Development of New Antimicrobial Peptides by Integrating Structural Motifs from Microbial-Derived Cyclic Lipopeptides

Microbial-derived cyclic-lipid antimicrobial peptides (CLAMPs) exhibit significant toxicity, which hinders their wide application in clinical practice. However, such AMPs generally possess high antimicrobial activity and high metabolic stability. The superiority of their molecular structures merits summarization and can be utilized in the design of novel AMPs. Therefore, a heptameric CLAMP template was designed from scratch in this study, with the general formula: R-Dab-(<i>x</i>)-<sup>D</sup>Tyr-<i>cyclo</i>[Lys-<i>y</i>-<i>y</i>-Trp-<i>z</i>-<i>z</i>-Glu]. Through modifying the <i>N</i>-terminal acyl group and amino acids at key positions inside and outside the ring, new CLAMPs with high antimicrobial activity, low toxicity, and high stability were screened out. Among these, the newly optimized CLAMPs, <b>CyLip-10</b> and <b>CyLip-20</b>, stand out for their broad-spectrum antimicrobial efficacy, low hemolytic activity, and excellent stability. Additionally, they have good safety and antimicrobial activity <i>in vivo</i>. In summary, designing novel CLAMPs based on those derived from microorganisms is feasible and effective.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-06-16
DOI
https://doi.org/10.1021/acs.jmedchem.5c00331
Citations
3
Primary Topic
Antimicrobial Peptides and Activities
Type
article
Field-Weighted Citation Impact
3.55

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article

Development of New Antimicrobial Peptides by Integrating Structural Motifs from Microbial-Derived Cyclic Lipopeptides

Zufang Ba, Xueting Liu, Pengyi Yan, Bingqian Ren et al.
3 citations
Journal of Medicinal Chemistry
Antimicrobial Peptides and Activities
3.55
article

Development of New Antimicrobial Peptides by Integrating Structural Motifs from Microbial-Derived Cyclic Lipopeptides

Zufang Ba, Xueting Liu, Pengyi Yan, Bingqian Ren, Tingting Yang, Sanhu Gou, Jingman Ni, Xu Ouyang, Yun Zhang, Hui Liu, Yu Wang, Beibei Li, Yao Liu, Chao Zhong, Yuhuan Zhao, Zhongwei Yu
article en
3 citations

Abstract

Microbial-derived cyclic-lipid antimicrobial peptides (CLAMPs) exhibit significant toxicity, which hinders their wide application in clinical practice. However, such AMPs generally possess high antimicrobial activity and high metabolic stability. The superiority of their molecular structures merits summarization and can be utilized in the design of novel AMPs. Therefore, a heptameric CLAMP template was designed from scratch in this study, with the general formula: R-Dab-(<i>x</i>)-<sup>D</sup>Tyr-<i>cyclo</i>[Lys-<i>y</i>-<i>y</i>-Trp-<i>z</i>-<i>z</i>-Glu]. Through modifying the <i>N</i>-terminal acyl group and amino acids at key positions inside and outside the ring, new CLAMPs with high antimicrobial activity, low toxicity, and high stability were screened out. Among these, the newly optimized CLAMPs, <b>CyLip-10</b> and <b>CyLip-20</b>, stand out for their broad-spectrum antimicrobial efficacy, low hemolytic activity, and excellent stability. Additionally, they have good safety and antimicrobial activity <i>in vivo</i>. In summary, designing novel CLAMPs based on those derived from microorganisms is feasible and effective.

Journal of Medicinal ChemistryVol. 68(12)
Macau University of Science and Technology (MO), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Lanzhou University (CN)
Lanzhou University, National Natural Science Foundation of China, Natural Science Foundation of Gansu Province, Chinese Academy of Medical Sciences, Program for Changjiang Scholars and Innovative Research Team in University
Openalex Percentile: Top 7%
Antimicrobial Peptides and Activities
3.55
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