Facile radiolabeling of monoclonal antibodies and other proteins with zirconium-89 or gallium-68 for PET imaging using p-isothiocyanatobenzyl-desferrioxamine

protocol.md

Authors: Lars Perk, Gerard Visser, Marianne Budde, Maria Vosjan, Paul Jurek, Garry Kiefer & Guus van Dongen 

Introduction

Presently, hundreds of monoclonal antibodies (mAbs) and mAb fragments are under clinical development because of their excellent potential for the systemic treatment of cancer and other pathological conditions (1, 2). Positron emission tomography (PET) offers an exciting imaging option to confirm and quantify selective tumor uptake of such targeting molecules (3).

To enable PET imaging of mAbs (immuno-PET), an appropriate positron emitter, with a half-life (t1/2) that is compatible with the time needed to achieve optimal tumor-to-nontumor ratios (typically 2-4 days for intact mAbs), has to be securely coupled to the targeting molecule. For this purpose we recently described the large scale production of pure zirconium-89 (89Zr; t1/2: 78.4 h) and a strategy for labeling mAbs with 89Zr via a multi-step synthesis using a succinylated-derivative of desferrioxamine B (Df) as bifunctional chelate (4). The utility of this approach was clearly demonstrated through high quality 89Zr-mAb-PET images reported in preclinical and clinical studies (5-11). The upcoming commercialization of 89Zr will make this radionuclide generally available for research and clinical development.

A shortcoming of the aforementioned approach is that the multi-step procedure is relatively complicated and time consuming. In this updated protocol we present the newly developed p-isothiocyanatobenzyl-derivative of Df (SCN-Bz-Df; Macrocyclics, TX) which provides an efficient and rapid preparation of 89Zr-labeled mAbs. First, SCN-Bz-Df is coupled to the amine groups of a protein at pH 9.0, followed by purification using gel filtration. Next, the conjugate is labeled at room temperature by addition of a solution of 89Zr oxalic acid followed by purification using gel filtration. SCN-Bz-Df can also be utilized to label proteins at room temperature with gallium-68 (68Ga; t1/2: 1.13 h). 68Ga is especially attractive for PET-imaging of fast kinetic targeting proteins like mAb fragments.

Reagents

1. Antibody or protein to be conjugated (typically 2-10 mg)

• p-isothiocyanatobenzyl-desferrioxamine (SCN-Bz-Df; Macrocyclics, cat. no. B-705; molecular weight=752.9 g/mol)
• Distilled, deionized water (Milli-Q; greater than 18 MΩ resistance)
• DMSO (Aldrich, cat. no. 494429)
• Sodium carbonate; 0.1 M and 2.0 M solutions in water (Aldrich, cat. no. 204420)
• Normal (0.9%) saline (B.Braun, cat. no. 5/12251178/1197)
• Gentisic acid (Fluka, cat. no. 37550)
• 0.9% NaCl/gentisic acid 5 mg ml (pH = 4.9-5.3; see REAGENT SETUP)
• Oxalic acid; 1.0 M solution in water (Fluka, cat. no. 75688)
• HEPES buffer solution (Invitrogen, cat. no. 15630-049; see REAGENT SETUP)
• Sodium hydroxide (NaOH); 1.0 M solution in water (Riedel-de Haën, cat. no. 30620)
• Citric acid monohydrate (Fluka, cat. no. 27491)
• Hydrochloric acid (HCl), Trace SELECT Ultra; 30% (9.5 M), 0.1 M, 1.0 M and 4.0 M solutions in water (Fluka, cat. no. 96208)
• Ammonium acetate (Fluka, cat. no. 73594)
• 3.0 M and 0.25 M ammonium acetate buffer (see REAGENT SETUP)
• Sodium dihydrogen phosphate monohydrate (Merck, cat. no. 1.06346.0500)
• Disodium hydrogen phosphate anhydrous (Merck, cat. no. 1.06566.0100)
• Sodium chloride (Merck, cat. no. 1.06404.0500)
• Sodium azide (Merck, cat. no. 1.06688.0100)
  • !CAUTION Highly toxic
• EDTA disodium salt (Sigma-Aldrich, cat. no. E1644)
• ITLC eluent (see REAGENT SETUP)
• HPLC eluent (see REAGENT SETUP)
• Zirconium-89 in 1.0 M oxalic acid (IBA molecular; www.iba.be/molecular)
• Gallium-68 (see EQUIPMENT)
  • !CAUTION: 89Zr and 68Ga are radionuclides emitting positrons and γ-radiations. 89Zr and 68Ga should be handled by following local radiation safety guidelines.

Equipment

1. Calibrated pH meter

• Eppendorf tubes, Protein LoBind Tubes, 1.5 ml (Eppendorf, order no. 0030 108.116)
• Disposable PD-10 desalting columns (GE Healthcare Life Sciences, cat. no. 17-0851-01)
• Thermomixer comfort (Eppendorf, order no. 5355 000.011)
• Sterile/clean glass reaction vials, 20 ml
• Polystyrene round-bottom test tubes, 5 ml, snap cap (BD Falcon, cat. no. 352058)
• Silica gel impregnated glass fiber sheets (ITLC; Pall Corp., cat. no. 61886), approximately 1×12 cm in size with a faint pencil mark 1.5 cm from one end.
• SPE cartridge Chromafix 30-PS-HCO3 (Macherey-Nagel, cat. no. 731 876)
• High performance liquid chromatograph with a UV and a γ-detector connected in series
• HPLC column: SuperdexTM 200 10/300 GL (GE Healthcare Life Sciences, cat. no. 17-5175-01)
• 68Ge/68Ga-generator (Eckert & Ziegler Isotope Products)

Reagent Setup

• 0.9% NaCl/gentisic acid 5 mg ml-1 (pH = 4.9-5.3) Dissolve 0.5 g gentisic acid in 100 ml normal (0.9%) saline, add 0.88 ml 2.0 M sodium carbonate. Homogenise until no more CO is formed (release pressure in bottle) and check pH. Acceptance range: pH 4.9-5.3.
• 0.5 M HEPES buffer (pH = 7.1-7.3) Add 18 ml of water to 20 ml 1 M HEPES solution. Check pH. pH < 7.1 adjust pH with 1 M NaOH. pH > 7.3 adjust pH with 1 M HCl. Adjust volume to 40 ml with water.
• 0.25 M ammonium acetate buffer (pH = 5.4 – 5.6) Dissolve 9.64 g of ammonium acetate in 0.5 liter of water, add 1.4 ml 30% HCl. Mix well and check the pH. Acceptance range: pH 5.4-5.6.
• 3.0 M ammonium acetate buffer (pH = 7.1-7.3) Dissolve 11.6 g of ammonium acetate in 50 ml of water. Mix well and check the pH. Acceptance range: pH 7.1-7.3.
• ITLC eluent (pH = 4.8-5.0) Dissolve 420 mg citric acid monohydrate in 100 ml Milli-Q water, add 0.98 ml 2.0 M sodium carbonate. Mix well and check the pH. Acceptance range: pH 4.8-5.0.
• HPLC eluent (pH = 6.2-7.0) Dissolve 13.8 g of sodium dihydrogen phosphate monohydrate, 14.2 g of disodium hydrogen phosphate, 17.4 g of sodium chloride, and 1.3 g of sodium azide in 2 l of water. Mix well and check the pH. Acceptance range: pH 6.2-7.0. Pass the eluent through a Millipore filter and rigorously degas before use.

Procedure

This procedure may be scaled up or down, maintaining the same molar ratios of reagents. A schematic representation of the procedure is shown in Figure 1.

Conjugation reaction

1. Pipette the required amount of protein solution (max. 1 ml; by preference between 2 and 10 mg ml protein) into an eppendorf tube. Adjust the reaction mixture to a total volume of 1 ml by adding a sufficient amount of normal saline into the tube.

• CRITICAL STEP Concentrations lower than 2 mg ml-1 will strongly decrease the efficiency of the conjugation reaction.
• Adjust pH of the protein solution to pH = 8.9 – 9.1 with 0.1 M NaCO (max. 0.1 ml).
  • CRITICAL STEP Alternatively, the desired pH for the reaction can be obtained by adding a stronger sodium carbonate buffer or by dialyzing the protein stock solution against 0.1 M sodium bicarbonate buffer (pH 9.0).
• Dissolve SCN-Bz-Df in DMSO at a concentration of between 2 and 5 mM (1.5-3.8 mg ml-1) depending on the amount of protein or antibody used. Add this to the protein solution to give a 3-fold molar excess of the chelator over the molar amount of protein and mix immediately. Keep the DMSO concentration below 5% in the reaction mixture.
  • CRITICAL STEP Typically, 20 µl 5 mM SCN-Bz-Df (100 nmol) in DMSO is added to 5 mg intact antibody (33 nmol). In that case, between 0.9-1.5 Df moieties will be coupled per antibody molecule.
• Incubate the reaction for 30 min at 37°C using a Thermomixer.
• This step can be performed using option A or option B depending on whether Df-conjugated proteins are radiolabeled with 89Zr or 68Ga, respectively.

A. Purification of Df-protein and subsequent labeling with 89Zr.

• i. Rinse a PD10 column with 20 ml 0.9% NaCl/gentisic acid 5 mg ml (pH = 4.9-5.3).
• ii. Pipette the conjugation reaction mixture onto the column and discard the flow-through.
• iii. Pipette 1.5 ml 0.9% NaCl/gentisic acid 5 mg ml-1 (pH = 4.9-5.3) onto the column and discard the flow-through.
• iv. Pipette 2 ml 0.9% NaCl/gentisic acid 5 mg ml-1 (pH = 4.9-5.3) onto the PD-10 column and collect the Df-protein.
  • PAUSE POINT The Df-protein can be stored at -20 °C until the day of planned use. The Df-protein should be stable in storage for at least several weeks.
• v. Pipette the required volume (= a) of 89Zr oxalic acid solution (max. 200 µl, between 37 and 185 MBq) into a glass “reaction vial”.
  • CAUTION Follow appropriate radiation safety measures for steps v. – xiii.
• vi. While gently shaking, add 200 µl – ________(= a, see v.) = _________ µl 1M oxalic acid into the reaction vial. Subsequently, pipette 90 µl 2 M Na2CO3 into the reaction vial and incubate for 3 minutes at room temperature.
• vii. While gently shaking, pipette successively 0.30 ml 0.5 M HEPES (pH = 7.2), 0.71 ml of modified protein (typically 1-3 mg), and 0.70 ml 0.5 M HEPES (pH = 7.2) into the reaction vial.
  • CRITICAL STEP The pH of the labeling reaction should be in the range of 6.8-7.2.
• viii. Incubate for 1 h at room temperature while gently shaking the reaction mixture. Radiolabeling efficiency (typically >85%) can be determined by instant thin-layer chromatography (ITLC) using silica-gel strips and 20 mM citric acid (pH 4.8-5.0)(ITLC eluent) as solvent. A 0.5-2.0 µl aliquot of the reaction solution can be directly applied to the ITLC sheet. Radiolabeled protein (Rf = 0.0 – 0.1) and unbound 89Zr (Rf = 0.4 – 1.0).
• ix. Meanwhile, rinse a PD10 column with 20 ml 0.9% NaCl/gentisic acid 5 mg ml-1 (pH = 4.9-5.3).
• x. After 1 h incubation, pipette the reaction mixture onto the column and discard the flow-through.
• xi. Pipette 1.5 ml 0.9% NaCl/gentisic acid 5 mg ml-1 (pH = 4.9-5.3) onto the column and discard the flow-through.
• xii. Pipette 2 ml 0.9% NaCl/gentisic acid 5 mg ml-1 (pH = 4.9-5.3) to the PD-10 column and collect the purified radiolabeled protein.
• xiii. Analyze the purified radiolabeled protein by ITLC and HPLC. When the radiochemical purity is greater than 95% it is ready for storage at 4 °C or dilution in 0.9% NaCl/gentisic acid 5 mg ml-1 (pH = 4.9-5.3) for in vitro or in vivo studies. The radiolabeled protein should be stable in storage for at least several days.
  • CRITICAL STEP Gentisic acid is introduced during labeling and storage to prevent deterioration of the protein integrity by radiation. Consideration should also be given to assessment of the biological function of the protein after the conjugation and labeling reaction.

B. Purification of Df-protein and subsequent labeling with 68Ga.

• i. Rinse a PD10 column with 20 ml 0.25 M ammonium acetate (pH = 5.5).
• ii. Pipette the conjugation reaction mixture onto the column and discard the flow-through.
• iii. Pipette 1.5 ml 0.25 M ammonium acetate (pH = 5.5) onto the column and discard the flow-through.
• iv. Pipette 2 ml 0.25 M ammonium acetate (pH = 5.5) onto the PD-10 column and collect the Df-protein.
  • PAUSE POINT The Df-protein can be stored at -20 °C until the day of planned use. The Df-protein should be stable in storage for at least several weeks.
• v. Pipette the required volume (= a) of preconcentrated and purified 68Ga (max. 200 µl) into a 5 ml test tube. For preconcentration and purification of 68Ga see Box 1.
  • CAUTION Follow appropriate radiation safety measures for steps v. – xiii.
• vi. While gently shaking, add 2 x ________(= a, see v.) = _________ µl 3 M ammonium acetate into the reaction vial and incubate for 3 minutes at room temperature.
• vii. While gently shaking, slowly add 0.2-1.0 ml of the modified protein (typically 0.5-2 mg) into the reaction vial. Adjust the reaction mixture to a total volume of 1.5 ml by adding a sufficient amount of 0.25 M ammonium acetate (pH = 5.5) into the tube.
  • CRITICAL STEP The pH of the labeling reaction should be in the range of 5-6.
• viii. Incubate for 5 min at room temperature while gently shaking the reaction mixture. Radiolabeling efficiency (typically >90%) can be determined by instant thin-layer chromatography (ITLC) using silica-gel strips and 20 mM citric acid (pH 4.8-5.0) containing 50 mM EDTA as solvent. A 0.5-2.0 µl aliquot of the reaction solution can be directly applied to the ITLC sheet. Radiolabeled protein (Rf = 0.0 – 0.1) and unreacted 68Ga (Rf = 0.4 – 1.0).
• ix. Meanwhile, rinse a PD10 column with 20 ml normal saline.
• x. After 5 min incubation, pipette the reaction mixture onto the column and discard the flow-through.
• xi. Pipette 2.0 ml normal saline onto the column and discard the flow-through.
• xii. Pipette 1.5 ml normal saline onto the PD-10 column and collect the purified radiolabeled protein.
• xiii. Analyze the purified 68Ga-labeled protein by ITLC and HPLC.

BOX 1 Purification and concentration of the 68Ga eluate using anion-exchange chromatography as described by Velikyan et al. (12)

1. Activate a Chromafix 30-PS-HCO3 cartridge by washing with 1 ml 100% ethanol, 1 ml Milli-Q water, and 1 ml 4 M HCl, successively.

• Elute the 68Ge/68Ga-generator with 0.1 M HCl according to the manufacturer protocol.
• Collect the generator eluate and add enough 30% HCl giving a final HCl concentration of 4.0 M HCl.
• Slowly load the generator eluate onto the activated Chromafix cartridge (flow rate of 0.5-1 ml/min). Discard the flow through.
• Wash the cartridge with 2 ml 4 M HCl and subsequently dry by sucking air through the cartridge.
• Elute with small fractions of Milli-Q water (50-100 µl). Collect the purified and concentrated 68Ga and measure the activity.

Timing

• Steps 1-4: 45 min
• Steps 5A i-iv: 15 min
• Steps 5A v-xiii: 1.5 h
• Steps 5B i-iv: 15 min
• Steps 5B v-xiii: 20 min

Troubleshooting

See Table 1

Anticipated Results

Typically, 0.9-1.5 Df moieties are coupled per antibody or protein molecule. Radiolabeling of the Df-conjugated mAb with 89Zr will result in overall labeling yields of >85%. Resulting 89Zr-mAb conjugates are optimal with respect to radiochemical purity (>95% according to ITLC and analytical HPLC), immunoreactivity, and in vivo stability. A representative HPLC chromatogram and SDS-PAGE gel of a 89Zr-labeled mAb (150 kDa) is shown in Figure 2a and 2c, respectively.

Radiolabeling of the Df-conjugated protein with 68Ga will result in overall labeling yields of >90%. The radiochemical purity of 68Ga-labeled proteins is >97% according to ITLC and analytic HPLC. A representative HPLC chromatogram and SDS-PAGE gel of a 68Ga-labeled nanobody13-15 (31 kDa) is shown in Figure 2b and 2d, respectively.

The positron emitters 89Zr and 68Ga can be applied to assess normal biodistribution, and confirm and quantitate selective tumor uptake of mAbs, mAb-fragments, non-traditional antibody-like scaffolds or other proteins of interest in animal and clinical studies using PET-imaging. A representative 89Zr-immuno-PET image is shown in Figure 3.

References

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• Reichert, J.M. & Valge-Archer, V.E. Development trends for monoclonal antibody cancer therapeutics. Nat. Rev. Drug. Discov. 6, 349-356 (2007).
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• Velikyan, I., Beyer, G.J. & Langstrom, B. Microwave-supported preparation of Ga-68 bioconjugates with high specific radioactivity. Bioconjug. Chem. 15, 554-560 (2004).
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Acknowledgements

This project was supported in part by grants from the European Union FP6 (LSHC-CT-2003-5032, STROMA) and the Dutch Technology Foundation (STW; VBC.6120). The authors want to thank the technical staff of BV Cyclotron and the Radionuclide Center for supply and processing of 89Zr.

Figures

Table 1: Troubleshooting Table

Figure 1: Schematic representation of mAb modification with SCN-Bz-Df (1) and subsequent labeling with 89Zr (2).

Figure 2: Representative HPLC chromatograms and SDS-PAGE gels of (a, c) 89Zr-labeled mAb U36 and (b, d) 68Ga-labeled anti-EGFR nanobody – www.ablynx.com

SDS-PAGE was performed on a Phastgel System (GE Healthcare Life Sciences) using preformed 7.5% (c) or high density (d) SDS-PAGE gels under non-reducing conditions.

Figure 3: Selective targeting of head and neck cancer xenografts in nude mice by 89Zr-labeled mAb U36.

PET images (coronal slices) were obtained at 24, 48, and 72 h after i.v. injection of 89Zr-mAb U36 (3.7 MBq, 100 µg mAb) with a double-crystal-layer high resolution research tomograph PET scanner. Images planes have been chosen where the right tumor is optimal visible. Tumors are indicated by arrows.

Author information

Lars Perk, Marianne Budde & Maria Vosjan, Departments of Otolaryngology/Head and Neck Surgery, VU University Medical Center, Amsterdam, The Netherlands

Gerard Visser, Department of Nuclear Medicine & PET Research, VU University Medical Center, Amsterdam, The Netherlands

Paul Jurek & Garry Kiefer, Macrocyclics, Dallas, Texas, USA

Guus van Dongen, Departments of Otolaryngology/Head and Neck Surgery, and Nuclear Medicine & PET Research, VU University Medical Center, Amsterdam, The Netherlands

Correspondence to: Guus van Dongen ([email protected])

Source: Protocol Exchange (2008) doi:10.1038/nprot.2008.22. Originally published online 24 January 2008.