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利用聚集蛋白染料YAT2150进行疟疾化疗。

Leveraging the Aggregated Protein Dye YAT2150 for Malaria Chemotherapy.

作者信息

Camarero-Hoyos Claudia, Bouzón-Arnáiz Inés, Avalos-Padilla Yunuen, Fallica Antonino Nicolò, Román-Álamo Lucía, Ramírez Miriam, Portabella Emma, Cuspinera Ona, Currea-Ayala Daniela, Orozco-Quer Marc, Ribera Maria, Siden-Kiamos Inga, Spanos Lefteris, Iglesias Valentín, Crespo Benigno, Viera Sara, Andreu David, Sulleiro Elena, Zarzuela Francesc, Urtasun Nerea, Pérez-Torras Sandra, Pastor-Anglada Marçal, Arce Elsa M, Muñoz-Torrero Diego, Fernàndez-Busquets Xavier

机构信息

Barcelona Institute for Global Health (ISGlobal), Hospital Clínic-Universitat de Barcelona, Rosselló 149-153, 08036 Barcelona, Spain.

Nanomalaria Group, Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology, Baldiri Reixac 10-12, 08028 Barcelona, Spain.

出版信息

Pharmaceutics. 2024 Sep 30;16(10):1290. doi: 10.3390/pharmaceutics16101290.

DOI:10.3390/pharmaceutics16101290
PMID:39458619
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11514582/
Abstract

: YAT2150 is a first-in-class antiplasmodial compound that has been recently proposed as a new interesting drug for malaria therapy. : The fluorescence of YAT2150 rapidly increases upon its entry into , a property that can be of use for the design of highly sensitive diagnostic approaches. YAT2150 blocks the in vitro development of the ookinete stage of and, when added to an infected blood meal, inhibits oocyst formation in the mosquito. Thus, the compound could possibly contribute to future transmission-blocking antimalarial strategies. Cell influx/efflux studies in Caco-2 cells suggest that YAT2150 is internalized by endocytosis and also through the OATP2B1 transporter, whereas its main export route would be via OSTα. YAT2150 has an overall favorable drug metabolism and pharmacokinetics profile, and its moderate cytotoxicity can be significantly reduced upon encapsulation in immunoliposomes, which leads to a dramatic increase in the drug selectivity index to values close to 1000. Although YAT2150 binds amyloid-forming peptides, its in vitro fluorescence emission is stronger upon association with peptides that form amorphous aggregates, suggesting that regions enriched in unstructured proteins are the preferential binding sites of the drug inside cells. The reduction of protein aggregation in the parasite after YAT2150 treatment, which has been suggested to be directly related to the drug's mode of action, is also observed following treatment with quinoline antimalarials like chloroquine and primaquine. : Altogether, the data presented here indicate that YAT2150 can represent the spearhead of a new family of compounds for malaria diagnosis and therapy due to its presumed novel mode of action based on the interaction with functional protein aggregates in the pathogen.

摘要

YAT2150是一种一流的抗疟化合物,最近被提议作为一种用于疟疾治疗的新型有趣药物。YAT2150进入[具体对象]后,其荧光迅速增强,这一特性可用于设计高灵敏度的诊断方法。YAT2150可阻断[疟原虫种类]卵囊期的体外发育,当添加到受感染的血餐中时,可抑制蚊子体内卵囊的形成。因此,该化合物可能有助于未来的传播阻断抗疟策略。在Caco-2细胞中进行的细胞内流/外流研究表明,YAT2150通过内吞作用以及OATP2B1转运蛋白进入细胞,而其主要的输出途径是通过OSTα。YAT2150具有总体良好的药物代谢和药代动力学特征,并且在封装于免疫脂质体中时,其适度的细胞毒性可显著降低,这导致药物选择性指数大幅提高至接近1000的值。尽管YAT2150与形成淀粉样蛋白的肽结合,但其与形成无定形聚集体的肽结合时,体外荧光发射更强,这表明富含无结构蛋白的区域是该药物在[细胞类型]细胞内的优先结合位点。用氯喹和伯氨喹等喹啉类抗疟药治疗后,也观察到YAT2150处理后寄生虫中蛋白质聚集的减少,这被认为与药物的作用方式直接相关。总之,此处呈现的数据表明,由于其基于与病原体中功能性蛋白质聚集体相互作用的推测新模式,YAT2150可代表用于疟疾诊断和治疗的新化合物家族的先锋。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/94b1078f4c9a/pharmaceutics-16-01290-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/f0cf36215935/pharmaceutics-16-01290-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/5ce5833224ef/pharmaceutics-16-01290-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/1326cf165f63/pharmaceutics-16-01290-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/521e1196f77f/pharmaceutics-16-01290-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/85ce30b2b5bb/pharmaceutics-16-01290-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/d2dcfe50c9bd/pharmaceutics-16-01290-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/94b1078f4c9a/pharmaceutics-16-01290-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/f0cf36215935/pharmaceutics-16-01290-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/5ce5833224ef/pharmaceutics-16-01290-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/1326cf165f63/pharmaceutics-16-01290-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/521e1196f77f/pharmaceutics-16-01290-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/85ce30b2b5bb/pharmaceutics-16-01290-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/d2dcfe50c9bd/pharmaceutics-16-01290-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d8/11514582/94b1078f4c9a/pharmaceutics-16-01290-g007.jpg

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