The binding behaviours between cyclopentanocucurbit[6]uril and three amino acids
Author(s) -
Siyuan Cheng,
Weiwei Zhao,
Xinan Yang,
Ye Meng,
Liantong Wei,
Zhu Tao,
Peihua Ma
Publication year - 2021
Publication title -
royal society open science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.84
H-Index - 51
ISSN - 2054-5703
DOI - 10.1098/rsos.202120
Subject(s) - isothermal titration calorimetry , cucurbituril , amino acid , lysine , glycine , leucine , chemistry , titration , alkyl , crystallography , stereochemistry , biochemistry , supramolecular chemistry , crystal structure , organic chemistry
Binding behaviours between cyclopentanocucurbit[6]uril (CyP 6 Q[6]) and three amino acids have been investigated by means of X-ray crystallography, proton nuclear magnetic resonance spectroscopy and isothermal titration calorimetry. The results showed that CyP 6 Q[6] forms a 1 : 2 inclusion complex with glycine, but 1 : 1 complexes with both leucine and lysine. Whereas the carboxyl group of glycine can enter the interior of the cavity of CyP 6 Q[6], only the alkyl chains of leucine and lysine can enter this cavity. Interestingly, leucine can adopt two different self-assembly modes upon its interaction with cucurbituril, depending on the external conditions, whereas glycine and lysine do not exhibit such behaviour.
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