In Vivo Immuno Imaging

Antibodies are powerful tools for in vivo immuno imaging applications. The quality and efficacy of the conjugated antibodies are crucial in order to obtain reliable and reproducible imaging results. GlyCLICK is a site-specific antibody conjugation technology that preserves the antigen binding affinity and increases tumor uptake in vivo while minimizing batch variations, delivering reliable imaging results.

 

 GlyCLICK technology In Vivo

Site-specific labeling using GlyCLICK

Reliable and quantitative conjugation is achieved with GlyCLICK for the generation of antibody conjugates with a consistent degree of label (DOL=2.0). Mass spec analysis was performed on trastuzumab conjugated with sDIBO-DFO using GlyCLICK (T-GlyCLICK-DFO) or randomly generated conjugates labeled at lysine residues using p-SCN-Bn-DFO (T-DFO) (Fig. 1). Results show a distinct mass shift for the intact antibody which verifies site-specific labeling by GlyCLICK with DOL of 2.0. Random labeling provided heterogenous conjugates with a varied DOL of zero to six.

In Vivo GlyCLICK

 

Figure 1. Intact mass analysis of non-conjugated, GlyCLICK and randomly DFO-conjugated trastuzumab. Trastuzumab and randomly conjugated material was deglycosylated with GlyCINATOR. All samples were separated by RP-LC on BEH C4 column (Waters) and analyzed on Bruker Impact II ESI-Q-TOF. Mass spectra were deconvoluted using the MaxEnt algorithm.

Decreased hydrophobicity of GlyCLICK conjugates

The site-specific labeling achieved with GlyCLICK results in less hydrophobic conjugates as compared to that of random (lysine) conjugates. The conjugates were analyzed to estimate the difference in hydrophobicity using hydrophobic interaction chromatography (HIC). GlyCLICK conjugates eluted as a single peak with only a minor shift in hydrophobicity compared to unlabeled and randomly labeled trastuzumab which displayed a broad peak with more hydrophobic and heterogenous material (Fig. 2).

GlyCLICK Technology In Vivo fig 3

Figure 2. Hydrophobic interaction analysis of trastuzumab, GlyCLICK and random DFO conjugates injected on TSKgel® Butyl-NPR column (Tosoh Bioscience) in 25 mM NaP pH 7, 1.5 M ammonium sulfate and eluted with a salt gradient with 20% isopropanol. The random lysine DFO-conjugates were more hydrophobic and not resolved in the analysis due to heterogeneity.

GlyCLICK enhances tumor uptake in vivo

ImmunoPET combines positron emission tomography (PET) with the target specificity of antibodies to visualize radioactive tracers in vivo. Tumor uptake and biodistribution are critical properties of labeled antibodies being used as targeting agents in immuno imaging applications. PET imaging was used to evaluate the effect of GlyCLICK conjugates in vivoby analyzing 89Zr-DFO-trastuzumab labeled using GlyCLICK conjugation (DAR=2) or random labeling at lysines (DAR=0-6, average 3). Tumor bearing mice were injected with 89Zr-DFO-trastuzumab and PET/CT images were obtained (Fig. 3). A fivefold increase in tumor uptake and a significantly longer circulation time was observed in mice injected with GlyCLICK conjugates (Fig. 4).

Figure 3. Longitudinal PET/CT imaging in coronal (top) and axial (bottom) images of SK-OV-3 tumor bearing mice (N=4/tracer).

GlyCLICK In Vivo fig 4

Figure 4. PET/CT imaging analysis of SK-OV-3 tumor bearing mice showing a) mean tumor uptake, b) image-derived biodistribution of 89Zr-DFO-trastuzumab in major organs and c) biodistribution ex vivo.

 

 

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2017_ATDC_Site-specific and Quantitative Conjugation of Functional Groups to Antibody N-glycans using the Novel GlyCLICKTM TechnologyDownload GlyCLICK Poster

Site-specific and Quantitative Conjugation of Functional Groups to Antibody N-glycans using the Novel GlyCLICK® Technology. Download the poster

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