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Purpose: Cystine knot (knottin) peptides, engineered to bind with high affinity to integrin receptors, have shown promise as molecular imaging agents in living subjects. The aim of the current study was to evaluate tumor uptake and in vivo biodistribution of 18F-labeled knottins in a U87MG glioblastoma model.
Procedures: Engineered knottin mutants 2.5D and 2.5F were synthesized using solid phase peptide synthesis and were folded in vitro, followed by radiolabeling with 4-nitrophenyl 2-18F-fluoropropionate (18F-NFP). The resulting probes, 18F-FP-2.5D and 18F-FP-2.5F, were evaluated in nude mice bearing U87MG tumor xenografts using microPET and biodistribution studies.
Results: MicroPET imaging studies with 18F-FP-2.5D and 18F-FP-2.5F demonstrated high tumor uptake in U87MG xenograft mouse models. The probes exhibited rapid clearance from the blood and kidneys, thus leading to excellent tumor-to-normal tissue contrast. Specificity studies confirmed that 18F-FP-2.5D and 18F-FP-2.5F had reduced tumor uptake when co-injected with a large excess of the peptidomimetic c(RGDyK) as a blocking agent.
Conclusions: 18F-FP-2.5D and 18F-FP-2.5F showed reduced gallbladder uptake compared with previously published 18F-FB-2.5D. 18F-FP-2.5D and 18F-FP-2.5F enabled integrin-specific PET imaging of U87MG tumors with good imaging contrasts. 18F-FP-2.5D demonstrated more desirable pharmacokinetics compared to 18F-FP-2.5F, and thus has greater potential for clinical translation.
Angiogenesis, the formation of new blood vessels from preexisting vasculature, plays a critical role in tumor growth and metastasis 1-2. To grow larger than 1-2 mm, a tumor needs sufficient blood flow, which provides oxygen and nutrients 3-4. Integrins are a family of heterodimeric transmembrane receptors that are involved in multiple steps of tumor angiogenesis and metastasis. In particular, overexpression of integrins αvβ3, αvβ5, and α5β1 is associated with malignancy and has been shown to play various roles in tumor growth and metastasis 5-8. Thus, integrin receptors have been attractive targets for developing molecular probes for non-invasive tumor imaging using different modalities including magnetic resonance imaging (MRI) 9, ultrasound 10-12, optical imaging 13-15, positron emission tomography (PET) 5, 16-18, and single-photon emission computed tomography (SPECT) 19-20.
Among the ligands that bind integrin receptors, arginine-glycine-aspartic acid (RGD)-containing peptides have been well validated for tumor imaging applications 21-22. Radiofluorinated RGD probes such as 18F-AH111585 and 18F-Galacto-RGD are currently undergoing clinical studies in humans 16, 23-25. In order to achieve higher tumor uptake, and better tumor-to-normal tissue contrasts, continued efforts to modify RGD-containing ligands remain an active area of research.
Cystine knots (also known as knottins) are small polypeptides with a common disulfide-bonded framework in which one disulfide bond threads through a macrocycle created by two other disulfide bonds and their connecting backbone segments 26-27, as illustrated in Figure Figure1A.1A. As a result, knottins have a high degree of thermal and proteolytic stability and thus provide a valuable framework for development of targeting agents for in vivo applications 28-31. Furthermore, the relatively small size of knottins (~30-50 amino acids) makes them accessible by standard solid-phase peptide synthesis, and would result in fast blood clearance, which is desirable for molecular imaging applications.
Previously, high affinity integrin binding was conferred upon Ecballium elaterium trypsin inhibitor (EETI-II) using yeast surface display 32. The 6-amino acid trypsin binding loop (PRILMR) of EETI-II was rationally substituted with an 11-amino-acid loop containing the RGD motif, and combinatorial methods were used to identify knottin mutants 2.5D and 2.5F, which bind to αvβ3/αvβ5 or αvβ3/αvβ5/α5β1 integrins, respectively, with high (low nM) affinity 32-33. The peptide sequences of knottins 2.5D and 2.5F are shown in Figure Figure1B.1B. Subsequently, 64Cu-labeled knottins were evaluated in mice bearing integrin-expressing U87MG glioblastoma xenografts, and microPET imaging and biodistribution studies showed rapid and high tumor accumulation, fast clearance from blood and normal organs, and low uptake in kidney and liver 33. Overall, these studies demonstrated that engineered knottins are promising probes for molecular imaging applications.
The physical properties of 18F (t½: 110 min, emits β+ particles at an energy of 635 keV, 99% abundant) complement the high target binding affinity and rapid blood clearance of knottin peptides. Previously, we radiolabeled the knottin 2.5D with 18F via the N-terminus of the peptide using N-succinimidyl-4-18F-fluorobenzoate (18F-SFB), and showed that this conjugate, 18F-FB-2.5D, could be used to image mice bearing U87MG tumor xenografts with good tumor-to-normal tissue contrast 34. To improve knottin-based probes for PET imaging and facilitate their clinical translation, we evaluated the use of an alternative 18F precursor, 4-nitrophenyl 2-18F-fluoropropionate (18F-NFP), which has shown enhanced metabolic stability and reduced hydrophobicity 16, 35-36. The resulting radio probes, 18F-FP-2.5D and 18F-FP-2.5F were evaluated for tumor uptake and tissue biodistribution in nude mice bearing U87MG tumor xenografts for comparison to our previous study.
All commercially available materials were used as provided unless noted. All 9-fluorenylmethyloxycarbonyl (Fmoc) protected amino acids were purchased from Novabiochem/EMD Chemicals Inc (La Jolla, CA) or CS Bio (Menlo Park, CA). 125I-labeled echistatin was purchased from GE Healthcare Life Sciences (Piscataway, NJ). All other chemicals were purchased from Fisher Scientific (Fair Lawn, NJ) unless otherwise specified. The U87MG human glioblastoma cell line was obtained from American Type Culture Collection (Manassas, VA). Nude mice (nu/nu) were purchased from Charles River Laboratory (Wilmington, MA). Semi-preparative reversed-phase high performance liquid chromatography (RP-HPLC), using a Vydac protein and peptide column (218TP510; 5µm, 250 × 10 mm), was performed on a Dionex 680 chromatography system with a UVD 170U absorbance detector and model 105S single-channel radiation detector (Carroll & Ramsey Associates). The recorded data were processed using Chromeleon version 7.1 software. With a flow rate of 5.0 mL/min, the mobile phase was changed from 95% solvent A [0.1% trifluoroacetic acid (TFA) in water] and 5% B [0.1% TFA in acetonitrile (MeCN)] (0-2 min) to 35% solvent A and 65% solvent B at 32 min. Analytical scale HPLC used the same gradient system except that the flow rate was 1.0 mL/min with a Vydac protein and peptide column (218TP510; 5 µm, 250 × 4.6 mm). UV absorbance was monitored at 218 nm and the identification of the peptides was confirmed based on UV spectrum acquired using a photodiode array detector. Instrumentation used for matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF-MS) is the same as described in our previous publication 37.
Chemistry and Radiochemistry Peptides corresponding to the sequence of 2.5D and 2.5F were synthesized on a CS Bio CS036 Peptide Synthesizer (Menlo Park, CA) using Fmoc-based solid phase peptide synthesis. Briefly, Rink amide resin was swollen in N,N-dimethylformamide (DMF) for 30 min. Fmoc groups were removed with 20% piperidine in DMF. Aliquots of amino acids (1 mmol) were activated in a solution containing 1 mmol hydroxybenzotriazole (HOBt) and 0.5 M diisopropylcarbodiimide (DIC) in DMF. Following synthesis, side-chain deprotection and resin cleavage were achieved by addition of a 94:2.5:2.5:1 (v/v) mixture of TFA/triisopropylsilane/ethanedithiol/water for 2 h at room temperature. The crude product was precipitated with cold anhydrous ether, and purified using semi-preparative RP-HPLC. Peptide purity was analyzed by analytical scale RP-HPLC.
Large scale folding reactions were performed by incubating the linear peptide with 4 M guanidine, 10 mM reduced glutathione, 2 mM oxidized glutathione, and 0.5 M dimethyl sulfoxide (DMSO) at pH 7.5. The correctly folded peptide was separated from unfolded and partly folded peptides by RP-HPLC, where it appeared as a single peak with a shorter retention time than that of unfolded or misfolded precursors. Following purification, folded peptides 2.5D and 2.5F were lyophilized and stored at room temperature prior to use. Peptide purity and molecular masses were determined by analytical scale HPLC and MALDI-TOF-MS, respectively.
The synthesis of 4-nitrophenyl 2-fluoropropionate (19F-NFP) is briefly described below. Bis(4-nitrophenyl) carbonate (15.2 mg, 50.0 µmol in 20 µL of diisopropylethylamine (DIPEA)) was added to a solution of 2-fluoropropionic acid (5.0 mg, 54.3 µmol in 200 µL of DMF). After incubating at 60 °C for 3 h, the reaction mixture was cooled to room temperature and diluted with 1 mL 5% acetic acid solution. The product 19F-NFP was isolated by semi-preparative HPLC. The collected fractions were combined and the solvent was removed under reduced pressure. The product was obtained as white powder (5.9 mg, 56%). ESI-MS: m/z 213.1 [M]+; 1H NMR (CDCl3, 300 MHz): δ = 8.24 (d, J = 9.0 Hz, 2H), 7.27 (d, J = 9.0 Hz, 2H), 5.21 (m, 1H), 1.70 (dd, J = 6.8 Hz, 23.4 Hz, 3H). 13C NMR (CDCl3, 75 MHz): δ = 18.9 (d, J = 22.5 Hz), 86.0 (d, J = 184.0 Hz), 122.9, 126.0, 146.4, 155.2, 168.5.
19F-NFP labeled 2.5D and 2.5F (19F-FP-2.5D, 19F-FP-2.5F) were prepared as reference standards. Briefly, 2.5D or 2.5F (0.5 mg, 0.15 μmol in 400 μL of DMSO) was mixed with 19F-NFP (0.3 mg, 1.5 μmol in 100 μL of DMSO and 10 μL of DIPEA) and reacted for 1 h at room temperature. The resulting conjugates, 19F-FP-2.5D and 19F-FP-2.5F were then purified by semi-preparative HPLC. Fractions containing the product were collected and lyophilized. The molecular masses of 19F-FP-2.5D and 19F-FP-2.5F were confirmed by MALDI-TOF-MS. Folded peptide 2.5D: m/z = 3244.0 for [MH]+ (C129H189N40O47S6, calculated [MH]+ = 3244.5). Retention time on analytical scale HPLC is 16.2 min; Folded peptide 2.5F: m/z = 3292.1 for [MH]+ (C131H201N42O46S6, calculated [MH]+ = 3292.6). Retention time: 15.2 min; 19F-FP-2.5D: m/z = 3317.5 for [MH]+ (C132H193FN40O48S6, calculated [MH]+ = 3317.4). Retention time: 17.5 min; 19F-FP-2.5F: m/z 3364.9 for [MH]+ (C134H203FN42O47S6, calculated [MH]+ = 3365.3). Retention time: 18.3 min.
18F-NFP was prepared and used for knottin radiolabeling based on a previously reported procedure (Figure (Figure1C)1C) 38. 18F-NFP (specific activity of 40-100 GBq/μmol at the end of synthesis, in 100 μL of DMSO) was added to the 2.5D or 2.5F peptide (100 μg) and 10 μL of DIPEA and reacted for 20 min at 60 °C. After adding 1 mL of water containing 50 μL of TFA to quench the reaction, the resulting conjugates were purified by semi-preparative HPLC using the same elution gradient as described for 19F-FP-knottin purification. The HPLC fractions containing 18F-FP-2.5D or 18F-FP-2.5F were collected, combined, and dried with a rotary evaporator. Radiolabeled peptides were reconstituted in PBS and sterilized using a 0.22 μm filter (Millipore) for in vitro and in vivo experiments.
Cell Culture: U87MG cells were cultured in DMEM containing high glucose (GIBCO, Carlsbad, CA), and supplemented with 10% fetal bovine serum (FBS) and 1% penicillin-streptomycin. Cells were expanded in tissue culture dishes and kept in a humidified atmosphere of 5% CO2 at 37 °C, with media changes every other day. Confluent monolayers were detached with 0.05% Trypsin-EDTA, 0.01M PBS (pH 7.4) and dissociated into single-cell suspensions for further cell culture and experimentation.
U87MG Cell Binding Assay: Cell binding assays were performed as previously described 37, 39. Briefly, 2 × 105 U87MG cells were incubated with 0.06 nM 125I-labeled echistatin and varying concentrations of peptides (2.5D, 2.5F, 19F-FP-2.5D or 19F-FP-2.5F) in integrin binding buffer [25 mM Tris pH 7.4, 150 mM NaCl, 2mM CaCl2, 1 mM MgCl2, 1 mM MnCl2, and 0.1% bovine serum albumin (BSA)] at room temperature for 3 h. The cell-bound radioactivity remaining after washing was measured by gamma-counting. Half-maximal inhibitory concentration (IC50) values were determined by nonlinear regression using GraphPad Prism (GraphPad Software, Inc.). Experiments were performed with quadruplicate samples.
MicroPET Imaging: All animal studies were carried out in compliance with Federal and local institutional regulations for the conduct of animal experimentation. Approximately 10 × 106 U87MG cells were suspended in 100 µL of PBS and subcutaneously implanted in the right shoulders of nude mice. Tumors were grown to a size of 0.5 cm in diameter (approximately 2-3 weeks). MicroPET scans were performed on a microPET R4 rodent model scanner (Concorde Microsystems Inc.). The scanner has a computer-controlled bed and 10.8-cm transaxial and 8-cm axial fields of view (FOVs). It has no septa and operates exclusively in the 3-dimensional (3D) list mode. Mice bearing U87MG xenografts were injected via tail vein with approximately 3.7 MBq (100 μCi) of 18F-FP-2.5D or 18F-FP-2.5F, with or without 10 mg/kg mouse body weight c(RGDyK). At 0.5, 1, and 2 h post injection (p.i.) mice were anesthetized with isoflurane (5% for induction and 2% for maintenance in 100% O2). With the help of a laser beam attached to the scanner, mice were placed in the prone position and near the center of the field of view of the scanner where the image resolution and sensitivity is highest. Three minute static scans were obtained, and images were reconstructed by use of a 2-dimensional ordered-subsets expectation maximization (OSEM) algorithm. No background correction was performed. Region of interests (ROIs) were drawn over the tumor on decay-corrected whole-body coronal images. The maximum counts per pixel per minute were obtained from the ROI and converted to counts per milliliter per minute by using a calibration constant. Based on the assumption of a tissue density of 1 g/ml, ROIs were converted to counts per gram per min. The percent injected dose per gram of tissue (%ID/g) was determined by dividing counts per gram per minute by injected dose. No attenuation correction was performed.
Animal Biodistribution Studies: For biodistribution studies, nude mice bearing U87MG xenografts (n = 3 for each group) were injected via tail vein with approximately 3.7 MBq (100 μCi) of 18F-FP-2.5D or 18F-FP-2.5F, with or without 10 mg/kg mouse body weight c(RGDyK). Mice were sacrificed at 2 h p.i., and tumor and normal tissues of interest were removed and weighed, and their radioactivity was measured in a gamma-counter. The radioactivity uptake in the tumor and normal tissues was expressed as % ID/g.
Statistical Method: Statistical analysis was performed using the Student's t-test for unpaired data. A 95% confidence level was chosen to determine the significance between groups, with P < 0.05 being designated as significantly different.
Chemistry and Radiochemistry: Peptides 2.5D and 2.5F were synthesized via solid phase peptide synthesis, followed by oxidative folding with a mixture of glutathione and DMSO. The final products were purified by semi-preparative RP-HPLC to achieve greater than 95% purity. Non-radioactive 19F analogs were used as standards for radiosynthesis and for cell binding assays. 19F-FP-2.5D and 19F-FP-2.5F were prepared by direct conjugation of 19F-NFP to knottin peptides 2.5D or 2.5F with yields of 92% and 95%, respectively. Product purities of greater than 95% were achieved as determined by analytical scale HPLC. MALDI-TOF-MS confirmed correct molecular masses for all peptides used in this study.
The total synthesis time for 18F-NFP was approximately 100 min using a modified GE synthetic module (TRACERlab FXFN) with decay corrected yields of 67 ± 11% (n = 10, Figure Figure1C)1C) 36, 38. The decay-corrected radiochemical yields of 18F-FP-2.5D and 18F-FP-2.5F based on 18F-NFP were 12.0 ± 2.7% and 10.5 ± 1.8% (n = 4), respectively. The radiochemical purities of 18F-FP-2.5D and 18F-FP-2.5F were greater than 99% according to analytical scale HPLC. The specific radioactivity of 18F-FP-2.5D and 18F-FP-2.5F was estimated to be 20-40 GBq/µmol at the end of synthesis.
In Vitro Cell Receptor-Binding Assay: Integrin positive U87MG human glioblastoma cells were used for binding studies. Binding affinities of 2.5D, 2.5F, 19F-FP-2.5D and 19F-FP-2.5F were determined by competitive displacement of 125I-echistatin, a potent integrin binder, from U87MG cells. All peptides inhibited the binding of 125I-echistatin to U87MG cells in a concentration-dependent manner. The IC50 values for 19F-FP-2.5D and 19F-FP-2.5F were 7.4 ± 1.9 and 7.5 ± 1.3 nM, respectively (n = 4) (Figure (Figure2).2). Comparison of binding values to unlabeled 2.5D and 2.5F (IC50 values = 6.9 ± 1.4 and 6.1 ± 1.6 nM, respectively) showed that fluoropropionate conjugation did not interfere with integrin receptor binding.
MicroPET Imaging Study: Static microPET scans were performed on U87MG tumor-bearing mice and representative decay-corrected coronal images at 0.5, 1, and 2 h after tail vein injection of 18F-FP-2.5D or 18F-FP-2.5F are shown in Figure Figure33 (n = 3 for each group). U87MG tumors were clearly visualized, as both tracers produced excellent tumor-to-background contrast. MicroPET quantification of tumors and other organs was obtained from ROI analysis and the results at 0.5, 1, and 2 h p.i. are shown in Figure Figure4A4A and B. No significant difference in tumor uptake between these two probes was observed at each time point (P > 0.05). For 18F-FP-2.5D, tumor uptake was 3.30 ± 1.08, 2.86 ± 1.11, and 2.37 ± 1.13 %ID/g at 0.5, 1, and 2 h p.i., respectively. For 18F-FP-2.5F, tumor uptake was 3.74 ± 0.88, 3.60 ± 0.25, and 1.71 ± 0.37 % ID/g at 0.5, 1, and 2 h p.i., respectively. Both probes were cleared rapidly from the blood, and moderate to low renal retention was observed (4.24 ± 1.94, 2.81 ± 1.42, and 2.68 ± 2.90 %ID/g for 18F-FP-2.5D at 0.5, 1, and 2 h p.i.; 13.39 ± 1.15, 5.25 ± 0.65, and 2.51 ± 0.16 %ID/g for 18F-FP-2.5F at 0.5, 1, and 2 h p.i.). Interestingly, liver uptake of 18F-FP-2.5F was significantly higher than 18F-FP-2.5D at 0.5 h p.i., (P < 0.05), while no significant difference was observed at 1 h and 2 h p.i. Nonspecific uptake in the muscle was very low for both probes (0.51 ± 0.30 %ID/g and 0.44 ± 0.08 %ID/g for 18F-FP-2.5D and 18F-FP-2.5F at 2 h p.i., respectively). Gallbladder uptake of 18F-FP-2.5D and 18F-FP-2.5F was 0.86 ± 0.33 and 1.08 ± 0.41 %ID/g at 2 h p.i., respectively; these values were similar to background muscle uptake level. Tumor-to-normal tissues ratios of both probes at 0.5, 1, and 2 h were calculated and are shown in Figure Figure4C.4C. At 0.5 h p.i., 18F-FP-2.5D had higher tumor to liver, kidneys, and muscle ratios than those of 18F-FP-2.5F (P < 0.05). This is consistent with the better tumor image quality of 18F-FP-2.5D compared to 18F-FP-2.5F at early time points (0.5 and 1 h p.i.), shown in Figure Figure3A3A and C.
The integrin targeting specificity of both probes was demonstrated by co-injection of an excess of c(RGDyK) as a blocking agent. Figure Figure3B3B and D show the microPET images of 18F-FP-2.5D and 18F-FP-2.5F at 0.5, 1, and 2 h p.i. with co-injection of c(RGDyK). The corresponding microPET quantification results are shown in Figure Figure4.4. Coinjection of c(RGDyK) resulted in significant decreases in tumor uptake for both 18F-FP-2.5D (3.91 ± 0.15 %ID/g without blocking vs. 1.96 ± 0.07 %ID/g with blocking, P < 0.05) and 18F-FP-2.5F (3.83 ± 0.51 %ID/g without blocking vs. 1.90 ± 0.21 %ID/g with blocking, P < 0.05).
Biodistribution Studies: To validate microPET imaging experiments, biodistribution studies of 18F-FP-2.5D and 18F-FP-2.5F were performed at 2 h p.i. in U87MG xenograft models. Probe uptake in tumors and other major organs was calculated and is shown in Figure Figure5.5. No significant differences were observed compared to microPET image quantification. In these studies, the in vivo tumor targeting specificity of the probes was further confirmed by co-injection of an excess of c(RGDyK) blocking agent. A significant decrease in tumor uptake was observed for both 18F-FP-2.5D (1.92 ± 0.65 %ID/g vs. 1.06 ± 0.10 %ID/g, P < 0.05) and 18F-FP-2.5F (2.24 ± 0.60 %ID/g vs. 1.25 ± 0.10 %ID/g, P < 0.05) upon co-injection with c(RGDyK).
Probe development is a central theme in cancer-specific molecular imaging applications. Historically, it has been challenging and time consuming to develop probes that bind tumor-related receptors with high affinity and specificity 40-42. Numerous efforts have sought to generalize binder development using a variety of molecular platforms. Recently, small protein scaffolds have become robust starting points for molecular probe development 39, 43-44. Knottins, which are generally 3-5 kDa in size, are highly stable scaffolds that have been shown to be amenable to rational and combinatorial engineering. Moreover, knottin engineering methods are maturing as new binders are being developed based on this versatile framework 30, 45. Recently, high-affinity integrin-binding knottins were successfully identified by yeast display technology 32-33. Radiolabeled knottins, using 64Cu or 18F for PET imaging, have shown great promise for imaging integrin expression in mouse tumor models 31, 44, 46.
In this study, we evaluated 18F-FP-labeled knottin 2.5D and 2.5F and explored potential advantages over 18F-FB analogs, including effects on tumor uptake and retention and uptake in non-target organs. 18F-fluoropropionate was chosen because it has relatively higher in vivo metabolic stability compared to 18F-fluorobenzoate, as indicated by a high percentage of intact 18F-FP-labeled probe in a metabolite analysis 38. Moreover, 18F-fluoropropionate is a less hydrophobic tag than that of 18F-fluorobenzoate. Methods for radiosynthesis of 18F-NFP have also been well established 38, 47-48. Importantly, 18F-NFP is practically the smallest 18F-radiolabeling group for peptides, and is currently being used in clinical trials in human subjects 16, 23, 35.
Figure Figure4A4A and B show the results of microPET image quantification of 18F-FP-2.5D and 18F-FP-2.5F, which exhibit rapid tumor targeting and good tumor retention. Both probes exhibited maximum tumor uptake at 0.5 h p.i., and sustained tumor accumulation was observed. For example, at 1 and 2 h p.i., tumor uptake values were 2.86 ± 1.11 and 2.37 ± 1.13 %ID/g for 18F-FP-2.5D, and 3.60 ± 0.25 and 1.71 ± 0.37 %ID/g for 18F-FP-2.5F, respectively. Comparatively, the previously published knottin, 18F-FB-2.5D demonstrated lower tumor uptake of 1.46 ± 0.35 %ID/g at 1 h p.i. 34. Furthermore, gallbladder uptake was lower for 18F-FP-2.5D (1.17 ± 0.47 %ID/g at 1 h p.i.), compared to 18F-FB-2.5D (2.82 ± 1.31 %ID/g), which could be due to lower in vivo stability of 18F-FB compared to 18F-FP. For example, in a previous study, high in vivo stability was reported for a 18F-FP labeled RGD dimer; more than 95% of the 18F-labeled RGD dimer was shown to be intact at 2 h p.i. 38. Importantly, 18F-FP-2.5D had higher tumor-to-normal tissue ratios than 18F-FB-2.5D, thus the 18F-FP label resulted in improved imaging quality. Tumor-to-organ ratios for liver, kidneys, lungs, and gallbladder were 2.56 ± 0.55, 0.83 ± 0.28, 3.74 ± 0.70, and 2.53± 0.39, respectively, at 0.5 h p.i. for 18F-FP-2.5D. In comparison, ratios for the same organs for 18F-FB-2.5D were 1.97 ± 0.75, 0.50 ± 0.16, 2.03 ± 0.40, and 0.71 ± 0.32, respectively (Figure (Figure4C).4C). Collectively, these results highlight advantages of using a FP prosthetic group versus FB for knottin radiolabeling and in vivo imaging.
The IC50 values of knottin 2.5D and 2.5F indicated higher affinity integrin binding compared to that of a cyclic RGD pentapeptide (c(RGDyK)) published in the literature 49; however, the tumor uptake for these probes were similar. For example, the U87MG tumor uptake of 18F-FB labeled c(RGDyK) was 2.56 ± 0.12 %ID/g 50, compared to tumor uptake values of 2.24 ± 0.60 %ID/g for 18F-FP-2.5F at 2 h p.i. in the biodistribution study. These results indicate that the in vivo performance of a peptide-based molecular imaging probe depends on not only binding affinity, but other parameters such as charge, size, or hydrophobicity.
64Cu-labeled knottin 2.5D and 2.5F analogs had similar tumor and normal tissue uptake, which resulted in comparable microPET contrast. However, different contrasts were observed for 18F-FP-2.5D and 18F-FP-2.5F (Figure (Figure3A3A and C). 18F-FP-2.5D showed better image quality compared to 18F-FP-2.5F at 0.5 and 1 h p.i., but at a later time point (2 h p.i.), the tumor-to-muscle ratios for 18F-FP-2.5D and 18F-FP-2.5F reached the same level. Despite having similar binding affinities, the amino acid residues flanking the RGD motif in the engineered integrin binding loops of 2.5D and 2.5F are very different (Figure (Figure1B),1B), which may have influenced their in vivo behavior in this study. These results further indicate the importance of evaluating different radiolabeling methods in order to optimize the in vivo performance of protein- or peptide-based imaging probes.
PET provides a sensitive technique to identify and characterize disease in living systems. For a newly-developed PET probe to be successfully translated into the clinic, it should have high tumor uptake with reasonable tumor-to-background ratios in support of clinical radioisotopes with relatively short half-lives, such as 18F. The PET probe should also be able to be prepared in high radiochemical yield, purity, and specific activity. The total radiosynthesis time for 18F-FP-2.5D and 18F-FP-2.5F was approximately 100 minutes. Furthermore, the 18F-FP labeled knottins developed here meet some of these basic criteria such as high labeling yield, high in vivo stability, high radiochemical purity and good tumor uptake with high tumor-to-background ratios. Together, these results suggest that 18F-FP-2.5D, and potentially 18F-FP-2.5F, may have clinical potential for integrin imaging.
In conclusion, radiolabeled knottin peptides, 18F-FP-2.5D and 18F-FP-2.5F showed integrin-specific PET imaging of U87MG tumors marked by good contrast, fast tumor targeting, rapid clearance from body and relatively low uptake in normal tissues. The 18F-FP-labeled knottin mutant 2.5D exhibited higher tumor-to-normal tissue contrast compared to 18F-FB-2.5D, perhaps due to increased in vivo stability of 18F-FP residue. Taken together, these results suggest that 18F-FP-2.5D may perform well in clinical applications.
This work was supported, in part, by the National Cancer Institute (NCI) 5R01 CA119053 (ZC), and the V Foundation for Cancer Research (JRC). The Stanford University cyclotron team is acknowledged for 18F production.