Jiao Yan, Lai Liu, Zhihao Chen, Qian Zhao, Xiaoqing Han, Yanjing Wang, Zhengzhi Mu, Xingbo Wang, Panpan Song, Yaqing Kang, Wenjie Lu, A.-M. Guo, Qing-Feng Sun, Haiyuan Zhang
Electron-spin dynamics represent an additional dimension in enzymatic catalysis, where most regulatory strategies focus on modulating active-site chemistry. Here, we present a spintronic approach that employs chiral gold nanohelices (CAu) as electron spin polarizers to enantiospecifically modulate cyclooxygenase-2 (COX-2) activity for rheumatoid arthritis intervention. Exploiting the chirality-induced spin selectivity (CISS) effect inherent to both COX-2 and CAu, we demonstrate that left-handed CAu (Lh-CAu) enhances, whereas right-handed CAu (Rh-CAu) suppresses COX-2 catalytic efficiency via spin-dependent electron transfer at the chiral nanoparticle-enzyme interfaces. To achieve targeted modulation in complex biological settings, we engineer molecularly imprinted CAu (CAu@MIP) for selectively regulating COX-2 in inflammatory cells and collagen-induced arthritis murine model (male DBA/1 J mice). Treatment with Rh-CAu@MIP significantly reduces prostaglandin E2 secretion and mitigates joint inflammation, achieving therapeutic efficacy comparable to conventional COX-2 inhibitors. Our findings introduce electron spin polarization as an orthogonal mechanism for enzymatic regulation, offering a bioelectronic strategy for inflammation-targeted therapy. Current strategies for regulating enzyme activity are often enzyme-specific. Here, the authors report a spintronic approach that uses chiral gold nanohelices as electron spin polarizers to enantiospecifically modulate cyclooxygenase-2 activity for rheumatoid arthritis intervention, and explore electron spin polarization as an orthogonal mechanism for enzymatic regulation.