- Methodology article
- Open Access
High yield production of pigeon circovirus capsid protein in the E. coliby evaluating the key parameters needed for protein expression
© Lai et al.; licensee BioMed Central Ltd. 2014
Received: 20 January 2014
Accepted: 1 May 2014
Published: 22 May 2014
Pigeon circovirus (PiCV) is considered to be a viral agent central to the development of young pigeon disease syndrome (YPDS). The Cap protein, a structural protein encoded by the cap (or C1) gene of PiCV, has been shown to be responsible for not only capsid assembly, but also has been used as antigen for detecting antibody when the host is infected with PiCV. The antigenic characteristics of the Cap protein potentially may allow the development of a detection kit that could be applied to control PiCV infection. However, poor expression and poor protein solubility have hampered the production of recombinant Cap protein in the bacteria. This study was undertaken to develop the optimal expression of recombinant full-length Cap protein of PiCV using an E. coli expression system.
The PiCV cap gene was cloned and fused with different fusion partners including a His-tag, a GST-tag (glutathioine-S-transferase tag) and a Trx-His-tag (thioredoxin-His tag). The resulting constructs were then expressed after transformation into a number of different E. coli strains; these then had their protein expression evaluated. The expression of the recombinant Cap protein in E. coli was significantly increased when Cap protein was fused with either a GST-tag or a Trx-His tag rather than a His-tag. After various rare amino acid codons presented in the Cap protein were optimized to give the sequence rCapopt, the expression level of the GST-rCapopt in E. coli BL21(DE3) was further increased to a significant degree. The highest protein expression level of GST-rCapopt obtained was 394.27 ± 26.1 mg/L per liter using the E. coli strain BL21(DE3)-pLysS. Moreover, approximately 74.5% of the expressed GST-rCapopt was in soluble form, which is higher than the soluble Trx-His-rCapopt expressed using the BL21(DE3)-pLysS strain. After purification using a GST affinity column combined with ion-exchange chromatography, the purified recombinant GST-rCapopt protein was found to have good antigenic activity when tested against PiCV-infected pigeon sera.
These findings shows that the E. coli-expressed full-length PiCV Cap protein has great potential in terms of large-scaled production and this should allow in the future the development of a serodiagnostic kit that is able to clinically detect PiCV infection in pigeons.
Pigeon circovirus (PiCV), is a non-enveloped virus and is considered to be the viral agent central to the development of young pigeon disease syndrome (YPDS). YPDS syndrome is a multifactorial disease that includes various unspecific clinical signs such as poor racing performance, weight loss, lethargy, anorexia, respiratory distress and diarrhea . At present, PiCV is classified as a tentative member of circovirus family based on its particle size, its associated histopathology and the fact that it shares low-level DNA homology with psittacine beak and feather disease virus (BFDV) . According to the previous reports on the genomic characterization of PiCV, PiCV has been characterized as having an ambisense single-stranded DNA genome of about 2.0 kb [3, 4]. There are five open reading frames (ORFs) present on the ss-DNA; V1, C2, C3 and C4; these partially overlap within the PiCV genome. ORF C1 encodes a 30 kDa protein, which is the putative major component responsible for assembly of the viral capsid protein (Cap) . ORF V1 encodes a non-structural protein with putative replication-associated protein (Rep) activity . The ORFs C2, C3 and C4 encodes hypothetical proteins, the biological functions of which remain unclear. To date, some conventional methods have been used to detect the PiCV infection. These include electron microscopy, histological observation and molecular diagnosis including polymerase chain reaction (PCR), in situ hybridization and nucleic acid-based dot blot hybridization [5–10]. Enzyme-linked immunosorbent assay (ELISA) is a convenient and popular assay for diagnosis of virus infections and allows the investigator to target virus-specific antibodies in the sera of the host. Nevertheless, very few ELISA assay systems for detecting PiCV infection have been established successfully. Development of an ELISA system relies on the availability of viral antigens that are then used as ELISA coating antigen or for antibody production. However, the propagation of PiCV in cell culture has never been described, and harvesting viral antigen from pigeons is a tedious, ineffective and time-consuming process that results in a low yield. Thus, using a recombinant DNA method to express a PiCV viral antigen has been suggested to be a better strategy for the development of an ELISA assay system. In previously reports, only two expression systems have been used to produce PiCV Cap protein; these were a E. coli expression system and a baculovirus-insect cell expression system [11, 12]. However, the production of the recombinant full-length Cap protein was found to be hampered in E. coli due to a failure to express the first 39 amino acid residues at the N-terminus of the Cap protein, the coding sequence of which includes a significant number of codons that are rarely used in E. coli. Moreover, in above system, most of the expressed recombinant Cap protein was found to be in the form of inclusion bodies . The information available on the baculovirus-insect cell expression system for Cap protein expression in Sf9 does not provide information on productivity on a large scale that would allow further evaluation. In the above context, the E. coli expression system is still easier to carry out and is more cost-effective when applied to viral antigen production than the baculovirus-insect cell system, although the E. coli system does have some limitations.
To develop the Cap protein as coating antigen of an ELISA system, the above mentioned limitations associated with using an E. coli expression system need to be overcome; these include making sure that the full-length of the Cap protein is expressed in E. coli and using an expression system in which the majority of Cap protein is produced in a soluble form rather than as inclusion bodies. If successful, this would not only allow the efficient purification of capsid protein on a scale that would allow an investigation of PiCV structural biology but also the purified recombinant protein would be potentially useful when developing diagnostic kits for the clinical detection of PiCV infection.
In this study, the PiCV cap gene was fused to a series of different fusion tags in order to improve recombinant Cap (rCap) protein expression. The rCap was then expressed attached to three different expression tags in order to evaluate rCap fusion protein expression and production across a number of different E. coli strains. Three expression vectors were used, one harboring a glutathione-S-transferase (GST) tag, another harboring a 6xHis tag and finally, a third harboring a thioredoxin-6xHis (Trx-His); these were investigated to explore the effect of these very different fusion tags on the expression of rCap protein across various E. coli strains. In addition, optimizations of codon usage for various amino acids within the Cap gene were also carried out to give the rCapopt sequence and then the effect of these changes on expression of rCapopt in the various E. coli strains was assessed. Finally, purified rCapopt protein was examined in order to determine its antigenicity and therefore its usefulness in further serodiagnostic applications. To the best of our knowledge, the yield of E. coli expressed full-length rCapopt in this study after codon optimization of the cap gene is the highest known to date.
The fusion tags and the strain preference falicitates the expression level of recombinant PiCV capsid protein in E. coli
As a result of the above findings, expression of the PiCV rCap fusion protein in E. coli was carried out in two other E. coli strains, BL21(DE3)-pLysS and BL21(DE3)-RIPL and their protein expression levels compared to that of E. coli BL21(DE3). The expression patterns of the rCap fusion protein in E. coli BL21(DE3)-pLysS and in E. coli BL21(DE3)-RIPL containing pHis-Cap, pGST-Cap, and pTrx-His-Cap are shown in Figures 2A, B, C, respectively,. The expression patterns for the rCap fusion protein were relatively poor in BL21(DE3)-pLysS. No matter whether the His-rCap or GST-rCap protein was being expressed, the protein products were almost undetectable. In contrast, the 48 kDa specific protein band for Trx-His-rCap could be detected using anti-His monoclonal antibody when the BL21(DE3)pLysS strain containing pTrx-His-Cap was induced with IPTG (Figure 2C, lane 3–4 of SDS-PAGE and Western blot). In addition, when pGST-Cap and pTrx-His-Cap were transformed into BL21(DE3)-RIPL strain, the GST-rCap and Trx-His-rCap protein could be successfully expressed and detected by both SDS-PAGE and Western-blot analysis (Figure 2B, lane 5–6; Figure 2C, lane 5–6 of SDS-PAGE and Western blot). Overall, expression level of the Trx-His-rCap protein, was significant higher than that of the GST-rCap protein in BL21(DE3)-RIPL strain. However, in the BL21(DE3)-RIPL strain containing the pHis-Cap plasmid, expression of His-rCap was still almost undetectable after IPTG induction (Figure 2A, lane 5–6 of SDS-PAGE and Western-blot, respectively). Thus the fusion tags GST and Trx-His seem to be able to facilitate expression of PiCV rCap protein in E. coli and, moreover, the E. coli strain used also plays a crucial role in expression and seems to affect the further application of these strains in large-scale production.
Optimization of the codon usage of the cap gene enhances of recombinant PiCV capsid protein expression in E. coli
Based on the results shown in Figure 2A, B and C, the expression levels of rCap were improved in E. coil when a Trx-His tag or GST tag on the N-terminus of rCap protein was used. The best expression was obtained using the strain BL21(DE3)-RIPL, which harbors extra copies of tRNAargU, proL, ileY, leuW. This is commercial E. coli host strain used for the gene expression of recombinant proteins that contain E. coli’s rare codons. The expression of Trx-His-rCap protein in strain BL21(DE3)-RIPL showing an expression level was significant higher than when the BL21(DE3) and BL21(DE3)-pLysS strains were used (Figure 2B, lane 5–6; Figure 2C, lane 5–6), this suggested that optimization of the codon usage in the rCap protein might further improve the expression level of rCap.
Furthermore, the quantitative yield for the Trx-His-rCapopt protein in the BL21(DE3)-pLysS strain after IPTG induction for 4 h reached 544.5 ± 33.2 µg/ml at the same optical density (OD) as the cultures, which represents a 5.07 fold increase over Trx-His-rCap in BL21(DE3)-pLysS by densitometric analysis (Figure 2C, panel 3–4 for Trx-His-rCap and panel 9–10 for Trx-His-rCapopt; right panel of Figure 3B). In addition, the yield of Trx-His-rCapopt protein in BL21(DE3)-pLysS was higher than that of Trx-His-rCapopt protein at 283.3 ± 9.0 µg/ml using BL21(DE3) strain and IPTG induction (right panel of Figure 3C). These findings confirm that the codon-optimized of the cap gene was able to improve protein expression significantly and allowed large amounts of intact rCapopt protein to be produced in E. coli BL21(DE3) or in BL21(DE3)pLysS with either the GST or the Trx-His fusion tag.
Chromatographic purification of recombinant PiCV capsid protein
Application of recombinant PiCV capsid protein on sero-diagnosis
PiCV infection is associated with development of young pigeon disease syndrome (YPDS). At present, no vaccine is available to prevent PiCV infection. Among circovirus, capsid proteins have been investigated as to their usefulness as immunogens for developing subunit vaccines [13–15]. The Cap protein is the only capsid protein encoded by PiCV. Generally speaking, PiCV Cap protein is thought to be a promising target for the production of a recombinant vaccine or the development of a sero-diagnostic kit [11, 12]. Recently, a truncated form of PiCV Cap protein has been shown to have been successful expressed in E. coli. However, expression of full-length recombinant PiCV Cap protein using an E. coli system has remained very difficult.
E. coli remains the most attractive expression system when assessing the expression of a heterologous protein for many different purposes . Using an E. coli expression system to express a heterologous recombinant protein has several advantages; these include cost-effectiveness, ease of production, time-saving and others. In this study, we have successfully produced for the first time the full-length Cap protein of PiCV using an E. coli expression system Previously, it has been suggested that the Cap protein is likely to be the sole structural protein of PiCV and this protein thus controls viral capsid assembly. Thus, have purified full-length Cap protein will help with the detailed study of PiCV's structure biology and it will also help with PiCV vaccine development and the production of a serodiagnostic kit for PiCV detection. The PiCV Cap protein has been demonstrated to have antigenic activity and to be able to recognize by PiCV specific antibodies [11, 12]. However, up to the present, a lack of highly purified full-length Cap protein has hindered research in these areas. The main problem with the E. coli approach to producing PiCV Cap protein has been poor protein expression and low protein solubility. Previous studies have shown that the production of recombinant Cap protein using an E. coli expression is relatively difficult and therefore this has become a bottle-neck . This study surmounts this problem and will allow the efficient production of recombinant PiCV Cap protein for future investigations.
A number of different strategies are available when improving protein expression and enhancing the protein solubility in E. coli. These factors include cultivation parameters, the fusing of an affinity tag of one type or another to the target protein and the optimization for E. coli of the codon usage of the foreign gene. [13, 17, 18]. This study explored how three different fusion tags, GST, His-tag and Trx-His tag, affected Cap protein expression; other fusion tag remain untested and may give further improvement in the future. Both a GST and a Trx-His fusion tag was found to significantly improve the yield of rCap protein compared to a 6 × His tag (Figure 2A, B and C). In a previous study, Liu et al. described how the expression of the Cap protein of porcine circovirus (PCV) was successfully improved in E. coli by fusing the maltose-binding protein (MBP) to the target protein , but the mechanism by which a fused MBP-8xHis tag is able to improve protein expression remains unclear. Nonetheless, one possibility is that protein solubility was improved . Similarly, in our previous study, the addition of a GST tag to the CAV VP1 protein also improved expression in E. coli significantly compared to a His × 6 tag . Thus some fusion tags would seem to be able to help improve the solubility of E. coli expressed proteins more than other tags; this occurs perhaps by promoting the correct folding of their selected fusion partner [13, 19].
Like porcine circovirus (PCV), beak and feather disease virus (BFDV) and chicken anemia virus (CAV), PiCV is also rich in basic amino acid residues close to the N-terminus of the capsid protein. This region has been predicted to be a nuclear localizing sequence and a nucleic acid binding domain via the DNAbinder software package (http://www.imtech.res.in/raghava/dnabinder/submit.html). In previous studies, this N-terminal regions of capsid proteins have often caused problems with recombinant protein expression using a prokaryotic system [11, 13, 20]. Deletion of the N-terminus of the capsid protein can often overcome this problem allowing the protein to be expressed successfully in E. coli; nonetheless, the usefulness of the truncated protein for diagnosis or for the development of a subunit vaccine is likely to be hampered. Obviously only the intact capsid protein contains all of the epitopes for elicitation of virus neutralizing antibodies by the host. Thus, it is best to express full-length PiCV capsid protein rather than a truncated form when developing a vaccine or a diagnostic kit.
The present study found that the E. coli strain BL21(DE3)-RIPL, when used to express Trx-His-rCap, gave the highest level of protein expression, significantly higher than any other combination (Figure 2B, lane 5–6; Figure 2C, lane 5–6). This demonstrated that extra copies of tRNAargU, proL, ileY, leuW are able to improve PiCV Cap protein expression usefully. In addition, it confirms that the E. coli rare codons with the cap gene have a significant effect on its expression. Using the GeneScript rare codon analysis tool, it was found that approximately 18% of the codons in the PiCV cap gene are rare E. coli codons. It had been suggested than when a target gene contains >10% rare cordons of E. coli, protein expression efficiency is likely to be decreased . Rosenberg et al. also described how the efficiency of protein translation might be affected by an abundance of rare codons near the 5’-end of the gene. Thus, when a codon-optimized cap gene was used, rCapopt, rather than rCap, expression of the Cap protein was significantly enhanced in E. coli compared to supplying extra copies of the rare tRNA genes via the expression strain.
We also investigated which of two different recombinant E. coli strains, BL21(DE3) and BL21(DE3)pLysS, was able to improve protein production and yield. With both GST-Capopt and Trx-His-Capopt, expression was better with BL21(DE3) and produced more Cap protein than BL21(DE3)-RIPL (right panel of Figure 3A and 3B). It is worth noted that BL21(DE3)pLysS has a higher growth rate than BL21(DE3) or BL21(DE3)-RIPL when expressing Trx-His-Capopt or Trx-His-Cap. (left panel of Figure 3B). This discrepancy may involve either higher protein stability or Trx-His-Capopt having a less cytotoxic nature when present in BL21(DE3)pLysS. However, these effect were not present during the production of GST-Capopt protein using E. coli BL21(DE3)pLysS at high expression levels. The superiority of Trx-His-Capopt expression in BL21(DE3)pLysS may be due to the presence in the strain of the pLysS plasmid during protein induction. The cytotoxicity tolerance of BL21(DE3)pLysS might be associated with the expression of T7 lysozyme which attenuates transcription leakage by T7 RNA polymerase. However, this phenomenon was not significant when GST-Capopt was expressed grown using BL21(DE3)pLysS. GST-Capopt was decreased when there was induction by IPTG. One possibility is that the cytotoxicity of GST-Capopt may be higher that that of Trx-His-Capopt in BL21(DE3)pLysS. In other words, a “protein burden” may not yet have been encountered when BL21(DE3)pLysS was used to express Trx-His-Capopt. Overall, we concluded that BL21(DE3)pLysS is the preferred choice for expressing Trx-His-Capopt.
The solubility of recombinant Cap protein is a potential problem and in this context the solubility of GST-Capopt protein is superior to that of Trx-His-Capopt. Furthermore, it is very easy to apply the protein to a GST-affinity column in order to carry out a protein purification. Moreover, the Cap protein contains basic amino acid residues rich at its N-terminus. Such highly positive charge amino acids within the recombinant Cap protein allow easy polishing by cation exchange column as part of down-stream processing. Therefore, it seems likely that, a higher purity of Cap protein can be obtained when an affinity column is combined with an ion-exchange chromatography during vaccine development.
In this study, positive PiCV-infected pigeon sera were used to evaluate the antigenic activity of the E. coli-expressed recombinant PiCV Cap protein. All tested PiCV-infected pigeon sera were able to demonstrate that E. coli-expressed recombinant PiCV Cap protein has the correct antigenic activities. This might be a result of the E. coli-expressed recombinant Cap protein displaying all of the appropriate protein antigenic regions on the protein surface for recognition by the pigeons' antibodies. However, rCap protein when used against some pigeon sera did not show very strong antigenicity. This perhaps suggests that the titers of antibodies against PiCV Cap protein have various levels in pigeons and such variation might explain in lower performance of antigenicity in certain birds.
In conclusion, using a prokaryotic system, the optimal expression of recombinant full-length PiCV Cap protein was established successfully during this study. Furthermore, by fusing the Cap protein to an affinity tag, by using the appropriate preferred E. coli and by optimizing the codon usage of the polypeptide, it was possible to increase the yield of Cap fusion protein significantly. In this context, a convenient and cost-effective strategy for increasing the expression of Cap protein, which was used herein, was the direct engineering of the codons of the Cap protein to fit the E. coli codon preferences. This approach paves the way for the large-scale efficient production of the PiCV Cap protein. In the future, this will also allow recombinant Cap protein to be used as a potential antigen for the development of a PiCV diagnostic test.
Bacterial strains and cell inoculation
Three commercial E. coli strains, BL21(DE3) (Invitrogen, Carlsbad, CA), BL21(DE3)CodonPlus-RIPL (Stratagene, La Jolla, CA) and BL21(DE3)pLysS (Stratagene, La Jolla, CA) were used and maintained at 37°C in the Luria-Bertani (LB) medium (1% tryptone, 0.5% yeast extract, 1% NaCl, pH 7.0). First, 0.5 mL of an overnight culture was inoculated into 50 mL LB medium to allow strain activation by growth at 37°C for around 3 hours, by which time the optical density of culture had reach 0.5 of OD600. These bacterial cells were then used for transformation.
Construction of the recombinant plasmids
A 822 bp of cDNA fragment consisting of the cap gene that encodes the full-length PiCV capsid protein was synthesized by Genemark Biosci & Tech Co. (Taichung, Taiwan) based on the published sequence (Columbid circovirus, isolate 9030; Accession No. AJ298229). This cDNA was cloned into either pET28a, pET32a (Novagen, Madison, WI) or pGEX-4T-1 (GE Healthcare, Piscataway, NJ) individually using EcoR1 and XhoI (Takara, Japan) restriction sites. The resulting recombinant plasmids were designated pHis-Cap, pTrx-His-Cap and pGST-Cap, respectively (Figure 1, panel a, e and c). To improve the codon usage of the cap gene from PiCV, a second cDNA sequence was synthesized by Genemark Biosci & Tech Co that contained the codons that were optimized for E. coli; this was also ligated individually into the same three E. coli expression vectors using the same restriction sites; these constructs were designated pHis-Capopt, pTrx-His-Capopt and pGST-Capopt, respectively (Figure 1, panel b, f and d). The six constructs were then individually transformed into One Shot® Top10 (Invitrogen, CA) chemically competent E. coli for maintenance of the recombinant plasmids. Transformants that containing a insert of the correct size were then confirmed as correct by restriction enzyme digestion and by DNA sequence analysis.
Expression of recombinant Cap protein (rCap) and codon optimized Cap protein (rCapopt) in E. coli
To express the recombinant rCap or rCapopt protein, all the constructed recombinant plasmids carrying either the cap gene or the codon-optimized cap gene, as described in Figure 1, were transformed into various E. coli strains to allow evaluation of protein expression. Three commercial E. coli host strains, BL21(DE3), BL21(DE3)CodonPlus-RIPL and BL21 (DE3)pLysS, each with a different recombinant construction, were used for protein induction and expression. The culture conditions, the composition of the LB medium and the protein induction condition of these recombinant strains have been described previously . After IPTG induction, samples of the cells were harvested and analyzed for protein expression. The total protein was measured by the procedure described in a previous study . Samples containing the expressed Cap or Capopt proteins were analyzed by 12.5% SDS-PAGE and Western-blotting using a monoclonal anti-His antibody (Invitrogen, Carlsbad, CA) or a monoclonal anti-GST antibody (GE healthcare, Piscataway, NJ).
Purification of recombinant Capoptprotein using GST affinity chromatography with on-column cleavage by thrombin
Recombinant rCapopt protein was purified from cells expressing the GST-rCapopt protein. This was carried out by spinning down 50 mL of culture supernatant and resuspended the pellet in GST resin binding buffer (140 mM NaCl, 2.7 mM KCl, 10 mM Na2HPO4, 1.8 mM KH2PO4, pH 7.3). The mixture was then sonicated on ice three times for 3 minutes using a 20% pulsed activity cycle (MISONIX Sonicator® 300). Next, the lysate was centrifuged for 10 min at 10,000 rpm to remove the cell debris. The resulting cell supernatant was loaded onto a GSTrap FF affinity column (GE healthcare, Piscataway, NJ) for protein purification using the standard procedure described in a previous study . The total protein concentration of each collected fraction from the column was determined using a Micro BCA kit (Pierce, Rockford, IL) with bovine serum albumin acting as the reference protein. The purity of the protein from each fraction was analyzed by 12.5% SDS-PAGE and then the resulting gels were Western blotted using monoclonal anti-GST antibody (GE Healthcare, Piscataway, NJ).
To confirm the identity of the recombinant Capopt protein, E. coli expressed GST-rCapopt protein that had been purified by GSTrap FF column was used. The rCapopt protein that had been eluted from the GSTrap FF column was loaded onto a SP cation exchange chromatography column (GE Healthcare) for further purification. The cation exchange column-purified rCapopt protein was then analyzed by 12.5% SDS-PAGE. The relevant band was then cut out from the 12.5% SDS-PAGE gel after coomassie blue staining and digested with trypsin. The resulting peptides were subjected to the MALDI-TOF-MS mass spectrometry (ESI-QUAD-TOF) to allow amino acid sequence identification of the protein, as described in a previous study .
This work was supported by the grant from China Medical University of Taiwan (CMU100-TS-05) and the National Science Council (NSC 95-2313-B-039-004-, NSC96-2313-B-276-001-MY3 and NSC102-2321-B-039-007-), Taiwan.
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