Summary
Human fibrinogen and purified plasmic degradation fragments X (stages 1 and 2), D
and E were labelled with 125-1 using the lactoperoxidase method. The chromatographic,
elec-trophoretic and immunologic properties of the labelled proteins were found to
be similar to those of non-labelled fragments. All the degradation products diffused
rapidly (T½ 0.27–0.75 hours) from the intravascular space of rabbits, as compared
with fibrinogen (4.26 hours). In addition, the metabolic half-life was found to be
49.3 hours for fibrinogen, as compared with only 5.1, 6.1, 2.3 and 1.4 for fragments
X (stage 1), X (stage 2), D and E, respectively. The metabolic half-life roughly reflects
the molecular size of the degradation products.