Smart Integration of Structural Biology and Medicinal Chemistry to Unlock Target‐Driven Drug Discovery

To enhance drug discovery efforts, medicinal chemists should evaluate, filter, and utilize relevant structural information about target proteins. Acquiring and interpreting protein structures is crucial for elucidating ligand-receptor interactions and addressing ADME-related considerations, making it an essential aspect of medicinal chemistry. Proteins exhibit diverse structural organizations, and their conformational variability poses challenges for drug design. Here we draw from our own experience how advances in structural biology have improved medicinal chemists' access to 3D protein structures and dynamics, while stressing the need for model validation and refinement. To highlight the influence of structural biology on drug discovery, we present case studies. Structural insights into P-glycoprotein have been crucial in addressing multidrug resistance, while the analysis of the oncoprotein β-catenin provides valuable guidance for developing future therapeutic strategies based on innovative technology like targeted protein degradation. Finally, we report about multimeric complexes of proteins (Alsin and AP-4) involved in rare HSPs and the contribution of protein-protein interaction analyses to discover mutation-specific drugs.

Authors

Institutions

Publication Details

Journal
Medicinal Research Reviews
Published
2026-03-16
DOI
https://doi.org/10.1002/med.70038
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Smart Integration of Structural Biology and Medicinal Chemistry to Unlock Target‐Driven Drug Discovery

Giuseppe Ermondi, Giulia Apprato, Giulia Caron, Serena Francisco et al.
Medicinal Research Reviews
Protein Degradation and Inhibitors
article

Smart Integration of Structural Biology and Medicinal Chemistry to Unlock Target‐Driven Drug Discovery

Giuseppe Ermondi, Giulia Apprato, Giulia Caron, Serena Francisco, Matteo Rossi Sebastiano
article en

Abstract

To enhance drug discovery efforts, medicinal chemists should evaluate, filter, and utilize relevant structural information about target proteins. Acquiring and interpreting protein structures is crucial for elucidating ligand-receptor interactions and addressing ADME-related considerations, making it an essential aspect of medicinal chemistry. Proteins exhibit diverse structural organizations, and their conformational variability poses challenges for drug design. Here we draw from our own experience how advances in structural biology have improved medicinal chemists' access to 3D protein structures and dynamics, while stressing the need for model validation and refinement. To highlight the influence of structural biology on drug discovery, we present case studies. Structural insights into P-glycoprotein have been crucial in addressing multidrug resistance, while the analysis of the oncoprotein β-catenin provides valuable guidance for developing future therapeutic strategies based on innovative technology like targeted protein degradation. Finally, we report about multimeric complexes of proteins (Alsin and AP-4) involved in rare HSPs and the contribution of protein-protein interaction analyses to discover mutation-specific drugs.

Medicinal Research Reviews
University of Turin (IT)
Industry, innovation and infrastructure
Openalex Percentile: Top 20%
Protein Degradation and Inhibitors
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.