Efficient Conjugation of Aflatoxin M1 With Bovine Serum Albumin through Aflatoxin M₁-(O-carboxymethyl) Oxime and Production of Anti-aflatoxin M1 Antibodies

3.1. Preparation of AFM1-(O-carboxymethyl) Oxime Derivative

Hsu and Chu (14) reported a useful method for coupling aflatoxin to protein. Here, we intend to describe a modification of the method proposed by Hsu and Chu. Since AFM₁ lacks a reactive group to conjugate with carrier proteins such as BSA, AFM₁ (Sigma, USA) was converted to AFM₁-(O-carboxymethyl) oxime (AFM₁-oxime) as follows: 152 μg of O-(Carboxymethyl) hydroxylamine hemihydrochloride (Sigma, USA) in 1 mL of deionized water was mixed with 100 μg of AFM₁ in 4 mL methanol, and then 1 mL of pyridine was added to the mixture. The mixture was refluxed for 3 hours and incubated at room temperature for an overnight. After reaction, the solvents were removed by rotary evaporator. The reaction product (AFM₁-oxime) was orange yellow in color, possessing a reactive carbonyl group and able to react with the amine groups of proteins.

The reaction product and aflatoxin standard were dissolved in chloroform and analyzed by thin-layer chromatography (TLC). TLC was performed by spotting the product and aflatoxin standard near the base of a silica gel plate followed by developing the TLC plate in acetone-chloroform (1:9). In addition, the product of the reaction was analyzed by Reversed-Phase High-Performance Liquid Chromatography (RP-HPLC) using a ODS column (150 mm × 4.6 mm). AFM₁ at the concentration of 10 ppb in methanol (as standard), carboxymethyl hydroxylamine at the concentration of 10 ppb in water and AFM₁-oxime at the concentration of 10 ppb in methanol were prepared. About 20 μL of each sample and standard were injected into the HPLC system. Isocratic solution of methanol-acetonitrile was used as the mobile phase. Elution was monitored by a spectroflurometric detector (RF-551, Shimadzu, Kyoto, Japan) operated at excitation and emission wavelengths of 365 and 420 nm, respectively. The column oven temperature was kept constant at 35°C and the mobile phase was filtered, degassed and pumped at a flow rate of 2.2 mL/min.

3.2. Conjugation of AFM1-(O-carboxymethyl) Oxime to Bovine Serum Albumin

One hundred microliter of AFM₁-oxime in 400 μL of 25% ethanol containing 6.5 mg EDS was mixed with 200 μg of BSA (Sigma, St. Louis, MO, USA) in 20 μL of 0.05 M sodium phosphate buffer (pH 7.2). The reaction mixture was stirred at room temperature for 48 hours in complete darkness. Two additional 6.5 mg portions of EDS were added to the reaction mixture during this period. After reaction, the mixture was dialyzed against deionized water for 24 hours, with 3 times water change, followed by centrifuging at 10000 × g for 10 minutes. The conjugation of AFM₁-oxime to BSA was analyzed by UV-VIS spectrophotometry against pure BSA.

3.3. Immunizations

Female rabbits, 6-8 weeks old, were obtained from Razi Institute (Tehran, Iran) and immunized with the AFM₁-BSA conjugate as follows: about 150 μL of AFM₁-BSA conjugate (500 μg/mL) was emulsified with equal volume of Complete Freund's adjuvant (CFA, Sigma) for the first injection and Incomplete Freund's adjuvant (IFA, Sigma) for the booster injections with 2-weeks intervals. The first injection was performed intradermally at 5 points on the animal’s back and sides. The booster injections were introduced intramuscularly. A normal rabbit was immunized with BSA as described previously. Starting at 3 or 4 weeks after the initial immunization, rabbits were bled on biweekly intervals and antibody titers were determined by an indirect ELISA. Rabbits were bled 3 weeks after final injection, the time when desirable titers of antibody were found. Antiserum was separated from the clot by centrifugation at 4000 × g (4°C) for 30 minutes and purified as follows.

3.4. Purification of IgG Fraction of Rabbit Serum

The serum was diluted thrice with PBS and half saturated (50%) with ammonium sulfate. The precipitated fraction was separated by centrifugation and dialyzed against 100 mM Tris-HCl buffer pH 7.8 and purified by a DEAE-Sephacel (Amersham Pharmacia Biotech) column equilibrated with the same buffer.

3.5. Affinity Chromatography With Bovine Serum Albumin Ligand

For further purification of BSA-AFM₁ antibody, the antibody produced against AFM₁ was negatively selected by a BSA-Sepharose 4B affinity column. In order to prepare affinity medium, CNBr-activated Sepharose 4B (Amersham Pharmacia Biotech) was swelled in adequate 1 mM HCl for two hours. For each milliliter of the swelled resin, 5 mg of BSA in 0.1 M carbonate buffer, pH 8.5 containing 0.5 M NaCl was added and the mixture was stirred for 2 hours at RT. Residual active sites were blocked with 0.2 M glycine containing 0.5 M NaCl. The resin was washed thrice with alternate buffers (50 mM acetate buffer pH 4 and 50 mM carbonate buffer pH 9 containing 0.5 M NaCl), then loaded on to a column and equilibrated with phosphate buffered saline (PBS) pH 7.2. The purified IgG fraction at concentration of 5 mg/mL was applied to the column, and the column was washed with PBS till the absorbance of effluents reached zero at 280 nm. Finally, 3 column volumes of 0.1 M glycine with pH 2.7 were used to elute bound antibodies from the column.

3.6. Enzyme-linked Immunosorbent Assay

ELISA method was used to determine the titers of prepared antiserums and purified antibodies as well as the cross reaction of purified antibodies with other aflatoxins (AFB₁, AFB₂, AFG₁, AFG₂). The optimal dilution of antigen pre-coated on the microtiter plate was determined by a checkerboard test. One hundred microliter of antigen (AFM₁-BSA or BSA at 5 µg/mL in PBS) was coated for 2 hours at 37°C. After 3 times of washing with PBS containing 0.05% (v/v) Tween 20 (PBS-T), nonspecific sites were blocked with PBS-BSA 2% (w/v) for 2 hours followed by 2 washes with PBS-T. 100 µL of 1:1000 to 1:64000 dilutions of the antiserums, purified antibodies or standard antiserums were added to each well and incubated for 1 hour at 37°C. The plates were washed 5 times with PBS-T and 100 µL of 1:10000 dilutions of secondary antibodies (goat anti-rabbit IgG conjugated with HRP, prepared in our laboratory) was added to each well. Plates were incubated for 45 minutes at 37°C and after 5 times of washing, 100 µL of TMB substrate solution (Sigma, St. Louis, MO, USA) was added. After 20 minutes of incubation in a dark place, the reaction was stopped with 100 µL of 5% solution of sulfuric acid. Absorbance of wells was read by a plate reader (Stat Fax 2100, Awareness Technology Inc. Palm City, USA) at 450 nm.

3.7. Analytical Methods

Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis (SDS-PAGE) was performed using 12.5% separating and 4% stacking gels containing 0.1% SDS (30). Protein samples were heated in boiling water for 5 minutes and resolved at 50 V for 30 minutes and 150 V for 1 hour followed by Coomassie Blue R250 staining. The protein concentrations were determined by the method of Bradford (31) using BSA as the standard protein.

4.1. Preparation of Aflatoxin M1-(O-carboxymethyl) Oxime

In order to confirm the coupling of AFM₁ to O-(Carboxymethyl) hydroxylamine hemihydrochloride, the reaction product was analyzed by TLC and RP-HPLC. Analysis of the product by TLC plate developed in acetone-chloroform (1:9) yielded two spots, using UV detector (Figure 1). The minor spot in the upper part of the gel had the same Rf value as the standard aflatoxin (Figure 1 lane A), and the major spot with lower Rf value was the AFM₁-oxime derivative (Figure 1 lane B).

For further confirmation of the AFM₁ coupling to O-(Carboxymethyl) hydroxylamine hemihydrochloride, the standard aflatoxin and the reaction product at the concentrations of 10 ppb were injected into the RP-HPLC system and retention times were measured. Figure 2 A shows the pattern of standard aflatoxin (retention time 9 minutes, peak B). The other peaks in this Figure correspond to the solvent. Figure 2 B shows the pattern of reaction product, which includes a major peak (retention time 6 minutes, peak A) and a minor peak (peak B) that eluted at the same retention time as standard aflatoxin peak. Peak B, which is negligible, corresponds to the free aflatoxin. By injection of O-(Carboxymethyl) hydroxylamine into the HPLC system, no peak appeared, indicating that it lacks any absorbance at the wave length of 365 nm and emission wavelength of 420 nm. Therefore, the peak eluted at 6-minute retention time corresponds to the AFM₁-oxim conjugate (peak A in Figure 2 B).

4.2. Conjugation of Aflatoxin M1-(O-carboxymethyl) Oxime to Bovine Serum Albumin

The UV spectrum of the reaction product from the wave length of 200 - 800 nm showed two peaks (Figure 3). The first peak at the wavelength of 280 nm corresponds to BSA. The peak at the wavelength of 365 nm corresponds to the coupled reaction product. The free AFM₁ molecule was separated from the reaction product by dialyzing against deionized water, so the peak at 365 nm corresponds to BSA-AFM₁ conjugate free of AFM₁ contaminants. The results obtained from spectrometric method indicated that about 12 moles of AFM₁-oxime were successfully coupled to 1 mole of BSA.

4.3. Preparation and Purification of Anti-AFM1 Antibodies

After each injection of antigen (BSA- AFM₁) to rabbit, the anti-AFM₁ antibody levels of the sera were monitored using a designed indirect ELISA. According to the ELISA results, the antibody titers were relatively weak after first and second injections and desirable titers were obtained 2 weeks after the third injection. The highest titers were observed after the fourth injection. Rabbits were bled two weeks after the last injection, when the maximum titers of antibody (64000 times) were found and the antiserum was prepared. The titers of prepared anti-AFM₁ antiserum were compared to the antiserum of immunized rabbit with standard BSA-AFM₁ conjugate and it was found that the titers of prepared antiserum in this study were suitable for use in immunological assays for the analysis of AFM₁.

The purity of prepared antibodies was estimated by SDS-PAGE (Figure 4). Ammonium sulfate fractionation caused partial purification of the antibody (Figure 4, lane 6). The first peak obtained from ion exchange chromatography contained IgG fraction with high purity. Reducing SDS-PAGE of this fraction included two intense bands at the MW of 26-27 and about 50 KDa, corresponding to the light and heavy chains of IgG, respectively (Figure 4, lanes 1-2). In Figure 4, lanes 4 and 5 show the protein content of second and third peaks of ion exchange chromatography, respectively that have been eluted from the column, with equilibrium buffer containing 0.1 and 1 M NaCl. They contained other impurities in addition to some parts of IgG.

In order to increase the specificity of antibody against AFM₁ and excluding anti-BSA antibodies, we used BSA-Sepharose 4B affinity chromatography. An indirect ELISA, using BSA or BSA-AFM₁ (5 µg/mL) as the coated antigen, was conducted to ensure that the antibody produced against protein carrier was completely removed by the BSA-Sepharose 4B affinity chromatography. The results showed that the column unbound antibody is very reactive and specific against BSA-AFM₁ (OD; 1 at 1:32000 dilution) and not reactive to BSA at the same dilution. These findings clearly show that the column unbound antibody includes specific antibody against AFM₁ and was successfully separated from the anti-BSA antibody by the affinity chromatography using BSA ligand.

4.4. Determination of Antibody Specificity

Specificity of purified antibodies obtained from rabbits immunized with BSA-AFM₁ was determined by a competitive ELISA. The antibody used in the assay was the BSA-Sepharose 4B affinity purified antibody. Results showed that the purified antibodies have the highest affinity to AFM₁ in comparison to related aflatoxins. Concentrations required to decrease absorbance by 50% (or to displace the bound AFM₁-proxidase) in the presence of different aflatoxins were 1, 70, 105, 240, 2500 ng/mL for AFM₁, AFB₁, AFB₂, AFG_1, and AFG₂, respectively.

Figure 1.

Lane A, standard aflatoxin; lane B, AFM1-(O-carboxymethyl) oxime conjugate.

Figure 2.

HPLC Chromatogram of Standard AFM1 (A) and AFM1-(O-carboxymethyl) Oxime Derivative (B)

Figure 3.

The peaks at wave lengths of 280 nm and 365 nm correspond to BSA and BSA-AFM1 conjugate, respectively.

Figure 4.

Lanes 1 and 2 shows the first peak containing purified antibody, lane 4 and 5 correspond to the second and third peaks respectively. M shows the protein markers with the MW of 94, 66, 45, 30, 20 and 14 KDa from up to down.