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Apoptin, a nonstructural protein encoded by the VP3 gene of chicken anemia virus (CAV), has been shown to not only induce apoptosis when introduced into the precursors of chicken thymocytes, but has been found to specifically kill human cancer cells, tumor cell and transformed cells without affecting the proliferation of normal cells. This tumor-specific apoptotic characteristic of the protein potentially may allow the development of a protein drug that has applications in tumor therapy. However, several major problems, which include poor expression and poor protein solubility, have hampered the production of apoptin in bacteria.
Significantly increased expression of recombinant full-length apoptin that originated from chicken anemia virus was demonstrated using an E. coli expression system. The CAV VP3 gene was fused with a synthetic sequence containing a trans-acting activator of transcription (TAT) protein transduction domain (PTD). The resulting construct was cloned into various different expression vectors and these were then expressed in various E. coli strains. The expression of the TAT-Apoptin in E. coli was significantly increased when TAT-Apoptin was fused with GST-tag rather than a His-tag. When the various rare amino acid codons of apoptin were optimized, the expression level of the GST-TAT-Apoptinopt in E. coli BL21(DE3) was significantly further increased. The highest protein expression level obtained was 8.33g/L per liter of bacterial culture after induction with 0.1mM IPTG for 4h at 25°C. Moreover, approximately 90% of the expressed GST-TAT-Apoptinopt under these conditions was soluble. After purification by GST affinity chromatography, the purified recombinant TAT-Apoptinopt protein was used to evaluate the recombinant protein’s apoptotic activity on tumor cells. The results demonstrated that the E. coli-expressed GST-TAT-apoptinopt showed apoptotic activity and was able to induce human premyelocytic leukemia HL-60 cells to enter apoptosis.
On expression in E. coli, purified recombinant TAT-Apoptinopt that has been fused to a GST tag and had its codons optimized, was found to have great potential. This protein may in the future allow the development of a therapeutic protein that is able to specifically kill tumor cells.
Chicken anemia virus (CAV), is a non-enveloped virus and the causative agent of chicken anemia disease. The disease results in aplastic anemia, lymph organ atrophy and immunosuppression in chickens [1-3]. The virus transcribes and translates three viral proteins, VP1, VP2 and VP3, which are respectively encoded by ORF3, ORF1 and ORF2 of the CAV genome. VP1 protein (51kDa) is the sole structural protein of CAV and is responsible for capsid assembly . The VP2 protein (30kDa) is a nonstructural protein that possesses a dual-specificity protein phosphatase (DSP) . The VP3 protein (13kDa), also called apoptin, is a strong inducer of apoptosis in precursor chicken thymocytes and various human transformed and tumor cell lines but not in normal cells . At present, the full anti-tumor mechanism of apoptin remains unclear. However, it is worth mentioning that apoptin-induced apoptosis in tumor cells is p53-independent and also is not suppressed by Bcl-2 or BCR-ABL protein . Thus, apoptin is thought to be a good candidate for use as a therapeutic protein and has potential to be developed as a cancer treatment, including those cancers that lack p53.
To develop apoptin as an anti-cancer drug, efficient transduction tools such as recombinant virus and a recombinant plasmid within liposomes have been used to deliver apoptin into tumor cells . However, these approaches have restrictions in terms of therapeutic application including a size limitation of the genes that can be delivered, insertional mutagenesis and transient expression [9-11]. Novel cell-penetrating peptides, such as the trans-acting activator of transcription (TAT) protein transduction domain (PTD), which consists of 11 amino acid residues (aa 47-57, YGRKKRRQRRR) have therefore been used as vectors for protein delivery [8,12]. With respect to apoptin, previously studies have been demonstrated that apoptin fused with a TAT peptide shows apoptotic activity against tumor cells because the TAT peptide’s delivery system is able to move apoptin into cells [13,14].
Up to the present, a number of different expression systems have been used to express apoptin, including E. coli, baculovirus-insect cells and plant cells [15-18]. However, production of recombinant full-length apoptin/VP3 protein has generally been possible only in E. coli. Several production problems involving the expression efficiency and protein solubility of apoptin in E. coli have been encountered [13,17,18]. Thus, there is a need to overcome these difficulties in order to scale-up production of full-length apoptin protein using an E. coli expression system. If successful, this would not only allow the efficient development of a therapeutic protein that is able to actively kill cancer cells specifically but the recombinant protein would also be potentially useful when developing diagnostic kits for the clinical detection of CAV infection .
It is clear that E. coli has a number of limitations and disadvantages in terms of the production of apoptin protein. However, expression of apoptin protein in E. coli is still an attractive alternative to the current production system when assessed in terms of cost, time and operational considerations. In this study, the CAV VP3 gene was fused to a synthetic gene containing the trans-acting activator of transcription (TAT) protein transduction domain (PTD). This protein, named TAT-Apoptin, was expressed using various different expression vectors in order to evaluate TAT-Apoptin expression and production by a number of different E. coli strains. Two expression vectors were used, one harboring a glutathione-S-transferase (GST) tag and the other a 6xHis tag; these were investigated to explore the effect of these fusion tags on the expression of TAT-Apoptin in the various E. coli strains. In addition, changes in codon usage for various amino acids within the VP3 gene were also assessed in terms of their effect on expression of TAT-Apoptinopt. Rare codons for E. coli within the VP3 gene of the TAT-Apoptin protein were optimized using prediction software and the preferred codon usage changed to that of E. coli. After this optimization, the expression levels of the modified VP3 genes were examined in various E. coli strains and the various production parameters for TAT-Apoptinopt protein expression assessed. To the best of our knowledge, the yield of E. coli expressed recombinant TAT-Apoptinopt in this study after codon optimization of the VP3 gene is the highest known to date.
To develop apoptin protein as anti-tumor drug, a composite cDNA of the CAV VP3 gene fused synthetic gene of TAT peptide was used to create two distinct expression constructs of TAT-Apoptin (Figure 1A, a and b). These constructs, pET-TAT-VP3 and pGEX-TAT-VP3, were transformed into three different E. coli strains in order to investigate the effect of the fusion tags on the expression of TAT-Apoptin. The 6×His and GST tags were fused with TAT-Apoptin at the N-terminus using the expression vectors pET28a and pGEX-4T-1, respectively. The expression of these two TAT-Apoptin constructs in various E. coli strains was explored (Figure (Figure2).2). When E. coli BL21(DE3) was used, significant amounts of full-length TAT-Apoptin protein were present in the whole cell lysate after IPTG induction for 4h with either pET-TAT-VP3 or pGEX-TAT-VP3 (Figure (Figure2B,2B, SDS-PAGE and Western-blotting). The 16kDa His-TAT-Apoptin and the 42kDa GST-TAT-Apoptin were detected using monoclonal anti-His antibody and anti-GST antibody, respectively (Figure (Figure2B,2B, lane 4 of Western-blot). Densitometric analysis of the blots showed that total expressed GST-TAT-Apoptin protein, both soluble and insoluble, from BL21(DE3) was approximately 19 fold greater than that of His-TAT-Apoptin produced under identical conditions (Figure 3A and C). When His-TAT-Apoptin and GST-TAT-Apoptin were induced for between 1 and 4h, the expression of both proteins continued to increase significantly over the 2-4h induction range (Figure 3A and C) with the highest amount of His-TAT-Apoptin protein produced being 0.34mg/ml at 4h of IPTG induction. In contrast, the highest amount of GST-TAT-Apoptin produced was 7.13mg/ml at 4h. A similar pattern of expression was observed for the two proteins in BL21(DE3)CodonPlus-RP and BL21(DE3)pLysS strains (Figure (Figure2).2). The highest amounts of GST-TAT-Apoptin produced by BL21(DE3)CodonPlus-RP and by BL21(DE3)pLysS were 2.43 and 1.15mg/ml, respectively, after 4h of IPTG induction (Figure 3A and C). The parallel results for His-TAT-Apoptin were 0.09 and 0.82mg/ml, respectively (Figure 3A and C). Thus the GST fusion tag improved protein expression significantly and allowed large amounts of intact TAT-Apoptin protein to be produced.
CAV VP3 gene that encodes the apoptin protein consists of 121 amino acid codons. The rare codons for E. coli within the VP3 gene were pinpointed using the GenScript Rare Codon Analysis Tool (http://www.genscript.com/cgi-bin/tools/rare_codon_analysis). The deduced amino acid sequence of apoptin was found to contain 15% basic amino acid residues such as arginine (R) and lysine (K) (Figure (Figure1B).1B). Overall, approximately 21% rare E. coli codons were present in the VP3 gene, including arginine, leucine, isoleucine, proline, cysteine, threonine, serine and glycine codons (Figure (Figure1B).1B). The presence of these codons is one possible reason for the relatively poor expression of apoptin in E. coli.
We have shown that expression of full-length TAT-Apoptin in E. coli is improved by fusing a GST tag to the N-terminus of the TAT-Apoptin protein. However, adding a His tag to give His-TAT-Apoptin did not produce such a yield improvement even when the optimal host strain BL21(DE3)pLysS is used (Figures2A and and3A).3A). Therefore, we next explored the effect on TAT-Apoptin productivity of optimizing the codon usage of the VP3 gene for E. coli. The TAT-Apoptin gene was engineered such that AGA/CGA/CGG were changed to CGT or CGC (R), CCC/CCT were changed to CCG or CCA (P), CTC/CTA/TTG were changed to CTG (L), ATA was changed to ATC (I), GGA/GGG were changed to GGT (G), ACT/ACA were changed to ACC (T), and CAA was changed to CAG (Q) (Figure (Figure1B).1B). The codon optimized VP3 gene was then linked to the TAT sequence at 5’ end of the VP3 gene to give an intact open reading frame. The new codon-optimized TAT-VP3 gene, denoted TAT-VP3opt, was then cloned into pGEX-4T-1 and pET28a to give pGEX-TAT-VP3opt and pET-TAT-VP3opt, respectively (Figure 1A, d and c). These plasmids were then individually expressed in E. coli. When expression in E. coli strain BL21(DE3) using whole cell lysate was analyzed by SDS-PAGE and Western blotting, both GST-TAT-Apoptinopt and His-TAT-Apoptinopt were successfully expressed after IPTG induction (Figure 4A and C) with a yield after 4h IPTG induction of about 9mg/ml and 0.65mg/ml, respectively. The yield of GST-TAT-Apoptinopt was almost 13 fold higher than His-TAT-Apoptinopt (0.65mg/ ml) (Figure 5A and C). BL21(DE3)-pLysS, similarly, gave increased expression of both His- TAT-Apoptinopt and GST-TAT-Apoptinopt (Figure 4A and C). The highest yields of GST-TAT-Apoptinopt and His-TAT-Apoptinopt in BL21(DE3)pLysS were obtained after 4h IPTG induction and were 6.38 and 1.2mg/ml, respectively (Figure 5A and C). These results confirm that the codon-optimized of TAT-Apoptin improved protein expression significantly and allowed large amounts of intact TAT-Apoptinopt protein to be produced in either E. coli BL21(DE3) or BL21(DE3)pLysS with either fusion tag.
In addition to the expression level of TAT-Apoptinopt, the solubility of TAT-Apoptinopt protein is also needs to examine and improved. To this end, the cultivation parameters and their effect on the TAT-Apoptinopt protein solubility were explored, namely cultivation temperature and the IPTG concentration for induction; GST-TAT-Apoptinopt was used as the model protein. Protein solubility and the expression levels of GST-TAT-Apoptinopt were determined using E. coli BL21 (DE3) at 25°C and 37°C. As shown in Figure Figure6A,6A, an increased amount of soluble GST-TAT-Apoptinopt was obtained after IPTG induction at 25°C. Approximately 15% and 65% of the GST-TAT-Apoptinopt in the whole cell lysate of the BL21(DE3) strain was soluble at 37°C and 25°C, respectively. In addition, the amounts of GST-TAT-Apoptinopt protein expressed in BL21(DE3) were 8.33mg/ml and 8.99mg/ml, respectively, at 25°C and 37°C after 4h IPTG induction (Figures5C and and7A);7A); thus the total amount of GST-TAT-Apoptinopt protein obtained at 25°C compared to 37°C was only very slightly lower (Figures5C and and7A7A).
When various IPTG induction concentration from 0.1 to 1mM were explored for protein induction, the highest amount of GST-TAT-Apoptinopt protein obtained was with 1mM IPTG induction using the BL21(DE3) strain (Figure (Figure6B)6B) and this gave about 65% soluble protein at 25°C (Figure (Figure6C).6C). The expression level of GST-TAT-Apoptinopt at 0.1 and 0.5mM IPTG was lower than for 1mM IPTG (Figure (Figure6B),6B), but the amount of soluble protein was highest at 0.1mM (95%) IPTG (Figure (Figure6C).6C). Thus a lower cultivation temperature of 25°C and an IPTG concentration of 0.1mM IPTG were able to produce the higher amount of soluble GST-TAT-Apoptinopt protein.
Using the approximately 95% soluble GST-TAT-Apoptinopt expressed by E. coli at 25°C and 0.1mM IPTG, the lysate was subjected to purification using a GST affinity column. After affinity chromatography, the eluted soluble GST-TAT-Apoptinopt protein was confirmed antigenically using anti-GST antibody and CAV-infected positive serum (Figure 8A, B and C). A typical elution profile of the protein fractions collected from a GST column is shown in Figure Figure8A8A after separation by SDS-PAGE. Fraction 4 contains the most eluted protein, has a significant absorbent peak at OD280 and was eluted at 12min (data not shown). The specific 42kDa band eluted in fraction 4 was almost purified to homogenicity (Figure (Figure8A,8A, lane 4 of elution). When the purified GST-TAT-Apoptinopt protein was examined by MALDI-TOF, seven peptides from GST-TAT-Apoptinopt could be identified after trypsin digestion and these demonstrated good alignment and a high score when compared to the predicted protein (data not shown). The longest peptide fragment, VNELKESLITTTPSRPR, consists of 17 amino acid residues and overall the coverage was 35.7% of the published amino acid sequence of apoptin (Accession No. AF212490) without any miss-match (Figure (Figure8D).8D). These MALDI-TOF results confirmed that the purified 42kDa protein is GST-TAT-Apoptinopt and that the E. coli preferred codon usage optimization within the VP3 gene has not altered either the amino acid sequence (Figure (Figure8C;8C; Figure Figure8B,8B, lane 4) or the antigenicity (Figure (Figure8C)8C) of the protein.
To investigate whether GST-TAT-Apoptinopt protein expressed by E. coli has apoptotic activity when introduced into tumor cells, purified GST-TAT-Apoptinopt protein was used to examine the protein's apoptotic activity when it was used to treat human premyelocytic leukemia HL-60 cells. As illustrated in Figure Figure9,9, flow cytometry analysis by Annexin-V FITC and propidium iodide staining showed an approximately 10% increase in the level of apoptotic levels among HL-60 cells that were co-cultured with GST-TAT-Apoptinopt compared to HL-60 cells only, HL-60 co-cultured with GST or chromatographic elution buffer. However, compared to the control, HL-60 cells co-cultured with GST-TAT-Apoptinopt induced less apoptosis than when HL-60 cells were induced into apoptosis by treatment with cyclohexamide (CHX). Nevertheless, GST-TAT-Apoptinopt was able to induce apoptosis in HL-60 cells to a meaningful degree. These results indicate that E.coli expressed GST-TAT-Apoptinopt retains the protein’s original apoptotic activity when used to treated HL-60 cells even after the modifications carried out in this study.
Apoptin from chicken anemia virus has been demonstrated to have apoptotic activity and to be able to specifically kill several types of tumor cells including the cell lines HeLa, Saos-2, lung cancer cells H1299 and HepG2 [9-11,13,14,19]. Apoptin is not only p53 and Bcl- independent, but also does not require specific post-modification in order to be able to induce apoptosis . Therefore, apoptin has great potential to be developed into a protein drug that will be useful as part of the cancer therapy armory. In this context, previously studies have shown that fusing the TAT peptide to apoptin, in order to create a recombinant protein vehicle, which allows protein uptake by cells, improves protein translocation into the cell and increases Saos-2 cell killing . This approach is a useful was of overcoming problems associated with the delivery of apoptin into cells without affecting the anti-cancer activity of the protein. However, up to the present, few studies have investigated anti-cancer activity using such a recombinant TAT-Apoptin protein. The main reason for this lack of progress is the poor expression and low protein solubility of TAT-Apoptin. Previous studies have shown that the large-scale production of recombinant TAT-Apoptin using a prokaryotic expression is difficult and therefore this has become a bottle-neck [17,18]. Even today, in spite of the fact that many eukaryotic expression systems are well established, various factors, such as cost-effectiveness, insertional mutagenesis and transient expression, still need to be resolved for these systems. Taking the above into consideration, the effective production of TAT-Apoptin protein using a prokaryotic system is a crucial key step in developing this protein drug as an anti-tumor therapy. Therefore, in this study, the specific aim was to develop a prokaryotic expression system that allowed the efficient production of recombinant TAT-Apoptin protein. Using a prokaryotic expression system to express heterologous recombinant protein has several advantages including time-savings, cost-effectiveness, ease of production, simplified characterization and others. It is for these reasons that E. coli is the most used expression system when evaluating the expression of a foreign protein . Indeed, the above points are some of the critical factors associated with choosing a suitable production system when developing a protein drug. To this end, problems associated with having a truly effective system for the large-scale production of apoptin protein still needed to be explored.
To improve protein expression and to enhance the solubility of any protein produced in an E. coli expression system, a number of strategies are available. These include cultivation parameters, the effect of fusing the protein to an affinity tag and the optimization of codon usage of foreign gene for E. coli. All of these have been frequently employed to improve the amount of recombinant protein recovered [17,18,21-23]. In the present study, we first explored the effect of two different fusion tags on TAT-Apoptin expression, although others remain available, are untested as yet and may further improve the yield in the future. The presence of a GST fusion tag was found to significantly improve the yield of TAT-Apoptin compared to a 6×His tag (Figures2 and and3).3). In a previous study, Liu et al successfully overcame the problem of less efficient expression in E. coli of porcine circovirus (PCV) by fusing the maltose-binding protein (MBP) to an 8xHis tag . The main mechanism by which the MBP-8xHis tag improved protein expression remains unclear. However, one possibility is improved protein solubility . 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 it would seem that some fusion tags are able to improve expression of soluble protein in E. coli compared to other tags, perhaps by aiding the correct folding of their fused partner [21,24].
Next we investigated which of three different E. coli strains, BL21(DE3), BL21(DE3)pLysS and BL21(DE3)Codonplus-RP, was able to improve protein production and yield. With both GST-TAT-Apoptin and His-TAT-Apoptin, BL21(DE3) was preferred and produced more TAT-Apoptin protein than either BL21(DE3)pLysS or BL21(DE3)Codonplus-RP (Figure 2A and C). It is worth noting that BL21(DE3)pLysS has a higher growth rate than BL21(DE3) or BL21(DE3)Codonplus-RP when expressing His-TAT-Apoptin (Figure 2B and D). This discrepancy may involve either poor protein stability or the cytotoxic nature of His-TAT-Apoptin when present in BL21(DE3) and BL21(DE3)Codonplus-RP. These results are similar to those obtained for the production of GST-VP1 protein from CAV in E. coli at low expression levels . BL21(DE3)pLysS superiority may be due to the presence in the strain of the pLysS plasmid during protein induction [17,21]. This difference may enable BL21(DE3)pLysS to tolerate cytotoxicity associated with the expression of T7 lysozyme by attenuating the transcription leakage by T7 RNA polymerase [17,21]. However, this phenomenon was not important when GST-TAT-Apoptin was expressed and the growth profiles of the three strains producing GST-TAT-Apoptin were almost identical on induction by IPTG. In this area, it is possible that the cytotoxicity of GST-TAT-Apoptin may be less that that of His-TAT-Apoptin in BL21(DE3) and BL21(DE3)Codonplus-RP . Furthermore, the phenomenon of “protein burden” may not have been encountered when BL21(DE3) was used to express GST-TAT-Apoptin . It was concluded that BL21(DE3) is the preferred choice for expression of GST-TAT-Apoptin.
Rosenberg et al have proposed that the abundance of a rare codon near the 5’-end of the gene might affect the efficiency of protein translation . If this is true, then the approach used in the present study to modify the codon usage in the gene ought to improve the expression of full-length apoptin protein. When Genscript OptimumGeneTM bioinformatic software was used to identify rare codons in E. coli that exist in the wild-type CAV VP3 gene, the pinpointed amino acid residues included arginine, leucine, proline and lysine; these are commonly found in the N-terminus and C-terminus regions of the apoptin protein. After codon optimization of CAV VP3 gene, TAT-Apoptinopt was fused with both tags and successful expressed in E. coli (Figure (Figure4A,4A, C). The amount of expressed GST-TAT-Apoptinopt in E. coli was substantially higher than that of GST-TAT-Apoptin and His-TAT-Apoptinopt when BL21(DE3) or BL21(DE3)pLysS were used (Figure (Figure5A,5A, C and Table1). Thus codon optimization within VP3 gene of the rare codons in E. coli was able to improve the expression level of TAT-Apoptin; specifically translation efficiency was improved without the need to supply extra copies of the rare tRNA genes [27,28]. Interestingly, in terms of growth, BL21(DE3) and BL21(DE3)pLysS performed almost identically when expressing GST-TAT-Apoptin (Figure (Figure3D).3D). However, the growth rate of BL21(DE3)pLysS was significantly slower than that of BL21(DE3) when expressing GST-TAT-Apoptinopt (Figure (Figure5D).5D). This might be explained in terms of the “protein burden” within BL21(DE3)pLysS when it is producing GST-TAT-Apoptinopt at a relatively high level early during induction and this protein burden may eventually result in BL21(DE3)pLysS undergoing growth arrest. The growth profile of BL21(DE3) expressing GST-TAT-Apoptinopt may involve the balancing of the steady-state growth conditions for the strain with the yield and also suggests that this strain had reached the maximum possible growth rate; as a result the growth profile of BL21(DE3) during the expression of GST-TAT-Apoptinopt did not significantly change (Table1, Figures3D and and5D).5D). In contrast, when producing His-TAT-Apoptinopt, the growth profiles of BL21(DE3) and BL21(DE3)pLysS were very similar to the situation when the strains were producing His-TAT-Apoptin (Figures3B and and5B).5B). One possible explanation for this is that the level of produced His-TAT-Apoptin or His-TAT-Apoptinopt did not reach the threshold value where there was a protein burden and therefore no growth arrest occurred.
The presence of a fusion tag and optimization of the codon usage within the gene were both useful strategies for improving the production of TAT-Apoptin (Table1). When compared, the increase level in yield obtained when a fusion tag was used seems to be greater than that derived from codon optimization (Table1). Specifically, the yield was only increased from 7.1mg/ml (GST-TAT-Apoptin) to 8.9mg/ml (GST-TAT-Apoptinopt) was expressed in BL21(DE3).
In order to improve the protein stability of TAT-Apoptin, various cultivation parameters were adjusted. Although a cultivation temperature of 37°C was able to produce a higher growth rate and greater protein yield, this temperature did not produce a high yield of soluble protein. When 25°C was used or when a lower IPTG concentration was used (0.1mM of IPTG), it was not only possible to obtain a similar expression level of TAT-Apoptin within 6hrs (compared to 4hrs), but there was also a significant improvement in protein solubility (Figures6A, ,7A).7A). Recovering soluble TAT-Apoptin using the GST tag as an affinity ligand during the purification process is highly convenient in terms of downstream processing. After GST affinity chromatography, approximately 80% of the GST-TAT-Apoptin produced by the E. coli was recovered and recovery of GST-TAT-Apoptin even reached over 90% with one batch (Figure (Figure8).8). The purified target protein can then be subjected to further purification steps in order to obtain a protein drug with high purity.
In this study, human premyelocytic leukemia HL-60 cells were used to evaluate the apoptotic activity of the E. coli-expressed TAT-Apoptin. Apoptosis was induced when the HL-60 cells were co-cultured with 90 ug/ml of GST column purified GST-TAT-Apoptinopt. There was a 10% increase in apoptosis compared to the non-apoptosis control (Figure 9A, B and C). However, this is less apoptosis than that induced by CHX, which is the positive apoptosis control. Previous studies have reported that approximately 70% of tumor cells undergoing apoptosis in the presence of apoptin . This discrepancy may be a result of differences in the tumor cell lines used, which may have different levels of tolerance with respect to apoptin. In addition, the TAT-Apoptin carried the GST fusion tag had not undergo protease cleavage before use and the presence of the tag may have affected the protein drug's apoptotic activity during co-culture with the tumor cells. Nevertheless, it is clear that the E. coli-expressed GST-TAT-Apoptinopt produced in the present study does retain its anti-tumor cell activity and the ability to induce apoptosis.
The expression of recombinant full-length TAT-Apoptin protein was established successfully herein using a prokaryotic system, and the yield was significantly improved by fusing the protein with an affinity tag and by optimizing the codon usage of the polypeptide for expression in E. coli. Direct engineering of the apoptin protein was a convenient and cost-effective strategy of increasing the expression of TAT-Apoptin protein in E. coli. This paves the way for the large-scale production of TAT-Apoptin protein using this approach. In the future, this will also allow TAT-Apoptin to be used for the development of a protein drug that has anti-cancer activity or as part of a CAV diagnostic test.
Three E. coli strains, BL21(DE3) (Invitrogen, Carlsbad, CA), BL21(DE3)CodonPlus-RP (Stratagene, La Jolla, CA) and BL21(DE3)pLysS (Stratagene, La Jolla, CA) were used and maintained at 37°C using 10ml Luria-Bertani (LB)medium (1% tryptone, 0.5% yeast extract, 1% NaCl, pH 7.0) in 50ml flasks. For strain activation, 0.5ml of an overnight culture were inoculated into 50ml LB medium and grown at 37°C for around 3h, by which time the optical density of culture had reach 0.5 of OD600. These bacterial cells could then be used for transformation or for protein expression.
A 420bp of synthetic cDNA encoding the full-length CAV apoptin protein that was fused to a trans-acting activator of transcription (TAT) protein transduction domain (PTD) at its N-terminus, the latter being synthesized by Genemark Biosci & Tech Co. (Taichung, Taiwan) and then ligated into pBluescript II SK(−) using Bam H1 (Takara, Japan) and Xho I (Takara, Japan) restriction sites. The resulting recombinant plasmid was designated pB-TAT-VP3. The TAT-VP3 gene then was subcloned into either pET28a (Novagen, Madison, WI) or pGEX-4T-1 (GE Healthcare, Piscataway, NJ) using Bam H1 and Xho I. The resulting constructs were designated pET-TAT-VP3 and pGEX-TAT-VP3 (Figure 1A, a and b), respectively. To generate the VP3 gene of CAV harboring the codon optimized nucleotide sequence, a codon optimized fragment of VP3 gene fused with the TAT PDT was also synthesized by Genemark Biosci & Tech Co. and then ligated into the pBluescript II SK(−) using Bam H1 and Xho I restriction sites. The TAT-VP3opt gene was then further subcloned into either pET28a or pGEX-4T-1 as described above and the resulting constructs were designated pET-TAT-VP3 opt and pGEX-TAT-VP3opt, respectively (Figure 1A, c and d). The constructs described above were then transformed into One Shot® Top10 (Invitrogen, CA) chemically competent E. coli for maintenance of the recombinant plasmids and for protein expression. Transformants that contained a gene of the correct size by PCR were then confirmed as correct by restriction enzyme digestion and by DNA sequence analysis.
To express the His-TAT-Apoptin, GST-TAT-Apoptin, His-TAT-Apoptinopt and GST-TAT-Apoptinopt proteins, the four constructed recombinant plasmids, pET-TAT-VP3, pGEX-TAT-Apoptin, pET-TAT-VP3opt and pGEX-TAT-VP3opt, were transformed into E. coli strain to allow evaluation of protein expression. Three E. coli host strains, BL21(DE3), BL21(DE3)CodonPlus-RP and BL21 (DE3)pLysS, each being a different recombinant constructions, were used for protein induction and expression. The recombinant strains were grown in LB medium in the presence of kanamycin (50μg/ml), ampicillin (50μg/ml) or chloramphenicol (34μg/ml) as appropriate at 37°C. When the culture had reached an optical density (OD600) of 0.5, isopropyl-β-D-thiogalactopyronoside (IPTG) at different concentrations was added to induce protein expression and then growth was continued for 4h. After IPTG induction, samples of the cells were harvested and analyzed for protein expression. Protein concentration was determined using the procedure described in a previous study . Samples containing the various expressed proteins, His-TAT-Apoptin or His-TAT-Apoptinopt and GST-TAT-Apoptin or GST-TAT-Apoptinopt, 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).
To purify the recombinant GST-TAT-Apoptinopt proteins, cells were spun down from 50mL of culture supernatant and resuspended in GST resin binding buffer (140mM NaCl, 2.7mM KCl, 10mM Na2HPO4, 1.8mM KH2PO4, pH 7.3). The mixture was then sonicated on ice three times for 3 minutes with a 20% pulsed activity cycle (MISONIX Sonicator® 300). Next, the lysate was centrifuged for 10min at 10,000rpm 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 apoptin protein, E. coli expressed GST-TAT-Apoptin was purified by GSTrap FF column, and then the eluted proteins containing in collected fraction were separated 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 samples 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 .
Human promyelocytic leukemia HL-60 cells (CCRC 60043) were purchased from the Food Industry Research and Development Institute (FIRDI) (Hsichu. Taiwan). These cells were used to evaluate the apoptotic activity of GST-TAT-Apoptinopt using an Annexin-V FITC apoptosis kit (BD Phaemingen, San Diego, CA). The cell was grown in the FIRDI-suggested medium, and all experiments were performed in 6-well culture plates. The cultured HL-60 cells were stained with Annexin-V FITC and propidium iodide (PI) according to manufacturer’s guidelines. Briefly, 2×105 cells were co-cultured with 90 ug/ml of GST-TAT-Apoptinopt for 24hrs, and then resuspended in 100 ul of 1× binding buffer, which was followed by incubation with 2.5 ul of Annexin-V FITC and PI at room temperature for 30min. Finally the cells were added to 200 ul of 1× binding buffer and assayed immediately using FACSCanto flow cytometry (BD Biosciences, San Jose, CA). A positive control was included and this consisted of treating the cells with 100mM cycloheximide (CHX) (Sigma-Aldrich, USA) for 24hrs. The negative controls were either cells treated with protein buffer (50mM Tris-HCl, 10mM reduced glutathione, pH 8.0) or cells treated with 90 ug/ml glutathione-S-transferase (GST) protein for 24hrs.
All of authors declare no competing interests.
MSL participated in this study design, performed the experiments and helped with the writing of the manuscript. SHF, GHL and FCS performed the experiments and participated in the construction of the plasmids. YYL participated in the experiments on protein antigenicity and GHL, CHH and JC participated in the protein purification. HJC and MSL6 participated in the data analysis and the writing of the manuscript. MSL, HYC and JTCT coordinated the study and participated in the writing of the manuscript. All authors read and approved the final manuscript.
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), Taiwan.