AJMB Avicenna Journal of Medical Biotechnology 2008-2835 2008-4625 Avicenna Research Institute AJMB-2-87 Original Article Conjugation of R-Phycoerythrin to a Polyclonal Antibody and F (ab')2 Fragment of a Polyclonal Antibody by Two Different Methods Mahmoudian Jafar 1 Jeddi-Tehrani Mahmood 1 2 Rabbani Hodjattallah 1 2 Mahmoudi Ahmad Reza 1 Akhondi Mohammad Mehdi 3 Zarnani Amir Hassan 4 Goli Leila Balaei 1 Babaei Mahdokht 1 Ghods Roya 1 * Monoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran Immune and Gene Therapy Lab, Cancer Center Karolinska, Karolinska Institute, Stockholm, Sweden Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran Nanobiotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran Corresponding author: Roya Ghods, M.Sc., Monoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran. P.O. Box: 19615-1177. Tel: +982122432020. Fax: +0982122432021. E-mail: ghods@avicenna.ac.ir April-June 2010 2 2 87 91 15 05 2010 19 06 2010 Copyright © 2010 Avicenna Research Institute 2010

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R-Phycoerythrin (R-PE), a fluorescent protein from phycobiliprotein family, is isolated from red algae. Conjugation of antibodies to R-PE facilitates multiple fluorescent staining methods. In the present study polyclonal antibodies and polyclonal F(ab')2 fragment antibodies were conjugated to R-PE by two different methods. The efficiency of the methods was evaluated using Immunocytochemistry (ICC) and Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis (SDS-PAGE). In the first conjugation method, PE was attached to SMCC linker followed by conjugation of antibody to PE-SMCC. In the second method, SH groups were added onto R-PE molecule, while the antibody was attached to SPDP linker. Then, the antibody-SPDP molecule was conjugated to R-PE. Our results showed that the two conjugation methods did not have any abrogative effects on the antibody binding activity.

 Antibody Conjugation Immunocytochemistry Phycoerythrin Introduction

R-Phycoerythrin (R-PE) is one of the most commonly-used fluorescent dyes for fluorescent staining and other immunoassays. R-PE is a large protein (approximately 240 kDa) containing 25 fluors (1). R-PE has three types of subunits: alpha (∼20,000 daltons), beta (∼20,000 daltons) and gamma (∼30,000 daltons) and its subunit structure [(alpha-beta) 6 gamma] has been determined (2). Typically, only one PE molecule is conjugated to one antibody molecule (3).

Nonetheless, by virtue of its huge absorption coefficient and almost perfect quantum efficiency it is one of the brightest dyes used today. It emits at about 570 nm, and is excited by an argon laser tuned to 488 nm; however, much more sensitive detection is obtained with a laser tuned to 533 nm (3).

In this study we conjugated R-PE to antibodies by two various methods. Firstly, R-PE was attached to SMCC linker; and then, the antibody was attached to PE-SMCC (3). Secondly, SH groups were added onto PE molecule, while the antibody was attached to SPDP linker. Then, the antibody-SPDP molecules were conjugated to R-PE (4–6).

 Materials and Methods Antibodies (Abs)

For the purpose of conjugation, three different antibodies were prepared at Avicenna Research Institute, Tehran, Iran.

These antibodies included sheep anti mouse immunoglobulins adsorbed against human immunoglobulins [ShαM Ig (human Ig ads)], F(ab')2 fragment of sheep anti mouse immunoglobulins adsorbed against human immunoglobulins [ShαM Ig F(ab')2 (human Ig ads)], sheep anti human immunoglobulins adsorbed against mouse immunoglobulins [ShαH (Mouse Ig Ads)].

 Conjugation of R- PE to a reduced antibody by SMCC linker

Sulfosuccinimidyl- 4-(N-maleimidomethyl) cyclohexane-1-carboxylate (Sulfo-SMCC) (Sigma- Aldrich, Wisconsin, USA) is a water-soluble heterobifunctional linker. It contains an amine-reactive N-hydroxysuccinimide (NHS ester) and a sulfhydryl-reactive maleimide group. First, 200 µg sulfo-SMCC was attached to 1 mg R-PE (2–3 mg/ml) by the amine-reactive end for 1 hr with shaking in Phosphate Buffered Saline (PBS); then, the excess sulfo-SMCC was removed by dialysis in PBS at 4 °C overnight. The antibody was reduced by 20 mM Dithiothreitol (DTT) for 30 min without shaking; and then, DTT was rapidly removed by dialysis in PBS. The reduced antibody was immediately added to PE-SMCC where the sulfhydryl-reactive maleimide end in PE-SMCC was used to attach PE- SMCC to the reduced antibody. Then, the mixture was mixed for 6 hr at Room Temperature (RT). Finally, free SH groups on the antibody molecules were blocked by 40 mM N- Ethylmaleimide (NEM) for 30 min at RT (3).

 Conjugation of thiolated PE to the antibody by SPDP linker

R-PE was thiolated by Traut's Reagent (2-Iminothiolane or 2-IT) (Sigma-Aldrich) for 1.5 hr at RT, while the antibody was attached to a heterobifunctional linker called SPDP (N -succinimidyl 3-(2-pyridyldithio)-propionate) (Uptima, Montiucon, Cedex, France) in PBS. Finally, thiolated R-PE was mixed with Ab-SPDP; resulting in Ab-SPDP-PE.

 Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis (SDS-PAGE)

To analyze conjugate quality, equal amounts of protein (10 µg) were run on 12.5% SDS-PAGE at 100 V for 2 hrs under discontinuous non-reducing condition using a Mini-Protean III electrophoresis apparatus (Bio-Rad, Hercules, CA).

 Cell culture

A mouse IgG-producing hybridoma cell line was grown in RPMI 1640 medium containing 10% (v/v) fetal calf serum (Invitrogen, California, USA) and 1% penicillin/ streptomycin (Sigma- Aldrich) at 37 °C in the presence of 5% Co2.

 Immunocytochemistry

Two different cell types were used in this experiment. A mouse IgG-producing hybrid-oma cell line and human B lymphocytes as part of Peripheral Blood Mononuclear Cells (PBMC) that were prepared from whole blood by Ficoll separation (7). Forty thousand cells were added onto glass slides. After drying for 2 hr at RT, they were fixed by 2% formaldehyde. The fixed cells were washed and then blocked by 5% sheep serum. R-PE conjugated antibodies were added. Cells were washed with PBS and then observed directly under a fluorescent microscope (Olympus, Tokyo, Japan).

 Results Electrophoretic pattern of both PE conjugated whole antibody and F(ab')2 fragments by SMCC linker

Figures 1 and 2 show electrophoretic mobility patterns of R-PE conjugated whole ShαM Ig and F(ab')2 fragment of ShαM Ig by SMCC linker in SDS-PAGE, respectively. Considering the fact that the conjugation of antibodies to R-PE may involve one or more R-PE subunits for each antibody molecule, the conjugation materials may show different electrophoretic mobility properties as reflected by a smear rather that a single sharp band in SDS-PAGE (2).

Electrophoretic pattern of R-PE conjugated ShαM Ig by SMCC linker in non-reduced 12.5% SDS-PAGE: Lane 1 shows R-PE conjugated ShαM Ig. Lane 2 shows unconjugated ShαM Ig. Lane 3 shows R-PE alone

Electrophoretic pattern of R-PE conjugated F(ab')2 fragment of ShαM Ig by SMCC linker in non-reduced 12.5% SDS-PAGE. Lane 1 shows F(ab')2 fragment of ShαM Ig (100 kDa). Lane 2 shows IgG molecule (150 kDa) as protein marker. Lane 3 shows R-PE alone. Lane 4 shows R-PE conjugated F(ab')2 fragment of ShαM Ig

 Electrophoretic pattern of both PE conjugated whole antibodies and F(ab')2 fragments by SPDP linker

Figure 3 shows electrophoretic mobility patterns of R-PE conjugated whole and F(ab')2 fragments of ShαM Ig by SPDP in SDS-PAGE. Similar to SMCC linker method, the conjugation method using SPDP linker also resulted in smears because of different numbers of R-PE subunits bound per Ab molecule.

Electrophoretic pattern of R-PE conjugated ShαM Ig and F(ab')2 fragment of ShαM Ig by SPDP linker in non-reduced 12.5% SDS-PAGE. Lane1 shows unconjugated F(ab')2 fragment of ShαM Ig. Lane 2 shows unconjugated ShαM Ig. Lane 3 shows R-PE alone. Lane 4 shows R-PE conjugated ShαM Ig. Lane 5 shows R-PE conjugated F(ab')2 fragment of ShαM Ig

 Immunocytochemistry analysis of antibodies conjugated by SMCC linker

To analyze the specific binding of R-PE conjugated antibodies by SMCC linker method, conjugated whole ShαM Ig and its F(ab')2 fragments were studied by ICC on a mouse IgG-producing hybridoma cell line. The R-PE conjugated ShαH Ig as the control antibody was tested for its specific reactivity on human B lymphocyte in ICC assay as depicted in Figures 4A and B. Both ShαM Ig – R-PE and its R-PE conjugated F(ab')2 fragments could successfully bind to the cells (Figures 5A and B) while the negative control, R-PE conjugated ShαH Ig (Figures 5C) did not bind to these cells.

Immunocytochemistry analysis of R-PE conjugated ShαH Ig on human B lymphocytes. A) ShαH (Mouse Ig Ads)-PE (1 mg/ml dilution: 1/100). B) ShαM Ig (Human Ig Ads)-PE (1 mg/ml dilution: 1/100)

Immunocytochemistry analysis of ShαM Ig – R-PE and its R-PE conjugated F(ab')2 fragments by SMCC linker on a mouse IgG-producing hybridoma cell line. A) ShαM Ig (Human Ig Ads)-PE (1 mg/ml dilution: 1/100). B) F(ab')2 fragment of ShαM Ig (Human Ig Ads)-PE (1 mg/ml dilution: 1/100). C) ShαH (Mouse Ig Ads)-PE (1 mg/ml dilution: 1/100)

 Immunocytochemistry analysis of antibodies conjugated by SPDP linker

Specific binding of whole R-PE conjugated ShαM Ig and its F(ab')2 fragments by SPDP linker was tested by ICC on the mouse IgG-producing hybridoma cell line. As shown in Figure 6 both antibody conjugates reacted to the cells (Figures 6A and B), while its negative control (ShαH Ig-R-PE) was negative as shown in Figure 6C.

Immunocytochemistry analysis of ShαM Ig – R-PE and its R-PE conjugated F(ab')2 fragments by SPDP linker on a mouse IgG-producing hybridoma cell line. A) ShαM Ig (Human Ig Ads)-PE (1 mg/ml dilution: 1/100). B) F(ab')2 fragment of ShαM Ig (Human Ig Ads)-PE (1 mg/ml dilution: 1/100). C) ShαH (Mouse Ig Ads)-PE (1 mg/ml dilution: 1/100)

 Discussion

Though there are different methods to conjugate R-PE to antibodies, optimization of an efficient method is crucial. Conjugating R-PE molecules to antibodies without other adverse byproducts is our main goal in this conjugation. Considering the fact that R-PE – R-PE and Ab – Ab conjugates are not useful, a proper conjugation should attach R-PE to antibody specifically. The commonly used homobifunctional linkers, like glutaraldehyde, have some disadvantages. They result in high levels of adverse byproducts such as Ab – Ab and R-PE – R-PE conjugates; in addition, their chemical process is hard to control and may lead to unwanted polymerization of materials (8). Hence, in order to conjugate R-PE to Abs, the most efficient method is using heterobifunctional linkers (9). These linkers usually have two different end groups, an amine reactive group and a sulfhydryl reactive group, which provide a feasible tool to conjugate different molecules.

Selecting an appropriate method to attach two different molecules depends on their structure or surface active groups. On account of the fact that the surface of R-PE molecule contains many amine groups (10), and anti-bodies contain many intra-disulfide bonds (11), these different properties could be used as a significant tool during an appropriate bioconjugation. Therefore, in our first conjugation method a heterobifunctional linker, sulfo-SMCC, was used to link the amine groups on R-PE molecule to the sulfhydryl groups in the reduced antibody molecules.

However, this notion is challenged by some researchers who prefer to use the amine groups of antibody (12). To examine this possibility in our system, we used the second conjugation method in which SPDP linker was used to conjugate thiolated R-PE to amine groups on the intact antibody molecules. The results of experiments showed that the antibodies retained their binding ability in both systems.

 Acknowledgment

This work was supported by a grant from Avicenna Research Institute.

 References Glazer AN Phycobilisomes: structure and dynamics Annu Rev Microbiol 1982 36 1 173 198 Jiang T Zhang J Chang W Liang D Crystal structure of R-phycocyanin and possible energy transfer pathways in the phycobilisome Biophys J 2001 81 2 1171 1179 Hardy RR Purification and coupling of fluorescent proteins for use in flow cytometry Handbook of experimental immunology 1986 4th ed Oxford Black-well Scientific Chambers JD Simon SI Berger EM Sklar LA Arfors KE Endocytosis of beta 2 integrins by stimulated human neutrophils analyzed by flow cytometry J Leukoc Biol 1993 53 4 462 469 Kronick MN Grossman PD Immunoassay techniques with fluorescent phycobiliprotein conjugates Clin Chem 1983 29 9 1582 1586 Oi VT Glazer AN Stryer L Fluorescent phycobili-protein conjugates for analyses of cells and molecules J Cell Biol 1982 93 3 981 986 Ferrante A Thong YH Optimal conditions for simultaneous purification of mononuclear and polymorphonuclear leucocytes from human blood by the hypaque-ficoll method J Immunol Methods 1980 36 2 109 117 Migneault I Dartiguenave C Bertrand MJ Wald-ron KC Glutaraldehyde: behavior in aqueous solution, reaction with proteins, and application to enzyme crosslinking BioTechniques 2004 37 5 790 802 Mattson G Conklin E Desai S Nielander G Savage MD Morgensen S A practical approach to crosslinking Mol Biol Rep 1993 17 3 167 183 Jiang T Zhang J Liang D Structure and function of chromophores in R-phycoerythrin at 1.9 A resolution Proteins 1999 34 2 224 231 Wang W Singh S Zeng DL King K Nema S Antibody structure, instability, and formulation J Pharm Sci 2006 96 1 1 26 Barbet J Machy P Leserman LD Monoclonal antibody covalently coupled to liposomes: specific targeting to cells J Supramol Struct Cell Biochem 2004 16 3 243 258