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. 2018 Nov 4;35(1):e2732. doi: 10.1002/btpr.2732

Figure 5.

Figure 5

Chromatographic behavior of Cathepsin L in bind‐and‐elute chromatography. (A) Fragmentation (during pH 3.4 incubation) of Fab A visualized by HP‐SEC profiles after purification from CCF by cation exchange, affinity and mixed mode chromatography. (B) Elution profiles of Fab A and Cathepsin L on different cation exchanger resins eluted in a 0–500 mM NaCl, 20 CV linear gradient at pH 5.0. (C) Elution profiles of Fab A and Cathepsin L on Fractogel® SO3(M) in a 0–500 mM NaCl, 20 CV linear gradient at different pH values. (D) The effects of washes on elution product protease level and step yield observed during Fab A purification with Fractogel® SO3(M). The elution product was acidified to pH 3.4 and incubated at 37°C for 3 h and fragment level was measured by HP‐SEC.