Your browser doesn't support javascript.
loading
Prioritizing Virtual Screening with Interpretable Interaction Fingerprints.
Fassio, Alexandre V; Shub, Laura; Ponzoni, Luca; McKinley, Jessica; O'Meara, Matthew J; Ferreira, Rafaela S; Keiser, Michael J; de Melo Minardi, Raquel C.
Affiliation
  • Fassio AV; São Carlos Institute of Physics, University of São Paulo, São Carlos, São Paulo 13563-120, Brazil.
  • Shub L; Department of Biochemistry and Immunology, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais 31270-901, Brazil.
  • Ponzoni L; Department of Pharmaceutical Chemistry, Department of Bioengineering & Therapeutic Sciences, Institute for Neurodegenerative Diseases, Kavli Institute for Fundamental Neuroscience, Bakar Computational Health Sciences Institute, University of California, San Francisco, San Francisco, California 9
  • McKinley J; Department of Pharmaceutical Chemistry, Department of Bioengineering & Therapeutic Sciences, Institute for Neurodegenerative Diseases, Kavli Institute for Fundamental Neuroscience, Bakar Computational Health Sciences Institute, University of California, San Francisco, San Francisco, California 9
  • O'Meara MJ; Gilead Sciences, Inc., Foster City, California 94404, United States.
  • Ferreira RS; Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Keiser MJ; Department of Biochemistry and Immunology, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais 31270-901, Brazil.
  • de Melo Minardi RC; Department of Pharmaceutical Chemistry, Department of Bioengineering & Therapeutic Sciences, Institute for Neurodegenerative Diseases, Kavli Institute for Fundamental Neuroscience, Bakar Computational Health Sciences Institute, University of California, San Francisco, San Francisco, California 9
J Chem Inf Model ; 62(18): 4300-4318, 2022 09 26.
Article in En | MEDLINE | ID: mdl-36102784
ABSTRACT
Machine learning-based drug discovery success depends on molecular representation. Yet traditional molecular fingerprints omit both the protein and pointers back to structural information that would enable better model interpretability. Therefore, we propose LUNA, a Python 3 toolkit that calculates and encodes protein-ligand interactions into new hashed fingerprints inspired by Extended Connectivity FingerPrint (ECFP) EIFP (Extended Interaction FingerPrint), FIFP (Functional Interaction FingerPrint), and Hybrid Interaction FingerPrint (HIFP). LUNA also provides visual strategies to make the fingerprints interpretable. We performed three major experiments exploring the fingerprints' use. First, we trained machine learning models to reproduce DOCK3.7 scores using 1 million docked Dopamine D4 complexes. We found that EIFP-4,096 performed (R2 = 0.61) superior to related molecular and interaction fingerprints. Second, we used LUNA to support interpretable machine learning models. Finally, we demonstrate that interaction fingerprints can accurately identify similarities across molecular complexes that other fingerprints overlook. Hence, we envision LUNA and its interface fingerprints as promising methods for machine learning-based virtual screening campaigns. LUNA is freely available at https//github.com/keiserlab/LUNA.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Proteins / Dopamine Type of study: Diagnostic_studies / Prognostic_studies / Screening_studies Language: En Year: 2022 Type: Article

Full text: 1 Database: MEDLINE Main subject: Proteins / Dopamine Type of study: Diagnostic_studies / Prognostic_studies / Screening_studies Language: En Year: 2022 Type: Article