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Fibrin(ogen) peptide B beta 15-42 inhibits platelet aggregation and fibrinogen binding to activated platelets
C S Chen1, S H Chou, P Thiagarajan
1Department of Medicine, University of Washington, Seattle 98195.
Abstract:
The binding of fibrinogen to activated platelets leads to platelet aggregation. Fibrinogen has multiple binding sites to platelet membrane glycoprotein IIb-IIIa complex. At least two well-defined sequences in fibrinogen, Arg-Gly-Asp sequence of A alpha 95-97 and A alpha 572-574 and gamma 400-411, have been shown to interact with glycoprotein IIb-IIIa. A possible binding site on the amino-terminal end of fibrinogen to platelet glycoprotein IIb-IIIa has also been reported. In this paper the effect of synthetic peptides derived from the amino-terminal end of the B beta chain on platelet aggregation and fibrinogen binding has been examined. B beta 15-42 peptide inhibits platelet aggregation and 125I-fibrinogen binding to activated platelets in a dose-dependent manner. Since B beta 15-42 contains a previously identified fibrinogen binding site, B beta 15-18, exposed by thrombin cleavage of native fibrinogen, we also examined the effect of B beta 15-18, B beta 19-42, and B beta 1-14 (fibrinopeptide B) on platelet aggregation and fibrinogen binding. Synthetic fibrinopeptide B and B beta 15-18 had no effect on platelet aggregation and fibrinogen binding while B beta 19-42 retained the inhibitory effect. When fibrinogen is chromatographed on a column of agarose-bound B beta 15-42, a cation-dependent retention of fibrinogen on the peptide column was observed, and fibrinogen was eluted from the column by B beta 15-42 but not by B beta 1-14. Under the same conditions, platelet glycoprotein IIb-IIIa was not retained in the column. Thus, the observed inhibitory effect is due to its interaction with fibrinogen rather than to platelet glycoprotein IIb-IIIa.(ABSTRACT TRUNCATED AT 250 WORDS)
Insights
Synthetic peptides from fibrinogen
Area of Science:
- Biochemistry
- Molecular Biology
- Hematology
Background:
- Platelet aggregation is crucial for hemostasis and thrombosis.
- Fibrinogen binding to platelet glycoprotein IIb-IIIa mediates this aggregation.
- Specific sequences in fibrinogen interact with this receptor.
Purpose of the Study:
- To investigate the effect of synthetic peptides from the B beta chain's amino-terminal end on platelet aggregation and fibrinogen binding.
- To identify the specific peptide sequences responsible for inhibiting these processes.
Main Methods:
- Synthesis of peptides derived from the B beta chain of fibrinogen.
- Assay of peptide effects on platelet aggregation and 125I-fibrinogen binding to activated platelets.
- Chromatographic analysis of fibrinogen interaction with immobilized peptides.
Main Results:
- The B beta 15-42 peptide significantly inhibited platelet aggregation and fibrinogen binding in a dose-dependent manner.
- The inhibitory effect was retained in the B beta 19-42 peptide fragment, but not in B beta 15-18 or fibrinopeptide B (B beta 1-14).
- Fibrinogen demonstrated cation-dependent retention on a B beta 15-42 peptide column, indicating direct interaction with fibrinogen, not the platelet receptor.
Conclusions:
- The B beta 19-42 sequence within fibrinogen is critical for inhibiting platelet aggregation and fibrinogen binding.
- The inhibitory mechanism involves direct interaction of the peptide with fibrinogen, not with the platelet glycoprotein IIb-IIIa receptor.