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B1CTcu5:一种具有抗结核活性的蛙源 Brevinin-1 肽。

B1CTcu5: A frog-derived brevinin-1 peptide with anti-tuberculosis activity.

机构信息

Chemical Biology Laboratory, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram, 695014, India.

Mycobacterium Research Group, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram, 695014, India.

出版信息

Peptides. 2020 Oct;132:170373. doi: 10.1016/j.peptides.2020.170373. Epub 2020 Jul 15.

Abstract

Tuberculosis (TB) is a devastating infectious disease that causes a high rate of mortality. Drugs with new modes of action are needed to overcome this scenario. Cationic antibacterial peptides can serve as a potential alternative to existing TB drugs as they target the entire bacterial membrane for activity, thereby reducing the probability of development of drug resistance. In this study, we report anti-tuberculosis activity of B1CTcu5, a peptide that belongs to brevinin-1 family of antimicrobial peptides. This peptide possesses potent in vitro inhibitory activity against M. tuberculosis at 12.5 μg/mL but was not active against M. smegmatis. B1CTcu5 successfully eliminated intracellular mycobacteria without inducing cytotoxicity to the human macrophages at the concentrations tested. This peptide can be used as a template to design peptide-based anti-tubercular agents.

摘要

结核病(TB)是一种具有高死亡率的破坏性传染病。需要具有新作用模式的药物来克服这种情况。阳离子抗菌肽可以作为现有结核病药物的潜在替代品,因为它们针对整个细菌膜发挥作用,从而降低了耐药性发展的可能性。在这项研究中,我们报告了 B1CTcu5 的抗结核活性,B1CTcu5 是一种属于抗菌肽 brevinin-1 家族的肽。该肽在 12.5μg/ml 时对结核分枝杆菌具有很强的体外抑制活性,但对耻垢分枝杆菌没有活性。在测试的浓度下,该肽可以成功清除细胞内分枝杆菌而不诱导人巨噬细胞的细胞毒性。该肽可用作设计基于肽的抗结核剂的模板。

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