BROAD-SPECTRUM ANTIMICROBIAL PEPTIDE FOR THE TREATMENT OF ACNE AND SKIN CANCER 
UCLA Technology Available For Licensing

BACKGROUND:  Conventional antibiotics are often used in the treatment of skin infections and inflammation. Topical and oral antibiotics are common in the treatment of acne, which is aimed at killing the Propionibacterium acnes, the bacteria linked to the pathogenesis of acne vulgaris. Erythromycin and tetracycline are frequently prescribed for reducing P. acnes, though the efficacy of antibiotics has been declining as the prevalence of this microbe has become widespread. Excessive utilization of antibiotics due to improper use and inaccurate diagnosis is contributing to microbes gaining resistance to conventional therapeutics. Due to random genetic mutations that occur from natural selection and evolution, microbes develop resistance genes that make it impervious to antibiotics, exposing many current compounds to obsolescence. The new generation of antimicrobial compounds must therefore eradicate microbes independent of its survival machinery, such as cell wall or RNA synthesis. Novel strategies for killing pathogenic cells can also yield alternative uses for treating other skin diseases.

INNOVATION:  Investigators at UCLA have modified the naturally occurring antimicrobial peptide, granulysin, which is known to possess antimicrobial activity against bacteria, parasites, and fungi. The length of the modified peptide has been shortened to 20 amino acids, yet it retains antimicrobial activity. A mutant of the peptide increases the in vitro cytotoxic activity to nearly 100x greater than wild-type granulysin. Crystal structure of the peptide suggests that it exerts its antimicrobial activity through a direct interaction with the microbial cell wall/membrane to increase permeability and induce lysis.

ADVANTAGES

APPLICATIONS:

DEVELOPMENT TO DATE:  In vitro studies have demonstrated that the modified peptide is effective in killing P. acnes. Various modifications have been tested to identify ones that produce the most cytolytic activity.

Related Papers (Selected)
  • McInturff JE, Wang SJ, Machleidt T, Lin TR, Oren A, Hertz CJ, Krutzik SR, Hart S, Zeh K, Anderson DH, Gallo RL, Modlin RL, Kim J. J Invest Dermatol. 2005 Aug;125(2):256-63. (Link)

Reference: UCLA Case Nos. 2005-351; 2004-087 Patent Applications: WO/2006/088945
WO/2005/026194

For additional technical details and current licensing
availability, please contact the following UCLA office:

UCLA Office of Intellectual Property
11000 Kinross Avenue, Suite #200
Los Angeles, CA 90095-7231
Tel: 310-794-0558 Fax: 310-794-0638
email: ncd@research.ucla.edu
NCD URL:   http://www.research.ucla.edu/tech/ucla05-351.htm

Lead Inventor: Jenny Kim

UCLA Technologies Available for Licensing
http://www.research.ucla.edu/tech

Copyright © 2003 The Regents of the University of California.

keywords: therapeutics antimicrobial acnes acne antibiotic resistant microbe peptide antiinflammatory inflammation skin cytolytic uclancd ucla technologies intellectual property patents technology transfer invention business card