计算生物学
化学
泛素
小分子
肽
细胞生物学
蛋白质-蛋白质相互作用
序列同源性
结构-活动关系
血浆蛋白结合
结合位点
生物化学
分子模型
生物
同源(生物学)
化学生物学
泛素连接酶
生物物理学
同源建模
机制(生物学)
杠杆(统计)
纳米技术
分子构象
蛋白质结构
癌细胞
癌症治疗
分子识别
HEK 293细胞
分子动力学
作者
Daniel H. O Donovan,Jon Winter-Holt,Gavin W. Collie,Maria Emanuela Cuomo,David John McGarry,Millie Fox,Bo Kyung A. Seong,Ursula Grazini,Peter Barton,David Longmire,Andrew Lister,Yong Xu,Hazel Mak,Evelyne Barrey,Marta Acebrón-García-de-Eulate,Magdalena Richter,Nisha Peter,Maxime Couturier,Gustavo J. Gutierrez,Ryan Guilbert
标识
DOI:10.1021/acschembio.5c01006
摘要
Inhibiting the oncogenic driver NRF2 in non-small cell lung cancer (NSCLC) represents a promising yet challenging clinical opportunity. Small molecules that enhance the NRF2:β-TrCP interaction ("molecular glues") could hold therapeutic potential by promoting the ubiquitination and proteasomal degradation of NRF2. NRX-252114 is a molecular glue previously reported to promote the interaction between β-catenin and β-TrCP. We now find that NRX-252114 can also enhance the association between β-TrCP and NRF2 phosphodegron peptides. To leverage this novel interaction for the development of NRF2:β-TrCP molecular glues, we synthesized and evaluated a library of chemical analogues, guided by homology modeling and subsequently by X-ray crystallography. Surprisingly, structural elucidation of the NRF2:β-TrCP complex revealed occlusion of the presumed molecular glue binding pocket. This mechanistic insight explains the limited affinity enhancement for analogues of NRX-252114, and provides a structural rationale for the lack of NRF2 degradation in cells. Our findings broaden the scope of β-TrCP-targeted molecular glues, demonstrate that NRF2 is "glueable" at the peptide level, and provide mechanistic guidance for future efforts to target the pharmacologically elusive NRF2 pathway in cancer.
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