Accelerating drug discovery and repurposing by combining transcriptional signature connectivity with docking

We present an in silico approach for drug discovery, dubbed connectivity enhanced structure activity relationship (ceSAR). Building on the landmark LINCS library of transcriptional signatures of drug-like molecules and gene knockdowns, ceSAR combines cheminformatic techniques with signature concordance analysis to connect small molecules and their targets and further assess their biophysical compatibility using molecular docking. Candidate compounds are first ranked in a target structure-independent manner, using chemical similarity to LINCS analogs that exhibit transcriptomic concordance with a target gene knockdown. Top candidates are subsequently rescored using docking simulations and machine learning-based consensus of the two approaches. Using extensive benchmarking, we show that ceSAR greatly reduces false-positive rates, while cutting run times by multiple orders of magnitude and further democratizing drug discovery pipelines. We further demonstrate the utility of ceSAR by identifying and experimentally validating inhibitors of BCL2A1, an important antiapoptotic target in melanoma and preterm birth-associated inflammation.

Authors

Institutions

Publication Details

Journal
Science Advances
Published
2024-08-30
DOI
https://doi.org/10.1126/sciadv.adj3010
Citations
12
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
3.98
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Accelerating drug discovery and repurposing by combining transcriptional signature connectivity with docking

Maria Czyzyk-Krzeska, Marcin Pilarczyk, Yi Zheng, Rafał Adamczak et al.
12 citations
Science Advances
Computational Drug Discovery Methods
3.98
article

Accelerating drug discovery and repurposing by combining transcriptional signature connectivity with docking

Maria Czyzyk-Krzeska, Marcin Pilarczyk, Yi Zheng, Rafał Adamczak, Michal Kouril, Mehdi Fazel‐Najafabadi, Somchai Chutipongtanate, Robert E. McCullumsmith, William Seibel, Alexander W. Thorman, Mario Medvedovic, Ardythe L. Morrow, Nicolas Nassar, Sarah A. Hummel, David A. Hildeman, Surbhi Bhatnagar, Behrouz Shamsaei, Andrew B. Herr, James Reigle, Jarek Meller, Juechen Yang, Wen Niu
article en
12 citations

Abstract

We present an in silico approach for drug discovery, dubbed connectivity enhanced structure activity relationship (ceSAR). Building on the landmark LINCS library of transcriptional signatures of drug-like molecules and gene knockdowns, ceSAR combines cheminformatic techniques with signature concordance analysis to connect small molecules and their targets and further assess their biophysical compatibility using molecular docking. Candidate compounds are first ranked in a target structure-independent manner, using chemical similarity to LINCS analogs that exhibit transcriptomic concordance with a target gene knockdown. Top candidates are subsequently rescored using docking simulations and machine learning-based consensus of the two approaches. Using extensive benchmarking, we show that ceSAR greatly reduces false-positive rates, while cutting run times by multiple orders of magnitude and further democratizing drug discovery pipelines. We further demonstrate the utility of ceSAR by identifying and experimentally validating inhibitors of BCL2A1, an important antiapoptotic target in melanoma and preterm birth-associated inflammation.

Science AdvancesVol. 10(35)
Cincinnati Children's Hospital Medical Center (US), Mahidol University (TH), Veterans Health Administration (US), Cincinnati Health Department (US), Nicolaus Copernicus University (PL), Ramathibodi Hospital (TH), University of Cincinnati (US), University of Toledo (US), University of Cincinnati Medical Center (US)
Good health and well-being
Openalex Percentile: Top 6%
Computational Drug Discovery Methods
3.98
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.