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小分子靶向 microRNAs 调控宿主-寄生虫相互作用。

Modulation of Host-Parasite Interactions with Small Molecules Targeting microRNAs.

机构信息

Institute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, 81675Munich, Germany.

Center for Global Health, TUM School of Medicine, Technical University of Munich, 81675Munich, Germany.

出版信息

ACS Infect Dis. 2022 Oct 14;8(10):2028-2034. doi: 10.1021/acsinfecdis.2c00360. Epub 2022 Sep 13.

Abstract

Parasites use different strategies of communication with their hosts. One communication channel that has been studied in recent years is the use of vesicle microRNAs to influence the host immune system by trematodes. sma-microRNA-10, secreted from , has been shown to influence the fate of host T-cells through manipulation of the NF-κB pathway. We have identified low molecular weight tool compounds that can interfere with this microRNA-mediated manipulation of the host immune system. We used a fragment-based screening approach by means of nuclear magnetic resonance (NMR) to identify binders to the precursor of the parasite sma-microRNA-10 present in their extracellular vesicles. The small fragments identified were used to select larger molecules. These molecules were shown to counteract the inhibition of NF-κB activity by sma-microRNA-10 in cell-based assays.

摘要

寄生虫利用不同的策略与宿主进行交流。近年来,研究人员发现了一种交流渠道,即吸虫利用囊泡 microRNA 影响宿主免疫系统。从 中分泌的 sma-microRNA-10 通过操纵 NF-κB 途径来影响宿主 T 细胞的命运。我们已经确定了可以干扰这种 microRNA 介导的宿主免疫系统操纵的低分子量工具化合物。我们使用基于片段的筛选方法,通过核磁共振 (NMR) 鉴定与寄生虫 sma-microRNA-10 前体结合的结合物,该前体存在于其细胞外囊泡中。鉴定出的小片段被用于选择更大的分子。这些分子在基于细胞的测定中显示出能够抵抗 sma-microRNA-10 对 NF-κB 活性的抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf0/9578036/0e77037740ad/id2c00360_0001.jpg

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