| Literature DB >> 24667070 |
Geoffrey A Mueller1, John A Ankney2, Jill Glesner3, Taruna Khurana4, Lori L Edwards2, Lars C Pedersen2, Lalith Perera2, Jay E Slater4, Anna Pomés3, Robert E London2.
Abstract
Bla g 1 is a major allergen from Blatella germanica and one of the primary allergens used to assess cockroach allergen exposure. The epitope of an anti-Bla g 1 scFv was mapped in order to better understand cross reactivity with other group 1 cockroach allergens and patient IgE epitopes. X-ray crystallography was used to determine the structure of the scFv. The scFv epitope on Bla g 1 was located by alanine scanning site-directed mutagenesis and ELISA. Twenty-six rBla g 1-GST alanine mutants were evaluated for variations in binding to the scFv compared to the wild type allergen. Six mutants showed a significant difference in scFv binding affinity. These mutations clustered to form a discontinuous epitope mainly comprising two helices of Bla g 1. The allergen-scFv complex was modeled based on the results, and the epitope region was found to have low sequence similarity with Per a 1, especially among the residues identified as functionally important for the scFv binding to Bla g 1. Indeed, the scFv failed to bind Per a 1 in American cockroach extract. The scFv was unable to inhibit the binding of IgE antibodies from a highly cockroach allergic patient to Bla g 1. Based on the surface area of Bla g 1 occluded by the scFv, putative regions of patient IgE-Bla g 1 interactions can be inferred. This scFv could be best utilized as a capture antibody in an IgE detection ELISA, or to differentiate Bla g 1 from Per a 1 in environmental exposure assays. Published by Elsevier Ltd.Entities:
Keywords: Allergen; Bla g 1; Cockroach; Epitope; Structure; scFv
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Year: 2014 PMID: 24667070 PMCID: PMC4097036 DOI: 10.1016/j.molimm.2014.02.003
Source DB: PubMed Journal: Mol Immunol ISSN: 0161-5890 Impact factor: 4.407