Issue 5, 2021

Effects of turn-structure on folding and entanglement in artificial molecular overhand knots

Abstract

The length and constitution of spacers linking three 2,6-pyridinedicarboxamide units in a molecular strand influence the tightness of the resulting overhand (open-trefoil) knot that the strand folds into in the presence of lanthanide(III) ions. The use of β-hairpin forming motifs as linkers enables a metal-coordinated pseudopeptide with a knotted tertiary structure to be generated. The resulting pseudopeptide knot has one of the highest backbone-to-crossing ratios (BCR)—a measure of knot tightness (a high value corresponding to looseness)—for a synthetic molecular knot to date. Preorganization in the crossing-free turn section of the knot affects aromatic stacking interactions close to the crossing region. The metal-coordinated pseudopeptide knot is compared to overhand knots with other linkers of varying tightness and turn preorganization, and the entangled architectures characterized by NMR spectroscopy, ESI-MS, CD spectroscopy and, in one case, X-ray crystallography. The results show how it is possible to program specific conformational properties into different key regions of synthetic molecular knots, opening the way to systems where knotting can be systematically incorporated into peptide-like chains through design.

Graphical abstract: Effects of turn-structure on folding and entanglement in artificial molecular overhand knots

Supplementary files

Article information

Article type
Edge Article
Submitted
26 okt 2020
Accepted
01 des 2020
First published
08 des 2020
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2021,12, 1826-1833

Effects of turn-structure on folding and entanglement in artificial molecular overhand knots

Y. Song, F. Schaufelberger, Z. Ashbridge, L. Pirvu, I. J. Vitorica-Yrezabal and D. A. Leigh, Chem. Sci., 2021, 12, 1826 DOI: 10.1039/D0SC05897A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements