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Oct 15, 2011 (Vol. 31, No. 18)

Identifying Promising Drug Candidates

Screening and Characterizing Therapeutic Antibodies Targeting Receptor Tyrosine Kinase

  • The development of potent and selective monoclonal antibodies (mAbs) is a significant challenge. More than 25 antibodies have been approved for human therapy and over 240 antibodies are being clinically developed worldwide for a wide range of diseases.

    The quest for better therapeutic antibodies has gained great momentum in recent years, driven by the development of new technologies to better understand the mechanisms of action of antibody-based drugs.

    Cisbio Bioassays has developed new tools for the screening and characterization of biotherapeutics using Tag-lite®, its recently launched cell-based technology based on HTRF® (Cisbio’s homogeneous fluorescence technology).

    Due to its critical involvement in tumor progression, the receptor tyrosine kinase (RTK) family represents a validated target class for anticancer therapy.

    How Tag-lite enables the screening of therapeutic antibodies for their binding to receptor tyrosine kinase and determination of their affinities is explained in this article. In addition, how the functional activity of the antibodies can be assessed through the measurement of ERK phosphorylation is shown.

  • Assay Principle

    Click Image To Enlarge +
    Figure 1. HTRF® assay principle: (A) cellular binding assay on RTK using a d2 labeled secondary antibody for detection; (B) cell-based immunosandwich assay to measure the ERK phosphorylation.

    Tag-lite starts with the cloning of the RTK sequence in frame with the SNAP-Tag® fragment in a mammalian expression vector. HEK293 cells are transfected with the SNAP tagged-RTK vector following the lipofectamine 2000 procedure, either in microplates or in T175 flasks. These cells are specifically labeled with the SNAP-Lumi4®-Terbium substrate and used for the antibody binding study in the presence of a d2-labeled antispecies antibody (mouse or human) or a d2-labeled anti-Tag antibody to capture the primary antibody (Figure1A).

    In parallel, wild-type RTK or SNAP-RTK expressing cells enabled the antibody functional test to be performed by measuring the ERK phosphorylation level using a cell-based sandwich immunoassay (Figure1B).

  • Materials & Methods

    Reagents: SNAP-Lumi4-Tb, anti-mouse Fc-d2, anti-human Fc-d2, anti-cMyc-d2, anti-His-d2, SNAP-RTK plasmids, and the labeling medium were from Cisbio Bioassays. Lipofectamin 2000 was purchased from Invitrogen, and the cell-dissociation buffer was from Sigma-Aldrich. Anti-RTK antibodies were obtained from different sources.

    Covalent labeling of SNAP-RTK cells: A solution of Tag-lite SNAP-Lumi4-Tb substrate at 100 nM was prepared in Tag-lite labeling medium. After aspiration of the cell culture medium, the SNAP-Lumi4-Tb solution was added to the cells expressing the SNAP-RTK in the T175 flask, followed by one hour incubation at 37ºC. The cells were then washed four times to remove the excess of SNAP-Lumi4-Tb and detached using the cell-dissociation buffer. The cells were frozen under 1 million cells/vial in culture medium and 10% DMSO.

    Antibody binding assay: The SNAP-Tb labeled cells were thawed and washed with PBS, then re-suspended in labeling buffer. Binding assays were performed in a total volume of 20 μL in 384 small volume white plates. 10,000 cells/well were incubated for two hours at room temperature with two different concentrations of primary antibodies (10 and 40 nM). Red labeled antispecies antibodies or Red-labeled antitag antibodies were added at a fixed and saturating concentration (100 nM) for the detection.

    Erk phosphorylation assay: SNAP-EGFR1 expressing cells were dispensed in 384 sv plates and pretreated or not with Cetuximab or erlotinib (tyrosine kinase inhibitor) for two hours, at 37°C, then stimulated with EGF for 10 minutes. After cell lysis, phosphorylated ERK was quantified by HTRF using the Cellul’erk kit.



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