SPR analysis requires purified ligands and analytes to be used. Solubilized An. quadrimaculatus BBMV proteins were separated by anion-exchange chromatography and all elution fractions were tested for APN activity. Fractions 19–21 and 24–34 showed APN activity. Fractions 19–21 were made up of a single peak, and fractions 24–34 were made up of at least two peaks (Fig. 1). Fractions 19–21 were pooled, concentrated, and purified further by size-exclusion chromatography. A single peak was eluted at around 75 ml of run volume that correspond to a protein size of about 100 kDa (Fig. 2A). This peak was collected and was determined to hold APN activity. SDS-PAGE analysis of the protein also indicated a size of 100 kDa (Fig. 2B) and the 100 kDa protein was highly purified. The 100 kDa protein was named APN_Anq 100.

Initially, APN_Anq 100 was evaluated for binding by SPR analysis to four Cry toxins (Cry2Aa, Cry4Ba, Cry11Aa and Cry11Ba), which were previously determined in this laboratory to have mosquitocidal activity towards An. quadrimaculatus (data not shown). Only Cry11Ba bound significantly to APN_Anq 100. Further analysis of real-time binding kinetic of Cry11Ba to APN_Anq 100 was performed at different analyte concentrations (Fig. 3), followed by global fitting of all the response curves. A 1:1 binding stoichiometry, including a drifting-baseline correction, produced the following apparent rate constants of the bimolecular interaction: k_a = 184.0 M^-1s^-1 (± 1.0) and k_d = 1.03 × 10^-7 s^-1 (± 4.01 × 10^-6), K_D = 0.56 nM. More complex binding models, such as 2-site independent binding (A + B1 ↔ AB1; A + B2 ↔ AB2), and 2-site sequential binding (A + B ↔ AB ↔ AB*) also gave as good fitting as the simple 1:1 binding (A + B ↔ AB) with χ² = 0.112 (data not shown).

A twenty amino acid residue sequence (AQLEDYRLNDDVRPTAYRIE) was obtained from N-terminal sequencing of purified APN_Anq 100. Data mining for similar sequences in the arthropod databases revealed high homology (80–85% identities) with 3 conceptual translated proteins from An. gambiae (Table 1). A BLAST search using the first protein's full amino acid sequence from An. gambiae (accession no. EAA08760.1) revealed homology with many aminopeptidases from organisms of other genera (data not shown). This would suggest that the three proteins from An. gambiae have aminopeptidase activity.

Analysis of the N-terminal region with the program SignalP (http://www.cbs.dtu.dk/) predicted that the most probable cleavage site for the signal peptide sequence was between position 25 and 26 for EAA08760.1; between position 27 and 28 for EAA08763.1; and between position 28 and 29 for EAA08929.1. However, the sequences of the proteins shown in Table 2 start at positions further downstream from the predicted cleavage sites, which suggested that there might have been further processing of the N-terminal region of the An. quadrimaculatus APN. Analysis of the C-terminal region for possible glycosylphosphatidylinositol (GPI) anchor sites using the program Big-PI Predictor (http://mendel.imp.univie.ac.at/gpi/gpi_server.html) found no potential GPI-modification site for EAA08760.1. Potential GPI-modification sites were found at position 930 and 920 for EAA08763.1 and EAA08929.1, respectively. Analysis of the sequences using the program NetOGlyc 2.0 (http://www.cbs.dtu.dk/services/NetOGlyc/) 20 to reveal potential GalNAc O-glycosylation sites found 5 sites in EAA08760.1, 7 sites in EAA08763.1, and 6 sites in EAA08929.1. Analysis of the sequences using NetNGlyc 1.0 (http://www.cbs.dtu.dk/services/NetNGlyc/) 21 to reveal potential N-glycosylation sites found 2 sites in EAA08760.1, 8 sites in EAA08763.1, and 3 sites in EAA08929.1.

Another protein BLAST search was performed using the sequence of a known conserved region for aminopeptidases (MAAVPDFSAGAMENWGLL) 22, which yielded 16 homologous proteins from the An. gambiae genomic database (Table 2). This indicated that there are a large number of aminopeptidase isomers in these mosquitoes.

Fourth instars An. quadrimaculatus larvae were filtered with a nylon mesh, washed in distilled water, separated from large residual food particles, and dried briefly on a filter paper (Fisher) under vacuum suction. Harvested larvae were frozen at -70°C until needed. About 4–6 g of frozen larvae were homogenized in 8–12 ml of cold buffer A (300 mM mannitol, 5 mM EGTA, 17 mM Tris-HCl, pH 7.5). Larvae were homogenized by 40 strokes of Potter-Elvehjem PTFE pestle in glass tube at speed number 5 (~6000 rpm). BBMV were enriched through differential centrifugation by selective divalent-cation precipitations as described by Silva-Filha, et al 34. The BBMV pellet was resuspended in 1 ml of ice-cold binding buffer (8 mM NaHPO₄ , 2 mM KH₂ PO₄ , 150 mM NaCl, pH 7.4) supplemented with COMPLETE™ (Roche) protease inhibitor and homogenized by10 extrusions using a small Teflon pestle.The protein concentration of the BBMV was measured with the Coomassie protein assay reagent (Pierce), using BSA as the standard. The BBMV was kept at -70°C until needed.

Approximately 20 mg of BBMV was solubilized overnight at 4°C in the binding buffer supplemented with 10 mg/ml of CHAPS (Roche). Later, the solution was vortexed briefly and centrifuged at 15,000 rpm in a JA-17 rotor at 4°C for 10 min. The supernatant was treated with PIPLC for 1 hr at 37°C. The supernatant was separated by anion-exchange chromatography (HiTrap 5 ml column, Pharmacia) by continuous salt gradient using two buffers: A, 20 mM Tris-Cl, pH 7.4, 0.4 mg/ml CHAPS; B, buffer A with 1 M NaCl. Two milliliters elution fractions were collected at a flow rate of 1 ml/min. A small fraction of each elution fraction was tested for the presence of APN activity using L-leucine p-nitroanilide (Sigma) as substrate. Neighboring fractions containing APN activities were pooled and concentrated using centricon (YM30, Millipore) according to the manufacturer. The pooled fractions were further purified by size exclusion chromatography (Superdex 200, Pharmacia) in 20 mM Tris, pH 7.4, 0.4 mg/ml CHAPS and concentrated as before. The quality of the sample was checked by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) as described by Laemmli 35.

An E. coli clone of Cry2Aa (a grateful gift from Takashi Yamamoto) was used as a source of this gene. The cry2Aa gene was extracted by PCR and cloned into plasmid pHT600 and transformed into B. thuringiensis 4Q7, a plasmidless Cry^- derivitive. The genes cry4Aa, cry4Ba, cry11Aa and cry11Ba were received in the same plasmid vector and host B. thuringiensis strain (gratefully donated by Armelle Delécluse). Single Bt colonies were inoculated into a 5 ml LB medium supplemented with 10 μg/ml erythromycin and grown overnight at 30°C in an incubator-shaker at 250 rpm. These cultures were inoculated into a 500 ml SSM medium 36 also supplemented with erythromycin and incubated a further 4 days until sporulation and autolysis. Bt crystals in the autolysed-cells suspension were purified as described previously 37 for purification of Cry toxins expressed in E. coli, except that the sonication steps were omitted. The crystals were solubilized in carbonate buffer (30 mM Na₂ CO₃ , 20 mM NaHCO₃ , pH 10.0) supplemented with 10 mM dithiothreitol (Roche) at 37°C for 3 hours. Next, the solubilized toxin was incubated with 1/20 (v/v) 10 mg/ml trypsin (Sigma) at 37°C for 3 hours. The activated toxin was purified by FPLC using a Superdex 200 (Pharmacia) column in the carbonate buffer. Protein concentration was measured using the Coomassie protein assay reagent (Pierce) with bovine serum albumin as standard.

All surface plasmon resonance (SPR) experiments were performed on a BIAcore 3000 machine (Biacore AB). An. quadrimaculatus APN in 20 mM ammonium acetate, pH 4.2, was immobilized on a CM5 sensor chip by amine-coupling method (Biacore AB). The flow buffer HBS-EP (10 mM HEPES, 150 mM NaCl, 3 mM EDTA, 0.005% polysorbate 20 (v/v), pH 7.4) (Biacore AB) was used at a flow rate of 30 μl/min. Multiple concentrations (4, 8, 16, and 32 μM) of Cry11Ba was injected across the flow cell containing the APN and one blank flow cell containing ethanolamine as a blocking agent. Surfaces were regenerated with 2 pulses of 10 μl of 10 mM NaOH, pH 11, at 100 μl/min or until the signal return to baseline. Signal responses from the blank flow cells were subtracted from all response curves and data were globally fitted using BIAevaluation Ver. 3.1 (Biacore AB). The curves were fitted to a simple 1:1 Langmuir binding model (A+B ↔ AB) to obtain apparent rate constants.

For N-terminal sequencing, proteins separated in SDS-PAGE were transferred onto PVDF membrane (Roche) by electro-transfer (Mini-PROTEAN™ II, Bio Rad) according to the manufacturer. The membrane was stained briefly with Coomassie Blue R-250 and destained in 50% methanol. Bands representing 100-kDa proteins were excised and sequencing was performed on an automated sequencer (Model 477A, Applied Biosystems) at USDA Forest Service Laboratory, Delaware, OH. Data mining was performed on the N-terminal sequence using the basic local alignment search tool (BLAST), an on-line tool, at the National Center for Biotechnology Information (NCBI) website. The search parameter was limited to arthropods. CLUSTAL W (http://npsa-pbil.ibcp.fr/cgi-bin/npsa_automat.pl?page=npsa_clustalw.html) was used to align the amino acid sequences.