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An in vitro system from Plasmodium falciparum active in endogenous mRNA translation


An in vitro translation system has been prepared from Plasmodium falciparum by saponin lysis of infected-erythrocytes to free parasites which were homogeneized with glass beads, centrifuged to obtain a S-30 fraction followed by Sephadex G-25 gel filtration. This treatment produced a system with very low contamination of host proteins (<1%). The system, optimized for Mg2+ and K+, translates endogenous mRNA and is active for 80 min which suggests that their protein factors and mRNA are quite stable.

Plasmodium falciparum; protein synthesis; cell free translation; parasite lysate

An in Vitro System from Plasmodium falciparum Active in Endogenous mRNA Translation

Vol. 95(2): 231-235, Mar./Apr. 2000

Ana Ferreras, Ledia Triana, Heriberto Correia, Erlinda Sánchez, Flor Herrera+

Centro de Investigaciones Biomédicas, Facultad de Ciencias de la Salud, Universidad de Carabobo-Núcleo Aragua, Apartado 2351, Maracay, Edo. Aragua, Venezuela

An in vitro translation system has been prepared from Plasmodium falciparum by saponin lysis of infected-erythrocytes to free parasites which were homogeneized with glass beads, centrifuged to obtain a S-30 fraction followed by Sephadex G-25 gel filtration. This treatment produced a system with very low contamination of host proteins (<1%). The system, optimized for Mg2+ and K+, translates endogenous mRNA and is active for 80 min which suggests that their protein factors and mRNA are quite stable.

Key words: Plasmodium falciparum - protein synthesis - cell free translation - parasite lysate

Very scarce information about the mechanism of protein synthesis in Plasmodia is available. It is mainly due to the difficulties of preparing an efficient cell-free translation system which would make possible the translation of parasite mRNAs. Achieving this goal is a basic requirement for the study of the biochemistry of translation and the regulatory mechanisms of these parasites. Moreover, this knowledge is of potential importance for the control of malaria since reports in the literature show that there are significant distinctions between the protein synthesis mechanism of the host and that of the parasite (Wallach & Kilejian 1982, Deans et al. 1983, Perkins 1988, Surolia & Padmanaban 1991, Cambie et al. 1991, Elmendorf et al. 1992, Li et al. 1994a, b).

Results obtained using an in vitro translation system from Plasmodium lophurae suggest that components of the protein synthesis mechanism may be essential for the specific translation of parasite mRNAs (Wallach 1982). It has also been reported that chloroquine inhibits heme-dependent protein synthesis in P. falciparum (Surolia & Padmanaban 1991) concomitantly with the phosphorylation of the parasite initiation factor 2alpha (eIF-2alpha). These data may also explain the vulnerability of the trophozoite stage (the most active in protein synthesis) to chloroquine (Cambie et al. 1991). Recently, it has been suggested that the antibiotics thiostrepton (McConkey et al. 1997) and micrococcin (Rogers et al. 1998) target protein synthesis in the plastid-like organelle of the parasite. Furthermore, some reports suggest the existence of metabolic interdependence between extracellular energy metabolism and protein synthesis activity within the parasite (Elmendorf et al. 1992).

One interesting feature of Plasmodium species is that structurally distinct ribosomal RNA genes are expressed at different stages of the parasite's life cycle (Li et al. 1994a, b, Rogers et al. 1996). It is possible that the structural alterations of ribosomes mediate the selection of specific families of mRNA for translation. Changes in proteins synthesized by P. falciparum, have been reported as it undergoes the morphological transitions from asexual as well as sexual blood stages (Deans et al. 1983, Perkins 1988, Baker et al. 1995, Schmidt et al. 1998) which possibly reflects different translational demands in varying intracellular environments or during distinct cellular activities.

The development of a cell-free translation system from P. falciparum also opens the possibility for identifying target antigens which may be relevant for the acquisition of protective immunity (Druilhe et al. 1997, Greenwood 1997). This issue is a major current goal in the global malaria control strategy.

In this study we describe a cell-free system from P. falciparum that retains active polysomes capable of carrying out the elongation and termination steps of parasite polypeptide synthesis.

Maintenance of the malarial parasite - P. falciparum FCB1 strain, a local isolate from Colombia, was cultured in vitro according to the candle jar method (Trager & Jensen 1976).

Isolation of malaria parasites from infected blood - Parasites were synchronized using 5% D-sorbitol (Freeman & Holder 1983) and the cultures were pooled at late trophozoite stage with 8-10% parasitaemia. The infected blood was centrifuged at 2,000 x g for 10 min at 4ºC. The pellet which contained the red cells was resuspended in 2 vol of buffer A [20 mM Hepes/KOH pH 7.4; 2 mM Mg(OAc)2; 120 mM KOAc]. Parasites were released from erythrocytes following a modified procedure described in Ruenwongsa (1985). The red cells were suspended in 2 vol of 0.15% saponin in buffer A. After incubation at 37ºC for 30 min, 3 vol of cold buffer A was added and the mixture was centrifuged 10,000 x g for 10 min at 4ºC. The pellet, containing the freed parasites was washed three times with the same buffer, and frozen at -70ºC.

Preparation of the parasite cell-free system - Free-parasites were resuspended in 2 vol of ice-cold lysis buffer [50 mM Tris/HCl pH 7.4; 100 mM KOAc; 7 mM Mg(OAc)2; 380 mM sucrose; 6.5 mM ß-mercaptoethanol; 0.14% vol/vol Triton X-100; 15 µM leupeptin and 20 units of placental ribonuclease inhibitor]. Acid-washed glass beads (0.1 mm) equivalent to 2 g/vol of parasites, were added and the suspension was stirred in a vortex for 1 min followed by 10 min incubation for cooling. After two-extra vortex-cooling cycles, the parasite homogenate was centrifuged at 12,000 x g for 30 min at 4ºC. The supernatant was filtered through a Sephadex G-25 medium column equilibrated with buffer B [20 mM Hepes/KOH pH 7.4; 100 mM KOAc; 3 mM Mg(OAc)2; 2 mM DTT and 20% glycerol]. Fractions with the highest absorbance at 260 nm were pooled and used as the S-30 fraction (7-9 µg/µl and 10-12 A260 units/ml). A similar extract was prepared as described above from uninfected erythrocytes. Due to the low protein concentration of this cell extract (0.015-0.025 µg/µl), it was necessary to concentrate it approximately 20 times by lyophilization.

Isolation of ribosomes - The ribosomes were isolated according to Herrera et al. (1984). Some aliquots were treated with high salt and were labeled as high salt ribosomes (HSR).

Ribosome analysis - Ribosomes and HSR were analyzed on linear sucrose density gradient following the methodology described by Gasior et al. (1979).

Protein synthesis - Cell-free protein synthesis was carried out in a standard reaction mixture contained the following components in a volume of 50 µl: 20 mM Hepes/KOH pH 7.4; 100 mM KOAc; 5 mM Mg(OAc)2; 2 mM DTT; 10% glycerol; 0.5 mM ATP; 0.1 mM GTP; 20 mM creatine phosphate; 10 µg of creatine phosphokinase; 40 µM (each) of 19 aminoacids (except methionine) and 1.7 µM L-[3H]methionine (77 cpm/pmol) and variable amounts of S-30 fraction as indicated in the legends to the Figures. Reactions were initiated with the addition of the S-30 fractions and incubated at 37ºC for 60 min. At the end of the incubation period the fractions insoluble in hot (90ºC) 10% trichloroacetic acid were prepared; the precipitates were collected on glass-fiber filters, washed, dried and counted in a scintillation counter.

Polyacrylamide gel electrophoresis - The proteins were analyzed by 12.5% SDS/PAGE according to Laemmli (1970). Some incubations for protein synthesis were performed using [35S] methionine (117,5 Ci/mmol). Radioactively labeled proteins were electrophoresed and visualized by autoradiography.

Protein concentration determination - Protein concentration was determined as described by Lowry et al. (1951).

To develop the cell-free translation system from P. falciparum, we first free the parasites from erythrocytes to eliminate most of the contaminants. We determined that with a ratio of 2 vol of 0.15% saponin to 1 vol of erythrocytes, more than 90% of the cells were lysed (data not shown).

Comparison of the polypeptide pattern of parasite S-30 and that of extract of uninfected erythrocytes (Fig. 1) indicated the existence of parasite specific proteins which were absent from the control (Mrs of the prominent bands: 98, 62, 56, 52, and 40 kDas). Densitometric scanning of lane 1 (parasite proteins) and lane 2 (uninfected erythrocyte proteins), detected five major polypeptides (Mr 15, 28, 30, 46 and 69 kDas) from the uninfected erythrocytes that may be important contaminants in the parasite S-30. The polypeptide with a Mr of about 15 kDa may represent the globin chain. Taking it as a marker, we calculated the contamination of host proteins in the parasite S-30 fraction to be < 1%.

Sedimentation of the ribosomes in sucrose gradients showed (Fig. 2A) that 55% of the total 260 nm absorbing material is heavier than 80S indicating the presence of polyribosomes. It was also found that the P. falciparum polyribosomal fraction was dissociated with high salt treatment (Fig. 2B). The large polyribosome and monosome peaks decrease from 55% and 45% to 22% in both cases, whereas the ribosomal subunit population (60S and 40S) previously undetected increases to 56% with high-salt treatment.

The effect of the lysate concentration was tested on polypeptide synthesis directed by endogenous mRNA (Fig. 3). The best polymerization rate was found at concentrations around 2.8 mg of protein/ml which obtained up to a 24-fold stimulation over the background activity. As the concentration of K+ and Mg2+ ions play key roles in the fidelity as well as in the extent of translation (Roberts & Paterson 1973) of several in vitro systems, we first optimized the K+ and then Mg2+ concentrations. The values found were 75 mM for K+ and 5 mM for Mg2+ (data not shown). Next we determined that the protein synthesis continues up to 80 min and that the best temperature for this process was 37°C (data not shown).

To determine the proteins synthesized by the parasite cell-free system, [35S]methionine was added to the incubation mix and products were analyzed by SDS/PAGE and autoradiography. Fig. 4 not only shows the clear presence of five main polypeptides of Mrs 60, 58, 55 , 45 and 29 kDas but also reveals three minor bands of Mrs 105, 86 and 68 kDas.

Since it has been reported that hemin is needed for Plasmodia protein synthesis (Surolia & Padmanaban 1991), the effect of hemin was examined in our parasite cell-free system. Addition of increasing amounts of hemin to the parasite lysate strikingly inhibits protein synthesis (Fig. 5).

The preparation of a cell-free system from the blood stages of malaria parasites involves the efficient lysis of the erythrocyte membrane with saponin which can apparently permeabilize (by intercalating with cholesterol) selectively the erythrocyte plasmatic and parasite vacuolar membranes without disrupting the parasite plasmatic membrane (Crary & Haldar 1992). However, it is well known that the parasites freed by the saponin-lysis method are enclosed within the collapsed red cell membrane (Aikawa & Cook 1972) and therefore, it is possible that proteins from this membrane or remnant hemoglobin could be present in the parasite S-30 fraction. In this study this possibility is unlikely to be a significant factor, since it was determined that more of 99% of the polypeptides of the parasite extract correspond to parasite proteins (Fig. 1).

Analysis of the polysomes of our cell-free system showed nearly equimolar quantities of monosomes and large polysomes (Fig. 2). This is in contrast to other Plasmodia cell-free systems in which the polyribosomes represented only 10% (Wallach & Kilejian 1982). This data suggest that the P. falciparum system is actively engaged in protein synthesis, since most cells studied which are highly active in mRNA translation have mainly large polysomes (Woodland 1974).

We determined the optimal conditions for parasite protein synthesis (Fig. 3). Using these conditions the parasite S-30 fraction is able to translate endogenous mRNA giving about 25-fold stimulation over the activity at time zero. This represents an activity significantly higher than that described for other Plasmodium systems (Surolia & Padmanaban 1991). This translation can continue up to 80 min which suggests that protein factors and mRNA of the system are quite stable.

In addition, the incorporation of [35S] methionine into polypeptides with high molecular masses suggests strongly that the parasite cell-free system contains sufficient amount of polyribosomes, tRNA, aminoacyltRNA synthetases and factors that allow the system to complete the steps of elongation and termination of the protein synthesis mechanism (Fig. 4).

We found that our in vitro translation system is not dependent upon exogenous hemin (Fig. 5). This finding is in apparent contradiction with the data reported by Surolia and Padmanaban (1991). They observed that addition of heme in vitro stimulated cell-free Plasmodium protein synthesis strikingly. Probably, in our conditions, the parasite lysate retains sufficient amounts of endogenous heme and therefore it is not rate-limiting for mRNA translation.

We have described a cell-free system prepared from P. falciparum trophozoites able to translate endogenous mRNA. Work is now in progress to determine the nature of the proteins synthesized by the system.

This Plasmodium cell-free system can provide an useful tool to investigate the biology of the parasite and from which potential benefits like evaluation of the effects of a variety of drugs in Plasmodia translation could be derived.

To Drs Ricardo Montoreano, Edmundo Cayama, Francisco Triana and Lic. Elizabeth Ferrer for helpful discussions, to Maria Briceño for culturing parasites and to Lic. Rafael Medina for helping us with the photographic technique.

Fig. 1 | Fig. 2 | Fig. 3 | Fig. 4 | Fig. 5

This research was supported in part by Fundacite-Aragua, by the Consejo de Desarrollo Científico y Humanístico of the Universidad de Carabobo and by the Consejo Nacional de Investigaciones Científicas y Tecnológicas.

+Corresponding author. Fax: 58-43-713456. E-mail:

Received 7 May 1999

Accepted 13 December 1999

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Figure 5

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  • Publication Dates

    • Publication in this collection
      30 Jan 2001
    • Date of issue
      Apr 2000


    • Accepted
      13 Dec 1999
    • Received
      07 May 1999
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