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Shark Variable New Antigen Receptor (VNAR) Single Domain Antibody Fragments: Stability and Diagnostic Applications

Author(s): Katherine Griffiths | Olan Dolezal | Kathy Parisi | Julie Angerosa | Con Dogovski | Miles Barraclough | Abdulmonem Sanalla | Joanne L. Casey | Iveth González | Matthew A. Perugini | Stewart Nuttall | Michael Foley

Journal: Antibodies
ISSN 2073-4468

Volume: 2;
Issue: 1;
Start page: 66;
Date: 2013;
Original page

Keywords: single-domain antibody | shark VNAR | thermal stability | pH stability | protease resistance | AMA-1 | Plasmodium | malaria | diagnosis

The single variable new antigen receptor domain antibody fragments (VNARs) derived from shark immunoglobulin new antigen receptor antibodies (IgNARs) represent some of the smallest known immunoglobulin-based protein scaffolds. As single domains, they demonstrate favorable size and cryptic epitope recognition properties, making them attractive in diagnosis and therapy of numerous disease states. Here, we examine the stability of VNAR domains with a focus on a family of VNARs specific for apical membrane antigen 1 (AMA-1) from Plasmodium falciparum. The VNARs are compared to traditional monoclonal antibodies (mAbs) in liquid, lyophilized and immobilized nitrocellulose formats. When maintained in various formats at 45 °C, VNARs have improved stability compared to mAbs for periods of up to four weeks. Using circular dichroism spectroscopy we demonstrate that VNAR domains are able to refold following heating to 80 °C. We also demonstrate that VNAR domains are stable during incubation under potential in vivo conditions such as stomach acid, but not to the protease rich environment of murine stomach scrapings. Taken together, our results demonstrate the suitability of shark VNAR domains for various diagnostic platforms and related applications.
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