Alternative Role of B/b Knob–Hole Interactions in the Fibrin Assembly

• Published in: Biochemistry (Easton) Vol. 64; no. 4; pp. 791 - 800
• Main Authors: Platonova, Tatyana, Hrabovskyi, Oleksii, Chernyshenko, Volodymyr, Stohnii, Yevhenii, Kucheriavyi, Yevhenii, Baidakova, Kateryna, Korolova, Daria, Urbanowicz, Anna, Komisarenko, Serhiy
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 18.02.2025
• Subjects: blood; computers; densitometry; electron microscopy; fibrin; Fibrin - chemistry; Fibrin - metabolism; Fibrin Fibrinogen Degradation Products - chemistry; Fibrin Fibrinogen Degradation Products - metabolism; Fibrinogen - chemistry; Fibrinogen - metabolism; gel chromatography; Humans; Models, Molecular; molecular dynamics; polyacrylamide gel electrophoresis; polymerization; turbidity
• ISSN: 0006-2960; 1520-4995; 1520-4995
• DOI: 10.1021/acs.biochem.4c00695

The self-assembly of fibrin is a vital process in blood clotting, primarily facilitated by the interactions between knobs “A” and “B” in the central E region of one molecule and the corresponding holes “a” and “b” in the peripheral D regions of two other fibrin molecules. However, the precise function of the interactions between knob “B” and hole “b” during fibrin polymerization remains a subject of ongoing debate. The present study focuses on investigating intermolecular interactions between knob “B” and hole “b”. We investigated the D–E–D interactions within the fibrin protofibril to accomplish this objective. Our investigation involved studying the formation of supramolecular complexes involving desAB fibrin with fibrin­(ogen) fragments, specifically the D-dimer and D fragment. The research utilized analytical size-exclusion chromatography, SDS-PAGE and densitometry of SDS-PAGE images, dynamic light scattering measurements, turbidity studies, electron microscopy, and computer modeling. Our findings indicate that the interference of the D fragment into classical D–E–D interaction occurs through knob “B” of the fibrin molecule. Molecular dynamics simulations elucidate the binding of only one D region, attributed to the shift of the D-dimer toward the fibrin desAB molecule. The formation of such a complex can be considered evidence supporting the potential mechanism of the branching of protofibrils. According to this theoretical mechanism, the inclusion of the D region from an external fibrin molecule into D–E–D interactions is facilitated through “B/b” contacts.