- Open Access
Solution structure of a Plasmodium falciparum AMA-1/MSP 1 chimeric protein vaccine candidate (PfCP-2.9) for malaria
© Peng et al; licensee BioMed Central Ltd. 2010
Received: 20 November 2009
Accepted: 18 March 2010
Published: 18 March 2010
The Plasmodium falciparum chimeric protein PfCP-2.9 is a promising asexual-stage malaria vaccine evaluated in clinical trials. This chimeric protein consists of two cysteine-rich domains: domain III of the apical membrane antigen 1 (AMA-1 [III]) and the C-terminal region of the merozoite surface protein 1 (MSP1-19). It has been reported that the fusion of these two antigens enhanced their immunogenicity and antibody-mediated inhibition of parasite growth in vitro.
The 15N-labeled and 13C/15N-labeled PfCP-2.9 was produced in Pichia pastoris for nuclear magnetic resonance (NMR) structure analysis. The chemical shift assignments of PfCP-2.9 were compared with those previously reported for the individual domains (i.e., PfAMA-1(III) or PfMSP 1-19). The two-dimensional spectra and transverse relaxation rates (R2) of the PfMSP1-19 alone were compared with that of the PfCP-2.9.
Confident backbone assignments were obtained for 122 out of 241 residues of PfCP-2.9. The assigned residues in PfCP-2.9 were very similar to those previously reported for the individual domains. The conformation of the PfMSP1-19 in different constructs is essentially the same. Comparison of transverse relaxation rates (R2) strongly suggests no weak interaction between the domains.
These data indicate that the fusion of AMA-1(III) and MSP1-19 as chimeric protein did not change their structures, supporting the use of the chimeric protein as a potential malaria vaccine.
Malaria is one of the most serious life-threatening tropical diseases in the world. Because of the rapid spread of drug-resistant parasites and insecticide-resistant mosquitoes [1–4], new tools for control malaria are urgently needed. The 200-kDa merozoite surface protein-1 (MSP 1) and the apical membrane antigen (AMA-1) of Plasmodium falciparum are attractive candidates for malaria vaccines [5–9]. These two antigens are located on the merozoite surface and have been proposed to play a role in the invasion process [10–15]. A portion of the MSP1 targeted by protective immunity antigen has been mapped to the 19 kDa carboxy-terminal region (MSP1-19) which contains two tandem repeat epidermal growth factor (EGF)-like domains while the most C-terminal of the disulphide-bonded domains in AMA-1 (Domain III) was also a target for inhibitory antibodies isolated from malaria patients [16–20].
A chimeric protein (PfCP-2.9) was constructed comprising the sequences of both AMA-1(III) and the MSP 1-19 from P. falciparum . The two proteins were fused via a hinge encoding a Gly-Pro-Gly motif repeat, and a secreted form of the PfCP-2.9 protein was expressed in Pichia pastoris. The fusion enhanced product yield, immunogenicity, and antibody-mediated inhibition of parasite growth in vitro. Sera from rabbits and rhesus monkeys immunized with the chimeric antigen almost completely inhibited parasite growth. Two phase I clinical trials of this vaccine candidate formulated in Montanide ISA 720 were completed recently, demonstrating the safety, tolerability, and immunogenicity of the vaccine in humans [22, 23].
The PfCP-2.9 chimeric protein contains 18 cysteine residues, six of which are located in AMA-1(III) region and the rest in the MSP 1-19 region, that form nine intramolecular disulfide bonds. Protective immunity conferred by this vaccine candidate was shown to be dependent on its disulfide backbone-based conformation. Immune sera containing reduced and alkylated PfCP-2.9 did not inhibit parasite growth, indicating that induction of the growth-inhibitory response required proper folding of this chimeric protein . Therefore, it is necessary to characterize the structure of the fusion protein. In the present study, the 15N- and 15N/13C-labeled PfCP-2.9 protein were expressed in P. pastoris to determine its solution structure.
15NH4SO4 and 13C-D-glucose was purchased from Cambridge Isotope Laboratories (Andover, MA, USA). 13C-methanol was purchased from Spetra (Columbia, MD, USA).
Preparation of 15N-labeled PfCP-2.9
The stock P. pastoris strain  expressing PfCP-2.9 with C-terminal 6 × His tags was streaked on a YPD agar plate (1% Yeast extract, 2% Peptone, 2% Glucose, 2% agar) containing the antibiotic G418 (0.25 mg/ml). Clones were incubated in 150 ml BMGY medium (1.34% yeast nitrogen base [YNB] without ammonium sulfate and amino acids, 1% yeast extract, 2% peptone, 1% glycerol, 4 × 10-5% biotin, and 100 mM potassium phosphate [pH 6.0]) and grown to an optical density of approximately 20 at 600 nm (OD600). The cells were then transferred into 3L of 15N salt base medium (2.67% [v/v] H3PO4 (85%), 0.0894% CaSO4, 1.52% K2SO4, 1.49% MgSO4· 7H2O, 0.413% KOH, 4% glycerol, 0.4% [v/v] PTM1 salts, 0.9% [NH4]2SO4) in a 5-L fermenter. OD600 reached 75 after 21 hr, and 180 g methanol was then added to induce expression of the chimeric protein. After 19 hr, the culture was centrifuged at 6000 × g for 20 min at 4°C, and the supernatant was collected for protein purification.
The target protein was purified by Ni-NTA agarose column (Qiagen, Hilden, Germany) affinity purification. Ten milliliters of Ni-NTA agarose was equilibrated with the loading buffer (50 mM NaH2PO4, 300 mM NaCl, pH 8.0) without a reducing agent. The cell culture supernatant was then applied to the column at 1 ml/min, and flow through was collected for analysis. The column was washed with 60 ml loading buffer followed by 120 ml washing buffer (50 mM NaH2PO4, 300 mM NaCl, 20 mM imidazole, pH 8.0). Bound proteins were eluted with 250 mM imidazole. Eluted proteins were concentrated into 1 ml using an Amicon Ultra-15 centrifugal filter unit (10 kDa, Millipore, Billerica, USA).
The NMR sample was prepared in a buffer containing 20 mM sodium phosphate in 90% H2O/10% D2O (pH 7.4). The sample was argon-flushed.
Preparation of 13C/15N-labeled PfCP-2.9
The stock P. pastoris strain was streaked on a YPD agar plate and grown in 3 L of 15N salt base as described above. The cell density reached OD600 of 60 after 17 hr, and 5 g of 13C-D-glucose was then added. After 2 hr, 50 g of 13C-methanol was added to induce chimeric protein expression. After 6 hr, the culture was centrifuged at 6,000 × g for 20 min at 4°C, and the supernatant was collected for protein purification.
The purification and NMR sample preparation of the target protein was same as for 15N-labeled PfCP-2.9. The final volume was 1.2 ml. Protein concentration was 10 mg/ml as determined by the Bradford method, and purity was > 90% as assessed by SDS-PAGE.
Preparation of 15N-labeled PfMSP1-19
The stock P. pastoris strain was streaked on a YPD agar plate containing 0.25 mg/ml G418, which was preserved in laboratory. A clone was incubated in 500 ml BAGY medium (0.34% YNB without ammonium sulfate and amino acids, 1% glycerol, 0.5% (NH4)2SO4, 4 × 10-5% biotin, and 100 mM potassium phosphate [pH 6.0]) and grown to OD600 of approximately 10. Cells were collected by centrifugation and transferred into 500 ml of 15N BMM medium (0.34% YNB without ammonium sulfate and amino acids, 0.5% methanol, 0.5% (NH4)2SO4, 4 × 10-5% biotin, and 100 mM potassium phosphate [pH 6.0]). Every 12 hr, 1.25 ml of methanol was added to the culture medium. After 72 hr, the culture was centrifuged at 6,000 × g for 20 min at 4°C to collect the supernatant for protein purification. The purification process and NMR sample preparation was the same as for PfCP-2.9.
Nuclear magnetic resonance data collection and analysis
The nuclear magnetic resonance (NMR) spectra were acquired at 25°C with a Bruker Avance 500 (with a CryoProbe) and 800 MHz spectrometers, equipped with four RF channels and a triple-resonance probe with pulsed field gradients. The three-dimensional (3D) HNCA, HNCACB, CBCA(CO)NH, HNCO, and HN(CA)CO experiments were carried out for the backbone assignments. HBHA(CO)NH, (H)CC(CO) NH, CC(CO)NH, and 15N-TOCSY-HSQC experiments were performed for side-chain assignments . 3D 15N-edited NOESY-HSQC spectrum (mixing time, 100 ms) was performed to confirm the chemical shift assignments. All spectra were processed using the software package NMRPipe  and analysed with the programme NMRView .
Backbone 15N transverse relaxation measurements
The backbone 15N transverse relaxation experiments of the PfCP-2.9 and MSP 1-19 domain were recorded  on a Bruker AVANCE 800-MHz NMR spectrometer at 25°C. For both samples, 512 (1H) and 70 (15N) complex data points were collected with 48 transients per increment and a recycle delay of 3.0 s. The delays were 4 (×2), 32, 60, 100, 160 ms for 15N-labeled MSP 1-19, and 4 (×2), 12, 28, 48, 72, 100, 160 ms for 15N-labeled PfCP-2.9. The transverse relaxation rate constants (R2) were obtained by fitting the peak intensities to a single exponential function by nonlinear least-squares method using MATLAB .
Chemical shift assignments of PfCP-2.9
Comparison of the assigned chemical shifts of PfCP-2.9 with those of PfAMA-1 (III) and Pf MSP1-19 domains
For the residues assigned in the PfMSP1-19 domain, the majority show only small chemical shift differences: |ΔHN| < 0.1 ppm, |ΔN| < 1.0 ppm, |ΔCα| < 0.5 ppm, |ΔCβ| < 1.0 ppm, |ΔCO| < 0.5 ppm. Few atoms show bigger chemical shift differences between the current results and previously published assignments of PfMSP1-19 (BMRB entry 4437) ; these include the backbone 15N atoms of Glu169, Glu171 and Ala203, and the Cα atom of Ser238. The Glu169 and Glu171 residues are acidic residues, whereas the Ala203 residues are located between two Asp residues. The larger 15N chemical shift differences for these three residues probably result from the pH differences of buffers used in the two studies (buffer pH used in the previous study of the PfMSP1-19 domain was 6.5).
Spectral comparison between PfCP-2.9 and MSP 1-19 domain
Comparison of transverse relaxation rates between PfCP-2.9 and PfMSP1-19 domain
The lack of change in chemical shifts of the PfMSP1-19 domain when expressed as a part of the fusion protein PfCP-2.9 excludes the possibility of strong interactions between PfMSP1-19 and PfAMA-1(III) domains; however, weak interactions between the two domains are possible. If weak interactions between the two domains exist, one or both of the following phenomena were expected to seen: (1) chemical shift differences for residues at the interaction surface; (2) line broadening due to chemical/conformational changes.
Neither chemical shift changes between the two spectra nor peak disappearance was observed; therefore, the transverse relaxation rates R2 of the two samples were measured to further investigate the possibility of line broadenings. For the data analysis of PfCP-2.9, only those residues present in PfMSP1-19 were analysed. The peaks that overlapped were excluded from the analysis. Further, residues His150, Glu171, Asp184, Gly213, Ser228, and Ser238 showed weak signals and poor relaxation curves in both samples, thus were also removed from the final analysis. The R2 values of a total of 36 residues (Cys152, Asn160-Gly162, Phe164, Asp168-Glu169, Leu177-Lys180, Cys186-Glu188, Asn191, Thr193-Glu196, Gly199-Gly200, Ala203-Asp204, Lys206-Thr208, Gly216, Ile219-Thr220, Cys223-Thr224, Asp227, and Asp233-Phe236) were finally obtained.
It has been reported that a panel of monoclonal antibodies recognizing conformational epitopes on PfMSP1-19 interacted with the chimeric protein with reduced sensitivity . Of these monoclonal antibodies, mAb2.2 and 12.8 bind to the first EGF domain of PfMSP1-19, whereas mAb111.2 requires the presence of both EGF-like domains . The mAb12.8 is an inhibitory antibody while mAb 2.2 and mAb 1E1 are blocking antibodies [32, 33]. These data indicated that the critical epitopes were retained after fusion of the two domains into one molecule; however, correct folding of the PfAMA-1(III) portion and other epitopes on the PfMSP1-19 and potential interactions between the two domains was not known.
In the present study, the chemical shift assignments of PfCP-2.9 was compared with those previously reported for individual domains and found that the structures of the two domains were unchanged. Further, comparison of the 2D spectra of PfMSP1-19 with the domain in the PfCP-2.9 also demonstrated that the conformation of the domain is essentially the same, while the PfAMA-1(III) domain showed better folding in the chimeric protein than it did alone.
Comparison of transverse relaxation rates R2 between the PfMSP1-19 domain in PfCP-2.9 and the domain alone strongly suggests no weak interactions between domains. Taken together, these data suggested that the structures of the PfAMA-1(III) and PfMSP1-19 domains were not altered by fusion into the chimeric protein.
Crystallization the chimeric protein were unsuccessful despite various efforts. Therefore, 15N-labeled and 13C/15N-labeled PfCP-2.9 were expressed in P. pastoris for NMR structure analysis. The backbone chemical shift assignments can be obtained for a reasonable portion of the residues in PfCP-2.9. By comparing with the previously reported studies of the two domains alone, high similarity of chemical shifts was observed. Relatively larger differences were observed for only a small number of residues, which may be due to different experimental conditions (e.g., buffer pH and temperature). In fact, almost all the residues that showed significant chemical shift changes in PfAMA-1(III) were charged residues, with the exception of Cys63, which is near charged residues according to the NMR structure of PfAMA-1 (III). In addition, PfCP-2.9 was modified in the following ways: three glycosylation sites were removed by changing Asn to Gln, a hinge consisting of 28 residues was inserted between the two domains , and a 6×His-tag was added to its C-terminus. These modifications can also influence the chemical shift of nearby residues.
The PfCP-2.9 chimeric protein induces antibodies that inhibit parasite growth in vitro, providing additional evidence for the unchanged protein conformation. Moreover, both components of the chimeric protein are able to generate inhibitory antibodies against parasite growth, indicating that both domains fold correctly . NMR findings in the present study were consistent with previous reports. The lack of interaction between the two domains greatly reduces the possibility that novel epitopes exist in the chimeric protein.
This work was supported by grants from, the National Natural Science Foundation of China (No.30430610), the National Basic Research Programme (973 Programme) in China (2007CB513100), the National 863 Programme in China (2006AA02A222) and the Shanghai Leading Academic Discipline Project(No. B901). We thank Dr. Meijin Guo for invaluable advice and technical assistance in fermentation.
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