Design, synthesis, and biological activity of a cyclic peptide: An inhibitor of HIV-1 tat–TAR interactions in human cells

Abstract

Replication of human immunodeficiency virus type 1 (HIV-1) requires specific interactions of Tat protein with the trans-activation responsive region (TAR) RNA, a 59-base stem-loop structure located at the 5′-end of all HIV mRNAs. A number of cyclic peptides are known to possess antibiotic activity and increased biological stability. Here we report the design, synthesis, and biological activity of a cyclic peptide (2 ), which inhibits transcriptional activation by Tat protein in human cells with an IC50 of ≈40 nM. Cyclic peptides that can target specific RNA structures provide a new class of small molecules that can be used to control cellular processes involving RNA–protein interactions in vivo.