1. N-Terminal Protein Binding and Disorder-to-Order Transition by a Synthetic Receptor.
- Author
-
Mockler NM, Ramberg KO, Flood RJ, and Crowley PB
- Subjects
- Crystallography, X-Ray, Protein Binding, Lectins chemistry, Lectins metabolism, Histones chemistry, Histones metabolism, Models, Molecular, Bacterial Proteins chemistry, Bacterial Proteins metabolism, Bacterial Proteins genetics, Protein Conformation, Calixarenes chemistry, Calixarenes metabolism, Ralstonia solanacearum chemistry, Ralstonia solanacearum metabolism
- Abstract
We describe the capture and structuring of disordered N-terminal regions by the macrocycle sulfonato-calix[4]arene ( sclx
4 ). Using the trimeric β-propeller Ralstonia solanacearum lectin (RSL) as a scaffold, we generated a series of mutants with extended and dynamic N-termini. Three of the mutants feature an N-terminal methionine-lysine motif. The fourth mutant contains the disordered 8-residue N-terminus of Histone 3, a component of the nucleosome. X-ray crystallography and NMR spectroscopy provide evidence for sclx4 binding to the flexible N-terminal regions. Three crystal structures reveal that the calixarene recognizes the N-terminal Met-Lys motif, capturing either residue. We provide crystallographic proof for sclx4 encapsulation of N-terminal methionine. Calixarene capture of intrinsically disordered regions may have applications in regulating protein secondary (and tertiary) structure.- Published
- 2025
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