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1
Effect of insertion of intein to Cryptococcus amylolentus, a nonpathogenic fungus closely related to causative agents of cryptococcosis.内含肽插入对浅白隐球菌(一种与隐球菌病病原体密切相关的非致病性真菌)的影响。
Microb Pathog. 2025 Feb;199:107267. doi: 10.1016/j.micpath.2024.107267. Epub 2024 Dec 28.
2
Small-molecule inhibitors for the Prp8 intein as antifungal agents.小分子抑制剂作为抗真菌剂对 Prp8 内含肽的作用。
Proc Natl Acad Sci U S A. 2021 Jan 12;118(2). doi: 10.1073/pnas.2008815118.
3
Cisplatin protects mice from challenge of by targeting the Prp8 intein.顺铂通过靶向 Prp8 内含肽保护小鼠免受 的挑战。
Emerg Microbes Infect. 2019;8(1):895-908. doi: 10.1080/22221751.2019.1625727.
4
Calcimycin Inhibits and by Targeting the Prp8 Intein Splicing.钙离子载体A23187通过靶向Prp8内含肽剪接来抑制和 。(原文中“and by Targeting the Prp8 Intein Splicing”前似乎少了内容,导致翻译不太完整准确)
ACS Infect Dis. 2022 Sep 9;8(9):1851-1868. doi: 10.1021/acsinfecdis.2c00137. Epub 2022 Aug 10.
5
The PRP8 inteins in Cryptococcus are a source of phylogenetic and epidemiological information.隐球菌中的PRP8内含肽是系统发育和流行病学信息的一个来源。
Fungal Genet Biol. 2005 May;42(5):452-63. doi: 10.1016/j.fgb.2005.01.011.
6
The distribution and evolutionary history of the PRP8 intein.PRP8内含肽的分布与进化史。
BMC Evol Biol. 2006 May 31;6:42. doi: 10.1186/1471-2148-6-42.
7
Spliceosomal Prp8 intein at the crossroads of protein and RNA splicing.剪接体 Prp8 内含肽处于蛋白质和 RNA 剪接的交汇点。
PLoS Biol. 2019 Oct 10;17(10):e3000104. doi: 10.1371/journal.pbio.3000104. eCollection 2019 Oct.
8
Preceding hydrophobic and beta-branched amino acids attenuate splicing by the CnePRP8 intein.前面的疏水氨基酸和β-分支氨基酸会减弱CnePRP8内含肽的剪接作用。
Biochim Biophys Acta. 2007 Aug;1774(8):995-1001. doi: 10.1016/j.bbapap.2007.05.015. Epub 2007 Jun 2.
9
Efficient splicing of the CPE intein derived from directed evolution of the PRP8 intein.高效拼接来自 PRP8 内含肽定向进化的 CPE 内含肽。
Acta Biochim Biophys Sin (Shanghai). 2023 Jul 23;55(8):1310-1318. doi: 10.3724/abbs.2023135.
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Inteins and introns within the prp8 -gene of four Eupenicillium species.四种青霉属物种的prp8基因中的内含肽和内含子。
J Basic Microbiol. 2009 Feb;49(1):52-7. doi: 10.1002/jobm.200800168.

本文引用的文献

1
Neighboring inteins interfere with one another's homing capacity.相邻的内含肽会相互干扰彼此的归巢能力。
PNAS Nexus. 2023 Oct 27;2(11):pgad354. doi: 10.1093/pnasnexus/pgad354. eCollection 2023 Nov.
2
Reciprocal modulation of ammonia and melanin production has implications for cryptococcal virulence.氨和黑色素生成的相互调节对隐球菌毒力有影响。
Nat Commun. 2023 Feb 15;14(1):849. doi: 10.1038/s41467-023-36552-7.
3
The WHO fungal priority pathogens list as a game-changer.世界卫生组织真菌优先病原体清单——改变游戏规则的因素。
Nat Rev Microbiol. 2023 Apr;21(4):211-212. doi: 10.1038/s41579-023-00861-x.
4
Prp8 Intein: An In Vivo Target-Based Drug Screening System in to Identify Protein Splicing Inhibitors and Explore Its Dynamics.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。
J Fungi (Basel). 2022 Aug 12;8(8):846. doi: 10.3390/jof8080846.
5
Calcimycin Inhibits and by Targeting the Prp8 Intein Splicing.钙离子载体A23187通过靶向Prp8内含肽剪接来抑制和 。(原文中“and by Targeting the Prp8 Intein Splicing”前似乎少了内容,导致翻译不太完整准确)
ACS Infect Dis. 2022 Sep 9;8(9):1851-1868. doi: 10.1021/acsinfecdis.2c00137. Epub 2022 Aug 10.
6
Secreted fungal virulence effector triggers allergic inflammation via TLR4.分泌型真菌毒力效应因子通过 TLR4 引发过敏炎症。
Nature. 2022 Aug;608(7921):161-167. doi: 10.1038/s41586-022-05005-4. Epub 2022 Jul 27.
7
Structural Basis for the Propagation of Homing Endonuclease-Associated Inteins.归巢内切核酸酶相关内含肽传播的结构基础。
Front Mol Biosci. 2022 Mar 16;9:855511. doi: 10.3389/fmolb.2022.855511. eCollection 2022.
8
Inteins as Drug Targets and Therapeutic Tools.内含肽作为药物靶点和治疗工具。
Front Mol Biosci. 2022 Feb 8;9:821146. doi: 10.3389/fmolb.2022.821146. eCollection 2022.
9
Cryptococcus neoformans melanization incorporates multiple catecholamines to produce polytypic melanin.新型隐球菌黑色素形成过程中涉及多种儿茶酚胺以产生多型黑色素。
J Biol Chem. 2022 Jan;298(1):101519. doi: 10.1016/j.jbc.2021.101519. Epub 2021 Dec 20.
10
Small-molecule inhibitors for the Prp8 intein as antifungal agents.小分子抑制剂作为抗真菌剂对 Prp8 内含肽的作用。
Proc Natl Acad Sci U S A. 2021 Jan 12;118(2). doi: 10.1073/pnas.2008815118.

内含肽插入对浅白隐球菌(一种与隐球菌病病原体密切相关的非致病性真菌)的影响。

Effect of insertion of intein to Cryptococcus amylolentus, a nonpathogenic fungus closely related to causative agents of cryptococcosis.

作者信息

Tharappel Anil Mathew, Li Zhong, Li Hongmin

机构信息

Department of Pharmacology and Toxicology, R Ken Coit College of Pharmacy, 1703 E Mabel St, Tucson, AZ, 85721-0207, USA.

Department of Pharmacology and Toxicology, R Ken Coit College of Pharmacy, 1703 E Mabel St, Tucson, AZ, 85721-0207, USA.

出版信息

Microb Pathog. 2025 Feb;199:107267. doi: 10.1016/j.micpath.2024.107267. Epub 2024 Dec 28.

DOI:10.1016/j.micpath.2024.107267
PMID:39736341
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11863799/
Abstract

Inteins are mobile elements within a host protein, with flanking exteins. Autocleavage of intein results in the fusion of exteins, leading to activation of protein. The presence of intein is species dependent. Pathogenic fungi Cryptococcus neoformans (Cne) and C. gattii (Cga) contain inteins in their inactive Prp8 protein precursor, whereas closely related nonpathogenic C. amylolentus (Cam) lacks inteins. Handling pathogenic fungi requires additional safety requirements. Studies on nonpathogenic but closely related fungal strains can expedite research on the role of inteins and potential changes in virulence or pathology. In this report, we have genetically modified and characterized Cam to possess intein (Cam-int). First, we inserted a selection marker into the Prp8 intein of Cne using an MIG vector and tested intein splicing efficiency in E. coli. The intein-selection marker fragment was then integrated into the prp8 gene of Cam, demonstrating in vivo splicing within Cam without affecting certain virulence factors. Intein splicing inhibitors, cisplatin and 6G-318S, showed increased sensitivity to Cam-int compared to the wild-type strain without the intein. This Cam-int fungal strain can serve as a valuable tool for further studying the role of inteins and holds potential for screening intein splicing inhibitors.

摘要

内含肽是宿主蛋白中的可移动元件,两侧为外显肽。内含肽的自切割导致外显肽融合,从而激活蛋白质。内含肽的存在具有物种依赖性。致病性真菌新型隐球菌(Cne)和格特隐球菌(Cga)在其无活性的Prp8蛋白前体中含有内含肽,而密切相关的非致病性淀粉样隐球菌(Cam)则缺乏内含肽。处理致病性真菌需要额外的安全要求。对非致病性但密切相关的真菌菌株进行研究可以加快对内含肽作用以及毒力或病理学潜在变化的研究。在本报告中,我们对Cam进行了基因改造并进行了表征,使其拥有内含肽(Cam-int)。首先,我们使用MIG载体将选择标记插入Cne的Prp8内含肽中,并在大肠杆菌中测试内含肽的剪接效率。然后将内含肽-选择标记片段整合到Cam的prp8基因中,证明其在Cam体内能够剪接,且不影响某些毒力因子。与不含内含肽的野生型菌株相比,内含肽剪接抑制剂顺铂和6G-318S对Cam-int表现出更高的敏感性。这种Cam-int真菌菌株可作为进一步研究内含肽作用的有价值工具,并具有筛选内含肽剪接抑制剂的潜力。