9KAS
Crystal structure of anti-sulfonylurea antibody scFv in complex with chlorpropamide
This is a non-PDB format compatible entry.
Summary for 9KAS
Entry DOI | 10.2210/pdb9kas/pdb |
Descriptor | anti-sulfonylurea antibody scFv, 1-(4-chlorophenyl)sulfonyl-3-propyl-urea (3 entities in total) |
Functional Keywords | antibody, immune system |
Biological source | Mus musculus |
Total number of polymer chains | 2 |
Total formula weight | 55552.86 |
Authors | |
Primary citation | Yu, X.,Zhou, T.,Pan, K.,Fan, M.H.,Yan, X.,Huang, X.A.,Zhang, H.,Shen, X.,Xie, H.,Gao, Y.G.,Lei, H. Structure Profiling of Broad-Specificity Immunoassays: Multitarget Recognition for Sulfonylurea Adulteration in Food. J.Agric.Food Chem., 73:9348-9358, 2025 Cited by PubMed Abstract: The limited understanding of the broad-specific antibody recognition mechanism significantly hinders the development of immunoassays for simultaneously detecting illegal adulterants. Herein, a recombinant antisulfonylureas (SUs) single-chain variable fragment (scFv), which retained the properties of its parental monoclonal antibody, was successfully generated. X-ray crystallography, molecular docking, functional assays, and mutation validation were used to investigate the structure-function relationships underlying antibody-SUs binding. Our study revealed three key mechanisms for broad specificity: (1) the conformational adaptability of the scFv, which enabled various SUs to access the binding pocket; (2) the role of the Trp98 residue in CDR-L3 in modulating binding affinities among multiple SUs; and (3) the design of haptens with common structures and more rigid R substituents, which emerged as a promising strategy for generating broad-specific antibodies. This study provides a comprehensive analysis of the broad-specific recognition mechanism, offering valuable insights for rational hapten design and targeted antibody evolution to advance multitarget immunoassays. PubMed: 40173361DOI: 10.1021/acs.jafc.5c00655 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.401 Å) |
Structure validation
Download full validation report
