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#protein folding Open access

Deposit formation in TGFBI corneal dystrophy as interface-limited precipitation on a non-renewing layer: model code and digitised source data

Sep 2026 · Zenodo (CERN European Organization for Nuclear Research)

Abstract

Model code, digitised source data and figure scripts for a forward model of deposit formation in granular corneal dystrophy type 2 (TGFBI R124H), treated as precipitation of a slightly supersaturated protein in a curved, partly non-renewing tissue rather than as a protein-folding disease. The work has no experimental data of its own. Every clinical value it is tested against is published, and every such value used is included here under data/digitised/ with its source in the file header, so that the reading itself can be checked. The central claim is reproduced by src/_arrest_exponent.py from those two digitised files and nothing else: writing the deposit radius as a ~ t^n and granting the published erosion budget in full, the median admissible exponent across all fifteen pairs of the six published ages is -0.03; one pair admits n > 1/2 and none admits n = 1. No fitted constant, no assumed observation error and no commitment to a growth law enters that comparison. A held-out test is reproduced by src/_mouse_incidence.py against a mouse the model was never fitted to: two constants fixed on the heterozygote incidence curve determine the whole homozygote curve with no free parameter, and it lands within one standard error at all five reported ages. Its expectations were pre-registered before the calculation, in prereg/PREREG_mouse.md. Negative results are kept deliberately (see src/_kappa_lit.py and the notes under prereg/). Three scripts additionally require public single-cell datasets that are too large to deposit; each names the file it needs and where to obtain it. Related patent application: KR 10-2026-0170403.

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