High-throughput selection of pathogen specific antimicrobials from random sequence peptide microarrays

Description

Antimicrobial resistance is one of the biggest healthcare challenges. Overuse and misuse of conventional antibiotics along with their broad spectra have triggered development of multi-drug resistant superbugs.

Researchers at Arizona State University have developed a novel process for producing alternative antimicrobial agents specific for any particular bacterial pathogen. The bacteria of interest are applied to an array of 10,000 random sequence peptides; combination of intracellular staining and membrane labeling of bacterial cells allows distinguishing between binding and lytic peptides directly from the array; active peptides are screened for specificity. This permits design of antibacterial synthetic antibodies that are targeted to specific bacteria without the broad toxicity of naturally-occurring antibacterial peptides.

This process has been demonstrated for E. coli O111:B4, Pseudomonas aeruginosa, Staphylococcus aureus, Streptococcus mutans, and Bacilus subtilis, but this system is generalizable to create antimicrobial agents with defined characteristics for any pathogen (bacterial, protozoan, fungal, yeast).

Potential Applications

High-throughput selection of antibacterial candidates specific for any particular pathogen Drug discovery Developing a treatment for antibiotic-resistant superbugs Developing a treatment for other pathogens like protozoa, fungi, yeast

Benefits and Advantages

  • High-throughput
  • Antimicrobial peptides have several advantages
  • relatively simple and inexpensive synthesis
  • Faster action due to external position of target molecules
  • few cases of developed resistance
  • selectivity for prokaryotic rather than eukaryotic cells
  • Protection of commensal flora
  • Possibility to develop a treatment for unknown pathogen in a case of invasion

For more information about the inventor(s) and their research, please see
Dr. Johnston's directory webpage

Case ID:
M12-025L
Published:
02-09-2012
Last Updated:
12-05-2018

Patent Information

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