Patent Application
20130067807
The present invention relates to methods of preparing plant-derived proteins. More specifically, the present invention provides methods to obtain proteins, including protein suprastructures, from plants and plant tissues.
Current recombinant expression strategies in host cells such as E. coli, insect cell culture, and mammalian cell culture express and secrete proteins at very high level in the culture media. Using these systems high levels of expression, proper protein folding and post-translational modification of proteins, is achieved. Furthermore, purification of the expressed protein is simplified since intracellular proteins may be readily segregated from other components (DNA, vesicle, membranes, pigments, and so on). For plant or yeast expression systems, the cell wall prevents secretion of expressed protein into the culture media.
Different approaches are widely used in science to generate cell-extracts. Mechanical approaches to disrupt cell wall and liberate its content are not usually selective for certain class of protein or cellular components. Directing expression of a protein of interest into the cell culture media, allowing intracellular contaminants to be removed by centrifugation or by filtration, allow simple and fast enrichment of the protein of interest. It may also be desirable to separate the a protein or a protein suprastructure of interest, including protein rosettes, nanoparticles, large protein complexes, antibodies or virus-like particles (VLPs), and the like, from some, or all of the proteins, DNA, membrane fragments, vesicles, pigments, carbohydrates, etc. present in the plant or plant matter before the protein suprastructure of interest is used in vaccine formulation.
Immunoglobulins (IgGs) are complex heteromultimeric proteins with characteristic affinity for specific antigenic counterparts of various natures. Today, routine isolation of IgG-producing cell lines, and the advent of technologies for IgG directed evolution and molecular engineering have profoundly impacted their evolution as biotherapeutics and in the general life science market. Therapeutic monoclonal IgG (monoclonal antibodies, mAbs) dominate the current market of new anti-inflammatory and anti-cancer drugs and hundreds of new candidates are currently under research and clinical development for improved or novel applications. The annual market demand for mAbs ranges from a few grams (diagnostics), a few kilograms (anti-toxin) to up to one or several hundreds of kilograms (bio-defense, anti-cancer, anti-infectious, anti-inflammatory). Methods to produce modified glycoproteins from plants is described in WO 2008/151440 (which is incorporated herein by reference).
A method for extracting protein from the intercellular space of plants, comprising a vacuum and centrifugation process to provide an interstitial fluid extract comprising the protein of interest is described in PCT Publication WO 00/09725 (to Turpen et al.). This approach is suitable for small proteins (of 50 kDa or smaller) that pass through network of microfibers under vacuum and centrifugation, but is not suitable for larger proteins, superstructure proteins, protein rosettes, nanoparticles, large protein complexes, such as antibodies or VLPs.
McCormick et al 1999 (Proc Natl Acad Sci USA 96:703-708) discloses use of a rice amylase signal peptide fused to a single-chain Fv (scFv) epitope to target the expressed protein to the extracellular compartment, followed by vacuum infiltration of leaf and stem tissue for recovery of the scFv polypeptides. Moehnke et al., 2008 (Biotechnol Lett 30:1259-1264) describes use of the vacuum infiltration method of McCormick to obtain a recombinant plant allergen from tobacco using an apoplastic extraction. PCT Publication WO 2003/025124 (to Zhang et al) discloses expression of scFv immunoglobulins in plants, targeting to the apoplastic space using murine signal sequences.
Virus-like particles (VLPs) may be employed to prepare influenza vaccines. Suprastructures such as VLPs mimic the structure of the viral capsid, but lack a genome, and thus cannot replicate or provide a means for a secondary infection. VLPs offer an improved alternative to isolated (soluble) recombinant antigens for stimulating a strong immune response. VLPs are assembled upon expression of specific viral proteins and present an external surface resembling that of their cognate virus but, unlike true viral particle, do not incorporate genetic material. The presentation of antigens in a particulate and multivalent structure similar to that of the native virus achieves an enhanced stimulation of the immune response with balanced humoral and cellular components. Such improvement over the stimulation by isolated antigens is believed to be particularly true for enveloped viruses as enveloped VLPs present the surface antigens in their natural membrane-bound state (Grgacic and Anderson, 2006, Methods 40, 60-65). Furthermore, Influenza VLPs, with their nanoparticle organization, have been shown to be better vaccine candidates compared to recombinant hemagglutinin HA (i.e. monomeric HA, or HA organized into rosettes; assembly of 3-8 trimers of HA), and they are able to activate both humoral and cellular immune response. (Bright, R. A., et. al., 2007, Vaccine 25, 3871-3878).
Influenza VLPs have been obtained in cultured mammalian cells from the co-expression of all 10 influenza proteins (Mena et al., 1996, J. Virol. 70, 5016-5024). Several viral proteins are dispensable for the production of VLPs, and influenza VLPs in vaccine development programs have been produced from the co-expression of the 2 major antigenic envelope proteins (HA and NA) with M1 or from the co-expression of HA and M1 only (Kang et al., 2009, Virus Res. 143, 140-146). Chen et al. (2007, J. Virol. 81, 7111-7123) have shown that HA alone is capable of driving VLP formation and budding and M1 co-expression could be omitted in their system. However, since HA was found to bind to sialylated glycoproteins on the surface of the mammalian cells producing the VLPs, a viral sialidase was co-expressed to allow the release of VLPs from the producing cell after budding.
PCT Publication WO 2006/119516 (to Williamson and Rybicki) discloses expression of full length and truncated human-codon optimized H5 HA of Influenza A/Vietnam/1194/2004 in plants. The truncated construct lacks the membrane anchoring domain. The highest accumulation of HA protein was obtained with constructs that targeted to the ER. Constructs lacking a membrane targeting domain did not yield detectable HA. The production of VLPs was not reported.
The production of influenza HA VLPs that comprise a lipid envelope has been previously described by the inventors in WO 2009/009876 and WO 2009/076778 (to D'Aoust et al.; both of which are incorporated herein by reference). For enveloped viruses, it may be advantageous for a lipid layer or membrane to be retained by the virus. The composition of the lipid may vary with the system (e.g. a plant-produced enveloped virus would include plant lipids or phytosterols in the envelope), and may contribute to an improved immune response.
The assembly of enveloped VLPs in transgenic tobacco expressing the HBV surface antigen (HBsAg) was described by Mason et al. (1992, Proc. Natl. Acad. Sci. USA 89, 11745-11749). Plant-produced HBV VLPs were shown to induce potent B- and T-cell immune responses in mice when administered parenterally (Huang et al., 2005, Vaccine 23, 1851-1858) but oral immunization through feeding studies only induced a modest immune response (Smith et al., 2003, Vaccine 21, 4011-4021). Greco (2007, Vaccine 25, 8228-8240) showed that human immunodeficiency virus (HIV) epitopes in fusion with HBsAg accumulated as VLP when expressed in transgenic tobacco and Arabidopsis, creating a bivalent VLP vaccine.
Expression of the viral capsid protein (NVCP) in transgenic tobacco and potato plants resulted in the assembly of non-enveloped VLPs (Mason et al., 1996, Proc. Natl. Acad. Sci. USA 93, 5335-5340). NVCP VLPs have been produced in agroinfiltrated N. benthamiana leaves (Huang et al. 2009, Biotechnol. Bioeng. 103, 706-714) and their immunogenicity upon oral administration demonstrated in mice (Santi et al., 2008, Vaccine 26, 1846-1854). Administration of 2 or 3 doses of raw potatoes containing 215-751 μg of NVCP in the form of VLPs to healthy adult volunteers resulted in development of an immune response in and 95% of the immunized volunteers (Tacket et al. 2000, J. Infect. Dis. 182, 302-305). Non-enveloped VLPs have also been obtained from the expression of HBV core antigen (HBcAg; Huang et al., 2009, Biotechnol. Bioeng. 103, 706-714), and the human papillomavirus (HPV) major capsid protein L1 (Varsani et al., 2003, Arch. Virol. 148, 1771-1786).
A simpler protein, or protein suprastructure production system, for example, one that relies on the expression of only one or a few proteins is desirable. Production of proteins, or protein suprastructures, for example but not limited to protein rosettes, nanoparticles, large protein complexes such as antibodies or VLPs, in plant systems is advantageous, in that plants may be grown in a greenhouse or field, and do not require aseptic tissue culture methods and handling.
Methods of preparing the proteins, or proteins, or suprastructure proteins, that are substantially free of, or easily separated from plant proteins, yet retain the structural and characteristics of the protein are desired.
The present invention relates to methods of preparing plant-derived proteins. More specifically, the present invention provides methods to obtain proteins, including protein suprastructures from plants and plant tissues.
It is an object of the invention to provide an improved method of preparing plant-derived proteins.
The present invention provides a method (A) of preparing plant-derived proteins, or proteins, or suprastructure proteins, comprising obtaining a plant or plant matter comprising the plant-derived proteins, or suprastructure proteins, localized within the apoplast; producing a protoplast and an apoplast fraction, the apoplast fraction comprising plant-derived proteins, or suprastructure proteins; and recovering the apoplast fraction. The method may further comprise a step of purifying the plant derived proteins, or proteins, or suprastructure proteins, from the apoplast fraction. The plant-derived proteins, or proteins, or suprastructure proteins, may be a chimeric plant-derived proteins, or suprastructure protein. The plant-derived proteins, or proteins, or suprastructure proteins, may be heterologous to the plant. The plant derived proteins, or proteins, or suprastructure proteins, may include a protein rosette, a protein complex, a proteasome, a metabolon, a transcription complex, a recombination complex, a photosynthetic complex, a membrane transport complex, a nuclear pore complex, a protein nanoparticle, a glycoprotein, an antibody, a polyclonal antibody, a monoclonal antibody, a single chain monoclonal antibody, a virus like particle, a viral envelope protein, a viral structural protein, a viral capsid protein, and a viral coat protein, a chimeric protein, a chimeric protein complex, a chimeric protein nanoparticle, a chimeric glycoprotein, a chimeric antibody, a chimeric monoclonal antibody, a chimeric single chain monoclonal antibody, a chimeric hemagglutinin, a viral envelope protein, a viral structural protein, a viral capsid protein, and a viral coat protein. The plant derived monoclonal antibody may comprise a chimeric mouse human monoclonal antibody, for example but not limited to C2B8. The plant derived VLPs may comprise influenza hemagglutinin.
The apoplast and protoplast fractions may be produced by treatment of the plant or plant matter by an enzyme composition. The enzyme composition may comprise one or more than one pectinase, one or more than one cellulase, or one or more than one pectinase and one or more than one cellulase. Furthermore, if desired, the enzyme composition does not include a lipase or protease, or the composition does not include an added lipase or protease.
Plant or plant matter may be obtained by growing, harvesting or growing and harvesting the plant. The plant matter may comprise some or all of the plant, one or more than one plant cell, leaves, stems, roots or cultured plant cells.
The present invention provides a method of preparing plant derived proteins, or proteins, or suprastructure proteins, as described above (Method A), wherein a nucleic acid encoding the proteins, or suprastructure proteins, is introduced into the plant in a transient manner. Alternatively, the nucleic acid is stably integrated within a genome of the plant.
The present invention provides a method of preparing plant derived proteins, or suprastructure proteins, as described above (Method A) further comprising a step of purifying the plant derived proteins, or suprastructure proteins, from the apoplast fraction. The step of purifying may comprise filtering the apoplast fraction using depth filtration to produce a clarified extract, followed by chromatography of the clarified extract using a cation exchange resin, affinity chromatography, size exclusion chromatography, or a combination thereof.
Without wishing to be bound by theory, proteins obtained from the apoplast are more homogenous, as the intermediate forms of post-translationally modified proteins, or proteins comprising other types of processing that occurs in various intracellular compartments, for example the mitochondria, chloroplast, and other organelles are not co-extracted. A higher degree of homogeneity of a recombinant protein typically results in a higher quality of a preparation comprising the protein, and may result in a product with beneficial properties including higher potency, longer half-life, or better immunogenic capacity. For example, blood proteins containing high-mannose glycosylation are eliminated in blood circulation more rapidly than proteins comprising complex glycosylation. A glycosylated protein produce in the apoplastic fraction exhibits more complex-type glycosylation. Therefore, an apoplast-derived protein prepared using the methods described herein, involving cell-wall digestion, exhibit, for example, a better half life in circulation.
The plant derived proteins, or suprastructure proteins, may include protein rosettes, protein complexes, protein nanoparticles, antibodies, monoclonal antibodies, VLPs. The VLPs may comprise one or more influenza HA polypeptides. The suprastructure protein may be a chimeric suprastructure protein, for example, the monoclonal antibody may be a chimeric monoclonal antibody, or the influenza HA polypeptide, may be a chimeric HA polypeptide. If the suprastructure protein is a VLP, then the plant-derived VLP may further comprise hemagglutinating activity. Plant or plant matter may be obtained by growing, harvesting or growing and harvesting the plant. The plant matter may comprise some or all of the plant, or one or more than one plant cell, leaves, stems, roots or cultured cells.
The present invention also provides a method (B) of preparing plant derived proteins, or suprastructure proteins, comprising obtaining a plant or plant matter comprising plant-derived proteins, or suprastructure proteins, digesting the plant matter using a cell wall degrading enzyme composition to produced a digested fraction, and filtering the digested fraction to produced a filtered fraction and recovering the plant-derived proteins, or suprastructure proteins, from the filtered fraction.
The enzyme composition may comprise one or more than one pectinase, one or more than one cellulose, or one or more than one pectinase and one or more than one cellulase. Furthermore, if desired, the enzyme composition does not include a lipase or protease, or the composition does not include an added lipase or protease. The plant-derived suprastructure protein may be a chimeric plant-derived suprastructure protein. The plant derived protein suprastructure may include a protein rosette, a protein complex, a proteasome, a metabolon, a transcription complex, a recombination complex, a photosynthetic complex, a membrane transport complex, a nuclear pore complex, a protein nanoparticle, a glycoprotein, an antibody, a polyclonal antibody, a monoclonal antibody, a single chain monoclonal antibody, a virus like particle, a viral envelope protein, a viral structural protein, a viral capsid protein, and a viral coat protein, a chimeric protein, a chimeric protein complex, a chimeric protein nanoparticle, a chimeric glycoprotein, a chimeric antibody, a chimeric monoclonal antibody, a chimeric single chain monoclonal antibody, a chimeric hemagglutinin, a viral envelope protein, a viral structural protein, a viral capsid protein, and a viral coat protein. The plant derived monoclonal antibody may comprise a chimeric mouse human monoclonal antibody, for example but not limited to C2B8. The plant derived VLPs may comprise influenza hemagglutinin.
The present invention provides a method of preparing plant derived proteins, or suprastructure proteins, as described above (Method B), wherein a nucleic acid encoding the proteins, or suprastructure proteins, is introduced into the plant in a transient manner. Alternatively, the nucleic acid is stably integrated within a genome of the plant.
The present invention provides a method of preparing plant derived VLPs as described above (Method B) further comprising a step of separating the proteins, or suprastructure proteins, in the filtered fraction from the cellular debris and insoluble materials. The step of separating may be performed by centrifugation, by depth filtration, or bother centrifugation and depth filtration to produce a clarified fraction. The plant derived proteins, or suprastructure proteins, may be further purified by chromatography, for example, the clarified extract may be purified using a cation exchange resin, an affinity resin, size exclusion chromatograph, or a combination thereof.
The plant derived proteins, or suprastructure proteins, may include protein rosettes, protein complexes, protein nanoparticles, glycoproteins, antibodies, monoclonal antibodies, VLPs. The VLPs may comprise one or more influenza HA polypeptides. The suprastructure protein may be a chimeric suprastructure protein, for example, the monoclonal antibody may be a chimeric monoclonal antibody, or the influenza HA polypeptide, may be a chimeric HA polypeptide. If the suprastructure protein is a VLP, then the plant-derived VLP may further comprise hemagglutinating activity.
Without wishing to be bound by theory, plant-made VLPs comprising plant derived lipids, may induce a stronger immune reaction than VLPs made in other manufacturing systems and that the immune reaction induced by these plant-made VLPs is stronger when compared to the immune reaction induced by live or attenuated whole virus vaccines.
The composition of a protein extract obtained from a host cell is complex and typically comprises intercellular and intracellular components along with a protein or suprastructure of interest that is to be isolated. Preparation of an apoplastic fraction, followed by a step to segregate the intracellular proteins and components is advantageous since the protein or suprastructure of interest can be enriched and increase efficiency within a manufacturing process. Having a simpler process, comprising fewer efficient steps, may result in significant yield increases, and cost reduction. It has also been found that the process of digesting the cell wall using cell wall degrading enzymes increases suprastructure protein yield even if protoplasts do not remain intact during the extraction procedure. Without wishing to be bound by theory, the step of cell wall digestion may loosen the polymeric components of the cells wall and assist in release of the proteins, or suprastructure proteins, otherwise associated within the cell wall. This protocol may also minimize contamination of the proteins, or suprastructure proteins, within intracellular components.
Methods to digest plant cell-wall are known, and enzyme cocktail mixtures that digest cell walls may vary. The present invention is not limited by the cell wall digestion method used.
The methods described herein result in less disruption, and contamination of a plant-derived suprastructure protein extract when compared to methods for preparing plant-derived suprastructure protein involving homogenization, blending or grinding. The methods described herein provide an apoplast fraction of the plant tissue and that may maintain the integrity of protoplasts and their components. The method as described herein is effective in purifying proteins, or suprastructure proteins, even if the protoplasts, or a portion of the protoplasts, lose their integrity and are no longer intact.
These methods provide a higher yield of proteins, or suprastructure proteins, when compared to methods of suprastructure protein extraction involving standard tissue disruption techniques, for example, homogenization, blending or grinding. The greater yield may be due to, in part, a reduction of the shearing forces that disrupt the structural integrity of the proteins, or suprastructure proteins, and in the case of VLPs, the lipid envelope. Preparation of proteins, or suprastructure proteins, from an apoplastic fraction may be advantageous, as apoplastic fractions are significantly reduced, or free of, cytoplasmic proteins. Therefore, separation of the suprastructure protein from other proteins and matter, including monomers, dimmers, trimers or fragments of the suprastructure protein, in the apoplastic fraction is easily carried out. However, increased yields of proteins, or suprastructure proteins, may also be obtained using the methods described herein, even if the protoplast preparation, or a portion of the protoplast preparation, is not intact.
Glycoproteins, including suprastructure glycoproteins, for example monoclonal antibodies, that are secreted into the apoplast comprises a higher percentage of N-glycans that have completed their maturation and comprise terminal N-acetyglucosamine or galactose residues (complex N-glycans), compared to extraction methods that do not digest the cell wall, for example blender extracted plants. Suprastructure glycoproteins, for example monoclonal antibodies, comprising complex N glycans have been found to exhibit the beneficial property of increased half life in the blood stream when compared to monoclonal antibodies comprising terminal mannose residues (immature N glycans).
Using enzymatic digestion of the cells wall, it may be possible to liberate a pool of apoplastic antibodies comprising N-glycans that have completed their maturation. This method of extraction may allow the recovery of an enriched population, or a homogeneous population of glycosylated antibodies bearing complex N-glycans, separating the immature forms of the glycosylated antibodies in the protoplast fraction. If the pool of antibodies bearing immature N-glycans is desired, the protoplast fraction can be retained and antibodies purified from the protoplast fraction.
The VLPs of the present invention are also characterized as exhibiting a greater hemagglutinating activity than those obtained using standard tissue disruption techniques. This improved hemagglutinating activity may result from a greater yield of intact VLPs (fewer HA monomers or trimers free in solution), a greater yield of intact VLPs with intact lipid envelopes, or a combination thereof.
Vaccines made using VLPs provide the advantage, when compared to vaccines made of whole viruses, that they are non-infectious. Therefore, biological containment is not an issue and it is not required for production. Plant-made VLPs provide a further advantage by allowing the expression system to be grown in a greenhouse or field, thus being significantly more economical and suitable for scale-up.
Additionally, plants do not comprise enzymes involved in synthesizing and adding sialic acid residues to proteins. VLPs may be produced in the absence of neuraminidase (NA), and there is no need to co-express NA, or to treat the producing cells or extract with sialidase (neuraminidase), to ensure VLP production in plants
This summary of the invention does not necessarily describe all features of the invention.
These and other features of the invention will become more apparent from the following description in which reference is made to the appended drawings wherein:
The present invention relates to methods of preparing plant-derived proteins. More specifically, the present invention provides methods to obtain proteins, or proteins, or proteins, or suprastructure proteins, from plants and plant tissues.
The following description is of a preferred embodiment.
The present invention provides a method for obtaining a protein, or protein suprastructure of interest. The protein of interest may be present in the apoplast or extracellular compartment, corresponding to the plant cell portion excluding the protoplast/spheroplast compartment. The method involves removing, digesting or both digesting and removing the cellulosic plant cell wall that surrounds plant cells. By digesting the cell wall the polymeric components of the cell wall are loosened, and the protein or proteins, or proteins, or suprastructure proteins, of interest may be more readily released. By using this method, the protein or proteins, or proteins, or suprastructure proteins, of interest is enriched since the protoplast/spheroplast compartment that contains a majorly host-cell proteins and components is segregated from the apoplast. As noted below, the method as provided herein is still effective in obtaining a protein or protein suprastructure of interest, if during the process the integrity of the protoplast/spheroplast compartment is lost, if the protoplast/spheroplast compartment is not intact, and if a portion of host cell proteins and components from the protoplast/spheroplast compartment are present in the apoplast fraction. Using the methods described below, if the integrity of the protoplast/spheroplast compartment is lost, the protein or protein suprastructure may still be separated from intact organelles, including the mitochondria, chloroplast and other organelles, and beneficial results may still be obtained.
By “protein” or “protein of interest” (these terms are used interchangeably), it is meant a protein, or protein subunit encoded by a nucleotide sequence, or coding region, that is to be expressed within a plant or portion of the plant. Proteins may have a molecular weight from about 1 to about 100 kDa or any amount therebetween, for example, 1, 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100 kDa, or any amount therebetween. A protein may be monomeric, dimeric, trimeric, or multimeric.
A protein suprastructure, also termed suprastructure protein, protein superstructure, or superstructure protein, is a protein structure comprised of two or more polypeptides. The polypeptides may be the same, or different; if different, they may be present in a ratio of about 1:1 to about 10:1 or greater. Suprastructure proteins, may include, but are not limited to protein rosettes, protein complexes, protein nanoparticles, glycoproteins, antibodies, polyclonal antibodies, monoclonal antibodies, single chain monoclonal antibodies, or virus like particles, proteasomes, metabolons, transcription complexes, recombination complexes, photosynthetic complexes, membrane transport complexes, nuclear pore complexes, chimeric proteins, chimeric protein complexes, chimeric protein nanoparticles, chimeric glycoproteins, chimeric antibodies, chimeric monoclonal antibodies, chimeric single chain monoclonal antibodies, or chimeric hemagglutinin (HA). If the protein suprastructure is a VLP, the VLP may be selected from the group of viral envelope proteins, viral structural proteins, viral capsid proteins, and viral coat proteins. The plant derived VLPs may comprise influenza (HA).
Typically a protein suprastructure (protein superstructure), when assembled, is large, for example having a molecular weight greater than 75 kDa, for example from about 75 to about 1500 kDa or any molecular weight therebetween. For example, the protein suprastructure may have a molecular weight from about 75, 80, 85, 90, 100, 110, 120, 130, 140, 150, 160, 170, 180, 200, 220, 240, 260, 280, 300, 320, 340, 360, 380, 400, 425, 450, 475, 500, 525, 550, 575, 600, 625, 650, 675, 700, 725, 750, 775, 800, 850, 900, 950, 1000, 1100, 1150, 1200, 1250, 1300, 1350, 1400, 1450, 1500 kDa, or any amount therebetween, Subunits that combine together to make up the protein suprastructure may be of a smaller molecular weight, for example each subunit having a molecular weight from about 1 kDa to about 500 kDa, or any amount therebetween. A protein suprastructure may comprise a protein exhibiting a secondary structure, with one or more amino acids hydrogen bonded, for example with residues in protein helices, a tertiary structure, having a 3-dimensional configuration, or a quaternary structure having an arrangement of multiple folded proteins or coiled protein molecules that form a multi-subunit complex.
A multiprotein complex (or a protein complex) may comprise a group of two or more associated polypeptide chains. If the different polypeptide chains contain different protein domains, then the resulting multiprotein complex can have multiple catalytic functions. The protein complex may also be a multienzyme polypeptide, comprising multiple catalyic domains within a single polypeptide chain. Protein complexes are typically in the form of quaternary structure. Examples of protein complexes that typically may not survive intact using standard protein isolation protocols, but that may be obtained using the methods described herein include proteasomes (for degradation of peptides and proteins), metabolons (for oxidative energy production), ribosomes (for protein synthesis; e.g. as described in Pereira-Leal, J. B.; et. al., 2006, Philos Trans R Soc Lond B Biol Sci., 361(1467):507-517), transcription complexes, recombination complexes, photosynthetic complexes, membrane transport complexes, nuclear pore complexes. The present method may be used to obtained protein complexes that are characterized as having stable or weaker protein domain—protein domain interactions.
Examples of a protein, or a protein suprastructure, include, for example but not limited to, an industrial enzyme for example, cellulase, xylanase, protease, peroxidase, subtilisin, a protein supplement, a nutraceutical, a value-added product, or a fragment thereof for feed, food, or both feed and food use, a pharmaceutically active protein, for example but not limited to growth factors, growth regulators, antibodies, antigens, and fragments thereof, or their derivatives useful for immunization or vaccination and the like. Additional proteins of interest may include, but are not limited to, interleukins, for example one or more than one of IL-1 to IL-24, IL-26 and IL-27, cytokines, Erythropoietin (EPO), insulin, G-CSF, GM-CSF, hPG-CSF, M-CSF or combinations thereof, interferons, for example, interferon-alpha, interferon-beta, interferon-gama, blood clotting factors, for example, Factor VIII, Factor IX, or tPA hGH, receptors, receptor agonists, antibodies, neuropolypeptides, insulin, vaccines, growth factors for example but not limited to epidermal growth factor, keratinocyte growth factor, transformation growth factor, growth regulators, antigens, autoantigens, fragments thereof, or combinations thereof.
A non-limiting example of a protein suprastructure is an antibody. Antibodies are glycoproteins that have a molecular weight from about 100 to about 1000 kDa, or any amount therebetween. Antibodies comprise four polypeptide chains, two light chains and two heavy chains, which are connected by disulfide bonds. For example, which is not to be considered limiting, each light chain may have a molecular weight of approx. 25 kDa, for example from about 20 to about 30 kDa or any amount therebetween, or more for example from about 20 to about 300 kDa or any amount therebewteen, and is composed of two domains, one variable domain (VL) and one constant domain (CL). Each heavy chain may have a molecular weight of approx. 50 kDa, for example from about 30 to about 75 kDa, or any amount therebetween, or more for example from about 30 to about 500 kDa or any amount therebewteen, and consists of a constant and variable region. The heavy and light chains contain a number of homologous sections consisting of similar but not identical groups of amino acid sequences. These homologous units consist of about 110 amino acids and are called immunoglobulin domains. The heavy chain contains one variable domain (VH) and either three or four constant domains (CH1, CH2, CH3, and CH4, depending on the antibody class or isotype). The region between the CH1 and CH2 domains is called the hinge region and permits flexibility between the two Fab arms of the Y-shaped antibody molecule, allowing them to open and close to accommodate binding to two antigenic determinants separated by a fixed distance.
Another non-limiting example of a protein suprastructure is a VLP. The VLP may comprise an HA0 precursor form, or the HA1 or HA2 domains retained together by disulphide bridges form. A VLP may have an average size of about 20 nm to 1 μm, or any amount therebetween, for example 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 120, 130, 140, 150 160, 170, 180, 190, or 200 nm, or any amount therebetween, for example 100 nm, and may include a lipid membrane.
The proteins, or suprastructure proteins, may further comprise one or more lipids, phospholipids, nucleic acids, membranes or the like. Two or more polypeptides may be connected by a covalent bond, a disulfide bridge, charge interaction, hydrophobic attraction, van der waals forces, hydrogen bonds or the like. An example of a protein suprastructure is a monoclonal antibody, a chimeric monoclonal antibody, a single chain monoclonal antibody, or a virus like particle (VLP) which may be enveloped, or non-enveloped, for example, a viral envelope protein, a viral structural protein, a viral capsid protein, or a viral coat protein.
Proteins, or suprastructure proteins, may be produced in suitable host cells including plant host cells, and if desired further purified. While a chimeric monoclonal antibody, an influenza VLP, and chimeric influenza VLP are exemplified herein, the methods described herein may be used for any cytosolic plant-derived protein or suprastructure protein, or any plant-derived protein or suprastructure protein that localize in, or are secreted to, the apoplast.
The present invention also provides a method of preparing plant-derived proteins, or suprastructure proteins. The method involves obtaining a plant or plant matter comprising plant-derived proteins, or suprastructure proteins, localized within the apoplast; producing a protoplast/spheroplast fraction, and an apoplast fraction from the plant matter, the apoplast fraction comprising plant-derived proteins, or suprastructure proteins, and recovering the apoplast fraction. If desired, the plant derived proteins, or suprastructure proteins, may be purified from the apoplast fraction.
The present invention also provides a method of preparing a protein or suprastructure protein, wherein the protein or suprastructure protein comprises a plant derived lipid envelope, for example a VLP comprising a plant-derived lipid envelope. The method includes obtaining a plant, or plant matter comprising the suprastructure protein of interest, for example the VLP, treating the plant or plant matter with an enzyme composition to produce one or more than one apoplastic protein complex and a protoplast/spheroplast fraction, and separating the one or more than one apoplastic protein complex from the protoplast fraction. The one or more than one apoplastic protein complex comprises the suprastructure protein or VLP comprising a plant derived lipid envelope.
The present invention also provides a method of preparing plant derived proteins, or suprastructure proteins, comprising obtaining a plant or plant matter that comprise the plant-derived proteins, or suprastructure proteins, digesting the plant matter using a cell wall degrading enzyme composition to produced a digested fraction, and filtering the digested fraction to produced a filtered fraction and recovering the plant-derived proteins, or suprastructure proteins, from the filtered fraction. In this method, integrity of the protoplasts may not be required.
A protoplast is a plant cell that has had its cell wall completely or partially removed. A spheroplast may have partial removal of the cell wall. A protoplast, a spheroplast, or both a protoplast and spheroplast (protoplast/spheroplast) may be used as described herein, and the terms as used herein are interchangable. The cell wall may be disrupted and removed mechanically (e.g. via homogenization, blending), the cell wall may be fully or partially digested enzymatically, or the cell wall may be removed using a combination of mechanical and enzymatic methods, for example homogenization followed by treatment with enzymes for digestion of the cell wall. Protoplasts may also be obtained from cultured plant cells, for example liquid cultured plant cells, or solid cultured plant cells.
Standard reference works setting forth the general principles of plant tissue culture, cultured plant cells, and production of protoplasts, spheroplasts and the like include: Introduction to Plant Tissue Culture, by MK Razdan 2nd Ed. (Science Publishers, 2003; which is incorporated herein by reference), or see for example, the following URL: molecular-plant-biotechnology.info/plant-tissue-culture/protoplast-isolation.htm. Methods and techniques relating to protoplast (or spheroplast) production and manipulation are reviewed in, for example, Davey M R et al., 2005 (Biotechnology Advances 23:131-171; which is incorporated herein by reference). Standard reference works setting forth the general methods and principles of protein biochemistry, molecular biology and the like include, for example Ausubel et al, Current Protocols In Molecular Biology, John Wiley & Sons, New York (1998 and Supplements to 2001; which is incorporated herein by reference); Sambrook et al, Molecular Cloning: A Laboratory Manual, 2d Ed., Cold Spring Harbor Laboratory Press, Plainview, N.Y., 1989 (which is incorporated herein by reference); Kaufman et al, Eds., Handbook Of Molecular And Cellular Methods In Biology And Medicine, CRC Press, Boca Raton, 1995 (which is incorporated herein by reference); McPherson, Ed., Directed Mutagenesis: A Practical Approach, IRL Press, Oxford, 1991 (which is incorporated herein by reference).
Enzymes useful for digesting or degrading plant cell walls for release or protoplasts or spheroplasts are known to one of skill in the art and may include cellulase (EC 3.2.1.4), pectinase (EC 3.2.1.15), xylanase (EC 3.2.1.8), chitinases (EC 3.2.1.14), hemicellulase, or a combination thereof. Non-limiting examples of suitable enzymes includes a multi-component enzyme mixture comprising cellulase, hemicellulase, and pectinase, for example MACEROZYME™ (containing approximately: Cellulase: 0.1 U/mg, Hemicellulase: 0.25 U/mg, and Pectinase: 0.5 U/mg). Other examples of commercial enzymes, enzyme mixtures and suppliers are listed in Table 1 (see: Introduction to Plant Tissue Culture, by MK Razdan 2nd Ed., Science Publishers, 2003).
Alternate names, and types of cellulases include endo-1,4-β-D-glucanase; β-1,4-glucanase; β-1,4-endoglucan hydrolase; cellulase A; cellulosin AP; endoglucanase D; alkali cellulase; cellulase A 3; celludextrinase; 9.5 cellulase; avicelase; pancellase SS and 1,4-(1,3;1,4)-β-D-glucan 4-glucanohydrolase. Alternate names, and types of pectinases (polygalacturonases) include pectin depolymerase; pectinase; endopolygalacturonase; pectolase; pectin hydrolase; pectin polygalacturonase; endo-polygalacturonase; poly-α-1,4-galacturonide glycanohydrolase; endogalacturonase; endo-D-galacturonase and poly(1,4-α-D-galacturonide) glycanohydrolase. Alternate names, and types of xylanases include hemicellulase, endo-(1→4)-β-xylan 4-xylanohydrolase; endo-1,4-xylanase; xylanase; β-1,4-xylanase; endo-1,4-xylanase; endo-β-1,4-xylanase; endo-1,4-β-D-xylanase; 1,4-β-xylan xylanohydrolase; β-xylanase; β-1,4-xylan xylanohydrolase; endo-1,4-β-xylanase; 3-D-xylanase. Alternate names, and types of chitinases include chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase.
Trichoderma
viride
T. viride
T. viride
T. viride
T. viride
Irpex locteus
T. viride
T. viride
T. viride
Helix pomatia
Aspergillus niger
Rhizopus sp.
Aspergillus niger
Rhizopus
arrhizus
R. arrhizus
A. niger
Bacillus
polymyza
Aspergillus sp.
Aspergillus
joponicus
Arthrobacter
luteus
Choice of a particular enzyme or combination of enzymes, and concentration and reaction conditions may depend on the type of plant tissue used from which the protoplast and apoplast fraction comprising the VLPs is obtained. A mixture of cellulase, hemicellulase and pectinase, for example, a pectinase MACEROZYME™ or Multifect, may be used in a concentration ranging from 0.01% to 2.5% (v/v), for example 0.01, 0.02, 0.04, 0.06, 0.08, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.1, 2.2, 2.3, 2.4, or 2.5% (v/v), or any amount therebetween. MACEROZYME™ or Multifect may be used alone, or in combination with other enzymes, e.g cellulase, pectinase, hemicellulase, or a combination thereof. Cellulase may be used in a concentration ranging from 0.1% to 5%, for example 0.1, 0.25, 0.5, 0.75, 1.0, 1.25, 1.5, 1.75, 2.0, 2.25, 2.5, 2.75. 3.0. 3.25, 3.5, 3.75, 4.0, 4.25, 4.5, 4.75, 5.0% (w/v) or any amount therebetween.
The enzyme solution (alternately referred to as a cell wall degrading composition, digesting solution) will generally comprise a buffer or buffer system, an osmoticum, and one or more than one salts, divalent cations or other additives. The buffer or buffer system is selected to maintain a pH in the range suitable for enzyme activity and the stability of the protein(s), or VLP, to purify, for example, within the range of about pH 5.0 to about 8.0, or any value therebetween. The selected pH used may vary depending upon the VLP to be recovered, for example the pH may be 5.0, 5.2, 5.4, 5.6, 5.8, 6.0, 6.2, 6.4, 6.6, 6.8, 7.0, 7.2, 7.4, 7.6, 7.8, 8.0, or any pH therebetween. Examples of buffers or buffer systems include, but are not limited to, MES, phosphate, citrate and the like. One or more buffers or buffer systems may be combined in an enzyme solution (digesting solution); the one or more buffers may be present at a concentration from 0 mM to about 200 mM, or any amount therebetween, for example 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 110, 120, 130, 140, 150, 160, 170, 180 or 190 mM or any amount therebetween. Depending on the suitability, an osmoticum component can be added if desired. The osmoticum and its concentration are selected to raise the osmotic strength of the enzyme solution. Examples of osmoticum include mannitol, sorbitol or other sugar alcohols, polyethylene glycol (PEG) of varying polymer lengths, and the like. Concentration ranges of osmoticum may vary depending on the plant species, the type of osmoticum used, and the type of plant tissue selected (species or organ of origin e.g. leaf or stem)—generally the range is from 0M to about 0.8 M, for example 0.05, 0.1, 0.15, 0.2, 0.25, 0.3. 0.35, 0.4, 0.5, 0.6, 0.7, or 0.75 M, or any amount therebetween, for example, 0, 50, 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600 nM mannitol, or any amount therebetween. The concentration of osmoticum may also be expressed as a percentage (w/v). For some plant or tissue types, it may be beneficial to employ a slightly hypertonic preparation, which may facilitate separation of plant cell plasma membrane from the cell wall. The osmoticum can also be omitted during digestion.
Another parameter to set for the plant digestion is the temperature. Temperature may be controlled if desired during the digestion process. Useful temperature range should be between 4° C. and 40° C. or any temperature therebetween, for example from about 4° C. to about 15° C., or any amount therebetween, or from about 4° C. to about 22° C., or any temperature therebetween. Depending to the temperature chosen, the other digestion experimental parameters may be adjusted to maintain optimal extraction conditions.
Cations, salts or both may be added to improve plasma membrane stability, for example divalent cations, such as Ca2+, or Mg2+, at 0.5-50 mM, or any amount therebetween, salts, for example CaCl2, NaCl, CuSO4, KNO3, and the like, from about 0 to about 750 mM, or any amount therebetween, for example 10, 20, 30, 40, 50, 100, 200, 300, 400, 500, 600, 700 or 750 mM. Other additives may also be added including a chelator for example, but not limited to, EDTA, EGTA, from about 0 to about 200 mM, or any amount therebetween, for example 5, 10, 15, 20, 25, 50, 75, 100, 125, 150, 175, 200 mM, or any amount therebetween, a reducing agent to prevent oxidation such as, but not limited to, sodium bisulfite or ascorbic acid, at 0.005-0.4% or any amount therebetween, for example 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4%, or any amount therebetween, specific enzyme inhibitors (see below), and if desired, an inhibitor of foliar senescence, for example, cycloheximide, kinetin, or one or more polyamines.
The digestion solution may also comprise one or more of mannitol from about 0 to about 600 mM, NaCl from about 0 to about 500 mM, EDTA from about 0 to about 50 mM, cellulose from about 1% to about 2% v/v, pectinase from about 0 to about 1% v/v, sodium metabisulfite from about 0.03 to about 0.04%, citrate from about 0 to about 125 mM or NaPO4 from about 0 to 75 mM.
The plant matter may be treated to enhance access of the enzymes or enzyme composition to the plant cell wall. For example, the epidermis of the leaf may be removed or ‘peeled’ before treatment with an enzyme composition. The plant matter may be cut into small pieces (manually, or with a shredding or cutting device such as an Urschel slicer); the cut up plant matter may be further infiltrated with an enzyme composition under a partial vacuum (Nishimura and Beevers 1978, Plant Physiol 62:40-43; Newell et al., 1998, J. Exp Botany 49:817-827). Mechanical perturbation of the plant matter may also be applied to the plant tissues (Giridhar et al., 1989. Protoplasma 151:151-157) before or during treatment with an enzyme composition. Furthermore, cultured plant cells, either liquid or solid cultures, may be used to prepare protoplasts or spheroplasts.
It may be desired to use an enzyme composition that lacks, or that has inactivated lipases or proteases. In some embodiments, one or more protease, or lipase inhibitors may be included in the enzyme composition. Examples of lipase inhibitors include RHC80267 (SigmaAldrich); examples of protease inhibitors include E-64, Na2EDTA, Pepstatin, aprotinin, PMSF, Pefabloc, Leupeptin, bestatin and the like.
Any suitable method of mixing or agitating the plant matter in the enzyme composition may be used. For example, the plant matter may be gently swirled or shaken in a tray or pan or via a rotary shaker, tumbled in a rotating or oscillating drum. Precaution should be taken in order to minimize the protoplast (and/or spheroplast) damage until they are removed form the digestion soup. The digestion vessel should be selected accordingly.
As a non-limiting example, an enzyme composition comprising 1.5% cellulase (Onozuka R-10) and 0.375% MACEROZYME™ in 500 mM mannitol, 10 m CaCl2 and 5 mM MES (pH 5.6) may be used for protoplast (or spheroplast) production from some Nicotiana tissues. As described herein, the concentration of mannitol may also be varied from about 0 to about 500 mM, or any amount therebetween. One of skill in the art, provided with the information disclosed herein, will be able to determine a suitable enzyme composition for the age and strain of the Nicotiana sp, or for another species used for production of VLPs.
Upon disruption of the cell wall, or partial digestion of the cell wall, a protoplast fraction (comprising protoplasts and/or spheroplasts), and an “apoplast fraction” are obtained. Alternatively, a “digested fraction” may be obtained. As noted below, integrity of the protoplast fraction may not be required to produce high yields of protein as described herein, therefore, an apoplast fraction or a digested fraction may be used for the extraction of proteins, for example, but not limited to, VLPs, viral envelope proteins, viral structural proteins, viral capsid proteins, viral coat proteins.
By “apoplast fraction” it is meant a fraction that is obtained following enzymatic digestion, or partial enzymatic digestion, using cell wall degrading enzymes of the plant matter in the presence of an osmoticum and/or other ingredients that may be used to assist in maintaining integrity of the protoplast. The apoplast fraction may comprise some components arising from disrupted protoplasts (or spheroplasts). For example, the apoplast fraction may comprise from about 0 to about 50% (v/v) or any amount therebetween, of the components from the protoplast fraction, or 0, 0.1, 0.5, 1, 5, 10, 15, 20, 25, 30, 35, 40, 45, or 50% (v/v) or any amount therebetween of the components from the protoplast fraction.
By a “digested fraction” it is meant the fraction that remains following enzymatic digestion, or partial enzymatic digestion, using cell wall degrading enzymes of the plant matter, however, integrity of the protoplast is not required, and the digested fraction may comprise intact, disrupted, or both intact and disrupted protoplasts. The composition comprising the cell wall degrading enzymes used to produce the digested fraction may comprise an osmoticum, or the osmoticum may be present at a reduced amount when compared to the amount present in standard procedures used to obtain protoplasts, or the osmoticum may be absent from the composition. The digested fraction comprises the apoplast fraction and the protoplast/spheroplast fraction, however, the protoplast/spheroplast fraction may or may not be intact. The digested fraction contains intracellular components and extracellular components. Intracellular components may be found in the form of protoplasts/spheroplasts if an osmoticum is used to maintain the protoplast/spheroplast intact. If no osmoticum is used in the digestion solution, then the protoplasts/spheroplasts may be disrupted and the intracellular and extracellular components may be combined in the digested fraction. As described herein, the proteins of interest, or protein suprastructures of interest, may be separated from components of the digested fraction using any suitable technique. Without wishing to be bound by theory, the step of cell wall digestion may loosen the polymeric components of the cells wall and assist in release of the proteins, or suprastructure proteins, otherwise trapped within the cell wall. This protocol also minimizes contamination of the proteins, or suprastructure proteins, with the intracellular components. The proteins or suprastructure proteins of interest may be separated from cellular debris following enzymatic digestion using low speed centrifugation followed by filtration, depth filtration, sedimentation, precipitation for example, but not limited to ammonium sulfate precipitation, or a combination thereof to obtain a separated fraction comprising the proteins or suprastructure proteins of interest.
If an osmoticum is used, the protoplast/spheroplast fraction, or fraction comprising protoplasts, may be separated from the apoplast fraction using any suitable technique, for example but not limited to, centrifugation, filtration, depth filtration, sedimentation, precipitation, or a combination thereof to obtain a separated fraction comprising the proteins or suprastructure proteins of interest and/or comprising protoplasts/spheroplasts that comprise the proteins or suprastructure proteins of interest.
The separated fraction may be for example a supernatant (if centrifuged, sedimented, or precipitated), or a filtrate (if filtered), and is enriched for proteins, or suprastructure proteins. The separated fraction may be further processed to isolate, purify, concentrate or a combination thereof, the proteins, or suprastructure proteins, by, for example, additional centrifugation steps, precipitation, chromatographic steps (e.g. size exclusion, ion exchange, affinity chromatography), tangential flow filtration, or a combination thereof. The presence of purified proteins, or suprastructure proteins, may be confirmed by, for example, native or SDS-PAGE, Western analysis using an appropriate detection antibody, capillary electrophoresis, or any other method as would be evident to one of skill in the art.
The apoplast is the portion of the plant cell outside the plasma membrane, and includes the cell wall and intercellular spaces of the plant. While it is preferred that the integrity of the protoplasts (and/or spheroplasts) be maintained during digestion and further processing, it is not required that the protoplasts remain intact in order to enrich for proteins, or suprastructure proteins.
During synthesis, proteins, or suprastructure proteins, may be secreted outside of the plasma membrane. If the suprastructure protein is a VLP, they are of an average size of about 20 nm to 1 μm, or any amount therebetween. If the suprastructure protein is an antibody, they are of a molecular weight from about 100 kDa to about 1000 kDa, or any amount therebetween. Due to their size, once synthesized, proteins, or suprastructure proteins, may remain trapped between the plasma membrane and cell wall and may be inaccessible for isolation or further purification using standard mechanical methods used to obtain plant proteins. In order to maximize yields, minimize contamination of the suprastructure protein fraction with cellular proteins, maintain the integrity of the proteins, or suprastructure proteins, and, where required, the associated lipid envelope or membrane, methods of disrupting the cell wall to release the proteins, or suprastructure proteins, that minimize mechanical damage to the protoplast and/or spheroplasts may be useful, such as the enzymatic methods described herein. However, it is not required that the integrity of all of the protoplasts be retained during the procedure.
A suprastructure protein, for example, a VLP produced in a plant may be complexed with plant-derived lipids. The plant-derived lipids may be in the form of a lipid bilayer, and may further comprise an envelope surrounding the VLP. The plant derived lipids may comprise lipid components of the plasma membrane of the plant where the VLP is produced, including, but not limited to, phosphatidylcholine (PC), phosphatidylethanolamine (PE), glycosphingolipids, phytosterols or a combination thereof. A plant-derived lipid may alternately be referred to as a ‘plant lipid’. Examples of phytosterols are known in the art, and include, for example, stigmasterol, sitosterol, 24-methylcholesterol and cholesterol (Mongrand et al., 2004, J. Biol Chem 279:36277-86).
Polypeptide expression may be targeted to any intracellular or extracellular space, organelle or tissue of a plant as desired. In order to localize the expressed polypeptide to a particular location, the nucleic acid encoding the polypeptide may be linked to a nucleic acid sequence encoding a signal peptide or leader sequence. A signal peptide may alternately be referred to as a transit peptide, signal sequence, or leader sequence. Signal peptides or peptide sequences for directing localization of an expressed polypeptide to the apoplast include, but are not limited to, a native (with respect to the protein) signal or leader sequence, or a heterologous signal sequence, for example but not limited to, a rice amylase signal peptide (McCormick 1999, Proc Natl Acad Sci USA 96:703-708), a protein disulfide isomerase signal peptide (PDI) having the amino acid sequence:
a plant pathogenesis related protein (PRP; Szyperski et al. PNAS 95:2262-2262), for example, Tobacco plant pathogenesis related protein 2 (PRP), a human monoclonal antibody signal peptide (SP, or leader sequence), or any signal peptide that is native with respect to the protein.
In some examples, an expressed polypeptide may accumulate in specific intercellular or extracellular space (such as the apoplast), organelle or tissue, for example when the polypeptide is expressed and secreted in the absence of a signal peptide or transit peptide.
The term “virus like particle” (VLP), or “virus-like particles” or “VLPs” refers to structures that self-assemble and comprise viral surface proteins, for example an influenza HA protein, or a chimeric influenza HA protein. VLPs and chimeric VLPs are generally morphologically and antigenically similar to virions produced in an infection, but lack genetic information sufficient to replicate and thus are non-infectious.
By “chimeric protein” or “chimeric polypeptide”, it is meant a protein or polypeptide that comprises amino acid sequences from two or more than two sources, for example but not limited to, two or more influenza types or subtypes, that are fused as a single polypeptide. The chimeric protein or polypeptide may include a signal peptide that is the same (i.e. native) as, or heterologous with, the remainder of the polypeptide or protein. The chimeric protein or chimeric polypeptide may be produced as a transcript from a chimeric nucleotide sequence, and remain intact, or if required, the chimeric protein or chimeric polypeptide may be cleaved following synthesis. The intact chimeric protein, or cleaved portions of the chimeric protein, may associate to form a multimeric protein. A chimeric protein or a chimeric polypeptide may also include a protein or polypeptide comprising subunits that are associated via disulphide bridges (i.e. a multimeric protein). For example, a chimeric polypeptide comprising amino acid sequences from two or more than two sources may be processed into subunits, and the subunits associated via disulphide bridges to produce a chimeric protein or chimeric polypeptide. A non-limiting example a chimeric protein is a chimeric monoclonal antibody, for example C2B8, or a chimeric VLP, for example but not limited to proteins and VLPs produced constructs numbered 690, 691, 696, 734, 737, 745 or 747 (Table 2) as described in U.S. provisional application US 61/220,161 and PCT/CA2010/000983 (which are incorporated herein by reference).
The protein or suprastructure protein maybe a glycoprotein, and the method as described herein involving extraction by cell wall digestion can be applied to plants co-expressing a glycoprotein and one or more enzymes for modifying N-glycosylation profile as described in WO 20008/151440 (Modifying glycoprotein production in plants; which is incorporated herein by reference) for favoring the recovery of glycoproteins bearing modified mature N-glycans. For example, mature N-glycans could be exempt of xylose and fucose residues, or exhibit reduced fucosylated, xylosylated, or both, fucosylated and xylosylated, N-glycans. Alternatively, a protein of interest comprising a modified glycosylation pattern may be obtained, wherein the protein lacks fucosylation, xylosylation, or both, and comprises increased galatosylation
The modified N-glycosylation profile may be obtained by co-expressing within a plant, a portion of a plant, or a plant cell, a nucleotide sequence encoding a first nucleotide sequence encoding a hybrid protein (GNT1-GalT), comprising a CTS domain (i.e. the cytoplasmic tail, transmembrane domain, stem region) of N-acetylglucosaminyl transferase (GNT1) fused to a catalytic domain of beta-1,4-galactosyltransferase (GalT), the first nucleotide sequence operatively linked with a first regulatory region that is active in the plant, and a second nucleotide sequence for encoding the suprastructure protein of interest, the second nucleotide sequence operatively linked with a second regulatory region that is active in the plant, and co-expressing the first and second nucleotide sequences to synthesize a suprastructure protein of interest comprising glycans with the modified N-glycosylation profile, as described in WO 20008/151440.
The suprastructure protein may be influenza hemagglutinin (HA), and each of the two or more than two amino acid sequences that make up the polypeptide may be obtained from different HA's to produce a chimeric HA, or chimeric influenza HA. A chimeric HA may also include a amino acid sequence comprising heterologous signal peptide (a chimeric HA pre-protein) that is cleaved after synthesis. Examples of HA proteins that may be used in the invention described herein may be found in WO 2009/009876; WO 2009/076778; WO 2010/003225 (which are incorporated herein by reference). A nucleic acid encoding a chimeric polypeptide may be described as a “chimeric nucleic acid”, or a “chimeric nucleotide sequence”. A virus-like particle comprised of chimeric HA may be described as a “chimeric VLP”. Chimeric VLPs are further described in PCT Application No. PCT/CA2010/000983 filed Jun. 25, 2010, and U.S. Provisional Application No. 61/220,161 (filed Jun. 24, 2009; which is incorporated herein by reference). VLPs can be obtained from expression of native or chimeric HA.
The HA of the VLPs prepared according to a method provided by the present invention, include known sequences and variant HA sequences that may be developed or identified. Furthermore, VLPs produced as described herein do not comprise neuraminidase (NA) or other components for example M1 (M protein), M2, NS and the like. However, NA and M1 may be co-expressed with HA should VLPs comprising HA and NA be desired.
Generally, the term “lipid” refers to a fat-soluble (lipophilic), naturally-occurring molecules. A chimeric VLP produced in a plant according to some aspects of the invention may be complexed with plant-derived lipids. The plant-derived lipids may be in the form of a lipid bilayer, and may further comprise an envelope surrounding the VLP. The plant derived lipids may comprise lipid components of the plasma membrane of the plant where the VLP is produced, including phospholipids, tri-, di- and monoglycerides, as well as fat-soluble sterol or metabolites comprising sterols. Examples include phosphatidylcholine (PC), phosphatidylethanolamine (PE), phosphatidylinositol, phosphatidylserine, glycosphingolipids, phytosterols or a combination thereof. A plant-derived lipid may alternately be referred to as a ‘plant lipid’. Examples of phytosterols include campesterol, stigmasterol, ergosterol, brassicasterol, delta-7-stigmasterol, delta-7-avenasterol, daunosterol, sitosterol, 24-methylcholesterol, cholesterol or beta-sitosterol (Mongrand et al., 2004, J. Biol Chem 279:36277-86). As one of skill in the art will readily understand, the lipid composition of the plasma membrane of a cell may vary with the culture or growth conditions of the cell or organism, or species, from which the cell is obtained.
Cell membranes generally comprise lipid bilayers, as well as proteins for various functions. Localized concentrations of particular lipids may be found in the lipid bilayer, referred to as ‘lipid rafts’. These lipid raft microdomains may be enriched in sphingolipids and sterols. Without wishing to be bound by theory, lipid rafts may have significant roles in endo and exocytosis, entry or egress of viruses or other infectious agents, inter-cell signal transduction, interaction with other structural components of the cell or organism, such as intracellular and extracellular matrices.
VLPs comprising a lipid envelope has been previously described in WO 2009/009876; WO 2009/076778, and WO 2010/003225 (which are incorporated herein by reference). With reference to influenza virus, the term “hemagglutinin” or “HA” as used herein refers to a structural glycoprotein of influenza viral particles. The HA of the present invention may be obtained from any subtype. For example, the HA may be of subtype H1, H2, H3, H4, H5, H6, H7, H8, H9, H10, H11, H12, H13, H14, H15, or H16, or of influenza types B or C. The recombinant HA of the present invention may also comprise an amino acid sequence based on the sequence of any hemagglutinin. The structure of influenza hemagglutinin is well-studied and demonstrates a high degree of conservation in secondary, tertiary and quaternary structure. This structural conservation is observed even though the amino acid sequence may vary (see, for example, Skehel and Wiley, 2000 Ann Rev Biochem 69:531-69; Vaccaro et al 2005; which is incorporated herein by reference). Nucleotide sequences encoding HA are well known, and are available for example, from the BioDefense and Public Health Database (now Influenza Research Database; Squires et al., 2008 Nucleic Acids Research 36:D497-D503) for example at URL: biohealthbase.org/GSearch/home.do?decorator=Influenza) or the databases maintained by the National Center for Biotechnology Information (NCBI; for example at URL: ncbi.nlm.nih.gov/sites/entrez?db=nuccore&cmd=search&term=influenza), both of which are incorporated herein by reference.
The present invention also pertains to methods of preparing, isolating, or both preparing and isolating VLPs, including influenza VLPs of viruses which infect humans, or host animals, for example primates, horses, pigs, birds, sheep, avian water fowl, migratory birds, quail, duck, geese, poultry, chicken, camel, canine, dogs, feline, cats, tiger, leopard, civet, mink, stone marten, ferrets, house pets, livestock, mice, rats, seal, whale and the like. Some influenza viruses may infect more than one host animal. Amino acid variation is tolerated in hemagglutinins of influenza viruses. This variation provides for new strains that are continually being identified. Infectivity between the new strains may vary. However, formation of hemagglutinin trimers, which subsequently form VLPs is maintained. The present invention also includes methods of preparing any plant-derived VLPs, regardless of the HA subtype or sequence, or chimeric HA comprising the VLP, or species of origin.
Correct folding of the suprastructure protein may be important for stability of the protein, formation of multimers, formation and function of the protein. Folding of a protein may be influenced by one or more factors, including, but not limited to, the sequence of the protein, the relative abundance of the protein, the degree of intracellular crowding, the availability of cofactors that may bind or be transiently associated with the folded, partially folded or unfolded protein, the presence of one or more chaperone proteins, or the like.
Heat shock proteins (Hsp) or stress proteins are examples of chaperone proteins, which may participate in various cellular processes including protein synthesis, intracellular trafficking, prevention of misfolding, prevention of protein aggregation, assembly and disassembly of protein complexes, protein folding, and protein disaggregation. Examples of such chaperone proteins include, but are not limited to, Hsp60, Hsp65, Hsp 70, Hsp90, Hsp100, Hsp20-30, Hsp10, Hsp100-200, Hsp100, Hsp90, Lon, TF55, FKBPs, cyclophilins, ClpP, GrpE, ubiquitin, calnexin, and protein disulfide isomerases (see, for example, Macario, A. J. L., Cold Spring Harbor Laboratory Res. 25:59-70. 1995; Parsell, D. A. & Lindquist, S. Ann. Rev. Genet. 27:437-496 (1993); U.S. Pat. No. 5,232,833). Chaperone proteins, for example but not limited to Hsp40 and Hsp70 may be used to ensure folding of a chimeric HA (PCT Application No. PCT/CA2010/000983 filed Jun. 25, 2010, and U.S. Provisional Application No. 61/220,161, filed Jun. 24, 2009; WO 2009/009876 and WO 2009/076778, all of which are incorporated herein by reference). Protein disulfide isomerase (PDI; Accession No. Z11499) may also be used.
Once recovered, proteins, or suprastructure proteins, may be assessed for structure, size potency or activity by, for example but not limited to, electron microscopy, light scattering, size exclusion chromatography, HPLC, Western blot analysis, electrophoresis, ELISA, activity based assays, e.g. hemagglutination assay, or any other suitable assay. These and other methods for assessing size, concentration, activity and composition of VLPs are known in the art.
For preparative size exclusion chromatography, a preparation comprising proteins, or suprastructure proteins, may be obtained by the methods described herein, and insoluble material removed by centrifugation. Precipitation with PEG or ammonium sulphate may also be of benefit. The recovered protein may be quantified using conventional methods (for example, Bradford Assay, BCA), and the extract passed through a size exclusion column, using for example SEPHACRYL™, SEPHADEX™, or similar medium, chromatography using an ion exchange column, or chromatography using an affinity column, and the active fractions collected. Protein complexes may also be obtained using affinity based magnetic separation for example, with Dynabeads™ (Invitrogen), and eluting the protein complex from the Dynabeads™. A combination of chromatographic and separation protocols may also be used. Following chromatography, or separation, fractions may be further analyzed by protein electrophoresis, immunoblot, ELISA, activity based assays as desired, to confirm the presence of the suprastructure protein.
If the suprastructure protein is a VLP, then a hemagglutination assay may be used to assess the hemagglutinating activity of the VLP-containing fractions, using methods well-known in the art. Without wishing to be bound by theory, the capacity of HA to bind to RBC from different animals is driven by the affinity of HA for sialic acids α2,3 or α2,3 and the presence of these sialic acids on the surface of RBC. Equine and avian HA from influenza viruses agglutinate erythrocytes from all several species, including turkeys, chickens, ducks, guinea pigs, humans, sheep, horses and cows; whereas human HAs will bind to erythrocytes of turkey, chickens, ducks, guinea pigs, humans and sheep (Ito T. et al, 1997, Virology, 227:493-499; Medeiros R et al, 2001. Virology 289:74-85).
A hemagglutination inhibition (HI, or HAI) assay may also be used to demonstrate the efficacy of antibodies induced by a vaccine, or vaccine composition comprising chimeric HA or chimeric VLP can inhibit the agglutination of red blood cells (RBC) by recombinant HA. Hemagglutination inhibitory antibody titers of serum samples may be evaluated by microtiter HAI (Aymard et al 1973). Erythrocytes from any of several species may be used—e.g. horse, turkey, chicken or the like. This assay gives indirect information on assembly of the HA trimer on the surface of VLP, confirming the proper presentation of antigenic sites on HAs.
Cross-reactivity HAI titres may also be used to demonstrate the efficacy of an immune response to other strains of virus related to the vaccine subtype. For example, serum from a subject immunized with a vaccine composition comprising a chimeric hemagglutinin comprising an HDC of a first influenza type or subtype may be used in an HAI assay with a second strain of whole virus or virus particles, and the HAI titer determined.
The influenza VLPs prepared by methods of the present invention may be used in conjunction with an existing influenza vaccine, to supplement the vaccine, render it more efficacious, or to reduce the administration dosages necessary. As would be known to a person of skill in the art, the vaccine may be directed against one or more than one influenza virus. Examples of suitable vaccines include, but are not limited to, those commercially available from Sanofi-Pasteur, ID Biomedical, Merial, Sinovac, Chiron, Roche, MedImmune, GlaxoSmithKline, Novartis, Sanofi-Aventis, Serono, Shire Pharmaceuticals and the like. If desired, the VLPs of the present invention may be admixed with a suitable adjuvant as would be known to one of skill in the art. Furthermore, the VLP produced according to the present invention may be co-expressed with other protein components or reconstituted with other VLPs or influenza protein components, for example, neuraminidase (NA), M1, and M2. It can also be co-expressed or reconstituted with other VLP made of vaccinal proteins such as malaria antigens, HIV antigens, respiratory syncytial virus (RSV) antigens, and the like.
Methods for transformation, and regeneration of transgenic plants, plant cells, plant matter or seeds comprising proteins, or suprastructure proteins, are established in the art and known to one of skill in the art. The method of obtaining transformed and regenerated plants is not critical to the present invention.
By “transformation” it is meant the interspecific transfer of genetic information (nucleotide sequence) that is manifested genotypically, phenotypically or both. The interspecific transfer of genetic information from a chimeric construct to a host may be heritable (i.e. integrated within the genome of the host) and the transfer of genetic information considered stable, or the transfer may be transient and the transfer of genetic information is not inheritable.
By the term “plant matter”, it is meant any material derived from a plant. Plant matter may comprise an entire plant, tissue, cells, or any fraction thereof. Further, plant matter may comprise intracellular plant components, extracellular plant components, liquid or solid extracts of plants, or a combination thereof. Further, plant matter may comprise plants, plant cells, tissue, a liquid extract, or a combination thereof, from plant leaves, stems, fruit, roots or a combination thereof. Plant matter may comprise a plant or portion thereof which has not been subjected to any processing steps. A portion of a plant may comprise plant matter. Plants or plant matter may be harvested or obtained by any method, for example, the whole plant may be used, or the leaves or other tissues specifically removed for use in the described methods. Transgenic plants expressing and secreting VLPs may also be used as a starting material for processing as described herein.
The constructs of the present invention can be introduced into plant cells using Ti plasmids, Ri plasmids, plant virus vectors, direct DNA transformation, micro-injection, electroporation, infiltration, and the like. For reviews of such techniques see for example Weissbach and Weissbach, Methods for Plant Molecular Biology, Academy Press, New York VIII, pp. 421-463 (1988); Geierson and Corey, Plant Molecular Biology, 2d Ed. (1988); and Miki and Iyer, Fundamentals of Gene Transfer in Plants. In Plant Metabolism, 2d Ed. D T. Dennis, D H Turpin, D D Lefebrve, D B Layzell (eds), Addison-Wesley, Langmans Ltd. London, pp. 561-579 (1997). Other methods include direct DNA uptake, the use of liposomes, electroporation, for example using protoplasts, micro-injection, microprojectiles or whiskers, and vacuum infiltration. See, for example, Bilang, et al. (Gene 100: 247-250 (1991), Scheid et al. (Mol. Gen. Genet. 228: 104-112, 1991), Guerche et al. (Plant Science 52: 111-116, 1987), Neuhause et al. (Theor. Appl Genet. 75: 30-36, 1987), Klein et al., Nature 327: 70-73 (1987); Howell et al. (Science 208: 1265, 1980), Horsch et al. (Science 227: 1229-1231, 1985), DeBlock et al., Plant Physiology 91: 694-701, 1989), Methods for Plant Molecular Biology (Weissbach and Weissbach, eds., Academic Press Inc., 1988), Methods in Plant Molecular Biology (Schuler and Zielinski, eds., Academic Press Inc., 1989), Liu and Lomonossoff (J. Virol Meth, 105:343-348, 2002), U.S. Pat. Nos. 4,945,050; 5,036,006; 5,100,792; 6,403,865; 5,625,136, (all of which are hereby incorporated by reference).
Transient expression methods may be used to express the constructs of the present invention (see Liu and Lomonossoff, 2002, Journal of Virological Methods, 105:343-348; which is incorporated herein by reference). Alternatively, a vacuum-based transient expression method, as described in PCT Publications WO 00/063400, WO 00/037663 (incorporated herein by reference) may be used. These methods may include, for example, but are not limited to, a method of Agro-inoculation or Agro-infiltration, however, other transient methods may also be used as noted above. With either Agro-inoculation or Agro-infiltration, a mixture of Agrobacteria comprising the desired nucleic acid enter the intercellular spaces of a tissue, for example the leaves, aerial portion of the plant (including stem, leaves and flower), other portion of the plant (stem, root, flower), or the whole plant. After crossing the epidermis the Agrobacterium infect and transfer t-DNA copies into the cells. The t-DNA is episomally transcribed and the mRNA translated, leading to the production of the protein of interest in infected cells, however, the passage of t-DNA inside the nucleus is transient.
The sequences described herein are summarized below.
The present invention will be further illustrated in the following examples. However it is to be understood that these examples are for illustrative purposes only, and should not be used to limit the scope of the present invention in any manner.
Constructs that may be used for the production of VLPs are described U.S. Provisional Application No. U.S. 61/220,161 and PCT/CA2010/000983 (which are incorporated herein by reference), WO 2009/009876, WO 2009/076778 and WO2010/003225 (all of which are incorporated herein by reference). Constructs may also include those listed in Table 2. Assembly of these constructs is described in WO 2009/009876, WO 2009/076778, WO2010/003225 and U.S. 61/220,161. However other constructs comprising known HA's, including but not limited to, those provided in Table 2, and combined with similar or different regulatory elements and promoters, may also be used for the production of VLPs as described herein.
CPMV-HT expression cassettes included the 35S promoter to control the expression of an mRNA comprising a coding sequence of interest flanked, in 5′ by nucleotides 1-512 from the Cowpea mosaic virus (CPMV) RNA2 with mutated ATG at positions 115 and 161 and in 3′, by nucleotides 3330-3481 from the CPMV RNA2 (corresponding to the 3′ UTR) followed by the NOS terminator. Plasmid pBD-05-1LC, (Sainsbury et al. 2008; Plant Biotechnology Journal 6: 82-92 and PCT Publication WO 2007/135480), was used for the assembly of CPMV-HT-based hemagglutinin expression cassettes. The mutation of ATGs at position 115 and 161 of the CPMV RNA2 was done using a PCR-based ligation method presented in Darveau et al. (Methods in Neuroscience 26: 77-85 (1995)). Two separate PCRs were performed using pBD-05-1LC as template. The primers for the first amplification were pBinPlus.2613c (SEQ ID NO: 3) and Mut-ATG115.r (SEQ ID NO: 4). The primers for the second amplification were Mut-ATG161.c (SEQ ID NO: 5) and LC-05-1.110r (SEQ ID NO: 6). The two fragments were then mixed and used as template for a third amplification using pBinPlus.2613c (SEQ ID NO: 3) and LC-05-1.110r (SEQ ID NO: 6) as primers. The resulting fragment was digested with PacI and ApaI and cloned into pBD-05-1LC digested with the same enzyme. The expression cassette generated was named 828.
The assembly of this cassette is described in WO 2009/009876, WO 2009/076778 and WO2010/003325, which are incorporated herein by reference.
Briefly, the coding sequence of H5 from A/Indonesia/5/2005 was cloned into CPMV-HT as follows: restriction sites ApaI (immediately upstream of the initial ATG) and StuI (immediately downstream of a stop codon) were added to the hemagglutinin coding sequence by performing a PCR amplification with primers ApaI-H5 (A-Indo).1c (SEQ ID NO: 7) and H5 (A-Indo)-StuI.1707r (SEQ ID NO: 8) using construct number 660 (D'Aoust et al., Plant Biotechnology Journal 6:930-940 (2008)) as template. Construct 660 comprises an alfalfa plastocyanin promoter and 5′ UTR, hemagglutinin coding sequence of H5 from A/Indonesia/5/2005 (Construct #660), alfalfa plastocyanin 3′ UTR and terminator sequences (SEQ ID NO: 9;
Post-transcriptional gene silencing (PTGS) may be involved in limiting expression of transgenes in plants, and co-expression of a suppressor of silencing from the potato virus Y (HcPro) may be used to counteract the specific degradation of transgene mRNAs (Brigneti et al., 1998). Alternate suppressors of silencing are well known in the art and may be used as described herein (Chiba et al., 2006, Virology 346:7-14; which is incorporated herein by reference), for example but not limited to, TEV-p1/HC-Pro (Tobacco etch virus-p1/HC-Pro), BYV-p21, p19 of Tomato bushy stunt virus (TBSV p19), capsid protein of Tomato crinkle virus (TCV-CP), 2b of Cucumber mosaic virus; CMV-2b), p25 of Potato virus X (PVX-p25), p11 of Potato virus M (PVM-p11), p11 of Potato virus S (PVS-p11), p16 of Blueberry scorch virus, (BScV-p16), p23 of Citrus tristeza virus (CTV-p23), p24 of Grapevine leafroll-associated virus-2, (GLRaV-2 p24), p10 of Grapevine virus A, (GVA-p10), p14 of Grapevine virus B (GVB-p14), p10 of Heracleum latent virus (HLV-p10), or p16 of Garlic common latent virus (GCLV-p16). Therefore, a suppressor of silencing, for example, but not limited to, HcPro, TEV -p1/HC-Pro, BYV-p21, TBSV p19, TCV-CP, CMV-2b, PVX-p25, PVM-p11, PVS-p11, BScV-p16, CTV-p23, GLRaV-2 p24, GBV-p14, HLV-p10, GCLV-p16 or GVA-p10, may be co-expressed along with the nucleic acid sequence encoding the protein of interest to further ensure high levels of protein production within a plant.
The construction of p19 is described in described in WO 2010/0003225 (which is incorporated herein by reference). Briefly, the coding sequence of p19 protein of tomato bushy stunt virus (TBSV) was linked to the alfalfa plastocyanin expression cassette by the PCR-based ligation method presented in Darveau et al. (Methods in Neuroscience 26: 77-85 (1995)). In a first round of PCR, a segment of the plastocyanin promoter was amplified using primers Plasto-443c:
and supP19-plasto.r
with construct 660 (described in WO 2010/0003225, which is incorporated herein by reference) as template. In parallel, another fragment containing the coding sequence of p19 was amplified with primers supP19-1c
using construct 35S:p19 as described in Voinnet et al. (The Plant Journal 33: 949-956 (2003)) as template. Amplification products were then mixed and used as template for a second round of amplification (assembling reaction) with primers Plasto-443c and SupP19-SacI.r. The resulting fragment was digested with BamHI (in the plastocyanin promoter) and Sad (at the end of the p19 coding sequence) and cloned into construct number 660, previously digested with the same restriction enzymes to give construct number R472. The plasmids were used to transform Agrobacteium tumefaciens (AGL1; ATCC, Manassas, Va. 20108, USA) by electroporation (Mattanovich et al., 1989). The integrity of all A. tumefaciens strains were confirmed by restriction mapping. The A. tumefaciens strain comprising R472 (
HcPro construct (35HcPro) was prepared as described in Hamilton et al. (2002). All clones were sequenced to confirm the integrity of the constructs. The plasmids were used to transform Agrobacteium tumefaciens (AGL1; ATCC, Manassas, Va. 20108, USA) by electroporation (Mattanovich et al., 1989). The integrity of all A. tumefaciens strains were confirmed by restriction mapping.
Nicotiana benthamiana plants were grown from seeds in flats filled with a commercial peat moss substrate. The plants were allowed to grow in the greenhouse under a 16/8 photoperiod and a temperature regime of 25° C. day/20° C. night. Three weeks after seeding, individual plantlets were picked out, transplanted in pots and left to grow in the greenhouse for three additional weeks under the same environmental conditions. After six weeks, plants have an average weight of 80 g and 30 cm in height.
Agrobacterium strain AGL1 was transfected (electroporation) with constructs as identified below, using the methods described by D'Aoust et al 2008 (Plant Biotechnology Journal 6:930-940). Transfected Agrobacterium were grown in YEB medium supplemented with 10 mM 2-(N-morpholino)ethanesulfonic acid (MES), 20 μM acetosyringone, 50 μg/ml kanamycin and 25 μg/ml of carbenicillin pH5.6 to an OD600 between 0.6 and 1.6. Agrobacterium suspensions were centrifuged before use and resuspended in infiltration medium (10 mM MgCl2 and 10 mM MES pH 5.6).
Plants were agroinfiltrated as described in D'Aoust et al (supra). Briefly, for vacuum-infiltration, A. tumefaciens suspensions were centrifuged, resuspended in the infiltration medium and stored overnight at 4° C. On the day of infiltration, culture batches were diluted in 2.5 culture volumes and allowed to warm before use. Whole plants of N. benthamiana were placed upside down in the bacterial suspension in an air-tight stainless steel tank under a vacuum of 20-40 Torr for 2-min. Unless otherwise specified, all infiltrations were performed as co-infiltration with a bacterial transformed with R472 (strain AGL1/R472) at a 1:1 ratio. Following vacuum infiltration, plants were returned to the greenhouse for a 4-6 day incubation period until harvest.
Following incubation of 4, 5, 6, 7 and 8 days, the aerial part of plants was harvested and used immediately. Total soluble proteins were extracted by homogenizing plant tissue in 3 volumes of cold 50 mM Tris pH 8.0, 0.15 M NaCl containing 1% Trition X-100 and 0.004% sodium metabisulfite. Plant tissue were mechanically homogenized using a POLYTRON™, grinding with mortar and pestle, or with a COMITROL™ in 1 volume of cold 50 mM Tris pH 8, 0.15 M NaCl. The buffer used with the COMITROL™ also contained 0.04% sodium metabisulfite. Following homogenization, the slurry of ground plant material was centrifuged at 5,000 g for 5 min at 4° C. and the crude extracts (supernatant) kept for analysis. The total protein content of clarified crude extracts was determined by the Bradford assay (Bio-Rad, Hercules, Calif.) using bovine serum albumin as the reference standard.
Leaf tissue was collected from the Nicotiana benthamiana plants and cut into ˜1 cm2 pieces. The leaf pieces were soaked in 500 mM mannitol for 30 minutes at room temperature (RT). The mannitol solution was then removed and changed with the enzyme mix (mixture of cellulases from Trichoderma viride (Onozuka R-10; 3% v/v) and a mixture of pectinases from Rhizopus sp. (MACEROZYME™; 0.75% v/v; both from Yakult Pharmaceuticals) in protoplasting solution (500 mM mannitol, 10 mM CaCl2 and 5 mM MES/KOH (pH 5.6)). The ratio used was 20 g of leaf pieces per 100 mL solution. This preparation was spread evenly into a shallow vessel (−11×18 cm) and incubated for 16 hours on a rotary shaker at 40 rpm and 26° C.
Alternately, VLP extraction may be performed as follows: plants were agroinfiltrated with AGL1/#685 as described in example 1. Leaf tissue was collected from the N. benthamiana plants at day 6 post-infiltration and cut into ˜1 cm2 pieces. Multifect Pectinase FE, Multifect CX CG and Multifect CX B (Genencor) were added to 1.0% each (v/v) in a 600 mM Mannitol, 75 mM Citrate, 0.04% sodium bisulfite pH 6.0 buffer using a ratio of 1:2.5 (w/v) fresh biomass; digestion buffer. The biomass was digested for 15 h at room temperature in a orbital shaker.
Following incubation, leaf debris was removed by filtration (nylon filter of 250 or 400 μm mesh). Protoplasts in suspension were collected by centrifugation at 200×g (15 min), followed by centrifugation of the supernatant at 5000×g (15 min) to further clarify the supernatant. Alternately, a single centrifugation step at 5000×g for 15 minutes may be employed. Seventy mL of the supernatant was then centrifuged at 70,000×g for 30 minutes. The resulting pellet was resuspended in 1.7 mL of PBS and analyzed immediately or frozen.
A hemagglutination assay for H5 was based on a method described by Nayak and Reichl (2004). Briefly, serial double dilutions of the test samples (100 μL) were made in V-bottomed 96-well microtiter plates containing 100 μL PBS, leaving 100 μL of diluted sample per well. One hundred microliters of a 0.25% turkey red blood cells suspension (Bio Link Inc., Syracuse, N.Y.) were added to each well, and plates were incubated for 2 h at room temperature. The reciprocal of the highest dilution showing complete hemagglutination was recorded as hemagglutination activity. In parallel, a recombinant HA5 standard (A/Vietnam/1203/2004 H5N1) (Protein Science Corporation, Meriden, Conn.) was diluted in PBS and run as a control on each plate.
HA5 standard was prepared with purified virus-like particles which were disrupted by treatment with 1% Triton X-100 followed by mechanical agitation in a Tissue Lyser™ (Qiagen) for 1 min. U-bottom 96-well microtiter plates were coated with 10 μg/mL of capture antibody (Immune Technology Corporation, #IT-003-0051) in 50 mM carbonate-bicarbonate coating buffer (pH 9.6) for 16-18 hours at 4° C. All washes were performed with 0.01 M PBS (phosphate-buffered saline), pH 7.4 containing 0.1% Tween-20. After incubation, plates were washed three times and blocked with 1% casein in PBS for 1 hour at 37° C. After the blocking step, plates were washed three times. The HA5 standard was diluted in a mock extract (prepared from leaf tissue infiltrated with AGL1/R472 alone) to generate a standard curve from 500 to 50 ng/mL. Samples to quantify were treated in 1% Triton X-100 prior to loading the microplate. Plates were further incubated for 1 hour at 37° C. After washing, sheep polyclonal antibody raised against HA5 (CBER/FDA) diluted 1:1000 was added and the plates were incubated for 1 hour at 37° C. After washing, horseradish peroxidase-conjugated rabbit anti-sheep antibody diluted 1:1000 was added and the plates were incubated for 1 hour at 37° C. After the final washes, the plates were incubated with SureBlue TMB peroxidase substrate (KPL) for 20 minutes at room temperature. Reaction was stopped by the addition of 1N HCl and A450 values were measured using a Multiskan Ascent plate reader (Thermo Scientific).
The quantity and relative activity of HA obtained from the present enzymatic extraction method were compared with that of HA obtained from common mechanical extraction methods. N. benthamiana plants were infiltrated with AGL1/685 and the leaves were harvested after a five to six-day incubation period. Leaf homogenates were prepared as follows: Two grams of leaves were homogenized with a Polytron homogenizer; 4 g of leaves were ground with a mortar and a pestle; and 25 kg of leaves were homogenized with a COMITROL™ processor (Urschel Laboratories) in an extraction buffer (50 mM Tris, 150 mM NaCl pH 8.0, ratio of 1:1 w/v). Enzymatic extraction was carried as follow: Twenty grams of harvested leaves were subjected to digestion with Macerozyme pectinases and Onozuka R-10 cellulases as described above. Following digestion, leaf debris were removed by filtration (nylon filter, 250 μm mesh). Protoplasts in suspension were removed by centrifugation at 200×g (15 min), and the supernatant further clarified by centrifugation at 5000×g (15 min).
The relative activity and quantity of HA in each of these plant extracts is shown in Table 3. The amount of HA released by enzymatic digestion of the cell wall is significantly superior when compared to the other techniques used.
A combination of differential centrifugation and size exclusion chromatography (SEC) was used to demonstrate that the HA obtained by the enzymatic extraction method described herein were organized as VLPs. N. benthamiana plants were agroinfiltrated with AGL1/685 as described in Example 1. Leaves were collected from the plants 6 days post-infiltration and cut into ˜1 cm2 pieces then digested, coarse-filtered and centrifuged as described in Example 1.
The clarified samples were then centrifuged at 70,000×g to allow for segregation of VLPs. The centrifugation pellet, containing the VLPs, was gently resuspended in 1/50 volume of Phosphate buffered saline (PBS; 0.1M sodium phosphate, 0.15M NaCl pH 7.2) before being loaded on a SEC column.
SEC columns of 32 ml SEPHACRYL™ S-500 high resolution beads (S-500 HR: GE Healthcare, Uppsala, Sweden, Cat. No. 17-0613-10) were prepared with equilibration/elution buffer (50 mM Tris, 150 mM NaCl, pH8). SEC chromatography was performed with the loading of a 1.5 mL VLP sample onto the equilibrated column, and its elution with 45 mL of equilibration/elution buffer. The eluate was collected in fractions of 1.7 mL, and the protein content of each fraction was evaluated by mixing 10 μL of the eluate fraction with 200 μL of diluted Bio-Rad protein dye reagent (Bio-Rad, Hercules, Calif.). Each separation was preceded by a calibration with Blue Dextran 2000 (GE Healthcare Bio-Science Corp., Piscataway, N.J., USA). Comparison of the elution profiles of both Blue Dextran 2000 and host proteins was performed for each separation to ensure uniformity of the separations.
Total protein content of clarified crude extracts was determined by the Bradford assay (Bio-Rad, Hercules, Calif.) using bovine serum albumin as the reference standard. Proteins present in SEC eluate fractions were precipitated with acetone (Bollag et al., 1996), resuspended in either 0.25 volume or 0.05 volume of denaturing sample loading buffer (0.1M Tris pH 6.8, 0.05% bromophenol blue, 12.5% glycerol, 4% SDS and 5% beta-mercaptoethanol) for SDS-PAGE analysis or immunoblot analysis, respectively. Separation by SDS-PAGE was performed under reducing conditions, and Coomassie Brillant Blue R-250 was used for protein staining.
Hemagglutination assay for H5 was performed based on a method described by Nayak and Reichl (2004). Briefly, successive double dilutions of the test samples (100 μL) were made in V-bottomed 96-well microtiter plates containing 100 μL PBS, leaving 100 μL of diluted sample per well. One hundred microliters of a 0.25% turkey red blood cells suspension (Bio Link Inc., Syracuse, N.Y.) were added to each well, and plates were incubated for 2 h at room temperature. The reciprocal of the highest dilution showing complete hemagglutination was recorded as hemagglutination activity. In parallel, a recombinant H5 standard (A/Vietnam/1203/2004 H5N1) (Protein Science Corporation, Meriden, Conn.) was diluted in PBS and run as a control on each plate.
N. benthamiana plants were agroinfiltrated with AGL1/685 as described in Example 1. Leaves were collected on day 6 post-infiltration, cut into ˜1 cm2 pieces, digested, coarse-filtered and centrifuged as described in Example 1.
The controlled enzymatic digestion of the leaves removed the cell walls, at least partially, thus allowing for the release of proteins and components presents in the space between the cell wall and the plasma membrane into the extraction medium. Since most intracellular proteins and components were still undamaged and contained within the mostly intact protoplasts, an initial centrifugation step allowed for their removal, thus providing a resulting solution comprising cell wall degrading enzymes, in addition of the extracellular plant proteins and components (apoplastic fraction), as shown in
The major contaminant present in lane 3 was found to be RubisCo (Ribulose-1,5-bisphosphate carboxylase oxygenase), which is made of two types of protein subunits: a large-chain (L, about 55 kDa) and a small-chain (S, about 13 kDa). A total of eight large-chain dimers and eight small-chains usually assemble with each other into a RubisCo 540 kDa larger complex. While this plant protein contaminant is found in large amount in plant extracts originating from mechanical extraction method (see arrow in
N. benthamiana plants were agroinfiltrated with AGL1/685 as described in Example 1. Leaves were collected on day 6 post-infiltration, cut into ˜1 cm2 pieces and digested for 15 h at room temperature in an orbital shaker. The digestion buffer contained 1.0% (v/v) Multifect Pectinase FE, 1.0% (v/v) Multifect CX CG or and 1.0% (v/v) Multifect CX B (all from Genencor), each in a solution of 600 mM Mannitol, 75 mM Citrate, 0.04% sodium bisulfite pH 6.0 buffer using a biomass: digestion buffer ratio of 1:2.5 (w/v).
Following digestion, the apoplastic fraction was filtered through a 400 μm nylon filter to remove coarse undigested vegetal tissue (<5% of starting biomass). The filtered extract was then centrifuged at room temperature for 15 min at 5000×g to remove protoplasts and intracellular contaminants (proteins, DNA, membranes, vesicles, pigments, etc). Next, the supernatant was depth-filtered (for clarification) using a 0.65 μm glass fiber filter (Sartopore2/Sartorius Stedim) and a 0.45/0.2 μm filter, before being subjected to chromatography.
The clarified apoplastic fraction was loaded over a cation exchange column (Poros HS Applied Biosystems) equilibrated with an equilibration/elution buffer (50 mM NaPO4, 100 mM NaCl, 0.005% Tween 80 pH 6.0). Once the UV was back to zero, the extract was step-eluted with the equilibration/elution buffer containing increasing concentrations of NaCl (500 mM). Where necessary, the chromatographic fractions were concentrated 10 times using Amicon™ devices equipped with 10 kDa MWCO. Protein analysis was performed as described in previous examples.
Under the above-mentioned conditions, most enzymes and plant proteins did not bind to the cation exchange resin whereas the HA-VLP did bind, thus providing a considerable enrichment in HA-VLPs in the eluted fraction (
N. benthamiana plants were agroinfiltrated with Agrobacterium AGL1 strains carrying a construct expressing a hemagglutinin of interest (H1/Cal WT, B/Flo, H5/Indo or H1/Cal X179A) as described in Example 1. Leaves were collected on day 6 post-infiltration, cut into ˜1 cm2 pieces and digested according to Example 4, except where noted below. Filtration, centrifugation and clarification were performed as described in Example 4.
NaCl was added to digestion buffer to evaluate its potential effect on the HA-VLP recovery rate. The suspected advantages were the potential prevention of non-specific association of HA with plant cells or with particle in suspension that are removed during clarification and potential effect on achievement and/or maintenance and/or improvement of colloidal stability of the HA-VLP.
Addition of 500 mM NaCl to the digestion buffer resulted in an increase of HA-VLP recovery yield per gram of biomass after removal of protoplasts and cellular debris by centrifugation. However, this increase was only noted with the for the H1/Cal WT and B/Flo strains, while the recovery yield for H5 was not significantly increased by this approach (Table 4).
1Yield (dil/g) with NaCl divided by Yield (dil/g) without NaCl
Addition of 500 mM NaCl during the digestion further resulted in an increase of the release of HA-VLP during digestion, which in turn resulted into increased recovery rate after clarification for both H1/Cal WT and H1/Cal X-179A strains (Table 5), but not for the H5/Indo strain.
1Recovery is expressed in percentage of hemagglutination activity obtained after depth filtration compared to the activity found in the centrifuged digested extract.
The association state of the HA-VLP, with and without the addition of NaCl during enzymatic digestion, was studied using Nanoparticle Tracking Analysis (NTA) for H5/Indo and H1/Cal WT (
N. benthamiana plants were agroinfiltrated with Agrobacterium AGL1 strains carrying a construct expressing a hemagglutinin of interest (H5/Indo) as described in Example 1. Leaves were collected on day 6 post-infiltration, cut into ˜1 cm2 pieces, and digested as described in Example 4, with addition of either 500 mM NaCl or 500 mM NaCl and 25 mM EDTA to the digestion buffer. Filtration, centrifugation and clarification were performed as described in Example 4.
Release of components having a green color during the enzymatic digestion step led to purified preparation of VLP having a greenish coloration. The composition of the cell wall digestion solution was therefore investigated and adjusted to obtain a VLP purified preparation having a reduced green coloration, and thus an increased purity. Without wishing to be bound by theory, since Ca2+ plays a critical role in the retention of constituents of the cell wall's middle lamellae together, and given the fact that there is usually a high concentration of Ca2+ in plant cell wall, the addition of Ca2+-chelator EDTA could facilitate the enzymatic depolymerisation of the cell wall, thereby preserving intact intracellular organelles, such as chloroplasts, and preventing the release green-pigments components.
As shown in Table 6, the addition of 25 mM EDTA to the digestion buffer allowed for the reduction of the green coloration of the purified H5-VLP preparation, as evaluated by measuring the difference in absorption of the preparation (OD677nm−OD650nm). When the green constituents were released in high quantity, or not suitably removed, VLP preparation exhibited a ΔOD>0.040.
N. benthamiana plants were agroinfiltrated with Agrobacterium AGL1 strains carrying a construct expressing a hemagglutinin of interest (H5/Indo) as described in Example 1. Leaves were collected on day 6 post-infiltration, cut into ˜1 cm2 pieces and digested according to Example 4, with modification of digestion buffer to include 0%, 0.25%, 0.5%, 0.75% or 1% v/v Multifect Pectinase FE, Multifect CX—CG cellulase and Multifect CX B cellulose as noted in Tables 7-9. Filtration, centrifugation and clarification were as described in Example 4.
As shown in following tables 7 and 8, pectinase has been demonstrated to be non-essential in the digestion buffer. Similar levels of H5/Indo or H1/Cal WT VLP can be extracted with the present method either in the presence or absence of pectinase. Furthermore, it has been found that reducing the concentration of cellulase when compared to previous examples had no significant impact on the quality of extraction (Table 9).
Controlling the pH during the digestion can be critical for the extraction of some VLPs. Taking into account that the depolymerisation of the cell wall occurring during the digestion step can release acid sugars that could acidify the solution (i.e. from pH 6 to 5) in the presence of appropriate buffers, and that some VLPs (such as those comprising H3/Bris and B/Flo HA) have already demonstrated a strong sensitivity to mildly acidic conditions, impact of such a potential acidification on the yield of VLP produced was investigated.
N. benthamiana plants were agroinfiltrated with Agrobacterium AGL1 strains carrying a construct expressing a hemagglutinin of interest (B/Flo, H5/Indo, H3/Bris) as described in Example 1. Leaves were collected on day 6 post-infiltration, cut into ˜1 cm2 pieces and digested according to Example 4, with modification of digestion conditions to include 500 mM NaCl; 25 or 50 mM EDTA; 0.03 or 0.04% sodium bisulfite; 0, 100, 200 or 600 mM mannitol, 75, 125 or 150 mM citrate; and/or 75 mM NaPO4; with the pH of the digestion buffer adjusted as set out in Tables 10-14. Filtration, centrifugation and clarification were as described in Example 4.
Various digestion buffer compositions were tested to achieve a pH of approximately 5.5 by the end of the enzymatic digestion, including increased concentration of citrate (buffer effect between pH 3.0 and 5.4) and addition of sodium phosphate (buffer effect at pH above 6.0). Table 10 shows that VLPs from the B strain were extracted more efficiently when post-digestion pH was close to pH 6.0.
1All buffers contained 600 mM mannitol, sodium metabisulfite 0.04%
Next, the effect of initiating the digestion at a higher pH in order to reach final pH value close to pH 6.0 was tested. As shown in Table 11, the digestion of plant cell wall with such near-neutral conditions was possible, and did not impaired the extraction yield for H5/Indo VLPs.
1All digestion buffers contained 600 mM mannitol, sodium metabisulfite 0.04%, 125 mM Citrate + 75 mM NaPO4 + 500 mM NaCl + 25 mM EDTA
Other components of the digestion solution were also shown to be modifiable without negatively affecting the extraction yield of VLPs. Table 12 illustrates modifications that can be applied to the digestion solution in order to enhance the extraction yield of B/Flo VLPs, while obtaining a post-digestion pH of 5.4-5.7. Such modifications include increasing the concentration of citrate and adding a PO4 buffer. It has been found that increasing the concentration of EDTA generally led to a more acidified extract and to lower VLP extraction yields.
1All buffers contained 500 mM NaCl, and sodium metabisulfite 0.04%.
Buffer composition was further modified to improve the extraction yield of H3/Brisbane VLPs (Table 13)
1All buffers containing 125 mM Citrate, 75 mM NaPO4, 500 mM NaCl,
As shown in Tables 12 and 13, mannitol concentration could be reduced to 200 mM without significantly affecting VLPs extraction yield. Further reduction of mannitol concentrations to 100 mM, and even the total omission of mannitol from the digestion solution, did not significantly affect the level of HA-VLP obtained (Table 14).
1All buffers containing 75 mM Citrate pH 6.0 + sodium metabisulfite 0.04%.
2Two trials were were performed to compare the extraction yields of VLPs without mannitol (Trial 1) and with 100 mM mannitol (Trial 2) versus 600 mM mannitol.
The enzymatic digestion method for plant biomass described herein has the potential to be applied to extracting of a broad variety of HA-VLPs. Adding to the extraction of HA-VLPs comprising H5/Indo, H1/Cal WT VLP, H3/Bris and B/Flo shown in previous examples, the method described herein was also shown to be suitable for the extraction of HA-VLPs from seasonal H1/Bris and H1/NC, as shown in Table 15.
Assembly of C2B8 expression cassette (construct #595) C2B8 is a chimeric (mouse/human) monoclonal antibody directed against the B-cell-specific antigen CD20 expressed on non-Hodgkin's lymphomas (NHL). C2B8 mediates complement and antibody-dependent cell-mediated cytotoxicity and has direct antiproliferative effects against malignant B-cell lines in vitro (N Selenko et. al., Leukemia, October 2001, 15 (10); 1619-1626).
A DNA fragment comprising 84 bp of the alfalfa plastocyanin promoter, the complete C2B8 light chain coding sequence and the complete alfalfa plastocyanin terminator was synthesized (LC fragment). The LC fragment was flanked by a DraIII restriction site (found in the plastocyanin promoter) and a EcoRI site downstream of the plastocyanin terminator. The sequence of LC fragment is presented in
The plasmid comprising a dual expression cassette for C2B8 expression (construct #595) was assembled as follows. Construct number 592 was digested with EcoRI, treated with Klenow fragment to generate blunt-ends and digested with SbfI. The resulting fragments, comprising the complete cassette for the expression of C2B8 heavy chain flanked by a SbfI site and a blunt-end, was inserted into construct #590 previously digested with SbfI and SmaI.
The construct R472, encoding p19 protein is described above (“Suppressors of silencing”; see
Nicotiana benthamiana plants were grown as described above (“Preparation of plant biomass, inoculum, agroinfiltration, and harvesting”) in a greenhouse under a 16/8 photoperiod and a temperature regime of 25° C. day/20° C. night. Three weeks after seeding, individual plantlets were picked out, transplanted in pots and left to grow in the greenhouse for three additional weeks under the same environmental conditions.
Agrobacteria bearing construct #595 or #R472 were grown in BBL Select APS LB broth medium supplemented with 10 mM 2-[N-morpholino]ethanesulfonic acid (MES), 50 μg/ml kanamycin and 25 μg/ml of carbenicillin pH5.6 until they reached an OD600>2.0. Agrobacterium suspensions were centrifuged before use and resuspended in infiltration medium (10 mM MgCl2 and 10 mM MES pH 5.6) and stored overnight at 4° C. On the day of infiltration, culture batches were diluted in 6.7 culture volumes and allowed to warm before use. Whole plants of N. benthamiana were placed upside down in the bacterial suspension in an air-tight stainless steel tank under a vacuum of 20-40 Torr for 1 min. Following infiltration, plants were returned to the greenhouse for a 5 day incubation period until harvest. Infiltrations were performed as co-infiltration with strains AGL1/595 and AGL1/R472 in a 1:1 ratio.
Following incubation, the aerial part of plants was harvested and used immediately. Total soluble proteins were extracted by homogenizing plant tissue in a domestic blender for 3 min. with 1.5 volumes of cold 20 mM NaPO4 pH 6.0, 0.15 M NaCl and 2 mM sodium metabisulfite. Following homogenization, the slurry of ground plant material was filtered on Miracloth to remove large insoluble debris. The pH of the extract was adjusted to 4.8 by addition of 1M HCl and the non-soluble materials were removed by centrifugation 18 000 g for 15 min (4° C.). The supernatant was collected and the pH was adjusted to 8.0 with Tris base 2M. The insoluble materials were removed by centrifugation at 18 000 g for 15 min at 4° C. and the crude extract (supernatant) was collected. The total protein content of clarified crude extracts was determined by the Bradford assay (Bio-Rad, Hercules, Calif.) using bovine serum albumin as the reference standard.
Leaf tissue was collected from the Nicotiana benthamiana plants and cut into ˜1 cm2 pieces. Leaf pieces were placed in 2.425 volumes of digestion solution (75 mM citrate pH 6.9, 600 mM mannitol, 1% Multifect Pectinase FE, 1% Multifect CXG, 1% Multifect B). This preparation was spread evenly into a shallow vessel and incubated for 16 hours on an orbital shaker at 120 rpm and 18° C. Following incubation, leaf debris were removed by filtration on a nylon filter (250 μm mesh). The extract was centrifuged at 5 000 g for 15 min. (22° C.) and the supernatant was collected and filtered on 0.65 μm glass fiber. The extract was adjusted to pH 6.0 with 0.5 M Tris base and filtered on PES membrane 0.45/0.22 μm.
Ammonium sulfate was slowly added to protein extracts to reach 45% saturation. The extract was kept on ice for 60 min and centrifuged at 18 000 g for 20 min. (4° C.). The supernatant was discarded and the pellet was kept frozen (−80° C.) until use.
The frozen protein pellet was thawed and resuspended in 1/10 volume (compared to the volume prior to precipitation) of protein resuspension solution (50 mM Tris pH 7.4, 150 mM NaCl). The protein solution was centrifuged at 12 000 g for 20 min. (4° C.) to remove non-solubilised materials. The protein solution was loaded onto MabSelect Sure resin (GE Healthcare, Baie d'Urfé, Canada). The column was washed with 10 CV of 50 mM Tris pH 7.4, 150 mM NaCl and the antibody was eluted with 6 CV of 100 mM sodium citrate pH 3.0. The elution volume was collected in 1 CV fractions in tubes containing 1/10 CV of 2 M Tris pH 7.4, NaCl 150 mM. Elution fractions were selected based on their protein content (measured by Bradford) and selected fractions were pooled and kept frozen (−80° C.) prior to analysis.
Total protein content was determined by the Bradford assay (Bio-Rad, Hercules, Calif.) using either bovine serum albumin (for crude protein extracts) or commercial rituximab (Rituxan®, Hoffmann-La Roche, Mississauga, Canada) (for purified antibodies) as the reference standard. Coomassie-stained SDS-PAGE was performed as described by Laemmli (Nature 1970, 227: 680-685).
Multiwell plates (Immulon 2HB, ThermoLab System, Franklin, Mass.) were coated with 2.0 μg/ml of monoclonal mouse anti-human IgG (Abcam, Ab9243) in 50 mM carbonate buffer (pH 9.6) at 4° C. for 16-18 h. Multiwell plates were then blocked through a 1 h incubation in 1% casein in phosphate-buffered saline (PBS) (Pierce Biotechnology, Rockford, Il) at 37° C. A standard curve was generated with dilutions of Rituximab (Rituxan®, Hoffmann-La Roche, Mississauga, Canada). When performing the immunoassays, all dilutions (control and samples) were performed in a plant extract obtained from plant tissue infiltrated and incubated with a mock inoculum (AGL1/R472 only) to eliminate matrix effect. Plates were incubated with protein samples and standard curve dilutions for 1 h at 37° C. After three washes with 0.1% Tween-20 in PBS (PBS-T), the plates were incubated with a peroxidase-conjugated dunkey anti-human IgG antibody (1/4000 dilution in blocking solution) (Jackson ImmunoResearch 709-035-149) for 1 h at 37° C. The washes with PBS-T were repeated and the plates were incubated with a 3,3′, 5,5′-Tetramethylbenzidine (TMB) Sure Blue peroxidase substrate (KPL, Gaithersburg, Md.). The reaction was stopped by adding 1N HCl and the absorbance was read at 450 nm. Each sample was assayed in triplicate and the concentrations were interpolated in the linear portion of the standard curve.
Samples comprising C2B8 (Rituxan™; 50 μg) were separated on 15% SDS/PAGE. Heavy and light chains were revealed with Coomassie blue and the protein band corresponding to the heavy chain was excised and cut into small fragments. Fragments were washed 3 times with 600 μL of a solution of 0.1M NH4HCO3/CH3CN (1/1) for 15 minutes each time and dried.
Reduction of disulfide bridges occurred by incubation of the gel fragments in 600 μL of a solution of 0.1M DTT in 0.1M NH4HCO3, at 56° C. for 45 minutes. Alkylation was carried out by adding 600 μL of a solution of iodoacetamide 55 mM in 0.1M NH4HCO3, at room temperature for 30 minutes. Supernatants were discarded and polyacrylamide fragments were washed once again in NH4HCO3 0.1M/CH3CN (1/1).
Proteins were then digested with 7.5 μg of trypsin (Promega) in 600 μL of 0.05M NH4HCO3, at 37° C. for 16 h. Two hundred μL of CH3CN were added and the supernatant was collected. Gel fragments were then washed with 200 μL of 0.1M NH4HCO3, then with 200 μL CH3CN again and finally with 200 μL formic acid 5%. All supernatants were pooled and lyophilized.
Glycopeptides were separated from peptides by chromatography on a Sep-Pack C18 cartridge. Glycopeptides were specifically eluted with 10% CH3CN in water and then analyzed by MALDI-TOF-MS on a Voyager DE-Pro MALDI-TOF instrument (Applied Biosystems, USA) equipped with a 337-nm nitrogen laser. Mass spectra were performed in the reflector delayed extraction mode using dihydrobenzoic acid (Sigma-Aldrich) as matrix.
Enzymatic digestion was compared to mechanical extraction for the extraction of C2B8 antibody. N. benthamiana plants were agroinfiltrated with AGL1/595 and AGL1/R472. After 6 days of incubation, the leaves were harvested and proteins were extracted by enzymatic digestion or mechanical extraction. Extractions were performed twice and the resulting extracts were compared for volume, protein concentration and antibody (C2B8) content. Results are presented in Table 16.
From 700 g of biomass, the mechanical extraction generated a average of 1440 ml of protein extract whereas the digestion generated 2285 ml of protein extract. The percentage of C2B8 antibody was higher in the extract from digestion (average value of 479% of extracted proteins) than in the extract produced in the blender (average value of 3.49% of extracted protein). Together, the higher volume of extract and the higher concentration of antibody found in the extract result in an 37% higher extraction yield for the digestion (240.75 mg C2B8/kg fresh weight) than the mechanical extraction (175.95 mg C2B8/kg fresh weight).
The C2B8 antibody was purified from the extracts by affinity chromatography on protein A as described in Example 10. The products purified from extracts obtained by mechanical extraction or digestion were compared on the basis of their protein content. The electrophoretic profile of the antibodies purified from each extraction lot is shown in
N-glycosylation of proteins consist in the addition of a complex glycan structure on the asparagine of secreted proteins bearing the N-X-S/T sequence, where N is the asparagine, X is any amino acid except a proline and S/T is a serine or a threonine. A precursor glycan is added early in the endoplasmic reticulum during the translation of the protein and, during their transit across the secretion pathway, N-glycans are subject to maturation. From a high-mannose type N-glycan in the endoplasmic reticulum (ER), N-glycan maturation in plants includes the addition and removal of glucose residues, the removal of mannoses in distal positions and the addition of N-acetylglucosamine, xylose, fucose and galactose residues. N-glycan maturation in plants is described by Gomord et al. in Post-translational modification of therapeutic proteins in plants (Curr. Opin. Plant Biol. 2004, 7: 171-181). Enzymes of the N-glycosylation pathway are positioned at precise locations in each compartment of the secretion pathway, namely the endoplasmic reticulum, the cis-Golgi, the medial Golgi and the trans-Golgi. Therefore, the N-glycosylation pattern of a protein will differ depending on its position at the moment of extraction. We have previously observed that a certain proportion of an antibody produced using agroinfiltration of N. benthamiana bore immature N-glycans of high mannose-type despite being targeted to the apoplast (Vézina et al., Plant Biotechnol. J. 2009 7: 442-455). A similar observation was reported elsewhere (Sriraman et al., Plant Biotechnol. J. 2004, 2, 279-287). In both cases, the presence of immature N-glycans on a certain proportion of antibodies was interpreted as the consequence of the presence of antibodies in early compartments of the secretion pathway at the moment of extraction.
The following study examined whether extraction of secreted glycoproteins by cell wall digestion was preferably extracting recombinant proteins bearing complex N-glycan. Antibodies and other glycoproteins secreted into the apoplast are expected to bear N-glycans having completed their maturation. Mature N-glycans most commonly bear terminal N-acetyglucosamine or galactose residues and are also named complex N-glycans. In contrast, immature N-glycans, mostly found on proteins en route in the secretory pathway, comprise terminal mannose residues. High mannose content of N-glycans on C2B8 (Rituxan™) has been associated with reduced half life in the blood stream (Kanda et al., Glycobiology 2006, 17: 104-118). In this context, an extraction method capable of favoring the extraction of apoplastic glycoproteins bearing complex N-glycans from plants would be desirable.
A comparative analysis of N-glycosylation on purified C2B8 antibodies was carried out as described in Example 10. The results demonstrate that the antibodies purified from digested biomass bore a significantly lower proportion of oligomannosidic N-glycans (
Extraction by cell wall digestion could also be applied to plants co-expressing a glycoprotein and one or more enzymes for modifying N-glycosylation profile as described in WO 20008/151440 (Modifying glycoprotein production in plants; which is incorporated herein by reference) for favoring the recovery of glycoproteins bearing modified mature N-glycans. For example, mature N-glycans could be reduced, or exempt of xylose and fucose residues.
The method to modify N-glycosylation may involve co-expressing the protein of interest along with a nucleotide sequence encoding beta-1.4galactosyltransferase (GalT; provided as SEQ ID NO:14 of WO 20008/151440), for example, but not limited to mammalian GalT, or human GalT however GalT from another sources may also be used. The catalytic domain of GalT (for example nucleotides 370-1194 of SEQ ID NO:14 as described in WO 20008/151440), may also be fused to a CTS domain of N-acetylglucosaminyl transferase (GNT1; for example, comprising nucleotides 34-87 of SEQ ID NO:17 as provided in WO 20008/151440), to produce a GNT1-GalT hybrid enzyme. The hybrid enzyme may be co-expressed with a sequence encoding the suprastructure protein of interest. Additionally, the sequence encoding the suprastructure of interest may be co-expressed with a nucleotide sequence encoding N-acetylglucosaminyltrasnferase III (GnT-III; SEQ ID NO:16 as described in WO 20008/151440). A mammalian GnT-III or human GnT-III, GnT-III from other sources may also be used. Additionally, a GNT1-GnT-III hybrid enzyme (SEQ ID NO:26; as described in WO 20008/151440), comprising the CTS of GNT1 fused to GnT-III may also be used.
All citations are herein incorporated by reference, as if each individual publication was specifically and individually indicated to be incorporated by reference herein and as though it were fully set forth herein. Citation of references herein is not to be construed nor considered as an admission that such references are prior art to the present invention.
One or more currently preferred embodiments of the invention have been described by way of example. The invention includes all embodiments, modifications and variations substantially as hereinbefore described and with reference to the examples and figures. It will be apparent to persons skilled in the art that a number of variations and modifications can be made without departing from the scope of the invention as defined in the claims. Examples of such modifications include the substitution of known equivalents for any aspect of the invention in order to achieve the same result in substantially the same way.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/CA10/01489 | 9/21/2010 | WO | 00 | 3/22/2012 |
| Number | Date | Country | |
|---|---|---|---|
| 61244786 | Sep 2009 | US |
