Papers

3

Total Citations

85

H-Index

2

About

Gilles Labesse is a structural biologist whose research lies at the intersection of X-ray crystallography, protein engineering, and fragment-based drug design. His most impactful contribution is the development of an innovative in-plate protein crystallization method, coupled with in situ ligand soaking and X-ray diffraction, detailed in a 2011 paper that has garnered 78 citations. This technique streamlines the traditionally laborious process of protein crystal handling, enabling high-throughput screening of small-molecule ligands directly within crystallization plates. By automating the structural determination of protein-ligand complexes, Labesse’s work has significantly advanced fragment-based drug design, offering a more efficient pathway for identifying lead compounds. His broader research, reflected in works like "From Molecular Modeling to Drug Design" and "Fragment and Conquer," underscores a commitment to bridging computational modeling and experimental structural biology. Labesse’s contributions have not only enhanced the automation and throughput of crystallographic methods but also provided a practical toolkit for researchers aiming to accelerate drug discovery, making him a notable figure in the field of structural biology and medicinal chemistry.

Research Focus

Key Achievements

2
H-Index
3
Papers
85
Total Citations
28
Avg Citations/Paper
🏆 Most Cited Paper
In-plate protein crystallization,<i>in situ</i>ligand soaking and X-ray diffraction
78 citations · 2011
📈 Most Prolific Year: 2011 (1 Papers)
🤝 Key Collaborators: 10
🏛 Institutions: Centre National de la Recherche Scientifique, Université de Montpellier

Top Papers

  1. 1
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  3. 3

Key Collaborators

Contact & Links

Available for collaboration
Content generated · 13 days ago