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8DPY

Synthetic Beta Sheet Macrocycle Stabilized by Hydrogen Bond Surrogates

Summary for 8DPY
Entry DOI10.2210/pdb8dpy/pdb
Descriptorbeta sheet-forming peptide with flexible linker (2 entities in total)
Functional Keywordssynthetic peptide, beta sheet, de novo protein
Biological sourcesynthetic construct
Total number of polymer chains2
Total formula weight2867.26
Authors
Lu, B.,Vecchioni, S.,Nazzaro, A.,Arora, P.S. (deposition date: 2022-07-18, release date: 2023-05-24, Last modification date: 2024-10-09)
Primary citationNazzaro, A.,Lu, B.,Sawyer, N.,Watkins, A.M.,Arora, P.S.
Macrocyclic beta-Sheets Stabilized by Hydrogen Bond Surrogates.
Angew.Chem.Int.Ed.Engl., 62:e202303943-e202303943, 2023
Cited by
PubMed Abstract: Mimics of protein secondary and tertiary structure offer rationally-designed inhibitors of biomolecular interactions. β-Sheet mimics have a storied history in bioorganic chemistry and are typically designed with synthetic or natural turn segments. We hypothesized that replacement of terminal inter-β-strand hydrogen bonds with hydrogen bond surrogates (HBS) may lead to conformationally-defined macrocyclic β-sheets without the requirement for natural or synthetic β-turns, thereby providing a minimal mimic of a protein β-sheet. To access turn-less antiparallel β-sheet mimics, we developed a facile solid phase synthesis protocol. We surveyed a dataset of protein β-sheets for naturally observed interstrand side chain interactions. This bioinformatics survey highlighted an over-abundance of aromatic-aromatic, cation-π and ionic interactions in β-sheets. In correspondence with natural β-sheets, we find that minimal HBS mimics show robust β-sheet formation when specific amino acid residue pairings are incorporated. In isolated β-sheets, aromatic interactions endow superior conformational stability over ionic or cation-π interactions. Circular dichroism and NMR spectroscopies, along with high-resolution X-ray crystallography, support our design principles.
PubMed: 37170337
DOI: 10.1002/anie.202303943
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1 Å)
Structure validation

237735

數據於2025-06-18公開中

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