Version 2 2023-06-29, 18:05Version 2 2023-06-29, 18:05
Version 1 2023-06-20, 14:08Version 1 2023-06-20, 14:08
journal contribution
posted on 2023-06-29, 18:05authored byJerre
M. Madern, Jim Voorneveld, Johannes G. M. Rack, Hans A. V. Kistemaker, Ivan Ahel, Gijsbert A. van der Marel, Jeroen D. C. Codée, Dmitri V. Filippov
Adenosine diphosphate (ADP) ribosylation is an important
post-translational
modification (PTM) that plays a role in a wide variety of cellular
processes. To study the enzymes responsible for the establishment,
recognition, and removal of this PTM, stable analogues are invaluable
tools. We describe the design and synthesis of a 4-thioribosyl APRr
peptide that has been assembled by solid phase synthesis. The key
4-thioribosyl serine building block was obtained in a stereoselective
glycosylation reaction using an alkynylbenzoate 4-thioribosyl donor.