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. 2016 Feb 6;8(3):501–512. doi: 10.1080/19420862.2016.1145865

Table 3.

Binding affinities of reverse-engineered 3H3 and LOB12.3 Fab variants to CD137.

Fab sample ka (x 105M−1s−1) kd (x 10−3s−1) KD (nM)
LOB12.3-Fab1 (VH-I100c) 4.29 3.68 8.60
LOB12.3-Fab2 (VH-L100c) 5.29 3.75 7.06
LOB12.3-Fabp 4.50 3.74 8.30
3H3-Fab1 (VH-I29) 25.4 4.63 1.82
3H3-Fab2 (VH-L29) 28.8 4.83 1.68
3H3-Fabp 22.1 4.51 2.05

LOB12.3-Fab1, -Fab2 and 3H3-Fab1, -Fab2 were reverse-engineered Fab variants, while LOB12.3-Fabp and 3H3-Fabp were Fabs derived by partial proteolysis of the parental (i.e., commercially obtained) IgGs. Standard errors for fitting of data to a 1:1 binding model were less than one unit in the third significant digit for all computed ka, kd and KD values.