Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/51920
Title: VHH (nanobody) directed against human glycophorin A: A tool for autologous red cell agglutination assays
Authors: Habib, Ibrahim
Smolarek, Dorota
Hattab, Claude
Grodecka, Magdalena
Hassanzadeh-Ghassabeh, Gholamreza
Muyldermans, Serge
Sagan, Sandrine
Gutiérrez, Carlos 
Laperche, Syria
Le-Van-Kim, Caroline
Aronovicz, Yves Colin
Wasniowska, Kazimiera
Gangnard, Stephane
Bertrand, Olivier
Colin Aronovicz, Yves
Keywords: Hiv-1 Infection
Chagas-Disease
Whole-Blood
Antibodies
Diagnosis, et al
Issue Date: 2013
Journal: Analytical biochemistry (Print) 
Abstract: The preparation of a VHH (nanobody) named IH4 that recognizes human glycophorin A (GPA) is described. IH4 was isolated by screening a library prepared from the lymphocytes of a dromedary immunized by human blood transfusion. Phage display and panning against GPA as the immobilized antigen allowed isolating this VHH. IH4, representing 67% of the retrieved VHH sequences, was expressed as a soluble correctly folded protein in SHuffle Escherichia coli cells, routinely yielding approximately 100 mg/L fermentation medium. Because IH4 recognizes GPA independently of the blood group antigens, it recognizes red cells of all humans with the possible exception of those with some extremely rare genetic background. The targeted linear epitope comprises the GPA Y52PPE55 sequence. Based on surface plasmon resonance results, the dissociation constant of the IH4-GPA equilibrium is 33 nM. IH4 is a stable protein with a transition melting temperature of 75.8 C (measured by differential scanning calorimetry). As proof of concept, we fused HIV p24 to IH4 and used the purified construct expressed in E. coli to show that IH4 was amenable to the preparation of autologous erythrocyte agglutination reagents: reconstituted blood prepared with serum from an HIV-positive patient was readily agglutinated by the addition of the bifunctional reagent.
URI: http://hdl.handle.net/10553/51920
ISSN: 0003-2697
DOI: 10.1016/j.ab.2013.03.020
Source: Analytical Biochemistry [ISSN 0003-2697], v. 438 (1), p. 82-89
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