体内
体外
度量(数据仓库)
兴奋剂
化学
小分子
药理学
计算生物学
细胞生物学
生物化学
生物
计算机科学
受体
数据挖掘
遗传学
作者
Olivia R. Shapiro,Clara Woods,Amanda M. Gleixner,Sara Sannino,Melanie Ngo,Michael D. McDaniels,Peter Wipf,Neil A. Hukriede,Christopher J. Donnelly,Jeffrey L. Brodsky
标识
DOI:10.1016/j.ab.2024.115712
摘要
Hsp70 prevents protein aggregation and is cytoprotective, but sustained Hsp70 overexpression is problematic. Instead, we developed small molecule agonists that augment Hsp70 activity. Because cumbersome assays were required to assay agonists, we developed cell-based and in vivo assays in which disease-associated consequences of Hsp70 activation can be quantified. One assay uses an optogenetic system in which the formation of TDP-43 inclusions can be controlled, and the second assay employs a zebrafish model for acute kidney injury (AKI). These complementary assays will facilitate future work to identify new Hsp70 agonists as well as other optimized MAL1-271 derivatives.
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