Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1986 Jan;83(2):299–302. doi: 10.1073/pnas.83.2.299

Affinity purification of human tissue factor: interaction of factor VII and tissue factor in detergent micelles.

A Guha, R Bach, W Konigsberg, Y Nemerson
PMCID: PMC322845  PMID: 3455766

Abstract

Tissue factor, a known initiator of blood coagulation, was found to be active in Triton X-100. A system consisting of tissue factor, factor VIIa, calcium ions, and coagulation factor X generated activated factor X at an appreciable rate. Based on this observation, we coupled human and bovine factor VII to a solid support. Each column bound tissue factor, solubilized in Triton X-100, in a species-specific manner. These interactions required calcium ions; when the columns were washed with detergent containing calcium ions, no tissue factor was eluted. When calcium ions were omitted from the eluant, tissue factor emerged as a sharp peak. Human tissue factor was extracted from an acetone brain powder into 2% Triton X-100. This extract, made 10 mM in CaCl2, was passed over a factor VII column. Human factor VII (1.2 mg) was coupled to 30 ml of Affi-Gel 15. This column bound approximately equal to 15 micrograms of human tissue factor. The eluted material was approximately equal to 25% pure. Final purification was achieved by gel filtration after chymotryptic digestion of contaminants. The tissue factor activity was stable to this treatment. The molecular weight determined by sodium dodecyl sulfate/PAGE (approximately equal to 46,000) was also unchanged by chymotrypsin. The final material was a single band on PAGE, demonstrated similar resistance to tryptic and chymotryptic digestion as bovine tissue factor, and had approximately the same specific coagulant activity as the previously purified bovine material. Tissue factor was also purified from human placenta, yielding a similar protein. A partial 28-residue sequence of the latter has been obtained.

Full text

PDF

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bach R., Nemerson Y., Konigsberg W. Purification and characterization of bovine tissue factor. J Biol Chem. 1981 Aug 25;256(16):8324–8331. [PubMed] [Google Scholar]
  2. Bach R., Oberdick J., Nemerson Y. Immunoaffinity purification of bovine factor VII. Blood. 1984 Feb;63(2):393–398. [PubMed] [Google Scholar]
  3. Barthels M., Seegers W. H. Substitution of lipids with bile salts in the formation of thrombin. Thromb Diath Haemorrh. 1969 Aug 31;22(1):13–27. [PubMed] [Google Scholar]
  4. Bjorklid E., Storm E., Prydz H. The protein component of human brain thromboplastin. Biochem Biophys Res Commun. 1973 Dec 10;55(3):969–976. doi: 10.1016/0006-291x(73)91237-0. [DOI] [PubMed] [Google Scholar]
  5. Bjorklid E., Storm E. Purification and some properties of the protein component of tissue thromboplastin from human brain. Biochem J. 1977 Jul 1;165(1):89–96. doi: 10.1042/bj1650089. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Broze G. J., Jr, Leykam J. E., Schwartz B. D., Miletich J. P. Purification of human brain tissue factor. J Biol Chem. 1985 Sep 15;260(20):10917–10920. [PubMed] [Google Scholar]
  7. Broze G. J., Jr, Majerus P. W. Purification and properties of human coagulation factor VII. J Biol Chem. 1980 Feb 25;255(4):1242–1247. [PubMed] [Google Scholar]
  8. Carson S. D., Bach R., Carson S. M. Monoclonal antibodies against bovine tissue factor, which block interaction with factor VIIa. Blood. 1985 Jul;66(1):152–156. [PubMed] [Google Scholar]
  9. Carson S. D., Konigsberg W. H. Cadmium increases tissue factor (coagulation factor III) activity by facilitating its reassociation with lipids. Science. 1980 Apr 18;208(4441):307–309. doi: 10.1126/science.7367861. [DOI] [PubMed] [Google Scholar]
  10. Dulley J. R., Grieve P. A. A simple technique for eliminating interference by detergents in the Lowry method of protein determination. Anal Biochem. 1975 Mar;64(1):136–141. doi: 10.1016/0003-2697(75)90415-7. [DOI] [PubMed] [Google Scholar]
  11. Hartree E. F. Determination of protein: a modification of the Lowry method that gives a linear photometric response. Anal Biochem. 1972 Aug;48(2):422–427. doi: 10.1016/0003-2697(72)90094-2. [DOI] [PubMed] [Google Scholar]
  12. Jesty J., Spencer A. K., Nemerson Y. The mechanism of activation of factor X. Kinetic control of alternative pathways leading to the formation of activated factor X. J Biol Chem. 1974 Sep 10;249(17):5614–5622. [PubMed] [Google Scholar]
  13. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  14. Makino S., Reynolds J. A., Tanford C. The binding of deoxycholate and Triton X-100 to proteins. J Biol Chem. 1973 Jul 25;248(14):4926–4932. [PubMed] [Google Scholar]
  15. Mimms L. T., Zampighi G., Nozaki Y., Tanford C., Reynolds J. A. Phospholipid vesicle formation and transmembrane protein incorporation using octyl glucoside. Biochemistry. 1981 Feb 17;20(4):833–840. doi: 10.1021/bi00507a028. [DOI] [PubMed] [Google Scholar]
  16. Nemerson Y., Bach R. Tissue factor revisited. Prog Hemost Thromb. 1982;6:237–261. [PubMed] [Google Scholar]
  17. Nemerson Y. Characteristics and lipid requirements of coagulant proteins extracted from lung and brain: the specifity of protein component of tissue factor. J Clin Invest. 1969 Feb;48(2):322–331. doi: 10.1172/JCI105988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Nemerson Y., Clyne L. P. An assay for coagulation factor VII using factor VII-depleted bovine plasma. J Lab Clin Med. 1974 Feb;83(2):301–303. [PubMed] [Google Scholar]
  19. Pitlick F. A., Nemerson Y. Purification and characterization of tissue factor apoprotein. Methods Enzymol. 1976;45:37–48. doi: 10.1016/s0076-6879(76)45007-3. [DOI] [PubMed] [Google Scholar]
  20. Silverberg S. A., Nemerson Y., Zur M. Kinetics of the activation of bovine coagulation factor X by components of the extrinsic pathway. Kinetic behavior of two-chain factor VII in the presence and absence of tissue factor. J Biol Chem. 1977 Dec 10;252(23):8481–8488. [PubMed] [Google Scholar]
  21. Zur M., Radcliffe R. D., Oberdick J., Nemerson Y. The dual role of factor VII in blood coagulation. Initiation and inhibition of a proteolytic system by a zymogen. J Biol Chem. 1982 May 25;257(10):5623–5631. [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES