N-末端六脒标记的盘尾丝虫巨噬细胞迁移抑制因子-1的晶体结构。

IF 1.1 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS Acta crystallographica. Section F, Structural biology communications Pub Date : 2024-12-01 DOI:10.1107/S2053230X24010550
Amber D Kimble, Omolara C O Dawson, Lijun Liu, Sandhya Subramanian, Anne Cooper, Kevin Battaile, Justin Craig, Elizabeth Harmon, Peter Myler, Scott Lovell, Oluwatoyin A Asojo
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引用次数: 0

摘要

盘尾丝虫会导致失明、盘尾丝虫病、皮肤感染和破坏性神经疾病,如点头综合征。由于目前使用的药物伊维菌素禁用于孕妇和同时感染 Loa loa 的患者,因此需要新的治疗方法。西雅图传染病结构基因组学中心(SSGCID)制备、结晶并确定了N-末端六联脒标记的伏虫巨噬细胞迁移抑制因子-1(His-OvMIF-1)的apo结构。OvMIF-1 是一个可能的药物靶点。His-OvMIF-1 具有独特的水母状结构,其 "头部 "是典型的巨噬细胞迁移抑制因子(MIF)三聚体,"尾部 "是独特的 C-端。去掉 N 端标签后,OvMIF-1 结构的空腔比在人类 MIF 中观察到的更大,可作为药物再利用和发现的目标。要确定 OvMIF-1 的实际生物寡聚体,就必须去除标签,因为 His-OvMIF-1 的尺寸排阻层析分析表明是单体,而 PISA 分析表明是由独特的 C 端尾部稳定的六聚体。
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Crystal structure of N-terminally hexahistidine-tagged Onchocerca volvulus macrophage migration inhibitory factor-1.

Onchocerca volvulus causes blindness, onchocerciasis, skin infections and devastating neurological diseases such as nodding syndrome. New treatments are needed because the currently used drug, ivermectin, is contraindicated in pregnant women and those co-infected with Loa loa. The Seattle Structural Genomics Center for Infectious Disease (SSGCID) produced, crystallized and determined the apo structure of N-terminally hexahistidine-tagged O. volvulus macrophage migration inhibitory factor-1 (His-OvMIF-1). OvMIF-1 is a possible drug target. His-OvMIF-1 has a unique jellyfish-like structure with a prototypical macrophage migration inhibitory factor (MIF) trimer as the `head' and a unique C-terminal `tail'. Deleting the N-terminal tag reveals an OvMIF-1 structure with a larger cavity than that observed in human MIF that can be targeted for drug repurposing and discovery. Removal of the tag will be necessary to determine the actual biological oligomer of OvMIF-1 because size-exclusion chomatographic analysis of His-OvMIF-1 suggests a monomer, while PISA analysis suggests a hexamer stabilized by the unique C-terminal tails.

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来源期刊
Acta crystallographica. Section F, Structural biology communications
Acta crystallographica. Section F, Structural biology communications BIOCHEMICAL RESEARCH METHODSBIOCHEMISTRY &-BIOCHEMISTRY & MOLECULAR BIOLOGY
CiteScore
1.90
自引率
0.00%
发文量
95
期刊介绍: Acta Crystallographica Section F is a rapid structural biology communications journal. Articles on any aspect of structural biology, including structures determined using high-throughput methods or from iterative studies such as those used in the pharmaceutical industry, are welcomed by the journal. The journal offers the option of open access, and all communications benefit from unlimited free use of colour illustrations and no page charges. Authors are encouraged to submit multimedia content for publication with their articles. Acta Cryst. F has a dedicated online tool called publBio that is designed to make the preparation and submission of articles easier for authors.
期刊最新文献
Crystal structure of N-terminally hexahistidine-tagged Onchocerca volvulus macrophage migration inhibitory factor-1. X-ray crystal structure of proliferating cell nuclear antigen 1 from Aeropyrum pernix. Human transforming growth factor β type I receptor in complex with kinase inhibitor SB505124. Multi-species cryoEM calibration and workflow verification standard.
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