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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Score 3
2016 pubmed 117 citations

pH Dependent Antimicrobial Peptides and Proteins, Their Mechanisms of Action and Potential as Therapeutic Agents.

Malik. Erum E; Dennison. Sarah R SR; Harris. Frederick F; Phoenix. David A DA

Key Findings

  • pH‑dependent antimicrobial peptides are most active in acidic environments such as the skin.
  • LL‑37 has passed clinical trials and shows promise for wound healing, anti‑infection, and anti‑cancer uses.
  • These peptides are usually delivered topically via creams, mouthwashes, or hydrogel patches.

Practical Outcomes

  • For biohackers, LL‑37 could be explored as a topical skin‑care or wound‑healing agent, but there are no clear dosage guidelines yet. Look for commercially available LL‑37 creams or gels that have been tested for safety, and start with low‑frequency use while monitoring skin response.

Summary

This review talks about natural antibiotics called antimicrobial peptides that work best in acidic places like the skin. One of these peptides, LL‑37, has been tested in humans and can help heal wounds, fight infections, and even target some cancers when applied on the surface of the body.

Abstract

Antimicrobial peptides (AMPs) are potent antibiotics of the innate immune system that have been extensively investigated as a potential solution to the global problem of infectious diseases caused by pathogenic microbes. A group of AMPs that are increasingly being reported are those that utilise pH dependent antimicrobial mechanisms, and here we review research into this area. This review shows that these antimicrobial molecules are produced by a diverse spectrum of creatures, including vertebrates and invertebrates, and are primarily cationic, although a number of anionic examples are known. Some of these molecules exhibit high pH optima for their antimicrobial activity but in most cases, these AMPs show activity against microbes that present low pH optima, which reflects the acidic pH generally found at their sites of action, particularly the skin. The modes of action used by these molecules are based on a number of major structure/function relationships, which include metal ion binding, changes to net charge and conformational plasticity, and primarily involve the protonation of histidine, aspartic acid and glutamic acid residues at low pH. The pH dependent activity of pore forming antimicrobial proteins involves mechanisms that generally differ fundamentally to those used by pH dependent AMPs, which can be described by the carpet, toroidal pore and barrel-stave pore models of membrane interaction. A number of pH dependent AMPs and antimicrobial proteins have been developed for medical purposes and have successfully completed clinical trials, including kappacins, LL-37, histatins and lactoferrin, along with a number of their derivatives. Major examples of the therapeutic application of these antimicrobial molecules include wound healing as well as the treatment of multiple cancers and infections due to viruses, bacteria and fungi. In general, these applications involve topical administration, such as the use of mouth washes, cream formulations and hydrogel delivery systems. Nonetheless, many pH dependent AMPs and antimicrobial proteins have yet to be fully characterized and these molecules, as a whole, represent an untapped source of novel biologically active agents that could aid fulfillment of the urgent need for alternatives to conventional antibiotics, helping to avert a return to the pre-antibiotic era.

Study Information

Provider

pubmed

Year

2016

Date

2016-11-01T00:00:00.000Z

DOI

10.3390/ph9040067

Citations

117

References

333