β-Lactamase Inhibitors Derived from Single-Domain Antibody Fragments Elicited in the Camelidae

Author:

Conrath Katja E.1,Lauwereys Marc1,Galleni Moreno2,Matagne André2,Frère Jean-Marie2,Kinne Jörg3,Wyns Lode1,Muyldermans Serge1

Affiliation:

1. Department of Ultrastructure, Vrije Universiteit Brussel, B-1640 St. Genesius Rode,1and

2. Institut de Chimie, Centre d'Ingénerie des Protéines, Université de Liège, B-4000 Sart-Tilman, Liège,2 Belgium, and

3. Central Veterinary Research Laboratories, Dubai, United Arab Emirates3

Abstract

ABSTRACT Small, soluble single-domain fragments derived from the unique variable region of dromedary heavy-chain antibodies (VHHs) against enzymes are known to be potent inhibitors. The immunization of dromedaries with the TEM-1 and BcII β-lactamases has lead to the isolation of such single-domain antibody fragments specifically recognizing and inhibiting those β-lactamases. Two VHHs were isolated that inhibit TEM-1 and one BcII inhibiting VHH was identified. All inhibitory VHHs were tight-binding inhibitors. The 50% inhibitory concentrations were determined for all inhibitors and they were all in the same range as the enzyme concentration used in the assay. Addition of the VHHs to the TEM-1 β-lactamase, expressed on the surface of bacteria, leads to a higher ampicillin sensitivity of the bacteria. This innovative strategy could generate multiple potent inhibitors for all types of β-lactamases.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference30 articles.

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5. Desmyter A. K. Decanniere S. Muyldermans and L. Wyns. One hypervariable loop of camel single-domain antibody sufficient for specific antigen recognition. J. Biol. Chem. in press.

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