绿色荧光蛋白
降级(电信)
抗体
化学
链条(单位)
细胞生物学
计算生物学
计算机科学
生物
生物化学
遗传学
物理
电信
基因
天文
作者
Moutushi Islam,Takefumi Negishi,Naomi Kitamoto,Yuki Hatoyama,Kanae Gamo,Ken‐ichiro Hayashi,Masato T. Kanemaki
标识
DOI:10.1101/2025.01.21.633519
摘要
Protein knockdown using an improved auxin-inducible degron (AID2) technology has proven to be a powerful tool for studying protein function. The current approach requires the fusion of target proteins with a degron tag, a process typically achieved through CRISPR knock-in. However, knock-in remains challenging in non-model organisms and humans, limiting the broader applicability of AID2. To overcome this limitation, we developed a single-chain antibody AID2 (scAb-AID2) system. This approach employs an adaptor composed of a single-chain antibody fused with a degron, which recognises a target protein and induces rapid degradation in the presence of the inducer 5-Ph-IAA. We demonstrated that scAb-AID2, in combination with an anti-GFP nanobody, degraded GFP-fused proteins in human cells and C. elegans. Furthermore, we showed that endogenous p53 and H/K-RAS were conditionally degraded in cells expressing an adaptor encoding an anti-p53 nanobody and -RAS monobody, respectively, and led to aphidicolin sensitivity in cell culture and growth inhibition in mouse xenografts. This study paves the way for broader application of AID2-based target depletion in model and non-model organisms and for advancing therapeutic strategies.
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