Subcell Biochem. 2026;113:413-473. doi: 10.1007/978-3-032-05273-5_13.
ABSTRACT
Fibrin is a fibrous biopolymer that plays a crucial role in hemostasis, thrombosis, wound healing, and various other biological functions and pathological conditions. The X-ray crystallographic structure of fibrinogen, along with computational reconstructions of missing regions and extensive biochemical and biophysical studies, has provided significant insights into the molecular mechanisms of fibrin formation, its structural organization, and its biological and mechanical properties. Upon cleavage of fibrinopeptides by thrombin, the blood protein fibrinogen is converted into fibrin monomers, which then interact through "knobs" exposed by the removal of fibrinopeptides in the central region and "holes" that are constitutively available at the ends of the molecules. The result is half-staggered, double-stranded oligomers that elongate into protofibrils, which then aggregate laterally to form fibers, and branch to create a three-dimensional network. Much has been learned about how the structure of fibrin contributes to the mechanical properties of the clot, including changes in fiber orientation, stretching, buckling, and the forced unfolding of molecular domains. Recent research into the mechanical stability of fibrin has enhanced our understanding of its rupture resistance, which is relevant to thrombotic embolization and mechanical thrombectomy. The fibrinolytic system, in which plasminogen, along with tissue-type plasminogen activator, binds to fibrin and is activated to plasmin, leads to the digestion of fibrin at specific lysine residues. Fibrin has been utilized in hemostatic fibrin sealants and as a biomaterial in tissue engineering and regenerative medicine. Despite significant advances in our understanding of these interconnected processes, much remains unknown about the molecular mechanisms underlying fibrin's biological functions, particularly concerning the molecular origins of its mechanical properties and the more complex structure and properties of hemostatic clots and pathological thrombi and their clinical implications.
PMID:41557239 | DOI:10.1007/978-3-032-05273-5_13