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The binding behaviours between cyclopentanocucurbit[6]uril and three amino acids

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...

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Detalles Bibliográficos
Autores principales: Cheng, Siyuan, Zhao, Weiwei, Yang, Xinan, Meng, Ye, Wei, Liantong, Tao, Zhu, Ma, Peihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8074881/
https://www.ncbi.nlm.nih.gov/pubmed/33959363
http://dx.doi.org/10.1098/rsos.202120
Descripción
Sumario: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.