Transferable excited-state dynamics enable screening of fluorescent protein chromophores
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arXiv
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| Format: | Preprint |
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2026
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| _version_ | 1866910128860561408 |
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| author | Barrett, Rhyan Wesely, Sophia Westermayr, Julia |
| author_facet | Barrett, Rhyan Wesely, Sophia Westermayr, Julia |
| contents | Transferable excited-state dynamics offer a route to efficient screening of photophysical behavior across molecular systems, but conventional nonadiabatic simulations remain prohibitively expensive. Here we introduce X-MACE, a transferable machine-learning potential for excited-state dynamics that predicts multiple potential energy surfaces, forces and oscillator strengths, and combine it with curvature-driven surface hopping to enable data-efficient screening of photochemical pathways. We apply this framework to fluorescent chromophores as an example application, using green fluorescent protein chromophore variants to demonstrate how subtle structural modifications reshape excited-state relaxation, lifetimes and photoisomerization yields. Fine-tuning a single pretrained model with fewer than 100 reference geometries per derivative yields accurate dynamics across a chemically diverse set of analogues. The screening reveals two governing design principles: steric crowding on the phenolate ring lowers the torsional barrier and accelerates access to twisted conical intersections, whereas conjugation extension stabilizes planar excited-state configurations, suppresses non-radiative decay and prolongs fluorescence. More broadly, this workflow provides a general framework for scalable excited-state screening and interpretable design of photophysical properties. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2604_12699 |
| institution | arXiv |
| publishDate | 2026 |
| record_format | arxiv |
| spellingShingle | Transferable excited-state dynamics enable screening of fluorescent protein chromophores Barrett, Rhyan Wesely, Sophia Westermayr, Julia Chemical Physics Computational Physics Transferable excited-state dynamics offer a route to efficient screening of photophysical behavior across molecular systems, but conventional nonadiabatic simulations remain prohibitively expensive. Here we introduce X-MACE, a transferable machine-learning potential for excited-state dynamics that predicts multiple potential energy surfaces, forces and oscillator strengths, and combine it with curvature-driven surface hopping to enable data-efficient screening of photochemical pathways. We apply this framework to fluorescent chromophores as an example application, using green fluorescent protein chromophore variants to demonstrate how subtle structural modifications reshape excited-state relaxation, lifetimes and photoisomerization yields. Fine-tuning a single pretrained model with fewer than 100 reference geometries per derivative yields accurate dynamics across a chemically diverse set of analogues. The screening reveals two governing design principles: steric crowding on the phenolate ring lowers the torsional barrier and accelerates access to twisted conical intersections, whereas conjugation extension stabilizes planar excited-state configurations, suppresses non-radiative decay and prolongs fluorescence. More broadly, this workflow provides a general framework for scalable excited-state screening and interpretable design of photophysical properties. |
| title | Transferable excited-state dynamics enable screening of fluorescent protein chromophores |
| topic | Chemical Physics Computational Physics |
| url | https://arxiv.org/abs/2604.12699 |