cAMP is produced in eukaryotic cells either by a transmembrane adenylyl cyclase (tmAC), which has a putative K⁺ channel at the N-terminus, or by a cytoplasmic soluble adenylyl cyclase (sAC). Homologs of both the tmAC (PF3D7_1404600) and sAC (PF3D7_0802600) (www.plasmodb.org) are encoded in P. falciparum genome [18], [19]. However, the gene encoding the P. berghei transmembrane AC (PbACα) has been knocked out with no deleterious effect on growth of blood stage parasites although sporozoites are impaired in hepatocyte infectivity [20]. Given that PbACα does not appear to have an essential role in blood stage growth we focused our attention on the soluble AC in P. falciparum (PfACβ).

Mouse antiserum raised against a synthetic peptide derived from PfACβ detects a protein of expected size (>250 kD) in schizont and merozoite lysates by Western blotting (S1 Figure). Detection of PfACβ by immunofluorescence assay (IFA) demonstrates that it co-localizes in late stage schizonts and merozoites with the cytoplasmic protein PfNapL [21] (Fig. 1). PfACβ is thus expressed in P. falciparum merozoites and is localized in the cytoplasm.

Exposure of P. falciparum merozoites to an ionic environment with low K⁺ as found in blood plasma triggers a rise in cytosolic Ca²⁺ and secretion of microneme proteins [5]. To determine if exposure of free merozoites to a low K⁺ environment also leads to a rise in cytosolic cAMP, we measured cAMP levels in purified merozoites suspended in a buffer that mimics the intracellular ionic environment (IC buffer – 140 mM KCl, 5 mM NaCl, 1 mM MgCl₂, 5.6 mM glucose, 25 mM HEPES, pH 7.2) and following transfer to a buffer that mimics extracellular ionic environment with low K⁺ levels (EC buffer – 5 mM KCl, 140 mM NaCl, 1 mM MgCl₂, 2 mM EGTA, 5.6 mM glucose, 25 mM HEPES, pH 7.2). cAMP levels were also measured before and after merozoites were transferred from IC to IC-K_low buffer (IC-K_low buffer – 5 mM NaCl, 5 mM KCl, 135 mM choline-Cl, 1 mM EGTA, 5.6 mM glucose, 25 mM HEPES, pH 7.2) to determine if change in environmental K⁺ level alone can trigger changes in cAMP levels. There is a distinct rise in cAMP when merozoites are transferred from IC to EC buffer, or from IC to IC-K_low buffer (Fig. 1B). Importantly, transfer of free merozoites to a low K⁺ buffer in the presence of KH7, which inhibits mammalian sAC [19], blocks the rise in cytosolic cAMP (Fig. 1C).

We monitored the secretion of microneme protein PfAMA1 following the transfer of free P. falciparum merozoites from IC to EC buffer with or without prior treatment with KH7. PfAMA1 is proteolytically cleaved into 48 kD and 44 kD fragments that are released into the supernatant following translocation to the merozoite surface [22]. PfAMA1 was detected in merozoite supernatants following transfer from IC to EC buffer by Western blotting using anti-PfAMA1 sera (Fig. 1D). Transfer of extracellular merozoites from IC to EC buffer in the presence of KH7 blocks the secretion of PfAMA1 (Fig. 1D). Treatment of merozoites with KH7 in the presence of 3-isobutyl-1-methylxanthine (IBMX), which inhibits 3’,5’-cAMP phosphodiesterase (PDE) and maintains high cAMP levels in cells [23], reverses the block in microneme secretion (Fig. 1D). Secretion of another microneme protein, EBA175, is also inhibited if merozoites are treated with KH7 prior to transfer from IC to EC buffer (S2 Figure).

Production of cAMP by soluble adenylyl cyclases is regulated by HCO₃⁻ ions in diverse organisms [24]–[26]. Incubation of P. falciparum merozoite lysates with ATP and different concentrations of HCO₃⁻ ions showed that increasing amounts of cAMP are produced in presence of increasing concentrations of HCO₃⁻ ions suggesting the presence of a HCO₃⁻ sensitive adenylyl cyclase activity (Fig. 2A). Moreover, cAMP production is inhibited by KH7 (Fig. 2A). These observations confirm the presence of a HCO₃⁻-sensitive ACβ in free P. falciparum merozoites.

Cytosolic pH (pH_i) is controlled in eukaryotic cells by carbonic anhydrase (CA), which catalyzes the reversible hydration of CO₂ to produce H⁺ and HCO₃⁻ (CO₂+H₂O↔HCO₃⁻+H⁺) [27]. Acetazolamide (ACTZ), a specific inhibitor of CA, can disrupt intracellular pH homeostasis [28], [29]. We tested whether the transfer of free merozoites from IC to EC buffer in presence of ACTZ affects pH_i. P. falciparum merozoites collected in IC buffer were loaded with the membrane permeable pH-sensitive fluorescent dye BCECF-AM [30] and transferred to EC buffer in the presence or absence of ACTZ. pH_i does not change when free merozoites are transferred from IC to EC buffer. In contrast, there is a rapid rise in pH_i when free merozoites are transferred from IC to EC buffer in presence of ACTZ (Fig. 2B). These observations indicate that PfCA activity is necessary for maintenance of pH_i when merozoites are transferred to a low K⁺ environment.

The observation that pH_i rises when merozoites are transferred to EC in presence of ACTZ is consistent with a model in which PfCA maintains pH_i by producing H⁺ and HCO₃⁻. To test whether the generation of HCO₃⁻ in free merozoites following transfer from IC to EC buffer leads to activation of PfACβ, we measured levels of cAMP in merozoites with or without treatment with ACTZ. Treatment of merozoites with ACTZ prior to transfer from IC to EC buffer inhibits rise in cAMP (Fig. 2C) as well as secretion of PfAMA1 (Fig. 2D). Treatment of P. falciparum merozoites with ACTZ in presence of IBMX reverses the block in microneme secretion (Fig. 2D). These results suggest that when free merozoites are exposed to an extracellular-like low K⁺ environment, the production of HCO₃⁻ by PfCA to maintain pH_i leads to activation of PfACβ and generation of cAMP, which triggers microneme secretion. Exposure of merozoites in IC buffer to increasing concentrations of HCO₃⁻ also leads to a dose-dependent increase in microneme secretion (S3 Figure) confirming that HCO₃⁻ plays a key role in regulating microneme secretion.

PKA commonly plays a role as a cAMP-responsive effector in signaling pathways [7]. To investigate the potential role of PfPKA in microneme discharge, we measured phosphorylation of kemptide, a specific substrate of PKA, by lysates of P. falciparum merozoites in IC and EC buffers with and without addition of KH7. There is a distinct increase in kemptide phosphorylation with lysates made from merozoites in EC buffer compared to IC buffer (Fig. 3A). Pre-treatment with KH7 inhibits this increase in kemptide phosphorylation by merozoite lysates in EC buffer suggesting that a cAMP-responsive kinase is activated when merozoites are transferred to EC buffer (Fig. 3A).

We used a molecular genetic approach to explore the regulatory role of PfPKA in microneme secretion. The P. falciparum transgenic line PHL dhfr-PfPKAr over-expresses the regulatory subunit (PfPKAr) (11, S4 Figure). Overexpression of PfPKAr results in reduced PKA activity and a parasite growth defect, which is restored by addition of the non-hydrolyzable cAMP analog dibutryl-cAMP (DiB) [11]. In contrast to wild type P. falciparum merozoites (Fig. 3A), lysates of P. falciparum PHL dhfr-PfPKAr merozoites in EC buffer do not phosphorylate kemptide at higher levels compared to lysates made in IC buffer (Fig. 3B). Treatment of P. falciparum PHL dhfr-PfPKAr merozoite lysates with DiB increases kemptide phosphorylation (Fig. 3B). These observations indicate that kemptide phosphorylation is primarily due to PfPKA and PfPKA activity increases when merozoites are transferred from IC to EC buffer.

Next, we followed secretion of PfAMA1 upon transfer of P. falciparum PHL dhfr-PfPKAr merozoites from IC to EC buffer with and without DiB treatment (Fig. 3C). PfAMA1 is not secreted when P. falciparum PHL dhfr-PfPKAr merozoites are transferred from IC to EC buffer (Fig. 3C). However, PfAMA-1 secretion is restored when P. falciparum PHL dhfr-PfPKAr merozoites are treated with DiB in EC buffer presumably due to the activation of PfPKA (Fig. 3C). These observations suggest that PfPKA plays a role in regulation of microneme secretion. Impairment of microneme secretion due to PfPKAr overexpression may be one of the reasons for poor growth of P. falciparum PHL dhfr-PfPKAr parasites.

Changes in the levels of cytosolic Ca²⁺ and cAMP control a variety of functions in diverse cell types [31]. We examined the crosstalk between these two ubiquitous second messengers in extracellular P. falciparum merozoites. We found that treatment of merozoites with the Ca²⁺ chelator, BAPTA-AM, or PLC inhibitor, U73122, does not affect the increase in cAMP levels when merozoites are transferred from IC to EC buffer (Fig. 4A). In contrast, treatment of merozoites with the ACβ inhibitor KH7 inhibits the increase in cytosolic Ca²⁺ levels when merozoites are transferred from IC to EC buffer (Fig. 4B) indicating that cAMP plays a key role in regulating cytosolic Ca²⁺ levels in P. falciparum merozoites.

Next, we found that Ca²⁺ levels increase in transgenic P. falciparum PHL dhfr-PKAr merozoites following their transfer from IC to EC buffer (Fig. 4B). Moreover, treatment of transgenic merozoites with DiB in IC buffer, which activates PfPKA, does not lead to further increase in cytosolic Ca²⁺ levels (Fig. 4C). These observations indicate that PfPKA does not play a role in generation of free cytosolic Ca²⁺ in P. falciparum merozoites following transfer from IC to EC buffer.

Alternative cAMP-responsive effectors, Epac 1 and Epac 2, have been shown to activate phospholipase C (PLC) in presence of cAMP leading to rise in cytosolic Ca²⁺ in mammalian cells [17], [32], [33]. P. falciparum codes for a single putative parasite PfEpac (PF3D7_1417400). Treatment of merozoites in IC buffer with the Epac agonist, 8-pCPT-2’-O-Me-cAMP [34], leads to a rise in cytosolic Ca²⁺ levels (Fig. 4D). This increase in Ca²⁺ is blocked if merozoites are treated with ESI-09, which inhibits both mammalian Epac 1 and Epac 2 [35] (Fig. 4D). ESI-05, which only inhibits mammalian Epac 2 [36], does not block increase in cytosolic Ca²⁺ following treatment with the Epac agonist (Fig. 4D). In mammalian cells, Epac activated by cAMP catalyzes the transfer of GTP to Rap1 [17]. Rap1-GTP activates PLC and triggers a rise in cytosolic Ca²⁺ through the PLC pathway [17]. Stimulation of merozoites with the Epac agonist in presence of GGTI298 [37], [38], which disrupts Rap1 activity, or the PLC inhibitor, U73122 [5], [39], inhibits rise in cytosolic Ca²⁺ (Fig. 4E). Moreover, treatment of merozoites with either ESI-09 or GGTI298 prior to transfer from IC to EC buffer also blocks rise in cytosolic Ca²⁺ (Fig. 4F) and inhibits PfAMA1 secretion (Fig. 5A, 5B). In contrast, ESI-05, which does not inhibit increase in cytosolic Ca²⁺ levels (Fig. 4F), does not block secretion of PfAMA1 (Fig. 5A). Treatment of merozoites with GGT1298 together with the Ca²⁺ ionophore A23187 restores microneme secretion (Fig. 5B). Thus, a cAMP-responsive Epac-Rap1 pathway is likely to be involved in regulating Ca²⁺ levels in P. falciparum merozoites.

To confirm the role of cAMP-responsive effectors PfPKA and PfEpac in microneme secretion, we treated merozoites in IC buffer with the Epac agonist, the Ca²⁺ ionophore A23187 and DiB, either individually or in combination. Treatment of merozoites in IC buffer with Epac agonist, A23187 or DiB individually does not trigger PfAMA1 secretion (Fig. 5C). However, treatment of merozoites in IC buffer with A23187 and DiB, or Epac-agonist and DiB triggers PfAMA1 secretion (Fig. 5C). The PLC inhibitor U73122 blocks PfAMA1 secretion induced by treatment of merozoites in IC buffer with Epac-agonist and DiB (Fig. 5D). However, the inactive analog, U73343 has no inhibitory effect. These observations suggest that Epac-agonist triggers rise in Ca²⁺ through the PLC pathway. Moreover, both Ca²⁺ and cAMP surges are required to trigger the secretion of microneme proteins in free merozoites.

Erythrocyte invasion assays were performed with purified extracellular merozoites in the presence of inhibitors of cAMP- and Ca²⁺-mediated signaling pathways. Merozoites were treated with ACβ inhibitor KH7, the CA inhibitor ACTZ, or Epac inhibitors ESI-09 and ESI-05, and allowed to invade human erythrocytes. Successful invasion events were scored by flow cytometry using DNA intercalating dye ethidium bromide to identify infected erythrocytes. KH7, ACTZ and ESI-09 inhibit invasion (Fig. 5E) adding to the evidence that both cAMP and Ca²⁺-dependent signaling pathways play critical roles in the process of red cell invasion by P. falciparum merozoites.

P. falciparum 3D7 was cultured in complete RPMI (RPMI 1640 (Invitrogen, USA), 27.2 mg/L hypoxanthine (Sigma, USA), 0.5 gms/L Albumax I (Gibco, USA) and 2 gm/L sodium bicarbonate (Sigma, USA) using O⁺ human erythrocytes under mixed gas (5% O₂, 5% CO₂ and 90% N₂) as described previously [49]. P. falciparum PHL dhfr-PfPKAr was cultured in complete RPMI according to the protocol described previously [11].

A peptide (1916–1930 aa) derived from PfACβ (PlasmoDB ID PF3D7_0802600) was synthesized, conjugated to keyhole limpet hemocyanin (KLH) and used to immunize mice to obtain anti-PfACβ specific antibodies.

The coding sequence of PfPKAr was amplified by PCR from P. falciparum cDNA with primers containing BamHI and XhoI restriction sites. The fragment was inserted into pCR2.1-TOPO and verified by sequencing. After digestion by XhoI and BamHI the insert was cloned into pGEX6P-1 (GE Healthcare) and transformed into E. coli BL21 that were grown in 50 mL of LB medium containing ampicillin (100 µg/mL, Euromedex). Recombinant protein expression was induced at 30°C for 4 h by addition of 0.2 mM IPTG (Euromedex). Cells were collected by centrifugation and lysed by sonication in lysis buffer (1× PBS-1 mM salt, 1% Triton, EDTA, protease inhibitors). The lysate was centrifuged (15000 rpm, 4°C, 60 min) and the soluble fraction incubated with glutathione sepharose beads (GE Healthcare) with stirring at 4°C for 90 min. Beads were washed with buffer (1× PBS, 1% Triton, 1 mM EDTA), the GST-tagged recombinant protein was eluted using increasing concentrations of glutathione. Purified recombinant antigen was used to immunize two rats to obtain anti-PfPKAr specific antibodies.

PfPKAc was cloned in the same way as PfPKAr. To increase stability of the recombinant catalytic subunit, we co-expressed PfPKAc-His with PfPKAr-GST in E. coli BL21. Transformed bacteria were grown in 50 mL of LB medium containing ampicillin (100 µg/mL, Euromedex). Recombinant protein expression was induced at 37°C for 4 h by addition of 0.5 mM IPTG (Euromedex). The bacterial pellet was washed once with 4 volumes of PBS and lysed using 4 volumes of Tris 20 mM at 4°C. After sonication, the lysate was centrifuged (6000 g, 4°C, 15 min) and the pellet resuspended in 3 volumes of inclusion body wash solution (2 M Urea, 500 mM NaCl, 2% NP40, 20 mM Tris-HCl, pH 8.0). The inclusion bodies were solubilised (5 mM Imidazole, 1 mM β-mercaptoethanol, 6 M Guanidine-HCl 6M, 20 mM Tris-HCl pH 8.0) and recombinant protein purified by metal affinity chromatography. His-tagged PfPKAc was eluted (8 M Urea to 0 M Urea, 20 mM imidazole to 500 mM imidazole, 500 mM NaCl, 1 mM β-mercaptoethanol, 20 mM Tris-Hcl pH 8.0) and used to immunize two rabbits to obtain anti-PfPKAc specific antibodies.

P. falciparum blood stage cultures were synchronized with 5% sorbitol for at least two successive cycles. Synchronized P. falciparum cultures were used to isolate merozoites as described previously [5], [43]. Briefly, when majority of infected erythrocytes reached mature schizont stage with prominent segmentation of merozoites, the culture was resuspended in IC buffer (IC buffer – 140 mM KCl, 5 mM NaCl, 1 mM MgCl₂, 5.6 mM glucose, 25 mM HEPES, pH 7.2) and schizonts were allowed to rupture to release merozoites over one hour at 37°C. Unruptured scizonts and uninfected erythrocytes were separated by centrifugation at 500 g for 5 min. The supernatant containing free merozoites was centrifuged at 3300 g for 5 min to collect merozoites. The merozoites were resuspended in IC buffer. The purity of merozoite preparations was confirmed by Giemsa staining (S5 Figure). Viability of merozoite preparations was estimated by labeling merozoites with dihydroethidine. Fluorescent merozoites were scored by flow cytometry and viability of merozoite preparations was estimated to be ∼65%.

P. falciparum merozoites were isolated in IC buffer and treated for 15 mins with the following at concentrations shown: 100 µM IBMX (3-isobutyl-1-methylxanthine, Calbiochem, USA), 50 µM KH7 (Calbiochem, USA), 100 µM ACTZ (acetazolamide, Sigma, USA), 20 µM DiB-cAMP (adenosine 3,5 cyclic monophosphate, N⁶, O²- dibutyryl sodium salt, Calbiochem, USA), 10 µM Ca²⁺ ionophore A23187 (Calbiochem, USA), 50 µM BAPTA-AM (Calbiochem, USA), 10 µM U73122 (Calbiochem, USA), 10 µM U73343 (Calbiochem, USA), 200 µM Epac agonist (8-pCPT-2’-O-Me-cAMP, Sigma, USA), 25 µM Epac antagonist ESI-05 (Biolog, Germany), 25 µM Epac antagonist ESI-09 (Biolog, Germany) and 50 µM geranyl geranyl transferase inhibitor, GGTI 298, which disrupts Rap1 function. Merozoites were then transferred to EC buffer (5 mM KCl, 140 mM NaCl, 1 mM MgCl₂, 2 mM EGTA, 5.6 mM glucose, 25 mM HEPES, pH 7.2) followed by either measurement of cytosolic cAMP and Ca²⁺ levels in merozoites or microneme secretion.

P. falciparum merozoites were isolated in IC buffer (140 mM KCl, 5 mM NaCl, 1 mM MgCl₂, 5.6 mM glucose, 25 mM HEPES, pH 7.2), incubated for 15 min at 37°C with or without various pharmacological inhibitors or agonists as described above and transferred to EC buffer (5 mM KCl, 140 mM NaCl, 1 mM MgCl₂, 2 mM EGTA, 5.6 mM glucose, 25 mM HEPES, pH 7.2) or IC-K_low buffer (5 mM NaCl, 5 mM KCl, 135 mM choline-Cl, 1 mM EGTA, 5.6 mM glucose, 25 mM HEPES, pH 7.2) with or without pharmacological inhibitors or agonists for 15 min at 37°C. Merozoites were separated by centrifugation as described above. Merozoite supernatants and merozoite pellets were separated by SDS-PAGE on a 12% gel under reducing conditions. Microneme proteins, PfAMA1 and EBA175, were detected in merozoite supernatants by Western blotting using anti-PfAMA1 and anti-EBA175 rabbit sera, respectively. Rabbit sera against cytoplasmic protein PfNapL were used to detect PfNapL in supernatants and merozoite pellets to estimate cell lysis and confirm that similar amounts of merozoites were used for each condition, respectively. Horseradish peroxidase (HRP)-conjugated anti-rabbit IgG goat antibodies (Sigma, USA) were used as secondary antibodies and detected by enhanced chemi-luminescence using ECL-Prime Western Blotting Detection reagent (GE Healthcare).

P. falciparum merozoites were lysed with 0.1 N HCl and clarified by centrifugation at 6000 g. Supernatants were used for measuring the cytosolic levels of cAMP using cAMP direct immunoassay kit (Calbiochem, USA) as per manufacturer’s protocol. The kit uses a polyclonal antibody to bind cAMP present in the sample in a competitive manner. A standard curve was generated using known amounts of cAMP standards provided in the kit. Quantitative measurement of cAMP was obtained from the equation derived from the standard curve. The total protein content in each merozoite lysate sample was determined using Pierce BCA Protein Assay Kit (Pierce, USA) based on bicinchoninic acid (BCA). The amount of cAMP per µg of protein in each merozoite lysate sample was determined and used to calculate fold increase in cAMP per µg of merozoite protein material in each sample compared to control (merozoites in IC buffer).

P falciparum merozoites were isolated in RPMI 1640 as described, washed twice with phosphate buffered saline (PBS) and resuspended in 50 mM Tris pH 7.5, 150 mM NaCl. Merozoites were lysed by repeated freeze-thaw cycles and the lysate was clarified by centrifugation at 6000 g for 1 min at 4°C. The supernatant was incubated with different concentrations of NaHCO₃ (0 mM, 10 mM, 20 mM and 40 mM) in the presence of 10 mM MgCl₂, 10 mM CaCl₂, 5 mM ATP and 500 µM IBMX for 30 min at 30°C. The soluble adenylyl cyclase inhibitor KH7 (50 µM) was used as negative control. The reactions were stopped by the addition of 0.1 N HCl and the level of cAMP produced was measured using the cAMP direct immunoassay kit as described above.

P. falciparum merozoites were isolated as described above and incubated with or without KH7 (50 µM) in IC buffer for 15 min prior to transfer to EC buffer. Merozoite pellets were collected by centrifugation at 3000 g and used immediately to measure cAMP-dependent protein kinase A (PKA) activity. Merozoites were resuspended in ice-cold TNET buffer (50 mM Tris 7.4, 150 mM NaCl, 1 mM EDTA, and 1% Triton, protease inhibitor cocktail (Pierce, USA), 50 mM Na₃VO₄, 50 mM NaF) and lysed by repeated freeze-thaw cycles (4 cycles). The lysates were cleared by centrifugation at 6000 g for 15 min at 4°C. Total amount of protein in the supernatant was determined by (bicinchoninic acid assay (BCA) (Pierce, USA) using known amounts of bovine serum albumin (BSA) as standard. PKA activity was measured by quantitating incorporation of ³²P in kemptide, a known peptide substrate of PKA (L-R-R-A-S-L-G, Kemptide PKA peptide substrate, Promega, USA) as described previously [9].

Intracellular pH (pH_i) of P. falciparum merozoites was measured using the pH-sensitive fluorescent dye BCECF (2′,7′-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein) [30], [50]. P. falciparum merozoites were isolated in RPMI 1640 and loaded with BCECF-AM (acetoxymethylester of BCECF, Invitrogen, USA) for 20 min at 37°C in IC buffer. The merozoites were washed to remove excess dye and incubated with or without ACTZ in IC buffer at 37°C for 10 min. Merozoites were collected by centrifugation and resuspended in IC or EC buffer in the presence or absence of ACTZ and transferred to a 96 well microtiter plate (200 µL/well). Samples were excited monochromatically with λ₁ = 440 nm and λ₂ = 492 nm in succession for 0–10 minutes and emission was recorded at 535 nm on a fluorimeter (Perkin-Elmer Victor, USA). A quantitative measure of the pH_i is provided by the ratio of the fluorescence measured at 535 nm following excitation at 492 nm and 440 nm. For each experiment, a pH calibration curve was prepared by resuspending merozoites in buffer containing 130 mm KCl, 25 mM HEPES, 20 mM glucose and 1 mM MgCl₂ with a pH range of 6.6 to 8.0 followed by the addition of 10 µm nigericin (Sigma). Nigericin equilibrates the intracellular and extracellular pH. The equation derived from the linear regression curve obtained by plotting the fluorescence ratio at different pH values (S6 Figure) was used to calculate pH_i of merozoites in different conditions.

P. falciparum merozoites were isolated as described above, loaded with 10 µM Fluo-4-AM for 20 min at 37°C, washed, resuspended in IC buffer and used for experiments within 5 min, as described earlier [5], [51]. Fluo-4-AM loaded P. falciparum merozoites were treated with cAMP or Ca²⁺ modulating agents and transferred from IC to EC buffer. Fluorescence signal from Fluo-4 in merozoites under different conditions was measured by flow cytometry using FACSCalibur (Becton Dickinson, USA) and analyzed using CellQuest software. Briefly, Fluo-4-AM loaded merozoites were excited at 488 nm and fluorescence signal was detected with a 430 nm/30 nm band pass filter for periods of 2–3 mins. Merozoites were gated on the basis of their forward scatter and side scatter. The mean fluorescence intensity (MFI), which reflects cytosolic Ca²⁺ levels in merozoites, was plotted against time using FlowJo software.

P. falciparum merozoites isolated as described above were either mock-treated or treated with 50 µm KH7 (Calbiochem, USA), 100 µm ACTZ (Sigma, USA), 25 µM ESI-05 (Biolog, Germany) or 25 µM ESI-09 (Biolog, Germany) for 15 min at 37°C, washed with IC buffer, resuspended in EC buffer and incubated with erythrocytes in EC buffer at 37°C under mixed gas environment for 2 h to allow invasion. EC buffer was then replaced with complete RPMI. After 18–20 h of incubation in complete RPMI under mixed gas environment to allow development of ring stages, the percentage of infected erythrocytes was scored by flow cytometry to determine invasion rates, as described earlier [52].

P. falciparum schizonts and merozoites were smeared on glass slides, dried and fixed with pre-chilled methanol. Smears were blocked with 3% BSA in 1× PBS for 2 h at room temperature (RT) and probed with anti-PfACβ mouse sera diluted 1∶100, followed by Alexa-Fluor 488 conjugated goat anti-mouse IgG antibody diluted 1∶200. For co-immuno-staining, smears were also probed with rabbit sera (1∶100 dilution) against the cytoplasmic protein PfNAPL [20]. After washing, smears were incubated with Alexa-Fluor 488-conjugated goat anti-mouse IgG (1∶200, Molecular Probes, USA) and Alexa-Fluor 594-conjugated goat anti-rabbit IgG (1∶200 dilution, Molecular Probes, USA), for 1 hr at RT. The slides were washed, mounted with 4′, 6-diamidino-2-phenylindole dihydrochloride (DAPI, Molecular Probes, USA) and antifade mounting media (Molecular Probes, USA) and analyzed using a Nikon A1-R confocal microscope.