Related Experiment Video
Updated: Jun 21, 2026

Chemically-blocked Antibody Microarray for Multiplexed High-throughput Profiling of Specific Protein Glycosylation in Complex Samples
Published on: May 4, 2012
Augmenting hepatitis C E1E2 glycoprotein antibody detection via an alternative lectin-assisted mannose-binding ELISA
Mena Youssef1, Mandy Döpke1, Corinne Ginkel1
1Institute for Experimental Virology, Centre for Experimental and Clinical Infection Research, a Joint Venture Between the Helmholtz Centre for Infection Research and the Hannover Medical School, TWINCORE, Feodor-Lynen-Str. 7-9, Hannover, 30625, Germany.
None:
In this study we compared several plant lectins for use in a lectin capture ELISAs to enrich HCV glycoproteins from cellular extracts for subsequent detection of HCV glycoprotein-specific antibodies. We selected various high-mannose plant lectins and assessed for their properties to capture HCV glycoproteins. Three lectins, Galanthus nivalis lectin (GNL), Narcissus Pseudonarcissus Lectin (NPL) and Hippeastrum hybrid lectin (HHL) demonstrated effective capturing properties. These were subsequently tested for specificity and sensitivity against viral isolates spanning diverse HCV genotypes. Furthermore, their performance was evaluated in detecting various HCV-specific monoclonal broadly neutralising antibodies, and polyclonal antibodies from both HCV-positive and negative donors. These three lectins share similar scaffold structures, which may be a critical factor in their capture efficacy. The results suggest that NPL and HHL are good candidates to replace the GNL in this glycan-capture assay.
