Poster Session 3.W - Pharmaceutical Sciences and Health Technologies
Balogh, Olivér, MSc
HYKT8D
Semmelweis University Department of Pharmacology and Pharmacotherapy
06203685079
balogh.oliver.marton@semmelweis.hu
ProteGAN: a Generative, Self-Supervised Model with Edge-Level Attention for Network-Based Protein–Protein Interaction Prediction
Olivér M. Balogh1, Lóránt Sagát1, András Horváth2, Péter Ferdinandy1, Bence Ágg1
1: Department of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest
2: Faculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest
Poszter
Poster Session 3.W - Pharmaceutical Sciences and Health Technologies
English
Pharmaceutical Sciences and Health Technologies
Introduction
Exploring protein–protein interactions (PPIs) remains a challenging task of drug target discovery due to the time and cost restrains of experimental methods. Numerous in silico prediction tools have been proposed to aid the selection of likely candidate protein pairs. In our prior work (DOI: 10.1186/s12859-022-04598-x), we introduced a conditional generative adversarial network model for the efficient prediction of PPIs, relying solely on the topology of PPI networks.
Aims
Here, our aim was to expand our model architecture with transformer-inspired encoder blocks in order to further improve the performance of our model.
Methods
ProteGAN, the next iteration of our model now includes several encoder blocks before the convolutional u-net part, providing context-aware information via edge-level attention. Version 12 of the STRING (Search Tool for the Retrieval of Interacting Genes/Proteins) database was used as the primary source of networks for training ProteGAN. The area under the precision-recall curve (AUPRC) and the precision in the top 500 predictions (P@500) were used as performance metrics.
Results
Our evaluations on the available PPI networks reveal the importance of simple image preprocessing techniques and state of the art neural architectures. On the H. sapiens network, utilizing 0.7 confidence threshold, our old model achieved AUPRC: 0.092 and P@500: 0.260, while with image preprocessing techniques and encoder blocks it improved to AUPRC: 0.415 and P@500: 0.966.
Conclusion
In conclusion, here we introduce ProteGAN, a generative adversarial network outfitted with transformer-inspired encoder blocks for the prediction of PPIs based on the topology of the interactome. ProteGAN shows considerable performance improvements compared to our previous model and as such, could be a valuable tool for the high throughput prediction of candidate PPIs, contributing to a more efficient drug target identification process.
Funding
Project no. RRF-2.3.1-21-2022-00003 has been implemented with the support provided by the European Union. This study was supported by the 2024-1.2.3.-HU-RIZONT-2024-00026 and the 2025-2.1.1-EKÖP-2025-00014 New National Excellence Program of the Ministry for Culture and Innovation from the source of the National Research, Development and Innovation Fund. O.M.B. was supported by Semmelweis 250+ Excellence Fellowship.
Semmelweis University
Dr. Bence Ágg
I do not give consent to the publication of my abstract on the website of the congress.
in doctoral studies after complex exam (PhD)
Szabad
elfogadva
poszter
nem rendelkezett róla
7403
14:36
14:39