Pharmaceutical Institute, Pharmaceutical Chemistry I , University of Bonn , An der Immenburg 4 , 53121 Bonn , Germany.
Department of Internal Medicine III , University Hospital Ulm , Albert-Einstein-Allee 23 , 89081 Ulm , Germany.
ACS Chem Biol. 2018 Sep 21;13(9):2771-2782. doi: 10.1021/acschembio.8b00693. Epub 2018 Sep 5.
The immunomodulatory drugs (IMiDs) thalidomide, lenalidomide, and pomalidomide, all approved for the treatment of multiple myeloma, induce targeted ubiquitination and degradation of Ikaros (IKZF1) and Aiolos (IKZF3) via the cereblon (CRBN) E3 ubiquitin ligase. IMiD-based proteolysis-targeting chimeras (PROTACs) can efficiently recruit CRBN to a protein of interest, leading to its ubiquitination and proteasomal degradation. By linking two pomalidomide molecules, we designed homobifunctional, so-called homo-PROTACs and investigated their ability to induce self-directed ubiquitination and degradation. The homodimerized compound 15a was characterized as a highly potent and efficient CRBN degrader with only minimal effects on IKZF1 and IKZF3. The cellular selectivity of 15a for CRBN degradation was confirmed at the proteome level by quantitative mass spectrometry. Inactivation by compound 15a did not affect proliferation of different cell lines, prevented pomalidomide-induced degradation of IKZF1 and IKZF3, and antagonized the effects of pomalidomide on multiple myeloma cells. Homobifunctional CRBN degraders will be useful tools for future biomedical investigations of CRBN-related signaling and may help to further elucidate the molecular mechanism of thalidomide analogues.
免疫调节药物(IMiDs)沙利度胺、来那度胺和泊马度胺均已获批用于多发性骨髓瘤的治疗,它们通过 cereblon(CRBN)E3 泛素连接酶诱导 Ikaros(IKZF1)和 Aiolos(IKZF3)的靶向泛素化和降解。基于 IMiD 的蛋白水解靶向嵌合体(PROTAC)可以有效地将 CRBN 募集到目标蛋白上,导致其泛素化和蛋白酶体降解。通过连接两个泊马度胺分子,我们设计了同型双功能,即所谓的同型 PROTAC,并研究了它们诱导自身泛素化和降解的能力。同二聚化合物 15a 被证明是一种高效且高活性的 CRBN 降解剂,对 IKZF1 和 IKZF3 的影响最小。通过定量质谱在蛋白质组水平上证实了化合物 15a 对 CRBN 降解的细胞选择性。化合物 15a 的失活不会影响不同细胞系的增殖,可防止泊马度胺诱导的 IKZF1 和 IKZF3 降解,并拮抗泊马度胺对多发性骨髓瘤细胞的作用。同型双功能 CRBN 降解剂将成为未来与 CRBN 相关信号转导相关的生物医学研究的有用工具,并可能有助于进一步阐明沙利度胺类似物的分子机制。