Revealing protein structures: crystallization of protein‐ligand complexes – co‐crystallization and crystal soaking
Protein crystallogenesis represents a key step in X-ray crystallography studies that employ co-crystallization and ligand soaking for investigating ligand binding to proteins. Co-crystallization is a method that enables the precise determination of binding positions, although it necessitates a significant degree of optimization. The utilization of microseeding can facilitate a reduction in sample requirements and accelerate the co-crystallization process. Ligand soaking is the preferred method due to its simplicity; however, it requires careful control of soaking conditions to ensure the successful integration of the ligands. This research protocol details the procedures for co-crystallization and soaking to achieve protein-ligand complex formation, which is essential for advancing drug discovery. Additionally, a simple protocol for demonstrating soaking for educational purposes is described.
Authors
- Barbora Kaščáková (ORCID: https://orcid.org/0000-0003-2709-4142)
- Ivana Kutá Smatanová (ORCID: https://orcid.org/0000-0002-1337-9481)
- Petra Havlíčková (ORCID: https://orcid.org/0000-0001-7622-3129)
- Anna Koutská (ORCID: https://orcid.org/0009-0006-7071-1045)
- Michaela Burdová
Institutions
- University of South Bohemia in České Budějovice (CZ)
Publication Details
- Journal
- FEBS Open Bio
- Published
- 2024-10-20
- DOI
- https://doi.org/10.1002/2211-5463.13913
- Citations
- 6
- Primary Topic
- Enzyme Structure and Function
- Type
- article
- Field-Weighted Citation Impact
- 0.70
Funders
- Federation of European Biochemical Societies
- HORIZON EUROPE Framework Programme
- HORIZON EUROPE Research Infrastructures