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Cyclotide Structures Revealed by NMR, with a Little Help from X‐ray Crystallography
Author(s) -
Handley Thomas N. G.,
Wang Conan K.,
Harvey Peta J.,
Lawrence Nicole,
Craik David J.
Publication year - 2020
Publication title -
chembiochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.05
H-Index - 126
eISSN - 1439-7633
pISSN - 1439-4227
DOI - 10.1002/cbic.202000315
Subject(s) - structural motif , chemistry , disulfide bond , peptide , combinatorial chemistry , stereochemistry , crystallography , biochemistry
This review highlights the predominant role that NMR has had in determining the structures of cyclotides, a fascinating class of macrocyclic peptides found in plants. Cyclotides contain a cystine knot, a compact structural motif that is constrained by three disulfide bonds and able to resist chemical and biological degradation. Their resistance to proteolytic degradation has made cyclotides appealing as drug leads. Herein, we examine the developments that led to the identification and conclusive determination of the disulfide connectivity of cyclotides and describe in detail the structural features of exemplar cyclotides. We also review the role that X‐ray crystallography has played in resolving cyclotide structures and describe how racemic crystallography opened up the possibility of obtaining previously inaccessible X‐ray structures of cyclotides.