| Literature DB >> 28087455 |
Abstract
Many parasites have evolved antigenic variation systems that alter surface proteins in order to evade recognition by presently expressed antibodies and subsequent death. Although the amino acid positions in antigens to which antibodies most commonly target are expected to be the most variable, this assumption has not been investigated. Using the vls antigenic variation system of Borrelia burgdorferi as a model, we first investigated this assumption computationally and then developed a sensitive immunoassay to experimentally validate the computational results. There was a strong correlation between variability at an amino acid position and each of the computational metrics associated with antibody reactivity. However, empirical measures of antibody reactivity were not consistently greater at the variable amino acid positions than at the invariant amino acid positions. The inconsistent experimental support for this hypothesis suggests that the biological effect of variability at an amino acid position is obfuscated by other factors.Entities:
Keywords: Antigenic variation; Borrelia burgdorferi; Epitope mapping; VlsE
Mesh:
Substances:
Year: 2017 PMID: 28087455 PMCID: PMC5403549 DOI: 10.1016/j.micinf.2017.01.001
Source DB: PubMed Journal: Microbes Infect ISSN: 1286-4579 Impact factor: 2.700