Chemical Biology, University of Duisburg-Essen, ZMB, Faculty of Biology, Universitätsstraße 2, 45117 Essen, Germany.
Chemical Biology, University of Duisburg-Essen, ZMB, Faculty of Biology, Universitätsstraße 2, 45117 Essen, Germany.
Cell Chem Biol. 2017 Jun 22;24(6):653-655. doi: 10.1016/j.chembiol.2017.06.005.
While proteasome inhibitors are now well-established research tools and chemotherapeutics, proteasome activators are much less explored. In this issue of Cell Chemical Biology, in a study from the groups of Berkers and Ovaa (Leestemaker et al., 2017), a chemical screen was used to identify a p38 MAPK inhibitor as a proteasome activator. This compound furthermore enhanced clearance of protein aggregates, thereby implicating alternative chemotherapeutic options for treating neurodegenerative diseases.
虽然蛋白酶体抑制剂现在已经成为成熟的研究工具和化疗药物,但蛋白酶体激活剂的研究要少得多。在本期《细胞化学生物学》中,Berkers 和 Ovaa 小组的一项研究(Leestemaker 等人,2017 年)通过化学筛选发现一种 p38 MAPK 抑制剂是一种蛋白酶体激活剂。该化合物还增强了蛋白质聚集体的清除,从而为治疗神经退行性疾病提供了另一种化学治疗选择。