Site-Selective Traceless Staudinger Ligation for Glycoprotein Synthesis Reveals Scope and Limitations

Making it traceless: A traceless Staudinger reaction between a specifically functionalized sugar phosphine and an azide‐tagged protein allows the construction of well‐defined reverse N‐linked glycoproteins (see scheme). This reaction was applied to different azidoprotein substrates and its potential...

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Veröffentlicht in:Chembiochem : a European journal of chemical biology 2011-06, Vol.12 (9), p.1383-1386
Hauptverfasser: Bernardes, Gonçalo J. L., Linderoth, Lars, Doores, Katie J., Boutureira, Omar, Davis, Benjamin G.
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container_issue 9
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container_title Chembiochem : a European journal of chemical biology
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creator Bernardes, Gonçalo J. L.
Linderoth, Lars
Doores, Katie J.
Boutureira, Omar
Davis, Benjamin G.
description Making it traceless: A traceless Staudinger reaction between a specifically functionalized sugar phosphine and an azide‐tagged protein allows the construction of well‐defined reverse N‐linked glycoproteins (see scheme). This reaction was applied to different azidoprotein substrates and its potentials and limitations are outlined.
doi_str_mv 10.1002/cbic.201100125
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subjects Aminobutyrates - chemistry
Azides - chemistry
glycoproteins
Glycoproteins - chemical synthesis
Glycoproteins - chemistry
Molecular Structure
Phosphines - chemistry
protein modification
Proteins - chemistry
Staudinger ligation
sugar phosphines
title Site-Selective Traceless Staudinger Ligation for Glycoprotein Synthesis Reveals Scope and Limitations
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