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Bioorganic hybrid OMS by straightforward grafting of trialkoxysilyl peptides

A novel strategy for the synthesis of peptide-bioorganic hybrid silica materials is reported. It relies on the design of hybrid peptides bearing a trialkoxysilane group. These reactive monomers are covalently attached to silica without requiring any prior surface modification. As an example, a bioor...

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Published in:Journal of materials chemistry 2013-06, Vol.1 (23), p.2921-2925
Main Authors: Jebors, Said, Enjalbal, Christine, Amblard, Muriel, Mehdi, Ahmad, Subra, Gilles, Martinez, Jean
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Language:English
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cited_by cdi_FETCH-LOGICAL-c354t-e93ae23ba9b0895deb1b23f7ea67dd2631f1ccdd3ea1ae6989897500ebaf74b53
cites cdi_FETCH-LOGICAL-c354t-e93ae23ba9b0895deb1b23f7ea67dd2631f1ccdd3ea1ae6989897500ebaf74b53
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container_issue 23
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creator Jebors, Said
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description A novel strategy for the synthesis of peptide-bioorganic hybrid silica materials is reported. It relies on the design of hybrid peptides bearing a trialkoxysilane group. These reactive monomers are covalently attached to silica without requiring any prior surface modification. As an example, a bioorganic-inorganic OMS aldolisation catalyst is prepared using the peptide sequence Pro-Pro-Asp-Lys.
doi_str_mv 10.1039/c3tb20122h
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ispartof Journal of materials chemistry, 2013-06, Vol.1 (23), p.2921-2925
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source Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list)
subjects Bearing
Biology
Chemical Sciences
Covalence
Material chemistry
Monomers
Peptides
Silicon dioxide
Strategy
Synthesis
title Bioorganic hybrid OMS by straightforward grafting of trialkoxysilyl peptides
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