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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 2
2022 pubmed 9 citations

Identification of heptapeptides targeting a lethal bacterial strain in septic mice through an integrative approach.

Zhang. Xiaoyan X; Li. Shan S; Luo. Haihua H; He. Shuyue S; Yang. Huangda H; Li. Lei L; Tian. Tian T; Han. Qizheng Q; Ye. Jiacong J; Huang. Chenyang C; Liu. Aihua A; Jiang. Yong Y

Key Findings

  • VTK‑LL37 binds the lethal E. coli strain with higher affinity than LL‑37 alone
  • VTK‑LL37 shows stronger bacteriostatic activity and blocks biofilm formation in vitro
  • In septic mice, VTK‑LL37 reduces bacterial load, lowers HMGB1 inflammation marker, protects organs, and improves survival

Practical Outcomes

  • The study suggests that adding a targeting sequence to antimicrobial peptides can markedly improve their anti‑infection power, which could guide future DIY peptide designs. However, it’s still animal research, so there’s no safe dosage or protocol for humans yet, and any self‑experimentation would be highly speculative and risky.

Summary

Researchers attached a short targeting piece (VTK) to the natural antimicrobial peptide LL‑37, creating VTK‑LL37. In lab tests and mouse sepsis models, this combo killed the harmful E. coli strain better than LL‑37 alone, stopped biofilm formation, lowered inflammation markers, and helped mice survive longer. The work is still early‑stage and not a ready‑to‑use treatment, but it shows that directing antimicrobial peptides to specific bugs can boost their effectiveness.

Abstract

Effectively killing pathogenic bacteria is key for the treatment of sepsis. Although various anti-infective drugs have been used for the treatment of sepsis, the therapeutic effect is largely limited by the lack of a specific bacterium-targeting delivery system. This study aimed to develop antibacterial peptides that specifically target pathogenic bacteria for the treatment of sepsis. The lethal bacterial strain Escherichia coli MSI001 was isolated from mice of a cecal ligation and puncture (CLP) model and was used as a target to screen bacterial binding heptapeptides through an integrative bioinformatics approach based on phage display technology and high-throughput sequencing (HTS). Heptapeptides binding to E. coli MSI001 with high affinity were acquired after normalization by the heptapeptide frequency of the library. A representative heptapeptide VTKLGSL (VTK) was selected for fusion with the antibacterial peptide LL-37 to construct the specific-targeting antibacterial peptide VTK-LL37. We found that, in comparison with LL37, VTK-LL37 showed prominent bacteriostatic activity and an inhibitive effect on biofilm formation in vitro. In vivo experiments demonstrated that VTK-LL37 significantly inhibited bacterial growth, reduced HMGB1 expression, alleviated lesions of vital organs and improved the survival of mice subjected to CLP modeling. Furthermore, membrane DEGP and DEGQ were identified as VTK-binding proteins by proteomic methods. This study provides a novel strategy for targeted pathogen killing, which is helpful for the treatment of sepsis in the era of precise medicine.

Study Information

Provider

pubmed

Year

2022

Date

2022-07-25T00:00:00.000Z

DOI

10.1038/s41392-022-01035-6

Citations

9

References

74