Mori Keita, Kuramochi Tsubura, Matsusaki Motonori, Hashiguchi Yuki, Okumura Masaki, Saio Tomohide, Furukawa Yoshiaki, Arai Kenta, Muraoka Takahiro
Department of Applied Chemistry, Graduate School of Engineering, Tokyo University of Agriculture and Technology 2-24-16 Naka-cho, Koganei, Tokyo, 184-8588, Japan.
Department of Chemistry, Massachusetts Institute of Technology 77 Massachusetts Avenue, Cambridge, MA, 02139, USA.
Angew Chem Int Ed Engl. 2025 Sep 1;64(36):e202502187. doi: 10.1002/anie.202502187. Epub 2025 Jun 30.
The stress-responsive up-regulation process is a sophisticated biological response to maintain cellular homeostasis. In intracellular anti-oxidant systems, the expression level of oxidoreductases is up-regulated under oxidative stress, mitigating oxidative damage on biomolecules and enhancing protein folding capacity. Herein, inspired by the biological system, we developed a synthetic folding promotor whose reactivity is up-regulated under stress conditions. We conjugated two metal-binding 1,4,7,11-tetraazacyclotetradecane (cyclam) ligands and a redox-active disulfide to obtain cyclam-SS, whose reactivity can be enhanced under metal-induced stress. Metal coordination increased the redox potential of cyclam-SS, activating it as an oxidant. While Cu ions severely hampered the oxidative folding of substrate polypeptides, cyclam-SS exhibited bifunctional folding-promoting properties, i) suppressing Cu-mediated misfolding and aggregation, and ii) harnessing Cu to enhance oxidative folding. Cyclam-SS was also useful for disulfide-bond formation to promote oxidative folding of pharmaceutical and pathological proteins, as demonstrated with proinsulin and superoxide dismutase 1 (SOD1). Furthermore, cyclam-SS protected cultured cells from copper-induced stress. Thus, we demonstrated the induction of the stress-responsive up-regulation process by a bifunctional folding promotor controlling the folding status of biologically important proteins under metal-induced stress. The strategy of "stress-responsive up-regulation" could aid the development of novel synthetic materials for treating intracellular stress and related disorders.
应激反应上调过程是一种复杂的生物反应,用于维持细胞内稳态。在细胞内抗氧化系统中,氧化还原酶的表达水平在氧化应激下会上调,减轻生物分子的氧化损伤并增强蛋白质折叠能力。在此,受生物系统启发,我们开发了一种合成折叠促进剂,其反应活性在应激条件下会上调。我们将两个金属结合的1,4,7,11-四氮杂环十四烷(环胺)配体和一个氧化还原活性二硫键共轭,得到环胺-二硫键(cyclam-SS),其反应活性在金属诱导的应激下可增强。金属配位增加了环胺-二硫键的氧化还原电位,使其作为氧化剂被激活。虽然铜离子严重阻碍底物多肽的氧化折叠,但环胺-二硫键表现出双功能折叠促进特性,即:i)抑制铜介导的错误折叠和聚集,以及ii)利用铜增强氧化折叠。如胰岛素原和超氧化物歧化酶1(SOD1)所示,环胺-二硫键也可用于促进药物和病理蛋白的二硫键形成以促进氧化折叠。此外,环胺-二硫键保护培养细胞免受铜诱导的应激。因此,我们证明了一种双功能折叠促进剂可在金属诱导的应激下控制生物学重要蛋白质的折叠状态,从而诱导应激反应上调过程。“应激反应上调”策略有助于开发用于治疗细胞内应激及相关疾病的新型合成材料。