蛋白酶体
蛋白酶体抑制剂
赫拉
细胞毒性
体外
化学
互补
蛋白质片段互补分析
抑制蛋白
生物化学
泛素
细胞培养
细胞生物学
伴侣(临床)
双分子荧光互补
分子生物学
生物
酶
表型
酵母
基因
病理
医学
遗传学
作者
Miho Izumikawa,Junko Hashimoto,Takatsugu Hirokawa,Satoshi Sugimoto,Taira Kato,Motoki Takagi,Kazuo Shin‐ya
摘要
Proteasome assembling chaperone (PAC) 3 acts as a homodimer and plays an important role in proteasome formation. We screened JBIR-22 (1) as an inhibitor for protein−protein interaction (PPI) of PAC3 homodimer from our natural product library using a protein fragment complementation assay (PCA) with monomeric Kusabira-Green fluorescent protein (mKG) in vitro and found that 1 exhibited potent inhibitory activity against PAC3 homodimerization. Compound 1 showed long-term cytotoxicity against the human cervical carcinoma cell line, HeLa. This is the first report of a PPI inhibitor for proteasome assembly factors.
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