QuPepFold: A python package for hybrid quantum-classical protein folding simulations with CVaR-optimized VQE

Akshay Uttarkar, Vidya Niranjan, Amit Saxena and Vinay Kumar

PLOS ONE, 2026, vol. 21, issue 2, 1-20

Abstract: Background and Objective: Protein folding, and especially the conformational sampling of intrinsically disordered regions (IDRs), remains a formidable challenge for classical computation. We introduce QuPepFold, a modular Python package designed to democratize hybrid quantum–classical simulations of peptide folding, with the specific aim of enabling exploration of IDR ensembles for therapeutic targeting. Methods: We compute ground-state energies using a variational quantum eigensolver (VQE) that has been tuned with a conditional value-at-risk (CVaR) objective. This CVaR approach focuses on the lowest-energy measurement results, which speeds convergence and helps the algorithm cope with noise. The software provides an interface suitable for biologists and is independent of any particular quantum hardware; it currently runs on Qiskit Aer, Braket’s tensor-network simulator, and IonQ’s Aria-1 device through the Amazon Braket service. Results: In tests on short peptides up to ten amino acids long, the CVaR-optimized VQE reached the ground state roughly 30 percent faster than a standard VQE based on expectation values. When run on the IonQ Aria-1 quantum computer, it reproduced ground-state energies with over 90 percent fidelity. The agreement of results across simulators and physical devices indicates that the package yields consistent and transferable energies. Conclusions: QuPepFold offers an approachable yet extendable framework for integrating quantum techniques into peptide folding studies, particularly for sampling the ensembles of intrinsically disordered regions. By hiding the technical details of circuit construction and error mitigation, it lowers the barrier to using quantum computers in structural biology and opens opportunities for drug discovery against disordered proteins that have long been considered difficult to target.

Date: 2026
References: Add references at CitEc
Citations:

Downloads: (external link)
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0342012 (text/html)
https://journals.plos.org/plosone/article/file?id= ... 42012&type=printable (application/pdf)

Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.

Export reference: BibTeX RIS (EndNote, ProCite, RefMan) HTML/Text

Persistent link: https://EconPapers.repec.org/RePEc:plo:pone00:0342012

DOI: 10.1371/journal.pone.0342012

Access Statistics for this article

More articles in PLOS ONE from Public Library of Science
Bibliographic data for series maintained by plosone ().