{
  "abstract": "Although ameliorative effects of molecular hydrogen (H₂) have been reported in a wide range of pathological conditions, it remained unresolved what molecular mechanism activates H₂ in animal cells, which lack the metal hydrogenases that dissociate the nonpolar, among-the-strongest-known H-H bond.Using first-principles calculations (geometries optimized with spin-unrestricted B3LYP-D3BJ/def2-SVP/CPCM, energies evaluated with ωB97M-V/def2-TZVPP) with active-site clusters of the Q-chamber of mitochondrial respiratory-chain Complex I (PDB 7QSK) and the Qo site of Complex III (PDB 1PP9), this study examined whether semiquinone could directly dissociate H₂ in the low-dielectric environment buried within the enzyme, and what changes when a conserved residue is added as a second hydrogen atom acceptor.At both sites, the anionic semiquinone Q• had no reaction pathway for cleaving ⁻ H-H, and only the neutral QH•, protonated by nearby residues, opened a homolytic hydrogen atom transfer (HAT) pathway with a well-defined transition state and a bound product.That the spin density on the transferring hydrogen shifts continuously from nearly 0 in the reactant to +0.99 for free H• confirmed at the electronic level that this is a true homolytic HAT, being neither proton transfer nor hydride transfer.The reaction energies (+21 to +26 kcal/mol) agree with an estimate from the difference between the bond dissociation free energies (BDFE) of the O-H bond of ubiquinol QH₂ and of the H-H bond that is broken.The same BDFE comparison also makes QH• a spin-allowed hydrogen-atom abstractor superior to superoxide by about 30 kcal/mol.For HAT with a single hydrogen atom acceptor the reaction energy of QH• + H₂ → QH₂ + H• is +28.3 kcal/mol, and the barrier cannot fall below that value.In the Q-chamber the conserved residue Tyr108 can act as a second acceptor, and for hydrogen atom transfer with H₂ held between QH• and TyrO• the barrier falls to +27.0 kcal/mol.However, this reactive QH• arises only under hyper-reductive pressure, where quinone-pool overreduction and high membrane potential coincide, upon occupation and protonation at the buried semiquinone reaction site.Therefore, H₂ dissociation itself is established only when the semiquinone reaction-site environment under hyper-reductive pressure is present as a necessary condition.Because H₂ has among the strongest σ bonds, the barrier is high and sharp, and quantum tunnelling makes a substantial contribution to crossing it at body temperature.At the onedimensional Eckart level that contribution does not exceed thermal activation, and it is obtained as a lower bound.The crossover temperatures, set by the imaginary frequency at the saddle, are 293.9K for Complex I and 264.7 K for Complex III.That the buried semiquinone reaction site makes a barrier against one of the strongest known σ bonds thin enough to bring the crossover temperature to within 16 K of body temperature is itself a quantitative result obtained here.The Marcus inverted region (bell-shaped kinetics) that we observed in solution in previous work shows that H₂ can be activated at all under metal-free conditions, but what tunnels there is the electron, along a coordinate distinct from the hydrogen nucleus analysed here.For the in-enzyme mechanism, the moderate primary isotope effect predicted at the same level (kH/kD ≈ 4) could be tested by detecting dissociated deuterium using D₂ as a tracer.Taken together, the above shifts the mechanistic account of H₂ medicine from classical antioxidant scavenging to redox regulation as a quantum-tunnelling-assisted conditional hydrogenase activity conditioned by reductive pressure, and positions it as a field of quantum biology.",
  "abstract_shown": true,
  "affiliations": [
    "Anicom Specialty Medical Institute (ASM",
    "Imabayashi Meiseikai Orthopedic Hospital",
    "Biotechnology Research Center and Department of Biotechnology",
    "Toyama Prefectural University"
  ],
  "article_type": null,
  "arxiv": null,
  "author_total": 2,
  "authors": [
    {
      "affs": [
        0,
        1
      ],
      "name": "Toru Ishibashi",
      "orcid": "0009-0001-7328-5524"
    },
    {
      "affs": [
        2,
        3
      ],
      "name": "Enjuro Harunari"
    }
  ],
  "bibtex": "https://research.draconitic.com/paper/9znvn605nzb85.bib",
  "cited_by": 0,
  "doi": "10.26434/chemrxiv.15006405/v2",
  "fulltext_url": null,
  "id": "9znvn605nzb85",
  "issns": [],
  "landing_url": "https://chemrxiv.org/doi/full/10.26434/chemrxiv.15006405/v2",
  "language": null,
  "licence": "CC-BY",
  "licence_label": "CC BY",
  "licence_source": "journal",
  "licence_url": "https://creativecommons.org/licenses/by/4.0/",
  "metadata_licence": null,
  "native_subjects": [
    [
      "openalex",
      "1604|Metal-Catalyzed Oxygenation Mechanisms"
    ]
  ],
  "openalex": "W7221150736",
  "pdf_url": "https://chemrxiv.org/doi/pdf/10.26434/chemrxiv.15006405/v2",
  "pmcid": null,
  "pmid": null,
  "published": "2026-10-09",
  "publisher": "American Chemical Society (ACS)",
  "ris": "https://research.draconitic.com/paper/9znvn605nzb85.ris",
  "sources": [
    {
      "first_seen": "2026-10-30T12:17:22Z",
      "native_id": "10.26434/chemrxiv.15006405",
      "source": "chemrxiv",
      "url": "https://chemrxiv.org/doi/full/10.26434/chemrxiv.15006405/v2"
    }
  ],
  "subjects": [
    {
      "field": "chemistry",
      "origin": "openalex:1604|Metal-Catalyzed Oxygenation Mechanisms",
      "subfield": "inorganic"
    }
  ],
  "title": "First-principles analysis of the metal-free H2 dissociation mechanism by semiquinone radicals in mitochondrial Complex I and III",
  "title_text": "First-principles analysis of the metal-free H2 dissociation mechanism by semiquinone radicals in mitochondrial Complex I and III",
  "type": "preprint",
  "updated_at": "2026-10-30T12:17:22Z",
  "url": "https://research.draconitic.com/paper/9znvn605nzb85",
  "venue": "ChemRxiv",
  "versions": [
    {
      "doi": "10.1039/d6cp02775j",
      "pid": null,
      "relation": "published-as",
      "title": null,
      "venue": null
    }
  ]
}