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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 2
2013 pubmed

Structural and functional characterization of CATH_BRALE, the defense molecule in the ancient salmonoid, Brachymystax lenok.

Li. Zheng Z; Zhang. Songyan S; Gao. Jiuxiang J; Guang. Huijuan H; Tian. Yuanyong Y; Zhao. Zongmao Z; Wang. Yipeng Y; Yu. Haining H

Key Findings

  • CATH_BRALE is a 199‑amino‑acid cathelicidin from Brachymystax lenok with high arginine and glycine content and a six‑amino‑acid repeat (RPGGGS).
  • It is mainly produced in the fish gills, with lower levels in gut and spleen.
  • Synthetic CATH_BRALE strongly inhibits gram‑negative fish pathogens (Aeromonas salmonicida and A. hydrophila) with MICs as low as 9.38 mM, outperforming human LL‑37.

Practical Outcomes

  • The peptide shows promise as a potent antimicrobial, but it’s not ready for human or consumer use. Biohackers would need extensive safety, dosing, and delivery research before considering it in protocols. For now, it serves as a lead for developing new antimicrobial agents.

Summary

Scientists discovered a new antimicrobial peptide called CATH_BRALE from an ancient fish. It’s highly positively charged, has a unique repeat sequence, and kills gram‑negative bacteria better than the human peptide LL‑37 in lab tests. However, it’s only been studied in fish and in test‑tube experiments, so there’s no human safety or dosage info yet.

Abstract

Thick-lipped lenok, Brachymystax lenok is one of the ancient fish species in China and northeast Asia countries. Due to the overfishing, the population of lenok has been declined significantly. Cathelicidins are innate immune effectors that possess both bactericidal activities and immunomodulatory functions. This report identifies and characterizes the salmonoid cathelicidin (CATH_BRALE) from this ancient fish. It consists of open reading frame (ORF) of 886 bp encoding the putative peptide of 199 amino acids. Sequence alignment with other representative salmonid cathelicidins displayed two distinctive features of current lenok cathelicidin: high level of arginine, resulting in high positive charge and glycine residues, which is significantly different from most acknowledged types of cathelicidins; and the six-aminoacid tandem repeated sequence of RPGGGS detected in a variable number of copies among fish cathelicidins, suggesting the existence of a genetically unstable region similar to that found in some mammalian cathelicidins. Expression of CATH_BRALE is predominantly found in gill, with lower levels in the gastrointestinal tract and spleen. The homology modeled structure of CATH_BRALE exhibits structural features of antiparallel b-sheets flanked by a-helices that are representative of small cationic cathelicidin family peptides. CATH_BRALE possesses much stronger antimicrobial activity against gram-negative bacteria than that of the human ortholog, LL-37. The growth of two typical fish bacterial pathogens, gram-negative bacterium of Aeromonas salmonicida and Aeromonas hydrophila was substantially inhibited by synthetic CATH_BRALE, with both MICs as low as 9.38 mM.

Study Information

Provider

pubmed

Year

2013

DOI

10.1016/j.fsi.2012.07.004