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Updated: Aug 7, 2026

Split-and-pool Synthesis and Characterization of Peptide Tertiary Amide Library
Published on: June 20, 2014
Identification of synthetic phosphatidylserine translocases from a combinatorial library prepared by directed
Rameshwer Shukla1, Yoshihiro Sasaki, Viktor Krchnák
1Department of Chemistry and Biochemistry and the Walther Center for Cancer Research, University of Notre Dame, Notre Dame, Indiana 46556, USA.
Abstract:
Simple sulfonamide and amide derivatives of tris(2-aminoethyl)amine (Tren) are known to promote the translocation or flip-flop of phosphatidylcholine, but not phosphatidylserine, across bilayer membranes. This paper describes the synthesis of a 300-member, spatially encoded library of Tren derivatives with appended peptide--sulfonamide and peptide--urea arms. The library was synthesized using the Encore method with SynPhase lanterns as the solid support. A high-throughput assay was developed to screen individual members of the library for an ability to translocate a fluorescent NBD derivative of phosphatidylserine across vesicle membranes. Several lead compounds were identified, and one was synthesized independently to confirm its high phosphatidylserine translocation activity.

