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Full-Text Articles in Medicine and Health Sciences
Identification And Characterization Of The Thrombin Binding Sites On Fibrin, David A. Meh, Kevin R. Siebenlist, Michael W. Mosesson
Identification And Characterization Of The Thrombin Binding Sites On Fibrin, David A. Meh, Kevin R. Siebenlist, Michael W. Mosesson
Biomedical Sciences Faculty Research and Publications
Thrombin binds to fibrin at two classes of non-substrate sites, one of high affinity and the other of low affinity. We investigated the location of these thrombin binding sites by assessing the binding of thrombin to fibrin lacking or containing γ′ chains, which are fibrinogen γ chain variants that contain a highly anionic carboxyl-terminal sequence. We found the high affinity thrombin binding site to be located exclusively in D domains on γ′ chains (Ka, 4.9 × 106−1; n, 1.05 per γ′ chain), whereas the low affinity thrombin binding site was in the fibrin E …
Plasma Factor Xiii Binds Specifically To Fibrinogen Molecules Containing Γ‘ Chains, Kevin R. Siebenlist, David A. Meh, Michael W. Mosesson
Plasma Factor Xiii Binds Specifically To Fibrinogen Molecules Containing Γ‘ Chains, Kevin R. Siebenlist, David A. Meh, Michael W. Mosesson
Biomedical Sciences Faculty Research and Publications
The difference between peak 1 and peak 2 fibrinogen lies in their γ chains. Peak 1 molecules contain 2 γA chains; peak 2 molecules contain 1 γA and 1 γ‘ chain, the latter of which contains a 20 amino acid extension (γ‘ 408−427) replacing the carboxyl-terminal 4 amino acids of the γA chain (γA 408−411). While the existence of γ‘ chains in plasma fibrinogen molecules has been known for many years, their function remains unknown. When fibrinogen is purified from plasma, the factor XIII zymogen (A2B2) copurifies with it and is found only in the peak …
The Relationship Between The Fibrinogen D Domain Self-Association/Cross-Linking Site (Gammaxl) And The Fibrinogen Dusart Abnormality (Aalpha R554c-Albumin): Clues To Thrombophilia In The "Dusart Syndrome", Michael W. Mosesson, Kevin R. Siebenlist, James F. Hainfeld, J. S. Wall, C. Soria, J. P. Caen
The Relationship Between The Fibrinogen D Domain Self-Association/Cross-Linking Site (Gammaxl) And The Fibrinogen Dusart Abnormality (Aalpha R554c-Albumin): Clues To Thrombophilia In The "Dusart Syndrome", Michael W. Mosesson, Kevin R. Siebenlist, James F. Hainfeld, J. S. Wall, C. Soria, J. P. Caen
Biomedical Sciences Faculty Research and Publications
Cross-linking of fibrinogen at its COOH-terminal gamma chain cross-linking site occurs in the presence of factor XIIIa due to self-association at a constitutive D domain site ("gammaXL"). We investigated the contribution of COOH-terminal regions of fibrinogen Aalpha chains to the gammaXL site by comparing the gamma chain cross-linking rate of intact fibrinogen (fraction I-2) with that of plasma fraction I-9, plasmic fraction I-9D, and plasmic fragment D1, which lack COOH-terminal Aalpha chain regions comprising approximately 100, approximately 390, and 413 residues, respectively. The cross-linking rates were I-2 > I-9 > 1-9D = D1, and indicated that the terminal 100 or more Aalpha …
Evidence For Intramolecular Cross-Linked Aα·Γ Chain Heterodimers In Plasma Fibrinogen, Kevin R. Siebenlist, Michael W. Mosesson
Evidence For Intramolecular Cross-Linked Aα·Γ Chain Heterodimers In Plasma Fibrinogen, Kevin R. Siebenlist, Michael W. Mosesson
Biomedical Sciences Faculty Research and Publications
A peptide band of ∼105 kDa migrating near the γ dimer position of disulfide bond reduced human plasma fibrinogen prepared from fresh single donor or outdated plasma was identified by SDS−PAGE. The band, amounting to ∼2% of the total Aα/γ chain population, was thrombin and plasmin sensitive and reacted with antibodies to Aα or γ chains but not with antibodies to Bβ chains, plasminogen, or factor XIII. Amino acid sequencing revealed a double sequence corresponding to that of Aα and γ chains, indicating that the band consists of covalently cross-linked Aα·γ chain heterodimers. Aα·γ heterodimers were identified as a component …