Data-Driven Virtual Screening of Conformational Ensembles of Transition-Metal Complexes

Transition-metal complexes serve as highly enantioselective homogeneous catalysts for various transformations, making them valuable in the pharmaceutical industry. Data-driven prediction models can accelerate high-throughput catalyst design but require computer-readable representations that account for conformational flexibility. This is typically achieved through high-level conformer searches, followed by DFT optimization of the transition-metal complexes. However, conformer selection remains reliant on human assumptions, with no cost-efficient and generalizable workflow available. To address this, we introduce an automated approach to correlate CREST(GFN2-xTB//GFN-FF)-generated conformer ensembles with their DFT-optimized counterparts for systematic conformer selection. We analyzed 24 precatalyst structures, performing CREST conformer searches, followed by full DFT optimization. Three filtering methods were evaluated: (i) geometric ligand descriptors, (ii) PCA-based selection, and (iii) DBSCAN clustering using RMSD and energy. The proposed methods were validated on Rh-based catalysts featuring bisphosphine ligands, which are widely employed in hydrogenation reactions. To assess general applicability, both the precatalyst and its corresponding acrylate-bound complex were analyzed. Our results confirm that CREST overestimates ligand flexibility, and energy-based filtering is ineffective. PCA-based selection failed to distinguish conformers by DFT energy, while RMSD-based filtering improved selection but lacked tunability. DBSCAN clustering provided the most effective approach, eliminating redundancies while preserving key configurations. This method remained robust across data sets and is computationally efficient without requiring molecular descriptor calculations. These findings highlight the limitations of energy-based filtering and the advantages of structure-based approaches for conformer selection. While DBSCAN clustering is a practical solution, its parameters remain system-dependent. For high-accuracy applications, refined energy calculations may be necessary; however, DBSCAN-based clustering offers a computationally accessible strategy for rapid catalyst representations involving conformational flexibility.

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Publication Details

Journal
Journal of Chemical Theory and Computation
Published
2025-05-09
DOI
https://doi.org/10.1021/acs.jctc.5c00303
Citations
1
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
1.50

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article

Data-Driven Virtual Screening of Conformational Ensembles of Transition-Metal Complexes

Adarsh V. Kalikadien, Evgeny A. Pidko, Sára Finta
1 citations
Journal of Chemical Theory and Computation
Computational Drug Discovery Methods
1.50
article

Data-Driven Virtual Screening of Conformational Ensembles of Transition-Metal Complexes

Adarsh V. Kalikadien, Evgeny A. Pidko, Sára Finta
article en
1 citations

Abstract

Transition-metal complexes serve as highly enantioselective homogeneous catalysts for various transformations, making them valuable in the pharmaceutical industry. Data-driven prediction models can accelerate high-throughput catalyst design but require computer-readable representations that account for conformational flexibility. This is typically achieved through high-level conformer searches, followed by DFT optimization of the transition-metal complexes. However, conformer selection remains reliant on human assumptions, with no cost-efficient and generalizable workflow available. To address this, we introduce an automated approach to correlate CREST(GFN2-xTB//GFN-FF)-generated conformer ensembles with their DFT-optimized counterparts for systematic conformer selection. We analyzed 24 precatalyst structures, performing CREST conformer searches, followed by full DFT optimization. Three filtering methods were evaluated: (i) geometric ligand descriptors, (ii) PCA-based selection, and (iii) DBSCAN clustering using RMSD and energy. The proposed methods were validated on Rh-based catalysts featuring bisphosphine ligands, which are widely employed in hydrogenation reactions. To assess general applicability, both the precatalyst and its corresponding acrylate-bound complex were analyzed. Our results confirm that CREST overestimates ligand flexibility, and energy-based filtering is ineffective. PCA-based selection failed to distinguish conformers by DFT energy, while RMSD-based filtering improved selection but lacked tunability. DBSCAN clustering provided the most effective approach, eliminating redundancies while preserving key configurations. This method remained robust across data sets and is computationally efficient without requiring molecular descriptor calculations. These findings highlight the limitations of energy-based filtering and the advantages of structure-based approaches for conformer selection. While DBSCAN clustering is a practical solution, its parameters remain system-dependent. For high-accuracy applications, refined energy calculations may be necessary; however, DBSCAN-based clustering offers a computationally accessible strategy for rapid catalyst representations involving conformational flexibility.

Journal of Chemical Theory and ComputationVol. 21(10)
Delft University of Technology (NL)
Nederlandse Organisatie voor Wetenschappelijk Onderzoek, Janssen Biotech
Climate action
Openalex Percentile: Top 17%
Computational Drug Discovery Methods
1.50
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