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On the Nature of Guest Complexation in Water: Triggered Wetting–Water-Mediated Binding

[Image: see text] The complexity of macromolecular surfaces means that there are still many open questions regarding how specific areas are solvated and how this might affect the complexation of guests. Contributing to the identification and classification of the different possible mechanisms of com...

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Detalles Bibliográficos
Autores principales: Suating, Paolo, Ernst, Nicholas E., Alagbe, Busayo D., Skinner, Hannah A., Mague, Joel T., Ashbaugh, Henry S., Gibb, Bruce C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059121/
https://www.ncbi.nlm.nih.gov/pubmed/35438501
http://dx.doi.org/10.1021/acs.jpcb.2c00628
Descripción
Sumario:[Image: see text] The complexity of macromolecular surfaces means that there are still many open questions regarding how specific areas are solvated and how this might affect the complexation of guests. Contributing to the identification and classification of the different possible mechanisms of complexation events in aqueous solution, and as part of the recent SAMPL8 exercise, we report here on the synthesis and conformational properties of TEEtOA 2, a cavitand with conformationally flexible ethyl groups at its portal. Using a combination of ITC and NMR spectroscopy, we report the binding affinities of a series of carboxylates to 2 and compare it to a related cavitand TEMOA 1. Additionally, we report MD simulations revealing how the wetting of the pocket of 2 is controlled by the conformation of its rim ethyl groups and, correspondingly, a novel triggered wetting, guest complexation mechanism, whereby the approaching guest opens up the pocket of the host, inducing its wetting and ultimately allows the formation of a hydrated host–guest complex (H·G·H(2)O). A general classification of complexation mechanisms is also suggested.