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. Author manuscript; available in PMC: 2013 Dec 29.
Published in final edited form as: Biochemistry. 2006 Apr 4;45(13):10.1021/bi052646f. doi: 10.1021/bi052646f

Figure 5.

Figure 5

Interaction of wild-type and mutant forms of ghA, ghB, and ghC with human CRP. The microtiter wells were coated with 1 µg/well of CRP. After blocking and washing, different quantities (0.063, 0.125, 0.25, 0.5, 1.0, and 2 µg/well) of (a) ghB, ArgB114Glu, ArgB129Ala, and ArgB163Glu; (b) ghB, HisB117Asp, LysB136Glu, and TyrB175Leu; and (c) ghC, LysC170Glu, ArgC156Ala, and HisC101Ala were added to the wells and incubated. Mouse anti-MBP antibodies, followed by the rabbit anti-mouse IgG–HRP conjugate detected the amount of bound globular-head modules or their mutants. The data shown is the mean ± SD of triplicate measurements. The result is presented in % residual binding. The values for the wild-type modules were taken as 100%.