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Development of novel LL-37 derived antimicrobial peptides with LPS and LTA neutralizing and antimicrobial activities for therapeutic application.

机译:具有LPS和LTA中和作用及抗菌活性的新型LL-37衍生抗菌肽的开发,可用于治疗应用。

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摘要

New peptides for lipopolysaccharide (LPS) and lipoteichoic acid (LTA) neutralization in upper respiratory tract infections were developed and evaluated in terms of efficacy and safety for application in humans. Based on the sequence of the human antimicrobial peptide LL-37 we developed and investigated length variants, substitution analogues and modifications to stabilize the peptides to prevent enzymatic degradation and to improve efficacy. The most promising peptide appears P60.4, a 24 amino acid peptide with similar efficacy as LL-37 in terms of LPS and LTA neutralization and lower pro-inflammatory activity. In addition, the acetylated and amidated version of this peptide shows no toxicity and displays higher or equal antimicrobial activity compared to LL-37.
机译:开发了用于中和上呼吸道感染的脂多糖(LPS)和脂磷壁酸(LTA)中和的新肽,并根据在人体中应用的功效和安全性进行了评估。基于人类抗微生物肽LL-37的序列,我们开发并研究了长度变体,取代类似物和修饰,以稳定该肽以防止酶促降解并提高功效。最有希望的肽是P60.4,它是一种24个氨基酸的肽,在LPS和LTA中和方面具有与LL-37相似的功效,并具有较低的促炎活性。另外,与LL-37相比,该肽的乙酰化和酰胺化形式没有毒性,并且显示出更高或相等的抗菌活性。

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