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This research introduces a logarithmic-scale variational quantum eigensolver that significantly reduces qubit requirements for off-lattice protein structure prediction, overcoming the limitations of current on-lattice simulations. By mapping torsional degrees of freedom to relative phases in statevector simulations, the architecture enables all-atom modeling with exponentially fewer qubits while successfully recovering native-like structures on existing IBM hardware. Although challenges like energy-ranking imbalances persist, this approach establishes a scalable foundation for hybrid quantum-classical algorithms in biophysics.
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Logarithmic-scale variational quantum eigensolver for off-lattice protein structure prediction in continuous torsional angle space

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arXiv:2609.02113v1 Announce Type: new Abstract: Classical and current quantum approaches to protein structure prediction (QPSP) face limitations, notably massive qubit requirements restricting near-term models to simplistic on-lattice simulations. We propose a logarithmic-scale variational quantum eigensolver (VQE) that reduces qubit requirements for N torsional degrees of freedom to O(log2N), enabling off-lattice, all-atom simulations. Our architecture extracts molecular torsions from relative phases in statevector simulations. On quantum hardware, a decoder maps the empirical cumulative distribution function (CDF) from basis-state probabilities to bounded torsional variables. These feed a classical algorithm to build heavy-atom coordinates. We use an EfficientSU2 ansatz and multi-stage relaxation to mitigate barren plateaus. Structures are evaluated via a custom hybrid quantum-classical Hamiltonian, alongside Rosetta and OpenMM benchmarks. Evaluation on chignolin and Trp-cage yielded native-like conformations. Chignolin reached a 0.623 {\AA} C{\alpha} RMSD in retained snapshots and 1.199 {\AA} in final models; Trp-cage achieved a 2.501 {\AA} RMSD among snapshots (3.512 {\AA} in final models). Execution on IBM processors (ibm_cleveland, ibm_miami) successfully recovered native-like structures with a best RMSD of 1.758 {\AA}. The custom energy function performed best overall, though energy-ranking imbalances persisted across sampled landscapes for all functions. This introduces the first all-atom, continuous-space quantum algorithm for QPSP. By converting physical qubit constraints into circuit depth constraints, it proves high-resolution prediction is feasible with exponentially fewer qubits. Despite current limits like computational overhead and energy function sensitivity, it establishes a scalable foundation for hybrid quantum biophysics.

Abstract:Classical and current quantum approaches to protein structure prediction (QPSP) face limitations, notably massive qubit requirements restricting near-term models to simplistic on-lattice simulations. We propose a logarithmic-scale variational quantum eigensolver (VQE) that reduces qubit requirements for N torsional degrees of freedom to O(log2N), enabling off-lattice, all-atom simulations. Our architecture extracts molecular torsions from relative phases in statevector simulations. On quantum hardware, a decoder maps the empirical cumulative distribution function (CDF) from basis-state probabilities to bounded torsional variables. These feed a classical algorithm to build heavy-atom coordinates. We use an EfficientSU2 ansatz and multi-stage relaxation to mitigate barren plateaus. Structures are evaluated via a custom hybrid quantum-classical Hamiltonian, alongside Rosetta and OpenMM benchmarks. Evaluation on chignolin and Trp-cage yielded native-like conformations. Chignolin reached a 0.623 Å C{\alpha} RMSD in retained snapshots and 1.199 Å in final models; Trp-cage achieved a 2.501 Å RMSD among snapshots (3.512 Å in final models). Execution on IBM processors (ibm_cleveland, ibm_miami) successfully recovered native-like structures with a best RMSD of 1.758 Å. The custom energy function performed best overall, though energy-ranking imbalances persisted across sampled landscapes for all functions. This introduces the first all-atom, continuous-space quantum algorithm for QPSP. By converting physical qubit constraints into circuit depth constraints, it proves high-resolution prediction is feasible with exponentially fewer qubits. Despite current limits like computational overhead and energy function sensitivity, it establishes a scalable foundation for hybrid quantum biophysics.

Quantum Physics (quant-ph); Chemical Physics (physics.chem-ph)

arXiv:2609.02113 [quant-ph]

(or arXiv:2609.02113v1 [quant-ph] for this version)

https://doi.org/10.48550/arXiv.2609.02113 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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