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. 2007 Jun 25;104(27):11227–11232. doi: 10.1073/pnas.0703714104

Fig. 4.

Fig. 4.

Mutations L81A and R122A stabilize cationic trypsin against chymotrypsin C-mediated degradation. Wild-type, L81A, and R122A cationic trypsins were incubated at 2 μM concentration with 300 nM chymotrypsin C in 0.1 M Tris·HCl (pH 8.0) and 25 μM CaCl2 (final concentrations). (A) At the indicated times, residual trypsin activity was measured as described in Fig. 1A. (B and C). Aliquots (100 μl) were precipitated with 10% trichloroacetic acid (final concentration) and analyzed by SDS/15% PAGE under reducing conditions.