A new linker based on the dibenzosuberyl system was developed in order to synthesis¢ peptide Cterminal semicarbazones which can b¢ readily converted into peptide (7-terminal aldehydes. The method uses Fmoc-methodoiogy and proceeds with no loss of stereochemical integrity.
Solid-phase Synthesis and Cellular Localization of a C- and/or N-terminal Labelled Peptide
✍ Scribed by P. Vidal; L. Chaloin; J. Méry; N. Lamb; N. Lautredou; R. Bennes; F. Heitz
- Book ID
- 105360392
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 672 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1075-2617
- DOI
- 10.1002/psc.58
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✦ Synopsis
We report the solid-phase synthesis by the Fmoc strategy of a peptide containing a cysteamide group at its C-terminus. This peptide was subjected to further modifications including the linkage of fluorophores, namely lucifer yellow and coumarin respectively, at the C- and/or N-terminals. After incubation with living cultured cells these two probes were localized and it is concluded that the post-synthesis modifications can strongly modify the localization of the peptide.
📜 SIMILAR VOLUMES
The solid-phase syntheses of enkephalin and somatostatin analogues with C-terminal OH functions instead of the normal carboxylates are described. The OH function of the N-terminal amino alcohol was acylated with succinic acid and esterified to the solid support. Normal Boc-TFA solid-phase strategy c