Variable Lymphocyte Receptor Recognition of the Immunodominant Glycoprotein of Bacillus anthracis Spores

• Published in: Structure (London) Vol. 20; no. 3; pp. 479 - 486
• Main Authors: Kirchdoerfer, Robert N., Herrin, Brantley R., Han, Byung Woo, Turnbough, Charles L., Cooper, Max D., Wilson, Ian A.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 07.03.2012
• Subjects: Animals; Bacillus anthracis; Bacillus anthracis - chemistry; Cloning, Molecular; Crystallography; Glycoproteins - chemistry; Glycoproteins - metabolism; Immunodominant Epitopes - chemistry; Immunodominant Epitopes - metabolism; Lampreys - immunology; Models, Molecular; Mutagenesis; Protein Binding; Receptors, Immunologic - chemistry; Spores, Bacterial - chemistry
• ISSN: 0969-2126; 1878-4186; 1878-4186
• DOI: 10.1016/j.str.2012.01.009

Variable lymphocyte receptors (VLRs) are the adaptive immune receptors of jawless fish, which evolved adaptive immunity independent of other vertebrates. In lieu of the immunoglobulin fold-based T and B cell receptors, lymphocyte-like cells of jawless fish express VLRs (VLRA, VLRB, or VLRC) composed of leucine-rich repeats and are similar to toll-like receptors (TLRs) in structure, but antibodies (VLRB) and T cell receptors (VLRA and VLRC) in function. Here, we present the structural and biochemical characterization of VLR4, a VLRB, in complex with BclA, the immunodominant glycoprotein of Bacillus anthracis spores. Using a combination of crystallography, mutagenesis, and binding studies, we delineate the mode of antigen recognition and binding between VLR4 and BclA, examine commonalities in VLRB recognition of antigens, and demonstrate the potential of VLR4 as a diagnostic tool for the identification of B. anthracis spores. [Display omitted] ► VLRBs use their C-terminal LRRs and the LRRCT-loop to interact with antigen ► Sequence-related VLRBs exhibit differential recognition of their BclA epitopes ► VLR4 binds a conserved protein epitope, yet is specific for B. anthracis spores