Quantum Approximated Graph Cutting: A Rapid Replacement for T-REMD?
Samarth SandeepiD, Sona Aramyan, Armen H. PoghosyaniD, Vaibhav Gupta
Abstract
Determining an optimal protein configuration for the employment of protein binding analysis as completed by Temperature based Replica Exchange Molecular Dynamics (T-REMD) is an important process in the accurate depiction of a proteins behavior in different solvent environments, especially when determining a proteins top binding sites for use in protein-ligand and protein-protein docking studies. However, the completion of this analysis, which pushes out top binding sites through configurational changes, is an polynomial-state computational problem that can take multiple hours to compute, even on the fastest supercomputers. In this study, we aim to determine if graph cutting provide approximated solutions the MaxCut problem can be used as a method to provide similar results to T-REMD in the determination of top binding sites of Surfactant Protein A (SP-A) for binding analysis. Additionally, we utilize a quantum-hybrid algorithm within Iff Technologys Polar+ package using an actual quantum processor unit (QPU), an implementation of Polar+ using an emulated QPU, or Quantum Abstract Machine (QAM), on a large scale classical computing device, and an implementation of a classical MaxCut algorithm on a supercomputer in order to determine the types of advantages that can be gained through using a quantum computing device for this problem, or even using quantum algorithms on a classical device. This study found that Polar+ provides a dramatic speedup over a classical implementation of a MaxCut approximation algorithm or the use of GROMACS T-REMD, and produces viable results, in both its QPU and QAM implementations. However, the lack of direct configurational changes carried out onto the structure of SP-A after the use of graph cutting methods produces different final binding results than those produced by GROMACS T-REMD. Thus, further work needs to be completed into translating quantum-based probabilities into configurational changes based on a variety of noise conditions to better determine the accuracy advantage that quantum algorithms and quantum devices can provide in the near future.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 1
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Utilizing Quantum Biological Techniques on a Quantum Processing Unit for Improved Protein Binding Site Determination
Samarth Sandeep, Vaibhav Gupta, Torin Keenan·bioRxiv·Mar 20, 2020
- A Pipeline for Solving Edge-Matching Puzzles and Their Implications for Protein Folding
Shahar Seifer·bioRxiv·May 24, 2026
- Quantum analysis of protein-ligand binding by integrating structural resolution, sequence homology, and ligand properties
Don Roosan, Samira Samrose, … Brian A. Provencher·bioRxiv·Jun 27, 2025
- Quantum Chemistry in a Pocket: A Multifaceted Tool to Link Structure and Activity
Filipe Menezes, Valeria Napolitano, … Grzegorz M. Popowicz·bioRxiv·Apr 22, 2024
- Designing Peptides on a Quantum Computer
V. K. Mulligan, H. Melo, … R. Bonneau·bioRxiv·Mar 11, 2020
- Quantum and Classical Graph Convolutional Neural Networks for Protein Ligand Dissociation Constant Prediction
Azamat Salamatov, Jun Bai, … Chaowen Guan·bioRxiv·Nov 20, 2025