Publication Cover
Amyloid
The Journal of Protein Folding Disorders
Volume 14, 2007 - Issue 3
387
Views
30
CrossRef citations to date
0
Altmetric
Original

Structural analyses of fibrinogen amyloid fibrils

, , &
Pages 199-203 | Published online: 06 Jul 2009

References

  • Benson M D. Amyloidosis. The Metabolic and Molecular Bases of Inherited Disease8th ed, C R Scriver, A L Beaudet, W S Sly, D Valle, B Childs, K W Kinzler, B Vogelstein. McGraw Hill Book Co., New York, NY 2000; IV: 5345–5378
  • Benson M D, Liepnieks J, Uemichi T, Wheeler G, Correa R. Hereditary renal amyloidosis associated with a mutant fibrinogen A-chain. Nature Genet 1993; 3: 252–255
  • Ostertag B. Demonstration einer eigenartigen familiaren “Paramyloidose”. Zentralbl Allg Pathol 1932; 56: 253–254
  • Ostertag B. Familiere Amyloid-Erkrankung. Z Menschl Vererbungs Konstit Lehre 1950; 30: 105–115
  • Hamidi Asl L, Liepnieks J J, Uemichi T, Rebibou J -M, Justrabo E, Droz D, Mousson C, Chalopin J -M, Benson M D, Delpech M, Grateau G. Renal amyloidosis with a frame shift mutation in fibrinogen Aα-chain producing a novel amyloid protein. Blood 1997; 90: 4799–4805
  • Gillmore J D, Booth D R, Madhoo S, Pepys M B, Hawkins P N. Hereditary renal amyloidosis associated with variant lysozyme in a large English family. Nephrol Dial Transplant 1999; 11: 2639–2644
  • Persey R P, Booth D R, Booth S E, van Zyl-Smit R, Adams B K, Fattaarr A B, Tennent G A, Hawkins P M, Pepys M B. Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I. Kidney Int 1998; 53: 276–281
  • Benson M D, Liepnieks J J, Yazaki M, Yamashita T, Hamidi Asl K, Guenther B, Kluve-Beckerman B. A new human hereditary amyloidosis: the result of a stop-codon mutation in the apolipoprotein AII gene. Genomics 2001; 72: 272–277
  • Uemichi T, Liepnieks J J, Benson M D. Hereditary renal amyloidosis with a novel variant fibrinogen. J Clin Invest 1994; 93: 731–736
  • Hamidi Asl L, Fournier V, Billerey C, Justrabo E, Chevet D, Droz D, Pécheux C, Delpech M, Grateau G. Fibrinogen Aα chain mutation (Arg554Leu) associated with hereditary renal amyloidosis in a French family. Amyloid: Int J Exp Clin Invest 1998; 5: 279–284
  • Uemichi T, Liepnieks J J, Alexander F, Benson M D. The molecular basis of renal amyloidosis in Irish-American and Polish-Canadian kindreds. Q J Med 1996; 89: 745–750
  • Uemichi T, Liepnieks J J, Yamada T, Gertz M A, Bang N, Benson M D. A frame shift mutation in the fibrinogen Aα chain gene in a kindred with renal amyloidosis. Blood 1996; 87: 4197–4203
  • Koopman J, Haverkate F, Grimbergen J, Lord S T, Mosesson M W, DiOrio J P, Siebenlist K S, Legrand C, Soria J, Soria C, Caen J P. Molecular basis for fibrinogen Dusart (Aα 554 → Cys) and its association with abnormal fibrin polymerization and thrombophilia. J Clin Invest 1993; 91: 1637–1643
  • Gillmore J D, Booth D R, Rela M, Heaton N D, Rahman V, Stangou A J, Pepys M B, Hawkins P N. Curative hepatorenal transplantation in systemic amyloidosis caused by the Glu526Val fibrinogen α-chain variant in an English family. Q J Med 2000; 93: 269–275
  • Zeldenrust S, Gertz M, Uemichi T, Björnsson J, Wiesner R, Schwab T, Benson M D. Orthotopic liver transplantation for hereditary fibrinogen amyloidosis. Transplantation 2003; 75: 560–561
  • Blake C CF, Serpell L C. Synchrotron X-ray studies suggest that the core of the transthyretin amyloid fibril is a continuous β-sheet helix. Structure 1996; 4: 989–998
  • Sunde M, Serpell L C, Bartlam M, Fraser P E, Pepys M B, Blake C CF. Common core structure of amyloid fibrils by synchrotron X-ray diffraction. J Mol Biol 1997; 273: 729–739
  • Pras M, Schubert M, Zucker-Franklin D, Rimon A, Franklin E C. The characterization of soluble amyloid prepared in water. J Clin Invest 1968; 47: 924–933
  • Shirahama T, Cohen A S. High-resolution electron microscopic analysis of the amyloid fibril. J Cell Biol 1967; 33: 679–708
  • Damas A M, Sebastião M P, Domingues F S, Costa P P, Saraiva M J. Structural studies on FAP fibrils: removal of contaminants is essential for the interpretation of X-ray data. Amyloid: Int J Exp Clin Invest 1995; 2: 173–178
  • Makin O S, Serpell L C. X-ray diffraction studies of amyloid structure. Methods Mol Biol 2005; 299: 67–80
  • Petkova A T, Leapman R D, Guo Z, Yau W M, Mattson M P, Tycko R. Self-propagating, molecular-level polymorphism in Alzheimer's beta-amyloid fibrils. Science 2005; 307: 262–265
  • Makin O S, Serpell L C. Structures for amyloid fibrils. FEBS J 2005; 272: 5950–5961
  • Westermark P. Aspects on human amyloid forms and their fibril polypeptides. FEBS J 2005; 272: 5942–5949
  • Eanes E D, Glenner G G. X-ray diffraction studies on amyloid filaments. J Histochem Cytochem 1968; 16: 673–677
  • Hamilton J A, Benson M D. Review. Transthyretin: a review from a structural perspective. Cell Mol Life Sci 2001; 58: 1491–1521
  • Doolittle R F. Structural basis of the fibrinogen-fibrin transformation: contributions from X-ray crystallography. Blood Rev 2003; 17: 33–41
  • Yang Z, Kollman J M, Pandi L, Doolittle R F. Crystal structure of native chicken fibrinogen at 2.7 Å resolution. Biochemistry 2001; 40: 12515–12523

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.