Crystallographic fragment screening of CDK2-cyclin A: FragLites map sites of protein-protein interaction

Sites of protein-protein interaction (PPI) are potentially more selective binding sites for therapeutics than protein substrate-binding sites. PPIs include distinct regions frequently called "hotspots," sites of key amino acid interactions. Prospective identification of these hotspots through X-ray crystallographic screening could assist in the identification of separation of function mutants for experimental validation, enhance confidence in AI-generated multiprotein complex predictions, and accelerate development of selective chemical probes. To explore these applications, we utilize the FragLite library to examine the binding surfaces of CDK2-cyclin A. The many protein- and peptide-CDK2-cyclin A complexes that have been structurally characterized make this complex an appropriate test case. We show that FragLites comprehensively map both known sites of protein-protein interaction on CDK2-cyclin A and identify a possible uncharacterized site, providing a structural method toward directing mechanistic studies and starting points for chemical probe design.

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Publication Details

Journal
Structure
Published
2025-08-15
DOI
https://doi.org/10.1016/j.str.2025.07.016
Citations
3
Primary Topic
Cancer-related Molecular Pathways
Type
article
Field-Weighted Citation Impact
3.14
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article

Crystallographic fragment screening of CDK2-cyclin A: FragLites map sites of protein-protein interaction

Natalie J. Tatum, Mathew P. Martin, Jane Endicott, Ian Hope et al.
3 citations
Structure
Cancer-related Molecular Pathways
3.14
article

Crystallographic fragment screening of CDK2-cyclin A: FragLites map sites of protein-protein interaction

Natalie J. Tatum, Mathew P. Martin, Jane Endicott, Ian Hope, Michael J. Waring, M.E.M. Noble, Ziwei Jiang
article en
3 citations

Abstract

Sites of protein-protein interaction (PPI) are potentially more selective binding sites for therapeutics than protein substrate-binding sites. PPIs include distinct regions frequently called "hotspots," sites of key amino acid interactions. Prospective identification of these hotspots through X-ray crystallographic screening could assist in the identification of separation of function mutants for experimental validation, enhance confidence in AI-generated multiprotein complex predictions, and accelerate development of selective chemical probes. To explore these applications, we utilize the FragLite library to examine the binding surfaces of CDK2-cyclin A. The many protein- and peptide-CDK2-cyclin A complexes that have been structurally characterized make this complex an appropriate test case. We show that FragLites comprehensively map both known sites of protein-protein interaction on CDK2-cyclin A and identify a possible uncharacterized site, providing a structural method toward directing mechanistic studies and starting points for chemical probe design.

StructureVol. 33(11)
Newcastle University (GB)
Openalex Percentile: Top 7%
Cancer-related Molecular Pathways
3.14
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