Prof Leslie Hicks

MoSE 3201A
Tuesday, May 1, 2018 - 11:00am to 12:00pm

PepSAVI-MS for natural product bioactive peptide discovery

As current methods for antibiotic drug discovery are being outpaced by the rise of antimicrobial resistance, new methods and innovative technologies are crucial to replenish our dwindling arsenal of antimicrobial therapeutics. While natural products are a well-studied source of biologically active small molecules, peptidyl factors contributing to their medicinal properties remain largely unexplored. To this end, we have developed the PepSAVI-MS (Statistically-guided bioactive peptides prioritized via mass spectrometry) pipeline1 to identify bioactive peptide targets from complex biological samples. MS/MS techniques such as CID, ETD, UVPD are implemented for de novo characterization. To validate this pipeline, we have demonstrated successful detection and identification of a known antimicrobial peptide, cycloviolacin O2 (cyO2), from the botanical species Viola odorata. Additionally, we have widened the known antimicrobial spectrum for V. odorata cyclotides, including antibacterial activity of cyO2 against A. baumannii and novel anticancer activities for cycloviolacins by their cytotoxicity against ovarian, breast and prostate cancer cell lines. The developed platform is highly versatile as it is adaptable to any natural product source of peptides and can test against diverse physiological targets, including bacteria, fungi, viruses, protozoans, and cancer cells for which there is a developed bioassay. As such, we demonstrate extension of this pipeline to fungal and bacterially-sourced AMPs through the identification of the killer toxin KP4 from Ustilago maydis2 and the bacteriocin Bac-21 from Enterococcus faecalis harboring pPD1. Bac-21 is identical in nucleotide sequence to another enterococcal bacteriocin, AS-48, but we have experimentally validated the protein sequence of Bac-21 for the first time. Additionally, we begin to probe the vast array of botanical natural product sources to prioritize highly active species for downstream analysis.

Professional Background

Dr. Hicks received her B.S. in Chemistry at Marshall University (summa cum laude) and Ph.D. in Analytical Chemistry at the University of Illinois, Urbana-Champaign where she was the recipient of an NSF Graduate Research Fellowship. She was an Assistant Member and Principal Investigator at the Donald Danforth Plant Science Center and an adjunct professor in the Department of Biology at Washington University in St. Louis prior to assuming her current role as an assistant professor in the Department of Chemistry at UNC.


Contact Information: 

Host:  Prof Ronghu Wu (

Map of Georgia Tech

School of Chemistry & Biochemistry

901 Atlantic Drive Atlanta, GA 30332-0400

(404) 894-4002 (phone) | (404) 894-7452 (fax)