Opportunity Overview
We will investigate the incorporation of geometric and physical constraints using constrained flow-matching. Generative models draw samples from a distribution to assess the likelihood match, but in protein-ligand binding mode prediction these distributions are typically single-point data obtained from co-crystallized complexes. We propose to develop more robust and generalizable methods by expanding our distributions using synthetic data, and will investigate samples drawn from (i) molecular dynamics trajectories, (ii) multiple binding modes produced by classical protein-ligand docking. We will also build on our recent results showing that data-guided regularization produces more accurate deep neural network models than standard regularization methods.
Supervised deep learning requires large amounts of expensive labelled data, but by exploiting contrastive learning using 3D-representations of protein-ligand complexes, we will develop fine-tuned self-supervised models that build on pre-trained models created using large unlabelled databases.
This interdisciplinary bioinformatics project cements links between industry and academia, spans multiple research areas within the EPSRC remit, and falls within the EPSRC's "Artificial intelligence technologies", "Biological informatics", "Chemical biology and...
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Start FreeSolicitation Details
| Issuing agency | EPSRC |
|---|---|
| Country | United Kingdom |
| Category | Research Development |
| Published | September 30, 2024 |
| Procurement stage | Active solicitation |
| Response due | March 30, 2028 |
| Status | Open — accepting responses |
| Official source | View original notice |
| Last verified | August 12, 2026 |
Source: UK Research and Innovation (UKRI) — Open Government Licence v3.0.
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