bioRxivBiochemistry
Improved Accuracy for Modeling PROTAC-Mediated Ternary Complex Formation and Targeted Protein Degradation via New In Silico Methodologies
Michael L Drummond, Andrew Henry, Huifang Li, Christopher I Williams
Abstract
Extending upon our previous publication (Drummond and Williams, J. Chem. Inf. Model. 2019, 59, 1634), in this work two additional computational methods are presented to model PROTAC-mediated ternary complex structures, which are then used to predict the efficacy of any accompanying protein degradation. Method 4B, an extension to one of our previous approaches, incorporates a clustering procedure uniquely suited for considering ternary complexes. Method 4B yields the highest proportion to date of crystal-like poses in modeled ternary complex ensembles, nearing 100% in two cases and always giving a hit rate of at least 10%. Techniques to further improve this performance for particularly troublesome cases are suggested and validated. This demonstrated ability to reliably reproduce known crystallographic ternary complex structures is further established through modeling of a newly released crystal structure. Moreover, for the far more common scenario where the structure of the ternary complex intermediate is unknown, the methods detailed in this work nonetheless consistently yield results that reliably follow experimental protein degradation trends, as established through seven retrospective case studies. These various case studies cover challenging yet common modeling situations, such as when the precise orientation of the PROTAC binding moiety in one (or both) of the protein pockets has not been experimentally established. Successful results are presented for one PROTAC targeting many proteins, for different possible PROTACs targeting the same protein, and even for degradation effected by an E3 ligase that has not been structurally characterized in a ternary complex. Overall, the computational modeling approaches detailed in this work should greatly facilitate PROTAC screening and design efforts, so that the many advantages of a PROTAC-based degradation approach can be effectively utilized both rapidly and at reduced cost.
- assay: protein structure
- research focus: drug response / drug discovery
- approach: deep learning
- approach: statistical model
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
- PRosettaC: Rosetta based modeling of PROTAC mediated ternary complexes
D. Zaidman, N. London·bioRxiv·May 27, 2020
- Efficient Sampling of PROTAC-Induced Ternary Complexes
Hongtao Zhao, Stefan Schießer, … Werngard Czechtizky·bioRxiv·Oct 30, 2024
- Rationalizing PROTAC-mediated ternary complex formation using Rosetta
N. Bai, P. Kirubakaran, J. Karanicolas·bioRxiv·May 27, 2020
- P4ward: an automated modelling platformfor Protac ternary complexes
Paula Jofily, Subha Kalyaanamoorthy·bioRxiv·Nov 28, 2024
- Benchmarking PROTAC docking and virtual screening tools
Evianne Rovers, Matthieu Schapira·bioRxiv·Aug 30, 2023
- PROTAC-induced Protein Structural Dynamics in Targeted Protein Degradation
Kingsley Y Wu, T. I. Hung, Chia‐en A. Chang·eLifePeer-reviewed·Sep 6, 2024