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. Author manuscript; available in PMC: 2018 Feb 23.
Published in final edited form as: Nature. 2017 Aug 23;548(7669):597–601. doi: 10.1038/nature23670

Figure 3. The influence of insert position and somatic mutations on antibody specificity.

Figure 3

a, Schematic representation of LAIR1-containing antibodies produced by different insertion modalities. b, Scheme of the constructs (C1-C10) containing LAIR1 or other Ig-like domains in different positions which were tested for binding to a set of antigens or anti-domain antibodies by ELISA or FACS. The construct domains and their binding values to the cognate ligands are color coded as depicted in the figure. The V and J segments that do not contribute to any binding are not colored. BKC3, in grey, is a negative control. LAIR1D21, LAIR1M1 and LAIR1J5 are the exons from MGD21, MGM1 and MGJ5 antibodies. LAIR1gen is the unmutated genomic sequence of LAIR1 encoded on chromosome 19. MGDUCA = unmutated common ancestor of donor D antibodies; GL = germline. Data are from one experiment out of two. c, Binding of LAIR1-containing antibodies to erythrocytes infected with nine parasite isolates and to human collagen (n=1). Values refer to binding at a concentration of 1 μg ml-1. The MGDUCA was also tested at 100 μg ml-1. The number of amino acid substitutions is reported in brackets next to the antibody names.