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  1. IPB Halle
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    • Trenner 0
    • Molecular Signal Processing
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    • Publication (3)
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    • 2012 (3)
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  • 1

Publications

Weissenborn, M. J.; Castangia, R.; Wehner, J. W.; Šardzík, R.; Lindhorst, T. K.; Flitsch, S. L.; Oxo-ester mediated native chemical ligation on microarrays: an efficient and chemoselective coupling methodology Chem. Commun. 48 4444-4446 (2012) DOI: 10.1039/C2CC30844D
  • Abstract
  • BibText
  • RIS

We report a highly efficient and selective method for the coupling of peptides and glycoconjugates bearing N-terminal cysteines to activated surfaces. This chemoselective method generates stable amide linkages without using any thiol additives.

Publications

Weissenborn, M. J.; Wehner, J. W.; Gray, C. J.; Šardzík, R.; Eyers, C. E.; Lindhorst, T. K.; Flitsch, S. L.; Formation of carbohydrate-functionalised polystyrene and glass slides and their analysis by MALDI-TOF MS Beilstein J. Org. Chem. 8 753-762 (2012) DOI: 10.3762/bjoc.8.86
  • Abstract
  • BibText
  • RIS

Glycans functionalised with hydrophobic trityl groups were synthesised and adsorbed onto polystyrene and glass slides in an array format. The adsorbed glycans could be analysed directly on these minimally conducting surfaces by MALDI-TOF mass spectrometry analysis after aluminium tape was attached to the underside of the slides. Furthermore, the trityl group appeared to act as an internal matrix and no additional matrix was necessary for the MS analysis. Thus, trityl groups can be used as simple hydrophobic, noncovalently linked anchors for ligands on surfaces and at the same time facilitate the in situ mass spectrometric analysis of such ligands.

Publications

Wehner, J. W.; Weissenborn, M. J.; Hartmann, M.; Gray, C. J.; Šardzík, R.; Eyers, C. E.; Flitsch, S. L.; Lindhorst, T. K.; Dual purpose S-trityl-linkers for glycoarray fabrication on both polystyrene and gold Org. Biomol. Chem. 10 8919-8926 (2012) DOI: 10.1039/C2OB26118A
  • Abstract
  • BibText
  • RIS

There is a wide range of immobilisation reactions to tether substrates to a variety of surfaces for array-based analysis. Most of these immobilisation strategies are specific for a particular surface and require an additional linker to be attached to the substrate or the surface. Furthermore, the analysis of functionalised surfaces is often restricted to certain analytical techniques and therefore, different immobilisation strategies for different surfaces are desirable. Here we have tested an S-tritylated linker for non-covalent or covalent immobilisation of mannosides to polystyrene or gold surfaces. S-Tritylated mannosides with varying linkers were readily synthesised and used to add to biorepulsive maleimide-terminated preformed SAMs after in situ deprotection of the S-trityl group. In addition, S-tritylated mannosides themselves formed stable glycoarrays on polystyrene microtiter plates. The glycoarrays were successfully analysed by MALDI-ToF mass spectrometry, SPR spectroscopy, and interrogated with GFP-transfected Escherichia coli cells. This work has shown that a dual purpose linker can be used on multiple surfaces to form arrays allowing for different testing as well as analytical approaches.

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