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首页> 外文期刊>Journal of peptide science: An official publication of the European Peptide Society >A review on anti-tuberculosis peptides: Impact of peptide structure on anti-tuberculosis activity
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A review on anti-tuberculosis peptides: Impact of peptide structure on anti-tuberculosis activity

机译:抗结核肽的综述:肽结构对抗结核活动的影响

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摘要

Antibiotic resistance is a major public health problem globally. Particularly concerning amongst drug-resistant human pathogens is Mycobacterium tuberculosis that causes the deadly infectious tuberculosis (TB) disease. Significant issues associated with current treatment options for drug-resistant TB and the high rate of mortality from the disease makes the development of novel treatment options against this pathogen an urgent need. Antimicrobial peptides are part of innate immunity in all forms of life and could provide a potential solution against drug-resistant TB. This review is a critical analysis of antimicrobial peptides that are reported to be active against the M tuberculosis complex exclusively. However, activity on non-TB strains such as Mycobacterium avium and Mycobacterium intracellulare, whenever available, have been included at appropriate sections for these anti-TB peptides. Natural and synthetic antimicrobial peptides of diverse sequences, along with their chemical structures, are presented, discussed, and correlated to their observed antimycobacterial activities. Critical analyses of the structure allied to the anti-mycobacterial activity have allowed us to draw important conclusions and ideas for research and development on these promising molecules to realise their full potential. Even though the review is focussed on peptides, we have briefly summarised the structures and potency of the various small molecule drugs that are available and under development, for TB treatment.
机译:全球抗生素抗性是一个主要的公共卫生问题。特别是在耐药性人病原体中是结核分枝杆菌,导致致命传染性结核病(TB)疾病。与抗药性结核病的当前治疗方案相关的重要问题和来自该疾病的高死亡率使得对这种病原体的新型治疗方案的发展迫切需要。抗微生物肽是各种类型的先天免疫的一部​​分,可以提供针对耐药TB的潜在溶液。本综述是对据报道的抗微生物肽专门针对M结核症复合物有效的抗微生物肽的关键分析。然而,每当可用时,可在可用的情况下包括非TB菌株的非TB菌株,例如可用的途径和分枝杆菌的菌株。讨论,讨论了各种序列的天然和合成抗微生物肽,以及其化学结构,并与其观察到的抗致细菌活性相关。缔结抗分泌活动的结构的批判性分析使我们能够为这些有希望的分子进行研究和开发的重要结论和想法,以实现其全部潜力。尽管审查侧重于肽,但我们简要概述了可在开发和正在开发的各种小分子药物的结构和效力,用于结核病治疗。

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