N Culver,et al.  Tobacco mosaic virus assembly and disassembly: determinants in pathogenicity and resistance. , 2002, Annual review of phytopathology.

[26]  W Wang,et al.  Instability, stabilization, and formulation of liquid protein pharmaceuticals. , 1999, International journal of pharmaceutics.

[27]  H. Jeske,et al.  Disassembly of African cassava mosaic virus. , 2008, The Journal of general virology.

[28]  T. Ranheim,et al.  Citrate-mediated disaggregation of rotavirus particles in RotaTeq vaccine. , 2006, Antiviral research.

[29]  J. Mena,et al.  Population kinetics during simultaneous infection of insect cells with two different recombinant baculoviruses for the production of rotavirus-like particles , 2007, BMC biotechnology.

[30]  F. Liprandi,et al.  Antibodies to Rotavirus Outer Capsid Glycoprotein VP7 Neutralize Infectivity by Inhibiting Virion Decapsidation , 2002, Journal of Virology.

[31]  Laura A Palomares,et al.  Strategies for manipulating the relative concentration of recombinant rotavirus structural proteins during simultaneous production by insect cells. , 2002, Biotechnology and bioengineering.

[32]  Adam Zlotnick,et al.  Observed Hysteresis of Virus Capsid Disassembly Is Implicit in Kinetic Models of Assembly* , 2003, The Journal of Biological Chemistry.

[33]  M. Estes,et al.  Rotavirus proteins: structure and assembly. , 2006, Current topics in microbiology and immunology.

[34]  K. Moe,et al.  The effects of relative humidity and temperature on the survival of human rotavirus in faeces , 2005, Archives of Virology.

[35]  M. Estes,et al.  Heterotypic protection from rotavirus infection in mice vaccinated with virus-like particles. , 1999, Vaccine.

[36]  L. Babiuk,et al.  Assembly of recombinant rotavirus proteins into virus-like particles and assessment of vaccine potential. , 1993, Vaccine.

[37]  L. Babiuk,et al.  In vitro assembly of the outer capsid of bovine rotavirus is calcium-dependent. , 1988, Virology.

[38]  Paula M Alves,et al.  Sodium dodecyl sulfate-capillary gel electrophoresis analysis of rotavirus-like particles. , 2008, Journal of chromatography. A.

[39]  L. Gilbert,et al.  Disassembly of structurally modified viral nanoparticles: characterization by fluorescence correlation spectroscopy. , 2005, Comptes rendus biologies.

[40]  A. Charpilienne,et al.  Cell lines susceptible to infection are permeabilized by cleaved and solubilized outer layer proteins of rotavirus. , 1997, The Journal of general virology.

[41]  W. Tan,et al.  Recombinant hepatitis B virus core particles: association, dissociation and encapsidation of green fluorescent protein. , 2008, Journal of virological methods.

[42]  Paula M Alves,et al.  Triple layered rotavirus VLP production: kinetics of vector replication, mRNA stability and recombinant protein production. , 2005, Journal of biotechnology.

[43]  S J Prestrelski,et al.  Factors affecting short-term and long-term stabilities of proteins. , 2001, Advanced drug delivery reviews.

[44]  A. Middelberg,et al.  Quantitative analysis of virus‐like particle size and distribution by field‐flow fractionation , 2008, Biotechnology and bioengineering.

[45]  R. Garcea,et al.  In vitro papillomavirus capsid assembly analyzed by light scattering. , 2004, Virology.

[46]  Manuel J T Carrondo,et al.  Purification of recombinant rotavirus VP7 glycoprotein for the study of in vitro rotavirus-like particles assembly. , 2008, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[47]  D. Leclerc,et al.  A method for in vitro assembly of hepatitis C virus core protein and for screening of inhibitors. , 2007, Analytical biochemistry.

[48]  T. Lin,et al.  Contribution of the surface free energy perturbation to protein-solvent interactions. , 1994, Biochemistry.

[49]  S. Ahmadian,et al.  Morphological study of the role of calcium in the assembly of the rotavirus outer capsid protein VP7. , 1999, Biotechnic & histochemistry : official publication of the Biological Stain Commission.

[50]  V. Vogt,et al.  Characterization of Rous Sarcoma Virus Gag Particles Assembled In Vitro , 2001, Journal of Virology.

[51]  Marcus Niebert,et al.  Towards the preparative and large-scale precision manufacture of virus-like particles. , 2005, Trends in biotechnology.

[52]  M. Estes,et al.  Rotavirus gene structure and function. , 1989, Microbiological reviews.

[53]  S. N. Timasheff,et al.  The control of protein stability and association by weak interactions with water: how do solvents affect these processes? , 1993, Annual review of biophysics and biomolecular structure.

[54]  A. Charpilienne,et al.  The concentration of Ca2+ that solubilizes outer capsid proteins from rotavirus particles is dependent on the strain , 1996, Journal of virology.

[55]  R Smith,et al.  Biochemical and immunologic comparison of virus-like particles for a rotavirus subunit vaccine. , 1999, Vaccine.

[56]  D. Skoog Fundamentals of analytical chemistry , 1963 .

[57]  J. Mccormick,et al.  Electrophoretic mobilities of RNA tumor viruses. Studies by Doppler-shifted light scattering spectroscopy. , 1975, Biochemistry.

[58]  Laurence Lavelle,et al.  The disassembly, reassembly and stability of CCMV protein capsids. , 2007, Journal of virological methods.

[59]  S. Harrison,et al.  Purified recombinant rotavirus VP7 forms soluble, calcium-dependent trimers. , 2000, Virology.