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人抗菌肽的高效流动合成

Efficient flow synthesis of human antimicrobial peptides.

作者信息

Albin John S, Pentelute Bradley L

机构信息

Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139.

Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA 02114.

出版信息

Aust J Chem. 2020 Apr;73(4):380-388. doi: 10.1071/CH20043. Epub 2020 Apr 8.

DOI:10.1071/CH20043
PMID:32431323
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7236790/
Abstract

Organisms from all kingdoms of life have evolved a vast array of peptidic natural products to defend against microbes. These are known collectively as antimicrobial peptides (AMPs) or host defense peptides, reflecting their abilities to not only directly kill microbes, but also to modulate host immune responses. Despite decades of investigation, AMPs have yet to live up to their promise as lead therapeutics, a reality that reflects, in part, our incomplete understanding of these diverse agents in their various physiological contexts. Toward improving our understanding of AMP biology and the ways in which this can be best leveraged for therapeutic development, we are interested in large-scale comparisons of the antimicrobial and immunological activities of human AMPs, an undertaking that requires an efficient workflow for AMP synthesis and subsequent characterization. We describe here the application of flow chemistry and reverse phase flash chromatography to the generation of 43 AMPs, approaches that, when combined, significantly expedite synthesis and purification, potentially facilitating more systematic approaches to downstream testing and engineering.

摘要

来自生命各个王国的生物体已经进化出大量肽类天然产物来抵御微生物。这些统称为抗菌肽(AMPs)或宿主防御肽,这反映了它们不仅能直接杀死微生物,还能调节宿主免疫反应的能力。尽管经过了数十年的研究,抗菌肽尚未实现其作为先导疗法的承诺,这一现实部分反映了我们对这些多样的物质在其各种生理环境中的不完全理解。为了增进我们对抗菌肽生物学的理解以及如何最好地利用其进行治疗开发,我们对人类抗菌肽的抗菌和免疫活性进行大规模比较感兴趣,这一工作需要一个高效的抗菌肽合成及后续表征工作流程。我们在此描述了流动化学和反相快速色谱法在生成43种抗菌肽中的应用,这些方法结合使用时能显著加快合成和纯化速度,有可能促进更系统的下游测试和工程方法。

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本文引用的文献

1
Automated Flow Synthesis of Tumor Neoantigen Peptides for Personalized Immunotherapy.自动化合成肿瘤新抗原肽用于个性化免疫治疗。
Sci Rep. 2020 Jan 20;10(1):723. doi: 10.1038/s41598-019-56943-5.
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Chimeric peptidomimetic antibiotics against Gram-negative bacteria.针对革兰氏阴性菌的嵌合肽模拟抗生素。
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Design of stapled antimicrobial peptides that are stable, nontoxic and kill antibiotic-resistant bacteria in mice.设计稳定、无毒且能杀死小鼠体内耐药菌的订书钉型抗菌肽。
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Engineering Selectively Targeting Antimicrobial Peptides.工程靶向抗菌肽。
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Reassessing the Host Defense Peptide Landscape.重新评估宿主防御肽格局。
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An Efficient Method for the Expression and Purification of Aβ(M1-42).一种表达和纯化Aβ(M1-42)的高效方法。
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Antimicrobial Peptides: An Emerging Category of Therapeutic Agents.抗菌肽:一类新兴的治疗药物。
Front Cell Infect Microbiol. 2016 Dec 27;6:194. doi: 10.3389/fcimb.2016.00194. eCollection 2016.
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The immunology of host defence peptides: beyond antimicrobial activity.宿主防御肽的免疫学:超越抗菌活性。
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APD3: the antimicrobial peptide database as a tool for research and education.APD3:作为研究与教育工具的抗菌肽数据库
Nucleic Acids Res. 2016 Jan 4;44(D1):D1087-93. doi: 10.1093/nar/gkv1278. Epub 2015 Nov 23.
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Rapid flow-based peptide synthesis.快速流动的肽合成。
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