ALDPI: adaptively learning importance of multi-scale topologies and multi-modality similarities for drug-protein interaction prediction.

Journal: Briefings in bioinformatics
Published Date:

Abstract

MOTIVATION: Effective computational methods to predict drug-protein interactions (DPIs) are vital for drug discovery in reducing the time and cost of drug development. Recent DPI prediction methods mainly exploit graph data composed of multiple kinds of connections among drugs and proteins. Each node in the graph usually has topological structures with multiple scales formed by its first-order neighbors and multi-order neighbors. However, most of the previous methods do not consider the topological structures of multi-order neighbors. In addition, deep integration of the multi-modality similarities of drugs and proteins is also a challenging task.

Authors

  • Kaimiao Hu
    School of Computer Science and Technology, Heilongjiang University, Harbin 150080, China.
  • Hui Cui
    Shanghai Center for Bioinformation Technology, Shanghai Academy of Science and Technology, 1278 Keyuan Road, Shanghai 201203, PR China; School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, PR China.
  • Tiangang Zhang
    School of Mathematical Science, Heilongjiang University, Harbin 150080, China. zhang@hlju.edu.cn.
  • Chang Sun
    Department of Gastroenterology, Changhai Hospital, Naval Medical University, Shanghai, China.
  • Ping Xuan
    School of Computer Science and Technology, Heilongjiang University, Harbin 150080, China.