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Prp8内含肽:一种基于体内靶点的药物筛选系统,用于鉴定蛋白质剪接抑制剂并探索其动力学。

Prp8 Intein: An In Vivo Target-Based Drug Screening System in to Identify Protein Splicing Inhibitors and Explore Its Dynamics.

作者信息

Fernandes José Alex Lourenço, Zatti Matheus da Silva, Arantes Thales Domingos, Souza Maria Fernanda Bezerra de, Santoni Mariana Marchi, Rossi Danuza, Zanelli Cleslei Fernando, Liu Xiang-Qin, Bagagli Eduardo, Theodoro Raquel Cordeiro

机构信息

Institute of Tropical Medicine, Federal University of Rio Grande do Norte (UFRN), Natal 59077-080, Rio Grande do Norte, Brazil.

Department of Biochemistry, Biosciences Center, Federal University of Rio Grande do Norte (UFRN), Natal 59078-900, Rio Grande do Norte, Brazil.

出版信息

J Fungi (Basel). 2022 Aug 12;8(8):846. doi: 10.3390/jof8080846.

Abstract

Inteins are genetic mobile elements that are inserted within protein-coding genes, which are usually housekeeping genes. They are transcribed and translated along with the host gene, then catalyze their own splicing out of the host protein, which assumes its functional conformation thereafter. As Prp8 inteins are found in several important fungal pathogens and are absent in mammals, they are considered potential therapeutic targets since inhibiting their splicing would selectively block the maturation of fungal proteins. We developed a target-based drug screening system to evaluate the splicing of Prp8 intein from the yeast pathogen (CnePrp8i) using Ura3 as a non-native host protein. In our heterologous system, intein splicing preserved the full functionality of Ura3. To validate the system for drug screening, we examined cisplatin, which has been described as an intein splicing inhibitor. By using our system, new potential protein splicing inhibitors may be identified and used, in the future, as a new class of drugs for mycosis treatment. Our system also greatly facilitates the visualization of CnePrp8i splicing dynamics in vivo.

摘要

内含肽是插入蛋白质编码基因(通常是管家基因)中的遗传移动元件。它们与宿主基因一起转录和翻译,然后催化自身从宿主蛋白中剪接出来,宿主蛋白随后呈现其功能构象。由于在几种重要的真菌病原体中发现了Prp8内含肽,而在哺乳动物中不存在,因此它们被认为是潜在的治疗靶点,因为抑制它们的剪接将选择性地阻断真菌蛋白的成熟。我们开发了一种基于靶点的药物筛选系统,以使用Ura3作为非天然宿主蛋白来评估酵母病原体(CnePrp8i)中Prp8内含肽的剪接。在我们的异源系统中,内含肽剪接保留了Ura3的全部功能。为了验证该药物筛选系统,我们检测了顺铂,它已被描述为一种内含肽剪接抑制剂。通过使用我们的系统,未来可能会鉴定出新的潜在蛋白质剪接抑制剂,并将其用作治疗真菌病的新型药物。我们的系统还极大地促进了体内CnePrp8i剪接动力学的可视化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3ef/9410109/8effef3b1bb1/jof-08-00846-g001.jpg

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