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白色念珠菌磷酸泛酰巯基乙胺基转移酶Ppt2作为潜在抗真菌药物靶点的特性研究

Characterisation of the Candida albicans Phosphopantetheinyl Transferase Ppt2 as a Potential Antifungal Drug Target.

作者信息

Dobb Katharine S, Kaye Sarah J, Beckmann Nicola, Thain John L, Stateva Lubomira, Birch Mike, Oliver Jason D

机构信息

F2G Ltd., Lankro Way, Eccles, Manchester, M30 0LX, United Kingdom.

Faculty of Life Sciences, The University of Manchester, Michael Smith Building, Oxford Road, Manchester, M13 9PT, United Kingdom.

出版信息

PLoS One. 2015 Nov 25;10(11):e0143770. doi: 10.1371/journal.pone.0143770. eCollection 2015.

Abstract

Antifungal drugs acting via new mechanisms of action are urgently needed to combat the increasing numbers of severe fungal infections caused by pathogens such as Candida albicans. The phosphopantetheinyl transferase of Aspergillus fumigatus, encoded by the essential gene pptB, has previously been identified as a potential antifungal target. This study investigated the function of its orthologue in C. albicans, PPT2/C1_09480W by placing one allele under the control of the regulatable MET3 promoter, and deleting the remaining allele. The phenotypes of this conditional null mutant showed that, as in A. fumigatus, the gene PPT2 is essential for growth in C. albicans, thus fulfilling one aspect of an efficient antifungal target. The catalytic activity of Ppt2 as a phosphopantetheinyl transferase and the acyl carrier protein Acp1 as a substrate were demonstrated in a fluorescence transfer assay, using recombinant Ppt2 and Acp1 produced and purified from E.coli. A fluorescence polarisation assay amenable to high-throughput screening was also developed. Therefore we have identified Ppt2 as a broad-spectrum novel antifungal target and developed tools to identify inhibitors as potentially new antifungal compounds.

摘要

迫切需要通过新作用机制发挥作用的抗真菌药物,以对抗由白色念珠菌等病原体引起的日益增多的严重真菌感染。由必需基因pptB编码的烟曲霉磷酸泛酰巯基乙胺基转移酶,此前已被确定为一个潜在的抗真菌靶点。本研究通过将一个等位基因置于可调控的MET3启动子控制下,并删除其余等位基因,研究了其在白色念珠菌中的直系同源物PPT2/C1_09480W的功能。该条件性无效突变体的表型表明,与烟曲霉一样,PPT2基因对白色念珠菌的生长至关重要,从而满足了高效抗真菌靶点的一个方面。使用从大肠杆菌中产生并纯化的重组Ppt2和Acp1,在荧光转移试验中证明了Ppt2作为磷酸泛酰巯基乙胺基转移酶的催化活性以及酰基载体蛋白Acp1作为底物的活性。还开发了一种适用于高通量筛选的荧光偏振试验。因此,我们已将Ppt2确定为一种广谱新型抗真菌靶点,并开发了工具来鉴定作为潜在新型抗真菌化合物的抑制剂。

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