Investigation of glycofullerene dynamics by NMR spectroscopy

© The Royal Society of Chemistry 2015. Glycofullerenes, in which carbohydrate molecules are attached via a linker to a [60]fullerene core, facilitate spherical presentation of glyco-based epitopes. We herein investigate the dynamics of two glycofullerenes, having 12 and 36 mannose residues at their...

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Detalles Bibliográficos
Autores: Engstrom, O., Muñoz, Antonio, Illescas, Beatriz M., Martín, Nazario, Ribeiro-Viana, Renato, Rojo, Francisco Javier, Widmalm, G.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2015
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/122379
Acceso en línea:http://hdl.handle.net/10261/122379
Access Level:acceso abierto
Descripción
Sumario:© The Royal Society of Chemistry 2015. Glycofullerenes, in which carbohydrate molecules are attached via a linker to a [60]fullerene core, facilitate spherical presentation of glyco-based epitopes. We herein investigate the dynamics of two glycofullerenes, having 12 and 36 mannose residues at their periphery, by NMR translational diffusion and quantitative <sup>13</sup>C relaxation studies employing a model-free approach for their interpretation. The sugar residues are shown to be highly flexible entities with S<sup>2</sup> < 0.2 in both compounds. Notably, the larger glycofullerene with longer linkers shows faster internal dynamics and higher flexibility than its smaller counterpart. The dynamics and flexibility as well as the slower translational diffusion of the larger glycofullerene, thereby favoring rebinding to a receptor, may together with its spatial extension explain why it is better than the smaller one at blocking the DC-SIGN receptor and inhibiting the infection by pseudotyped Ebola virus particles.