and to the bb¢ domains and inhibits PDI reductase activity.
Reversal of quercetin-3-rutinoside inhibition of thrombus
formation in a mouse model is observed with infusion of the
PDI b¢x domain (65).
A role for the chaperone function of PDI in thrombosis has
been suggested. Versteeg used S-methyl methanethiosulfonate
(MMTS) to inactivate the catalytic sites of PDI (109).