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9OT9

Crystal structure of the Galectin-3 complex with FN3con-7, an mRNA display-derived binding protein

Summary for 9OT9
Entry DOI10.2210/pdb9ot9/pdb
DescriptorGalectin-3,FN3con-7 (2 entities in total)
Functional Keywordscarbohydrate binding biosensor, carbohydrate
Biological sourceHomo sapiens (human)
More
Total number of polymer chains1
Total formula weight30570.02
Authors
Primary citationMutschler, R.,Caputo, A.T.,Guo, Z.,Fiorito, M.M.,Hayat, I.F.,Newton, S.,Zhang, X.,Karunathilaka, N.,Duval, C.,Brazel, H.,Chan, W.,Kostner, K.,Korczyk, D.,Abankwa, D.K.,Atherton, J.J.,Coats, A.J.S.,Punyadeera, C.,Alexandrov, K.,Cui, Z.
Cooperative Binding Domains Enhance Sensitivity and Overcome the Hook Effect in Two-Component Protein Biosensors.
ACS Sens, 11:2870-2879, 2026
Cited by
PubMed Abstract: Protein biosensors are important tools in research, bioengineering, and diagnostics. Unlike fully integrated single-component biosensors, two-component biosensors are modular and can be rapidly adapted to new targets by replacing binding elements. However, their utility is limited by a "hook effect," where high analyte concentrations lead to dissociation of the signalling complex and signal loss. We address this challenge by utilizing sequential mRNA display selection campaigns to develop high-affinity, cooperative FN3con (monobody) binding domains to Galectin-3, a protein biomarker of heart failure. Two-component biosensors equipped with such cooperative binders were devoid of the hook effect and demonstrated 5-fold higher sensitivity to Galectin-3 compared to systems based on non-cooperative binding domains. High-resolution crystal structures of cooperative and non-cooperative binding domains revealed how interactions between the two domains establish a cooperative Galectin-3 binding interface. The results and experimental approaches presented in this work enable the construction of high-performance biosensors for diverse applications.
PubMed: 41801969
DOI: 10.1021/acssensors.6c00488
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.923 Å)
Structure validation

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