1. Hydrodynamic characterization of recombinant human fibrinogen species
- Author
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Jos Grimbergen, Susan T. Lord, Bertrand Raynal, Patrick England, Mattia Rocco, Aldo Profumo, Barbara Cardinali, Biophysique des macromolécules et leurs interactions, Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), University of North Carolina [Chapel Hill] (UNC), University of North Carolina System (UNC), Istituto Nazionale per la Ricerca sul Cancro, Istituti di Ricovero e Cura a Carattere Scientifico (IRCCS), Institut Pasteur [Paris] (IP), Work partially supported by a grant from MIUR, Italy (PRIN 2008HAFF7X), and by NIH grant HL031048 (to S.T.L.)., and We thank J. Koopman (ProFibrix, The Netherlands) for reviewing the manuscript.
- Subjects
[SDV]Life Sciences [q-bio] ,MESH: Chromatography, Reverse-Phase ,FpA ,FpB ,Fibrinogen ,human plasma FG fragment X ,law.invention ,MESH: Recombinant Proteins ,human recombinant FG with Aα chains truncated after residue 251 ,law ,analytical ultracentrifugation sedimentation velocity ,chemistry.chemical_classification ,Chromatography, Reverse-Phase ,Chemistry ,AUC-SV ,Protein primary structure ,hpHMW-FG ,Hematology ,Recombinant Proteins ,fibrinopeptide A ,fibrinopeptide B ,Biochemistry ,Recombinant DNA ,Electrophoresis, Polyacrylamide Gel ,Ultracentrifuge ,medicine.drug ,Recombinant Fibrinogen ,chicken plasma FG ,Fibrinopeptide B ,Blotting, Western ,Article ,FG ,MESH: Hydrodynamics ,Fibrin Fibrinogen Degradation Products ,hpFrX-FG ,MESH: Fibrin Fibrinogen Degradation Products ,medicine ,Humans ,MESH: Blotting, Western ,Analytical Ultracentrifugation ,Blood Coagulation ,Messenger RNA ,human plasma high molecular weight FG ,MESH: Humans ,hrα251-FG ,MESH: Ultracentrifugation ,Human fibrinogen ,MESH: Fibrinogen ,Hydrodynamics ,cpFG ,fibrinogen ,human recombinant high molecular weight FG ,hrHMW-FG ,Glycoprotein ,Ultracentrifugation ,MESH: Electrophoresis, Polyacrylamide Gel - Abstract
International audience; Introduction: Fibrinogen is a key component of the blood coagulation system and plays important, diverse roles in several relevant pathologies such as thrombosis, hemorrhage, and cancer. It is a large glycoprotein whose three-dimensional molecular structure is not fully known. Furthermore, circulating fibrinogen is highly heterogeneous, mainly due to proteolytic degradation and alternative mRNA processing. Recombinant production of human fibrinogen allows investigating the impact on the three-dimensional structure of specific changes in the primary structure. Methods: We performed analytical ultracentrifugation analyses of a full-length recombinant human fibrinogen, its counterpart purified from human plasma, and a recombinant human fibrinogen with both Aα chains truncated at amino acid 251, thus missing their last 359 amino acid residues. Results: We have accurately determined the translational diffusion and sedimentation coefficients (D t(20,w) 0 , s (20,w) 0) of all three species. This was confirmed by derived molecular weights within 1% for the full length species, and 5% for the truncated species, as assessed by comparison with SDS-PAGE/Western blot analyses and primary structure data. No significant differences in the values of D t(20,w) 0 and s (20,w) 0 were found between the recombinant and purified full length human fibrinogens, while slightly lower and higher values, respectively, resulted for the recombinant truncated human fibrinogen compared to a previously characterized purified human fibrinogen fragment X obtained by plasmin digestion. Conclusions: Full-length recombinant fibrinogen is less polydisperse but hydrodynamically indistinguishable from its counterpart purified from human plasma. Recombinant Aα251-truncated human fibrinogen instead behaves differently from fragment X, suggesting a role for the Bβ residues 1-52 in inter-molecular interactions. Overall, these new hydrodynamic data will constitute a reliable benchmark against which models of fibrinogen species could be compared.
- Published
- 2013
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