Astrochemistry

Spatial Confinement And Boundary Constraints Governing Biological Chirality: A Simulation Study

By Keith Cowing
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q-bio.OT
June 2, 2026
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Spatial Confinement And Boundary Constraints Governing Biological Chirality: A Simulation Study
Geometry-dependent collective stereochemical organization under varying compatibility and fluctuation conditions. Upper-left heatmap: final mean enantiomeric excess measured after 36 h across different compatibility strengths and stochastic fluctuation amplitudes. Upper-middle heatmap: the corresponding same-handed spatial agreement index, quantifying local stereochemical coherence among neighboring regions. Upper-right inset: relationship between spatial organization and global handedness, indicating increased stereochemical asymmetry in simulations with stronger same-handed spatial correlations. Lower-left inset: radial profile of local enantiomeric excess from the center toward the domain boundary, revealing spatial heterogeneity associated with geometrical constraints. Lower-middle inset: boundary-dependent compatibility bias field applied to the simulated domain, expressed as a local bias rate in h⁻¹. Lower-right inset: the final spatial organization of chiral domains after 36 h, highlighting the coexistence of spatially distinct stereochemical regions shaped by compatibility interactions and finite geometrical boundaries. — q-bio.OT

Biological systems exhibit marked molecular asymmetry, with proteins based predominantly on L-amino acids and nucleic acids and carbohydrates largely composed of D-sugars.

Explanations for homochirality include asymmetric photochemistry, autocatalytic amplification, stochastic symmetry breaking and mineral-surface stereoselectivity, but these mechanisms only partially address the influence of finite geometry and collective spatial interactions on stereochemical stabilization.

Inspired by recent developments in condensed-matter physics, we investigated whether coherent chirality could emerge from the interplay among nonlinear stereochemical amplification, stochastic fluctuations and boundary-dependent spatial constraints. We developed a reaction-diffusion simulation in which local stereochemical populations evolved within finite two-dimensional domains under spatial coupling and weak geometrical bias fields.

Our model combined bistable autocatalytic dynamics, nearest-neighbor interactions and suppression of locally inconsistent stereochemical configurations in order to quantify temporal evolution of enantiomeric excess, same-handed neighbor agreement and radial stereochemical organization under varying interaction strengths and fluctuation amplitudes.

Our results showed progressive formation of chiral domains, segregation of opposite-handed regions and geometry-dependent modulation of local stereochemical organization. Spatial coupling increased local coherence and modified persistence of mixed stereochemical states, while finite boundaries influenced radial organization and anisotropic stabilization of molecular populations.

Potential applications include geometrically controlled asymmetric synthesis, confined stereoselective catalytic systems, adaptive chiral materials and characterization of heterogeneous stereochemical distributions in microstructured reaction environments.

Arturo Tozzi

Comments: 10 pages, 2 figures
Subjects: Other Quantitative Biology (q-bio.OT)
Cite as: arXiv:2605.24582 [q-bio.OT] (or arXiv:2605.24582v1 [q-bio.OT] for this version)
https://doi.org/10.48550/arXiv.2605.24582
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Submission history
From: Arturo Tozzi
[v1] Sat, 23 May 2026 13:46:44 UTC (747 KB)
https://arxiv.org/abs/2605.24582

Astrobiology, Astrochemistry, Genomics,

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