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A mechanistic model of in vitro plasma activation to evaluate therapeutic kallikrein-kinin system inhibitors

Fig 3

FXII activation versus DXS concentration via two alternative FXII activation mechanisms.

Comparison of the Røjkjær and Schousboe [44] experimental data with simulations using optimised kinetic parameters for FXII activation, via either a combination of FXII autoactivation (reaction 3) and FXII self-activation (reaction 4), or just FXII self-activation in the presence of background αFXIIa.

Fig 3

doi: https://doi.org/10.1371/journal.pcbi.1012552.g003