Minimalistic peptides composed of d - and l -amino acids are attractive building blocks for functional supramolecular materials, including catalysts. d -Amino acids have long been known to promote turn conformations in peptides, yet unexpected twists continue to emerge on their effects on self-assembly. The combination of single-crystal X-ray diffraction and full-atom molecular dynamics have finally unraveled fine details of how l-d-l -tripeptides visit different conformations in solution and establish key interactions in supramolecular structures.

Self-Assembling l-d-l -Tripeptides Dance the Twist

Vargiu A. V.
;
2020-01-01

Abstract

Minimalistic peptides composed of d - and l -amino acids are attractive building blocks for functional supramolecular materials, including catalysts. d -Amino acids have long been known to promote turn conformations in peptides, yet unexpected twists continue to emerge on their effects on self-assembly. The combination of single-crystal X-ray diffraction and full-atom molecular dynamics have finally unraveled fine details of how l-d-l -tripeptides visit different conformations in solution and establish key interactions in supramolecular structures.
2020
Chirality; d -amino acids; Hydrogels; Peptides; Self-assembly
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11584/297050
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