Installation of Metal-Binding Functionality at Lysine Residues via Azide-Alkyne "Click Chemistry"
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Date
2015-04-29
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Authors
Baucom, Matthew
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Abstract
A novel non-natural amino acid designed to bind divalent metal ions, dubbed Lys(PYRIT), was prepared in a “click reaction” by treating Fmoc-Lys(N3)-OH with 2-ethynylpyridine and Cu(I). It was incorporated into a 12-residue peptide using standard Fmoc solid phase synthesis protocols. Multiple spectroscopic techniques (NMR, ESI-QToF-MS, UV-vis, and CD) confirm that the PYRIdinyl/Triazolyl side-chain binds Zn(II) and Cu(II) in the presence of competing natural residues such as histidine and glutamic acid. It remains unclear whether metal ions mediate the oligomerization of the Y2K PYRIT peptide, as is believed to be important in neurodegenerative diseases.
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Baucom, Matthew. (2015). Installation of Metal-Binding Functionality at Lysine Residues via Azide-Alkyne "Click Chemistry". Unpublished manuscript, Honors College, East Carolina University, Greenville, N.C.