DocumentCode
3443685
Title
Expression of human fibrinogen in transgenic mice
Author
Subramanian, Anuradha ; Butler, Stephen P. ; Gwazdauskas, Frank C. ; Lubon, Henryk ; Velander, William H.
Author_Institution
Dept. of Chem. Eng., Virginia Polytech. Inst. & State Univ., Blacksburg, VA, USA
fYear
1997
fDate
4-6 Apr 1997
Firstpage
57
Lastpage
60
Abstract
Human fibrinogen (hfib) is a 340 kDa plasma protein which is a complex precursor substrate to fibrin during clot formation. The present work evaluates the potential of the mammary gland of transgenic mice to coordinately express three separate cDNAs for hfib and then assemble hexameric, functional recombinant human fibrinogen (rhfib). Trigenic mice were made by pronuclear co-microinjection of separate constructs for each cDNA of the Aα, Bβ and γ hfib polypeptides. Each transgene contained a 2.6 kb promoter sequence from the murine whey acidic protein (mWAP). Trigenic mice expressing rhfib at about 5-35 μg/ml milk were generated. The rhfib showed an apparent molecular weight by SDS-PAGE similar to that of hfib under non-reducing conditions. Under reducing conditions, the α-chain of rhfib had slightly greater mobility than α-chain from hfib. The rhfib was converted to fibrin by thrombin in a manner similar to that of hfib where a normal fibrin clot and a lower apparent mobility of the α-chain from the clot relative to the starting precursor chains were observed for both rhfib and hfib. In summary, these results show that functional fibrinogen can be synthesized and secreted by the mammary gland of transgenic mice
Keywords
DNA; blood; genetics; molecular biophysics; proteins; α-chain; 340 kDa plasma protein; cDNAs; clot formation; complex precursor substrate; fibrin; hexameric functional recombinant human fibrinogen; human fibrinogen expression; mammary gland; murine whey acidic protein; nonreducing conditions; pronuclear comicroinjection; reducing conditions; transgenic mice; Animals; Assembly; Bioreactors; Humans; Mammary glands; Mice; Nuclear and plasma sciences; Plasma chemistry; Protein engineering; Trigeneration;
fLanguage
English
Publisher
ieee
Conference_Titel
Biomedical Engineering Conference, 1997., Proceedings of the 1997 Sixteenth Southern
Conference_Location
Biloxi, MS
ISSN
1086-4105
Print_ISBN
0-7803-3869-3
Type
conf
DOI
10.1109/SBEC.1997.583213
Filename
583213
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