Search arXivSearch

arXiv · 2604.07844

Platelet plug microstructure and flow modulate fibrin gelation dynamics: Insights from computational simulations

Abstract

During the formation of a thrombus, the architecture of the growing platelet aggregate is heterogeneous, with areas of dense and loosely packed platelets. The surface of activated platelets facilitate biochemical coagulation reactions that ultimately result in the formation of a fibrin network which stabilizes the thrombus. How platelet-plug microstructure and flow jointly govern the onset and development of fibrin is incompletely understood. We developed a novel 2D computational framework that integrates (1) a pre-adhered, discrete platelet aggregate, (2) a reduced coagulation model that generates thrombin, and (3) a fibrin polymerization model. Three platelet-plug configurations were constructed with prescribed interplatelet gaps and simulations were performed with various wall shear rates. We quantified spatiotemporal clotting metrics, including coagulation factor concentrations, fibrin evolution, and gelation onset. Across geometries, gelation initiation accelerated with increasing plug density. For more dense geometries, gelation emerged first near the plug periphery. As the platelet density increased, intraplug transport was increasingly restricted and the thrombin concentrations in between platelets increased. In contrast, the loose plug supported fibrinogen replenishment deeper into the plug core. Despite slower coagulation initiation due to reduced platelet surface area, monomer generation persisted in the interior, causing gelation to begin at the vessel wall. These results suggest a mechanistic tradeoff: rapid sealing of the injured vessel wall by early platelet contraction, i.e. plug densification, may impede the intraplug fibrin formation needed for durable stabilization. The proposed model provides a basis for studies of platelet-coagulation interactions under flow, including therapeutic developments relevant to prevention of cardiovascular disease.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Janneke M. H. Cruts, Frank J. H. Gijsen, Aaron L. Fogelson, Anna C. Nelson. 2026-04-09. Platelet plug microstructure and flow modulate fibrin gelation dynamics: Insights from computational simulations. https://arxiv.org/abs/2604.07844

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

In Vivo Length Distributions as Mechanistic Fingerprints of Pathological Protein Aggregation

Modern imaging techniques can resolve individual pathological protein aggregates in postmortem human samples, providing detailed measurements of aggregate size distributions that are inaccessible with conventional bulk approaches. These distributions represent mechanistic fingerprints of the microscopic processes that generated the observed pathology, but extracting this mechanistic information requires a quantitative theoretical framework. Here, we develop the mathematical tools needed to interpret aggregate length distributions in living systems, where aggregate growth competes with active removal. We show that, across a class of models, the length distribution of sufficiently large aggregates approaches a geometric decay. Crucially, the decay rate is determined by the balance between aggregate elongation and removal, providing a direct quantitative readout of these competing processes from a single time point measurement. This enables mechanistic comparisons between healthy and diseased human samples without requiring longitudinal measurements of aggregate dynamics. We further analyse how additional aggregation and removal processes modify the observed length distributions. Together, these results establish the mathematical foundations and tools to use aggregate length distributions as an experimentally accessible route for inferring microscopic aggregation dynamics directly from human tissue.

q-bio.BM

Decoding enzyme-substrate interaction topology reveals principles underlying catalytic efficiency and mutational outcomes

The enzyme turnover number (kcat) defines catalytic efficiency and constrains quantitative models of metabolism, yet the molecular determinants governing kcat and its response to mutation remain poorly understood. Measurements are sparse and labor-intensive, and most computational approaches provide numerical predictions without explaining how enzyme-substrate interactions shape catalytic outcomes. A central challenge is therefore to identify the topological principles that determine where mutations act and how their functional outcomes are encoded within the enzyme-substrate interaction network. Here, we show that catalytic efficiency and mutational effects can be interpreted through enzyme-substrate interaction topology. We developed Interkcat, an interpretable bidirectional cross-attention framework that captures reciprocal coordination between protein residues and substrate atoms. Optimized on a unified benchmark, Interkcat achieves state-of-the-art predictive performance (R2 = 0.701). From its learned representations, we derive an Interaction Topology Score (ITS) that identifies sequence regions statistically enriched for mutation-sensitive sites without explicit structural inputs. We further demonstrate that higher-order topological features distinguish opposing mutational outcomes: lethal mutations disrupt coordinated networks, whereas activity-preserving or enhancing mutations retain sparse, globally organized coupling. These findings establish interaction topology as a unifying principle linking enzyme sequence, catalytic efficiency, and evolutionary perturbation.

q-bio.BM

Adapting Boltz-2 with limited experimental activity data improves early enrichment in virtual screening

Virtual screening aims to prioritize active compounds from large chemical libraries within a limited experimental budget. When applying Boltz-2 to virtual screening, a key challenge is how to use limited experimental data from the target assay to improve the prioritization of active compounds. We investigated whether fine-tuning the Boltz-2 affinity heads with a small number of binary activity labels could improve early enrichment of active compounds in hit discovery. We compared fine-tuning with 40-300 labels in a retrospective evaluation on eight MF-PCBA targets. With 300 activity measurements, fine-tuning increased the number of actives in the top 1% by a geometric mean of 1.77-fold across the eight targets and improved average precision (AP) by 2.14-fold relative to the control without fine-tuning. We also investigated whether rescoring a subset of candidates could retain the improvement in hit recovery by reranking only the top-ranked Boltz-2 candidates with the fine-tuned head. Restricting rescoring to approximately 10% of the evaluation set retained hit recovery comparable to full rescoring. These findings show that affinity-head fine-tuning with limited activity labels improves early enrichment with Boltz-2 and that this benefit can be retained when rescoring a restricted set of candidates.

q-bio.BM