After intravenous and subcutaneous injection, heparins and low-molecul
ar-weight heparins release tissue factor pathway inhibitor (TFPI) into
the blood stream. Protamine immediately reverses the plasma levels of
TFPI to pretreatment values. A low-molecular-weight dermatan sulphate
releases only very small amounts of TFPI after intravenous injection
without a clear dose-dependent effect. Together with other data from l
iterature, it seems likely that TFPI is rather specifically released b
y acidic glycosaminoglycans. In the present paper a binding region for
heparins is reported to be located in the C-terminal end. A basic ami
no acid cluster occurs between 256-lysine and 261-lysine. This propose
d heparin recognition region in TFPI is similar to the recognition reg
ion in antithrombin III and other proteins. The binding between the ba
sic region at the C-terminal end of TFPI and the negatively charged su
lphate or carboxyl-groups of glycosaminoclycans may occur in a linear
manner. A comparison of a helical wheel diagram of antithrombin III an
d tissue factor pathway inhibitor support also the proposal of this fo
rm of a heparin recognition region in TFPI. Further studies are now re
quired to analyse these interactions.