Vinyl sulfone functionalized silica: a ‘‘ready to use’’ pre-activated material for immobilization of biomolecules
Metadatos
Afficher la notice complèteAuteur
Ortega Muñoz, Mariano; Morales Sanfrutos, Julia; Megía Fernández, Alicia; López Jaramillo, Francisco Javier; Hernández Mateo, Fernando; Santoyo González, FranciscoEditorial
The Royal Society of Chemistry
Materia
Immobilization Silica vinyl sulfone
Date
2010Referencia bibliográfica
J. Mater. Chem., 2010, 20, 7189–7196
Patrocinador
Junta de Andalucía (P07-FQM-02899); Dirección General de Investigación Científica y Técnica (DGICYT) (CTQ2008-01754)Résumé
The combination of silica as support and vinyl sulfone as reactive group led to a pre-activated material
that readily reacts to form covalent bonds by Michael-type addition with both amine and thiol groups
naturally occurring in biomolecules in mild conditions compatible with the biological nature of the
enzymes. A simple two step synthetic strategy was designed to access this functionalized hybrid
material. Two types of vinyl sulfone silicas (N-type and S-type) differing in the chemical nature of the
linkers between the silica particle and the reactive vinyl sulfone group were prepared by implementation
of this strategy. The capabilities of those vinyl sulfone silicas were evaluated with the model enzymes
invertase, lactase and lysozyme. Both S-type and N-type vinyl sulfone silicas coupled efficiently with the
model enzymes even at 4 C by simple combination of the species and the immobilized enzymes retained
the enzymatic activity. The linker showed to play a major role in the non covalent interactions between
the enzymes and the silicas. In terms of capacity, the S-type material is the best option although its poor
flow rate when packed in columns invalidates its applications for low pressure liquid chromatography.
The capabilities of the N-type material were successfully put to the test as a pre-packed column for the
immobilization of invertase and further demonstrated with two real cases of relevance in proteomics: (i)
purification of glutathione-S-transferase (GST) and (ii) identification of proteins that interact with
thioredoxin h2 from Pisum sativum