Sequence Representations and Their Utility for Predicting Protein-Protein Interactions

Protein-Protein Interactions (PPIs) are a crucial mechanism underpinning the function of the cell. So far, a wide range of machine-learning based methods have been proposed for predicting these relationships. Their success is heavily dependent on the construction of the underlying feature vectors, with most using a set of physico-chemical properties derived from the sequence. Few work directly with the sequence itself. In this paper, we explore the utility of sequence embeddings for predicting protein-protein interactions. We construct a protein pair feature vector by concatenating the embeddings of their constituent sequence. These feature vectors are then used as input to a binary classifier to make predictions. To learn sequence embeddings, we use two established Word2Vec based methods - Seq2Vec and BioVec - and we also introduce a novel feature construction method called SuperVecNW. The embeddings generated through SuperVecNW capture some network information in addition to the contextual information present in the sequences. We test the efficacy of our proposed approach on human and yeast PPI datasets and on three well-known networks: CD9, the Ras-Raf-Mek-Erk-Elk-Srf pathway, and a Wnt-related network. We demonstrate that low dimensional sequence embeddings provide better results than most alternative representations based on physico-chemical properties while offering a far simple approach to feature vector construction.

Automated summary

Protein-protein interactions play a crucial role in cell function. This paper explores the use of sequence embeddings to predict these interactions. The authors propose a method that constructs a feature vector by combining the embeddings of the constituent sequences. The results show that low dimensional sequence embeddings outperform alternative representations based on physico-chemical properties.