Computer modeling of fibrin polymerization kinetics correlated with electron microscope and turbidity observations: clot structure and assembly are kinetically controlled

• Published in: Biophysical journal 1992-07, Vol.63 (1), p.111-128
• Main Authors: Weisel, J.W., Nagaswami, C.
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Biophysical Phenomena; Biophysics; Blood Coagulation - physiology; Blood coagulation. Blood cells; Computer Simulation; Fibrin - chemistry; Fibrin - metabolism; Fibrin - ultrastructure; Fundamental and applied biological sciences. Psychology; General aspects, investigation methods, hemostasis, fibrinolysis; Humans; In Vitro Techniques; Kinetics; Microscopy, Electron, Scanning; Models, Biological; Molecular and cellular biology; Nephelometry and Turbidimetry; Platelet Factor 4 - pharmacology; Platelet Membrane Glycoproteins - metabolism; Polymers - metabolism; Thrombospondins
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1016/S0006-3495(92)81594-1

Although much is known about fibrin polymerization, because it is complex, the effects of various modifications are not intuitively obvious and many experimental observations remain unexplained. A kinetic model presented here that is based on information about mechanisms of assembly accounts for most experimental observations and allows hypotheses about the effects of various factors to be tested. Differential equations describing the kinetics of polymerization were written and then solved numerically. The results have been related to turbidity profiles and electron microscope observations. The concentrations of intermediates in fibrin polymerization, and fiber diameters, fiber and protofibril lengths have been calculated from these models. The simplest model considered has three steps; fibrinopeptide A cleavage, protofibril formation, and lateral aggregation of protofibrils to form fibers. The average number of protofibrils per fiber, which is directly related to turbidity, can be calculated and plotted as a function of time. The lag period observed in turbidity profiles cannot be accurately simulated by such a model, but can be simulated by modifying the model such that oligomers must reach a minimum length before they aggregate. Many observations, reported here and elsewhere, can be accounted for by this model; the basic model may be modified to account for other experimental observations. Modeling predicts effects of changes in the rate of fibrinopeptide cleavage consistent with electron microscope and turbidity observations. Changes only in the rate constants for initiation of fiber growth or for addition of protofibrils to fibers are sufficient to account for a wide variety of other observations, e.g., the effects of ionic strength or fibrinopeptide B removal or thrombospondin. The effects of lateral aggregation of fibers has also been modeled: such behavior has been observed in turbidity curves and electron micrographs of clots formed in the presence of platelet factor 4. Thus, many aspects of clot structure and factors that influence structure are directly related to the rates of these steps of polymerization, even though these effects are often not obvious. Thus, to a large extent, clot structure is kinetically determined.