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派昔加南(MSI-78)衍生类似物的相互作用可减轻炎症和TLR4介导的细胞因子分泌:一项比较研究。

Interaction of Pexiganan (MSI-78)-Derived Analogues Reduces Inflammation and TLR4-Mediated Cytokine Secretion: A Comparative Study.

作者信息

Cohen Hadar, Wani Naiem Ahmad, Ben Hur Daniel, Migliolo Ludovico, Cardoso Marlon H, Porat Ziv, Shimoni Eyal, Franco Octavio Luiz, Shai Yechiel

机构信息

Department of Biomolecular Sciences, The Weizmann Institute of Science, Rehovot 76100, Israel.

Departamento de Engenharia Sanitária e Ambiental, Universidade Católica Dom Bosco, Campo Grande 79117-900, Brazil.

出版信息

ACS Omega. 2023 May 12;8(20):17856-17868. doi: 10.1021/acsomega.3c00850. eCollection 2023 May 23.

Abstract

Antibiotic-resistant bacterial infections have increased the prevalence of sepsis and septic shock mortality worldwide and have become a global concern. Antimicrobial peptides (AMPs) show remarkable properties for developing new antimicrobial agents and host response modulatory therapies. A new series of AMPs derived from pexiganan (MSI-78) were synthesized. The positively charged amino acids were segregated at their N- and C-termini, and the rest of the amino acids created a hydrophobic core surrounded by positive charges and were modified to simulate the lipopolysaccharide (LPS). The peptides were investigated for their antimicrobial activity and LPS-induced cytokine release inhibition profile. Various biochemical and biophysical methods were used, including attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, microscale thermophoresis (MST), and electron microscopy. Two new AMPs, MSI-Seg-F2F and MSI-N7K, preserved their neutralizing endotoxin activity while reducing toxicity and hemolytic activity. Combining all of these properties makes the designed peptides potential candidates to eradicate bacterial infection and detoxify LPS, which might be useful for sepsis treatment.

摘要

抗生素耐药性细菌感染在全球范围内增加了败血症和感染性休克的死亡率,已成为全球关注的问题。抗菌肽(AMPs)在开发新型抗菌剂和宿主反应调节疗法方面表现出显著特性。合成了一系列源自派昔加南(MSI-78)的新型AMPs。带正电荷的氨基酸在其N端和C端被分隔开,其余氨基酸形成一个被正电荷包围的疏水核心,并进行了修饰以模拟脂多糖(LPS)。研究了这些肽的抗菌活性以及LPS诱导的细胞因子释放抑制情况。使用了各种生化和生物物理方法,包括衰减全反射傅里叶变换红外(ATR-FTIR)光谱、微尺度热泳(MST)和电子显微镜。两种新型AMPs,MSI-Seg-F2F和MSI-N7K,在降低毒性和溶血活性的同时保留了其对内毒素的中和活性。综合所有这些特性,使得所设计的肽成为根除细菌感染和使LPS解毒的潜在候选物,这可能对败血症治疗有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec42/10210221/7954f3ec47c4/ao3c00850_0002.jpg

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