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鉴定针对动力蛋白样 EHD4 的 ATP 酶活性的类药分子。

Identification of drug-like molecules targeting the ATPase activity of dynamin-like EHD4.

机构信息

Structural Biology, Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.

Institute of Chemistry and Biochemistry, Freie Universität Berlin, Berlin, Germany.

出版信息

PLoS One. 2024 Jul 29;19(7):e0302704. doi: 10.1371/journal.pone.0302704. eCollection 2024.

Abstract

Eps15 (epidermal growth factor receptor pathway substrate 15) homology domain-containing proteins (EHDs) comprise a family of eukaryotic dynamin-related ATPases that participate in various endocytic membrane trafficking pathways. Dysregulation of EHDs function has been implicated in various diseases, including cancer. The lack of small molecule inhibitors which acutely target individual EHD members has hampered progress in dissecting their detailed cellular membrane trafficking pathways and their function during disease. Here, we established a Malachite green-based assay compatible with high throughput screening to monitor the liposome-stimulated ATPase of EHD4. In this way, we identified a drug-like molecule that inhibited EHD4's liposome-stimulated ATPase activity. Structure activity relationship (SAR) studies indicated sites of preferred substitutions for more potent inhibitor synthesis. Moreover, the assay optimization in this work can be applied to other dynamin family members showing a weak and liposome-dependent nucleotide hydrolysis activity.

摘要

Eps15(表皮生长因子受体途径底物 15)同源结构域蛋白(EHDs)是一类真核与动力蛋白相关的 ATP 酶家族,参与各种内吞膜运输途径。EHDs 功能失调与各种疾病有关,包括癌症。缺乏能够急性靶向单个 EHD 成员的小分子抑制剂,阻碍了对其详细细胞内膜运输途径及其在疾病过程中功能的研究进展。在这里,我们建立了一种与高通量筛选兼容的孔雀绿基础测定法来监测 EHD4 的脂质体刺激 ATP 酶活性。通过这种方式,我们鉴定出一种抑制 EHD4 的脂质体刺激 ATP 酶活性的类药性分子。结构活性关系(SAR)研究表明,更有效的抑制剂合成的首选取代位点。此外,本工作中的测定优化可应用于其他显示弱脂质体依赖性核苷酸水解活性的动力蛋白家族成员。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14ff/11285977/641397cc224e/pone.0302704.g001.jpg

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