Literature DB >> 17487187

An efficient Mitsunobu protocol for the one-pot synthesis of S-glycosyl amino-acid building blocks and their use in combinatorial spot synthesis of glycopeptide libraries.

Thomas Ziegler1, Carsten Schips.   

Abstract

Complex glycosylation patterns on cell surfaces are involved in many fundamental biological processes like specific cell-cell interactions and signal transduction. Furthermore, the glycon part of glycopeptides and glycosylated proteins play a crucial role in numerous ligand-receptor interactions of biological significance. However, the distinct function of complex carbohydrate structures associated with cell surfaces and proteins is still only poorly understood at a molecular level with regard to specific carbohydrate-protein interaction. Here, we present an efficient Mitsunobu protocol for the convenient chemical one-pot preparation of S-glycosyl amino-acid building blocks suitable for automated combinatorial syntheses of highly glycosylated beta-peptides, which, in turn, can serve as potential mimics for complex oligosaccharides or for studying carbohydrate-protein interactions. The protocol also describes the use of the S-glycosyl amino-acid building blocks for combinatorial spot syntheses of glycopeptide libraries and can be used for the construction of other combinatorial peptide libraries as well. This is a procedure that can be completed in approximately 7 days.

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Year:  2006        PMID: 17487187     DOI: 10.1038/nprot.2006.307

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  5 in total

1.  Parallel Glyco-SPOT Synthesis of Glycopeptide Libraries.

Authors:  Akul Y Mehta; Ravi Kumar H Veeraiah; Sucharita Dutta; Christoffer K Goth; Melinda S Hanes; Chao Gao; Kathrin Stavenhagen; Robert Kardish; Yasuyuki Matsumoto; Jamie Heimburg-Molinaro; Michael Boyce; Nicola L B Pohl; Richard D Cummings
Journal:  Cell Chem Biol       Date:  2020-06-30       Impact factor: 8.116

2.  Synthesis of aromatic glycoconjugates. Building blocks for the construction of combinatorial glycopeptide libraries.

Authors:  Markus Nörrlinger; Thomas Ziegler
Journal:  Beilstein J Org Chem       Date:  2014-10-22       Impact factor: 2.883

3.  Efficient Method for the Concentration Determination of Fmoc Groups Incorporated in the Core-Shell Materials by Fmoc-Glycine.

Authors:  Elżbieta Szczepańska; Beata Grobelna; Jacek Ryl; Amanda Kulpa; Tadeusz Ossowski; Paweł Niedziałkowski
Journal:  Molecules       Date:  2020-09-01       Impact factor: 4.411

4.  Dimerization of propargyl and homopropargyl 6-azido-6-deoxy-glycosides upon 1,3-dipolar cycloaddition.

Authors:  Nikolas Pietrzik; Daniel Schmollinger; Thomas Ziegler
Journal:  Beilstein J Org Chem       Date:  2008-08-13       Impact factor: 2.883

5.  Synthesis and NMR studies of malonyl-linked glycoconjugates of N-(2-aminoethyl)glycine. Building blocks for the construction of combinatorial glycopeptide libraries.

Authors:  Markus Nörrlinger; Sven Hafner; Thomas Ziegler
Journal:  Beilstein J Org Chem       Date:  2016-08-30       Impact factor: 2.883

  5 in total

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