Published November 25, 2024 | Version v1
Journal article Open

ProteinReDiff: Complex-based ligand-binding proteins redesign by equivariant diffusion-based generative models

  • 1. FPT Software AI Center
  • 2. University of Chicago
  • 3. University of Alabama at Birmingham

Description

Proteins, serving as the fundamental architects of biological processes, interact with ligands to perform a myriad of functions essential for life. Designing functional ligand-binding proteins is pivotal for advancing drug development and enhancing therapeutic efficacy. In this study, we introduce ProteinReDiff, an diffusion framework targeting the redesign of ligand-binding proteins. Using equivariant diffusion-based generative models, ProteinReDiff enables the creation of high-affinity ligand-binding proteins without the need for detailed structural information, leveraging instead the potential of initial protein sequences and ligand SMILES strings. Our evaluations across sequence diversity, structural preservation, and ligand binding affinity underscore ProteinReDiff's potential to advance computational drug discovery and protein engineering.

Data availability

The data that support the findings of this study are available from the corresponding author upon reasonable request. The data that support the findings of this study are openly available in Ref. 106. ( V. T. D. Nguyen, N. D. Nguyen, and T. S. Hy (2024). "Complex-based ligand-binding proteins redesign by equivariant diffusion-based generative models," Cold Spring Harbor Laboratory. https://github.com/HySonLab/Protein_Redesign.)

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Additional details

Identifiers

DOI
10.1063/4.0000271
Other
oai:uchicago.tind.io:14236

UChicago Information

Division(s)
Pritzker School of Molecular Engineering