FIG.2.
“Reverse” ALBI analyses: analysis of the abilities of recombinant OspE, OspF, and Elp proteins to bind to immobilized serum proteins. Serum proteins from different animals (indicated in each panel) were separated by SDS-PAGE with either 7.5% or 12.5% Criterion precast gels under nonreducing conditions. The proteins were immunoblotted and incubated with individual recombinant S-tagged proteins (100 μg ml−1), as indicated in each panel. Note that the blots shown in panels C and D were screened with BBO39 and BBN39, respectively. Identical results were obtained with BBM38, BBR42, BBO40, and BBP39 (data not shown). In all assays, bound recombinant protein was detected using HRP-conjugated (conj.) S protein. All methods were as described in the text. Purified human factor H (FH) was included as a positive control with all immunoblots. The location of factor H on the immunoblots presented in panels A and B is indicated by an arrow for reference. Note that in panel E the serum proteins were separated using reducing conditions and were screened with goat α-human factor H antiserum. With longer exposure, factor H was detected in all animals except duck, horse, rat, and chicken.
