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PMID: 6946434 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Structure of the fibrin protofibril.

Fowler WE, Hantgan RR, Hermans J, Erickson HP

Abstract

We identified the two-stranded fibrin protofibril and studied its structure in electron micrographs of negatively stained specimens. Based on these images and on considerations of symmetry, we constructed a model of the protofibril in which the two strands of trinodular fibrin molecules are related by a two-fold screw axis between the strands and two-fold axes perpendicular to them. The two strands are held together by staggered lateral contacts between the central nodules of one strand and outer nodules of the other. The molecules within a strand are joined by longitudinal contacts between outer nodules. This interpretation of the structure of protofibrils is supported by images of trimer complexes whose preparation and structure are described here, in which the central nodule of a fibrin monomer is attached to the crosslinked outer nodules of two other molecules. We conclude that the association of protofibrils to form thicker fibers must involve a second type of lateral contact, probably between outer nodules of adjacent, in-register strands. In total, we identify three intermolecular contacts involved in the polymerization of fibrin.

MeSH Terms
Fibrin Humans Macromolecular Substances Microscopy, Electron Models, Biological Protein Binding
Chemicals
Macromolecular Substances Fibrin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Fowler W E
Hantgan R R
Hermans J
Erickson H P
References (21)
21 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1981-08-00
Pages
4872-6
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC320279
Subset
IM
Grants
NHLBI NIH HHS · HL-20319 · United States
NHLBI NIH HHS · HL-23454 · United States
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