Publication

Article Metrics

Citations


Online attention

Structural Basis for the Specific Neutralization of Stx2a with a Camelid Single Domain Antibody Fragment

DOI: 10.3390/toxins10030108 DOI Help

Authors: Robert Alvin Bernedo-navarro (University of Campinas (UNICAMP)) , Ema Romão (Vrije Universiteit Brussel) , Tomomasa Yano (University of Campinas (UNICAMP)) , Joar Pinto (Vrije Universiteit Brussel) , Henri De Greve (Vlaams Instituut voor Biotechnologie (VIB); Vrije Universiteit Brussel) , Yann G.-j. Sterckx (Vrije Universiteit Brussel) , Serge Muyldermans (Vrije Universiteit Brussel)
Co-authored by industrial partner: No

Type: Journal Paper
Journal: Toxins , VOL 10

State: Published (Approved)
Published: March 2018
Diamond Proposal Number(s): 12718

Open Access Open Access

Abstract: Background: Shiga toxin-producing Escherichia coli (STEC) are a subset of pathogens leading to illnesses such as diarrhea, hemolytic uremic syndrome and even death. The Shiga toxins are the main virulence factors and divided in two groups: Stx1 and Stx2, of which the latter is more frequently associated with severe pathologies in humans. Results: An immune library of nanobodies (Nbs) was constructed after immunizing an alpaca with recombinant Shiga toxin-2a B subunit (rStx2aB), to retrieve multiple rStx2aB-specific Nbs. The specificity of five Nbs towards rStx2aB was confirmed in ELISA and Western blot. Nb113 had the highest affinity (9.6 nM) and its bivalent construct exhibited a 100-fold higher functional affinity. The structure of the Nb113 in complex with rStx2aB was determined via X-ray crystallography. The crystal structure of the Nb113–rStx2aB complex revealed that five copies of Nb113 bind to the rStx2aB pentamer and that the Nb113 epitope overlaps with the Gb3 binding site, thereby providing a structural basis for the neutralization of Stx2a by Nb113 that was observed on Vero cells. Finally, the tandem-repeated, bivalent Nb1132 exhibits a higher toxin neutralization capacity compared to monovalent Nb113. Conclusions: The Nb of highest affinity for rStx2aB is also the best Stx2a and Stx2c toxin neutralizing Nb, especially in a bivalent format. This lead Nb neutralizes Stx2a by competing for the Gb3 receptor. The fusion of the bivalent Nb1132 with a serum albumin specific Nb is expected to combine high toxin neutralization potential with prolonged blood circulation.

Journal Keywords: nanobody; Shiga toxin; Stx2; B domain; neutralization; crystal structure

Subject Areas: Biology and Bio-materials


Instruments: I24-Microfocus Macromolecular Crystallography