Abstract
Side-chain oligo- and polyglutamylation represents an important posttranslational modification in tubulin physiology. The particular number of glutamate units is related to specific regulatory functions. In this work, we present a method for the synthesis of building blocks for the Fmoc synthesis of peptides containing main chain glutamic acid residues that carry side-chain branching with oligo-glutamic acid. The two model peptide sequences CYEEVGVDSVEGEG-E(E x)-EEGEEY and CQDATADEQG-E(E x)-FEEEEGEDEA from the C-termini of mammalian α1- and β1-tubulin, respectively, containing oligo-glutamic acid side-chain branching with lengths of 1 to 5 amino acids were assembled in good yield and purity. The products may lead to the generation of specific antibodies which should be important tools for a more detailed investigation of polyglutamylation processes. © 2010 Werner Tegge et al.
Cite
CITATION STYLE
Tegge, W., Bonafe, C. F. S., Teichmann, A., & Erck, C. (2010). Synthesis of peptides from α- And β-tubulin containing glutamic acid side-chain linked oligo-glu with defined length. International Journal of Peptides, 2010. https://doi.org/10.1155/2010/189396
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.