

|
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基本情報 |
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氏名 |
林 謙一郎 |
氏名(カナ) |
ハヤシ ケンイチロウ |
氏名(英語) |
Hayashi Kenichiro |
所属 |
生命科学部 生物科学科 |
職名 |
教授 |
researchmap研究者コード |
5000032366 |
researchmap機関 |
岡山理科大学 |
A single-chain antibody-based AID2 system for conditional degradation of GFP-tagged and untagged proteins
Islam M, Negishi T, Kitamoto N, Hatoyama Y, Gamo K, Hayashi KI, Kanemaki MT.
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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 recognizes 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 Caenorhabditis 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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