Evaluation of competition binding experiments. The calculations were
performed using Model 2 (see “Experimental Procedures”).
A, inhibition of monovalent p85 C-SH2 domain binding to
Tyr(P)751 of PDGF β-receptor by different competitor peptides
as indicated. Fig. 6A of Ref.
17 was recapitulated with
ST = KD,C1 = 10
nm and KD,C2 = 75 nm,
where ST is the total concentration of C-SH2. B,
inhibition of p85 tandem SH2 construct by different competitor peptides as
indicated. In the case of the bisphosphorylated competitor, the value of χ
is varied as indicated. Fig. 6 (B and C) of Ref.
17 compares favorably with
these results when χ > 10 μm.