Hofmann V, Gati W P, Straub P W
Schweiz Med Wochenschr. 1977 Oct 15;107(41):1468.
Fibrinogen Zurich I (FZI) is characterized by delayed fibrin monomer aggregation. It has been previously shown that the patient fibrinogen is composed of two populations of molecules, one aggregating normally and the other not aggregating at all but interfering with the aggregation of the normal population. By use of a radioimmunoassay for fibrinopeptide A (FPA), only approximately half of the expected FPA could be recovered after thrombin and Defibrase proteolysis. Even after exhaustive proteolysis with 2 thrombin units of Defibrase, no further release of FPA could be obtained. The defective FPA release was confirmed by measurement of the N-terminal Gly/Tyr ratio. It may be assumed that the abnormal aggregation of one fraction of FZI is due to the defective FPA release from this fraction.
苏黎世纤维蛋白原I(FZI)的特征是纤维蛋白单体聚集延迟。先前已表明,患者的纤维蛋白原由两种分子群体组成,一种正常聚集,另一种根本不聚集,但会干扰正常群体的聚集。通过使用纤维蛋白肽A(FPA)的放射免疫测定法,凝血酶和去纤酶蛋白水解后仅能回收约一半预期的FPA。即使使用2个凝血酶单位的去纤酶进行彻底的蛋白水解,也无法获得更多的FPA释放。通过测量N端甘氨酸/酪氨酸比率证实了FPA释放存在缺陷。可以推测,FZI一部分的异常聚集是由于该部分FPA释放存在缺陷所致。