Virginia Tech. Department of ChemistryCenter for Drug DiscoveryZhang, WenyuBryson, David I.Crumpton, Jason B.Wynn, Jessica E.Santos, Webster L.2015-04-202015-04-202013-08-02Zhang, W., Bryson, D. I., Crumpton, J. B., Wynn, J., & Santos, W. L. (2013). Targeting folded RNA: a branched peptideboronic acid that binds to a large surface area of HIV-1 RRE RNA. Organic & Biomolecular Chemistry, 11(37), 6263-6271. doi: 10.1039/C3OB41053F1477-0520http://hdl.handle.net/10919/51701On-bead high-throughput screening of a medium-sized (1000_2000 Da) branched peptideboronic acid (BPBA) library consisting of 46 656 unique sequences against HIV-1 RRE RNA generated peptides with binding affinities in the low micromolar range. In particular, BPBA1 had a Kd of 1.4 _M with RRE IIB, preference for RNA over DNA (27 fold), and selectivity of up to >75 fold against a panel of RRE IIB variants. Structure_activity studies suggest that the boronic acid moiety and ͐branching in peptides are key structural features for efficient binding and selectivity for the folded RNA target. BPBA1 was efficiently taken up by HeLa and A2780 cells. RNA-footprinting studies revealed that the BPBA1 binding site encompasses a large surface area that spans both the upper stem as well as the internal loop regions of RRE IIB.application/pdfapplication/pdfen-USCreative Commons Attribution-NonCommercial 3.0 UnportedRibonucleic acid (RNA)Boronic acid groupsPeptidesArticle - Refereedhttp://pubs.rsc.org/en/content/articlelanding/2013/ob/c3ob41053fhttps://doi.org/10.1039/C3OB41053F