Bacterial resistance to antibiotics is a growing problem and even newly generated antibiotics are often ineffective against multi-drug resistant (MDR) bacteria. An increasing number of MDR bacterial infections are occurring in clinical settings, creating life threatening infections for patients already dealing with other conditions. This has driven the development of new antibiotics in an arms race of sorts between antibiotic development and bacterial resistance evolution, with antibiotic development lagging behind. However, a new class of antibiotics is being developed by mimicking a naturally occurring defense in many organisms known as AMPs. These AMP mimics are termed antimicrobial peptoids and work has indicated that they are potent in killing harmful bacteria, capable of disrupting bacterial biofilms, and relatively stable in the body. Although promising, the work in discovery of these antibiotics has been limited and slow, producing relatively few compounds. The overall goal of this project is to develop a screening method capable of rapidly identifying antimicrobial peptoids for nearly any type of bacteria. Specific work will involve the synthesis o libraries of antimicrobial peptoids on beads. These libraries will be screened in a unique method that allows for rapid identification of compounds capable of preventing bacterial growth. The structures of the best compounds from this screening will be determined by mass spectrometry and their antimicrobial properties characterized to determine how effective this method is at identifying potent antimicrobial agents. It is expected that completion of this proposal and the development of methods to screen large numbers of antimicrobial peptoids rapidly against nearly any bacteria will provide the ability to address dangerous MDR bacteria in a timely fashion.

Public Health Relevance

Bacterial resistance to antibiotics is a growing problem, necessitating antibiotics that act in unique ways. Antimicrobial peptoids are an emerging class of antibiotics that could serve to address this growing problem. The proposed research will develop methods for rapidly identifying antimicrobial peptoids for a wide range of bacteria.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Small Research Grants (R03)
Project #
5R03AI112861-02
Application #
9107813
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Xu, Zuoyu
Project Start
2015-07-10
Project End
2017-06-30
Budget Start
2016-07-01
Budget End
2017-06-30
Support Year
2
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Middle Tennessee State University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
077648780
City
Murfreesboro
State
TN
Country
United States
Zip Code
37132
Middleton, Madyson P; Armstrong, Scott A; Bicker, Kevin L (2018) Improved potency and reduced toxicity of the antifungal peptoid AEC5 through submonomer modification. Bioorg Med Chem Lett 28:3514-3519
Turkett, Jeremy A; Bicker, Kevin L (2017) Evaluating the Effect of Peptoid Lipophilicity on Antimicrobial Potency, Cytotoxicity, and Combinatorial Library Design. ACS Comb Sci 19:229-233
Fisher, Kevin J; Turkett, Jeremy A; Corson, Ashley E et al. (2016) Peptoid Library Agar Diffusion (PLAD) Assay for the High-Throughput Identification of Antimicrobial Peptoids. ACS Comb Sci 18:287-91