Immunological applications of single-domain llama recombinant antibodies isolated from a naïve library
Open Access
- 4 February 2009
- journal article
- research article
- Published by Oxford University Press (OUP) in Protein Engineering, Design and Selection
- Vol. 22 (4) , 273-280
- https://doi.org/10.1093/protein/gzp002
Abstract
We describe the rapid isolation of single-domain recombinant antibodies in VHH format from a pre-immune llama library created in our laboratory. Such naïve library has demonstrated to be a versatile tool and enabled the isolation of several different antibodies for any of the six proteins panned in parallel. The binders specific for human fibroblast growth factor receptor 1 (FGFR1) were successively analyzed in more detail and resulted suitable for both western blot and immunofluorescence analyses. Several milligrams per liter of antibodies were purified by affinity chromatography and used for kinetic and thermodynamic characterization. Their KD was in the nanomolar range and they apparently bound a FGF receptor 1 domain not overlapping the region recognized by its physiological ligand FGF. Altogether, the collected data indicate that the new library can enable the recovery of binders of high affinity, specificity and functionality in the conventional immunological tests, avoiding the necessity of further maturation steps. Such results confirmed recent reports of high affinity pre-immune IgNARs and supported the choice of using large single-domain recombinant antibody naïve libraries as an alternative to the preparation of immune libraries for selecting monoclonal antibodies, at convenient cost and time conditions.Keywords
This publication has 36 references indexed in Scilit:
- Generation of llama single-domain antibodies against methotrexate, a prototypical haptenMolecular Immunology, 2007
- Facile Generation of Heat-Stable Antiviral and Antitoxin Single Domain Antibodies from a Semisynthetic Llama LibraryAnalytical Chemistry, 2006
- Llama Single-Chain Antibody That Blocks Lipopolysaccharide Binding and Signaling: Prospects for Therapeutic ApplicationsClinical and Vaccine Immunology, 2006
- Formatted anti–tumor necrosis factor α VHH proteins derived from camelids show superior potency and targeting to inflamed joints in a murine model of collagen‐induced arthritisArthritis & Rheumatism, 2006
- Molecular basis for the preferential cleft recognition by dromedary heavy-chain antibodiesProceedings of the National Academy of Sciences, 2006
- Regulation of Endocytosis, Nuclear Translocation, and Signaling of Fibroblast Growth Factor Receptor 1 by E-CadherinMolecular Biology of the Cell, 2005
- Chemical Basis for the Affinity Maturation of a Camel Single Domain AntibodyJournal of Biological Chemistry, 2004
- β-Lactamase Inhibitors Derived from Single-Domain Antibody Fragments Elicited in the CamelidaeAntimicrobial Agents and Chemotherapy, 2001
- Selection and identification of single domain antibody fragments from camel heavy‐chain antibodiesFEBS Letters, 1997
- A new antigen receptor gene family that undergoes rearrangement and extensive somatic diversification in sharksNature, 1995