# Fast and Slow Signal Propagation in Abiotic Polypeptide Assemblies

**Authors:** Panagiotis Mougkogiannis, Andrew Adamatzky

PMC · DOI: 10.1002/cbic.202500943 · Chembiochem · 2026-03-23

## TL;DR

Abiotic proteinoid microspheres show complex electrical behaviors, including oscillations and responses to light, which could inform prebiotic systems and bio-inspired computing.

## Contribution

Quantification of electrical dynamics and morphological diversity in abiotic proteinoid assemblies using novel analytical frameworks.

## Key findings

- Proteinoid microspheres exhibit rapid voltage oscillations and long-term drifts with correlated signals across electrodes.
- Optical stimulation induces reproducible voltage responses and stabilization in proteinoid networks.
- Diverse morphologies in mixed amino acid systems correlate with unique electrical signatures.

## Abstract

Proteinoid microspheres—abiotically synthesized by thermal polymerization of amino acids—exhibit spontaneous electrical potential fluctuations despite lacking genetic material, membranes, or ion channels. Here, we quantify the electrical and structural dynamics of five proteinoid compositions using multi‐electrode differential recordings and high‐resolution electron microscopy. The assemblies display rapid voltage oscillations (timescales ≪1 min), long‐timescale drifts (hours to days), exponential relaxation, and correlated potential shifts across spatially separated electrode pairs (Pearson correlations 0.147–0.601, significantly above baseline noise levels, r<0.05), suggesting composition‐dependent patterns of electrical coupling. Optical stimulation induces reproducible voltage responses characterized by logarithmic drift and stimulus‐specific stabilization, indicating that proteinoid networks can modulate electrical pathways in response to external perturbations. Morphological analysis reveals that single‐amino‐acid systems create uniform microspheres (2–3 μm). In contrast, mixed compositions lead to varied structures. These include hollow spheres, lamellar extensions, and crystalline aggregates that can reach 129 μm. Each structure shows unique electrical signatures. We develop a quantitative framework based on algorithmic complexity (Lempel–Ziv), spatial coherence (phase‐locking value), and graph‐theoretical metrics (global efficiency, clustering coefficient) to characterize emergent dynamics in these abiotic networks. These results show that proteinoid assemblies have unique electrical properties based on their composition. This may help us understand prebiotic organization and inspire new types of bioinspired computing materials.

Proteinoid microspheres formed by thermal polymerization of amino acids exhibit spontaneous electrical potential fluctuations without genetic material, membranes, or ion channels. Multi‐electrode recordings and electron microscopy reveal composition‐dependent voltage oscillations, long‐term drifts, and correlated signals across electrodes. Optical stimulation produces reproducible responses and stabilization. Diverse microsphere morphologies show distinct electrical signatures, supporting emergent electrical coupling in abiotic networks.© 2026 WILEY‐VCH GmbH

## Full-text entities

- **Genes:** CHDH (choline dehydrogenase) [NCBI Gene 55349], CLTC (clathrin heavy chain) [NCBI Gene 1213] {aka CHC, CHC17, CLH-17, CLTCL2, Hc, MRD56}, TCFL5 (transcription factor like 5) [NCBI Gene 10732] {aka CHA, E2BP-1, Figlb, SOSF1, bHLHe82}, ASPM (assembly factor for spindle microtubules) [NCBI Gene 259266] {aka ASP, Calmbp1, MCPH5}, RMRP (RNA component of mitochondrial RNA processing endoribonuclease) [NCBI Gene 6023] {aka CHH, NME1, RMRPR, RRP2}, GYPA (glycophorin A (MNS blood group)) [NCBI Gene 2993] {aka CD235a, GPA, GPErik, GPSAT, HGpMiV, HGpMiXI}, BCAR1 (BCAR1 scaffold protein, Cas family member) [NCBI Gene 9564] {aka CAS, CAS1, CASS1, CRKAS, P130Cas}
- **Diseases:** seizure (MESH:D012640)
- **Chemicals:** polymers (MESH:D011108), L-Lys (MESH:D008239), L-Phe (MESH:D010649), Regime I (-), hydrogen (MESH:D006859), methane (MESH:D008697), silicon (MESH:D012825), L- (MESH:D007930), dipeptide (MESH:D004151), amino acid (MESH:D000596), acid (MESH:D000143), Glu (MESH:D018698), carbon (MESH:D002244), aromatic amino acid (MESH:D024322), L-Arg (MESH:D001120), Pt (MESH:D010984), L-Aspartic acid (MESH:D001224), ammonia (MESH:D000641), nitrogen (MESH:D009584), Ir (MESH:D007495), Water (MESH:D014867)
- **Species:** Badhamia polycephala (species) [taxon 5791], Chlamydomonas (genus) [taxon 3052], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Armillaria (genus) [taxon 47424], C. elegans [taxon 328850], Homo sapiens (human, species) [taxon 9606], PX clade (clade) [taxon 569578], Mimosa pudica (sensitive-plant, species) [taxon 76306]
- **Mutations:** C to H, Phe-Lys, PHE-LYS

## Full text

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## Figures

22 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13007495/full.md

## References

96 references — full list in the complete paper: https://tomesphere.com/paper/PMC13007495/full.md

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Source: https://tomesphere.com/paper/PMC13007495