巨噬细胞移动抑制因子
卷盘尾丝虫
盘尾丝虫病
低聚物
生物
免疫学
化学
病毒学
有机化学
细胞因子
作者
Amber D. Kimble,Omolara C. O. Dawson,Lijun Liu,Sandhya Subramanian,Anne Cooper,K.P. Battaile,Justin K. Craig,Elizabeth K. Harmon,Peter J. Myler,Scott Lovell,Oluwatoyin A. Asojo
标识
DOI:10.1107/s2053230x24010550
摘要
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- Ov MIF-1). Ov MIF-1 is a possible drug target. His- Ov MIF-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 Ov MIF-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 Ov MIF-1 because size-exclusion chomatographic analysis of His- Ov MIF-1 suggests a monomer, while PISA analysis suggests a hexamer stabilized by the unique C-terminal tails.
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