Publication details for Professor Paul DennyBolt, H.L., Denny, P.W. & Cobb, S.L. (2016). An Efficient Method for the Synthesis of Peptoids with Mixed Lysine-type/Arginine-type Monomers and Evaluation of Their Anti-leishmanial Activity. Journal of Visualized Experiments 117: e54750.
- Publication type: Journal Article
- ISSN/ISBN: 1940-087X
- DOI: 10.3791/54750
- Further publication details on publisher web site
- Durham Research Online (DRO) - may include full text
Author(s) from Durham
This protocol describes the manual solid-phase synthesis of linear peptoids that contain two differently functionalized cationic monomers. In
this procedure amino functionalized 'lysine' and guanido functionalized 'arginine' peptoid monomers can be included within the same peptoid
sequence. This procedure uses on-resin (N-(1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl) or Dde protection, orthogonal conditions to the Boc
protection of lysine monomers. Subsequent deprotection allows an efficient on-resin guanidinylation reaction to form the arginine residues. The
procedure is compatible with the commonly used submonomer method of peptoid synthesis, allowing simple peptoids to be made using common
laboratory equipment and commercially available reagents. The representative synthesis, purification and characterization of two mixed peptoids
is described. The evaluation of these compounds as potential anti-infectives in screening assays against Leishmania mexicana is also described.
The protozoan parasite L. mexicana is a causative agent of cutaneous leishmaniasis, a neglected tropical disease that affects up to 12 million